Publications

Samples and/or data from the National Cell Repository for Alzheimer’s Disease (NCRAD), which receives government support under a cooperative agreement grant (U24 AG21886) awarded by the National Institute on Aging (NIA), were utilized by the following publications. We thank contributors who collected samples and data used in these studies, as well as patients and their families, whose help and participation made this work possible.

Please feel free to click through the publications below. We have made available all publications which have been released publicly. Those which are not downloadable will be made available as soon as possible.

Vardarajan, B. and K. Faber, Age-specific incidence rate for dementia and Alzheimer's disease in NIA-LOAD/NCRAD and EFIGA families. 2014.
Download
Title
Age-specific incidence rate for dementia and Alzheimer's disease in NIA-LOAD/NCRAD and EFIGA families
Authors
B. Vardarajan and K. Faber
Journal
Year
2014
Volume
Issue
Pages
Wang, L., et al., Rarity of the alzheimer disease–protective app a673t variant in the united states. JAMA Neurology, 2015. 72(2): p. 209-216.
Download
Title
Effect of EPHA1 genetic variation on cerebrospinal fluid and neuroimaging biomarkers in healthy, mild cognitive impairment and Alzheimer's disease cohorts
Authors
H. F. Wang, L. Tan, X. K. Hao, T. Jiang, M. S. Tan, Y. Liu, D. Q. Zhang and J. T. Yu
Journal
J Alzheimers Dis
Year
2015
Volume
44
Issue
1
Pages
115-23
Wang, H.F., et al., Effect of EPHA1 genetic variation on cerebrospinal fluid and neuroimaging biomarkers in healthy, mild cognitive impairment and Alzheimer's disease cohorts. J Alzheimers Dis, 2015. 44(1): p. 115-23.
Download
Title
Rarity of the alzheimer disease–protective app a673t variant in the united states
Authors
L. Wang, A. C. Naj, R. R. Graham and et al.
Journal
JAMA Neurology
Year
2015
Volume
72
Issue
2
Pages
209-216
Vardarajan, B.N., et al., Coding mutations in SORL1 and Alzheimer disease. Annals of Neurology, 2015. 77(2): p. 215-227.
Download
Title
Coding mutations in SORL1 and Alzheimer disease
Authors
B. N. Vardarajan, Y. Zhang, J. H. Lee, R. Cheng, C. Bohm, M. Ghani, C. Reitz, D. Reyes-Dumeyer, Y. Shen, E. Rogaeva, P. St George-Hyslop and R. Mayeux
Journal
Annals of Neurology
Year
2015
Volume
77
Issue
2
Pages
215-227
Sun, Y., et al., An Integrated Bioinformatics Approach for Identifying Genetic Markers that Predict Cerebrospinal Fluid Biomarker p-tau181/Abeta1-42 Ratio in APOE4-Negative Mild Cognitive Impairment Patients. J Alzheimers Dis, 2015. 26: p. 26.
Download
Title
An Integrated Bioinformatics Approach for Identifying Genetic Markers that Predict Cerebrospinal Fluid Biomarker p-tau181/Abeta1-42 Ratio in APOE4-Negative Mild Cognitive Impairment Patients
Authors
Y. Sun, A. Bresell, M. Rantalainen, K. Hoglund, T. Lebouvier and H. Salter
Journal
J Alzheimers Dis
Year
2015
Volume
26
Issue
Pages
26
Shi, J., et al., Studying ventricular abnormalities in mild cognitive impairment with hyperbolic Ricci flow and tensor-based morphometry. Neuroimage, 2015. 104: p. 1-20.
Download
Title
Studying ventricular abnormalities in mild cognitive impairment with hyperbolic Ricci flow and tensor-based morphometry
Authors
J. Shi, C. M. Stonnington, P. M. Thompson, K. Chen, B. Gutman, C. Reschke, L. C. Baxter, E. M. Reiman, R. J. Caselli and Y. Wang
Journal
Neuroimage
Year
2015
Volume
104
Issue
Pages
42024
Nho, K., et al., Comprehensive Gene- and Pathway-Based Analysis of Depressive Symptoms in Older Adults. Journal of Alzheimer's Disease, 2015.
Download
Title
Comprehensive Gene- and Pathway-Based Analysis of Depressive Symptoms in Older Adults
Authors
K. Nho, V. K. Ramanan, E. Horgusluoglu, S. Kim, M. H. Inlow, S. L. Risacher, B. C. McDonald, M. R. Farlow, T. M. Foroud, S. Gao, C. M. Callahan, H. C. Hendrie, A. B. Niculescu and A. J. Saykin
Journal
Journal of Alzheimer's Disease
Year
2015
Volume
Issue
Pages
Nho, K., et al., Protective variant for hippocampal atrophy identified by whole exome sequencing. Annals of Neurology, 2015. 77(3): p. 547-552.
Download
Title
Protective variant for hippocampal atrophy identified by whole exome sequencing
Authors
K. Nho, S. Kim, S. L. Risacher, L. Shen, J. J. Corneveaux, S. Swaminathan, H. Lin, V. K. Ramanan, Y. Liu, T. M. Foroud, M. H. Inlow, A. L. Siniard, R. A. Reiman, P. S. Aisen, R. C. Petersen, R. C. Green, C. R. Jack, M. W. Weiner, C. T. Baldwin, K. L. Lunetta, L. A. Farrer, M. S. for the, S. J. Furney, S. Lovestone, A. Simmons, P. Mecocci, B. Vellas, M. Tsolaki, I. Kloszewska, H. Soininen, C. for the AddNeuroMed, B. C. McDonald, M. R. Farlow, B. Ghetti, M. for the Indiana, S. Aging, M. J. Huentelman, A. J. Saykin and I. for the Alzheimer's Disease Neuroimaging
Journal
Annals of Neurology
Year
2015
Volume
77
Issue
3
Pages
547-552
Nelson, P.T., et al., Reassessment of risk genotypes (GRN, TMEM106B, and ABCC9 variants) associated with hippocampal sclerosis of aging pathology. J Neuropathol Exp Neurol, 2015. 74(1): p. 75-84.
Download
Title
Reassessment of risk genotypes (GRN, TMEM106B, and ABCC9 variants) associated with hippocampal sclerosis of aging pathology
Authors
P. T. Nelson, W. X. Wang, A. B. Partch, S. E. Monsell, O. Valladares, S. R. Ellingson, B. R. Wilfred, A. C. Naj, L. S. Wang, W. A. Kukull and D. W. Fardo
Journal
J Neuropathol Exp Neurol
Year
2015
Volume
74
Issue
1
Pages
75-84
Moradi, E., et al., Machine learning framework for early MRI-based Alzheimer's conversion prediction in MCI subjects. Neuroimage, 2015. 104: p. 398-412.
Download
Title
Machine learning framework for early MRI-based Alzheimer's conversion prediction in MCI subjects
Authors
E. Moradi, A. Pepe, C. Gaser, H. Huttunen and J. Tohka
Journal
Neuroimage
Year
2015
Volume
104
Issue
Pages
398-412
McIntyre, J.A., et al., Antiphospholipid autoantibodies as blood biomarkers for detection of early stage Alzheimer’s disease. Autoimmunity, 2015. 0(0): p. 1-8.
Download
Title
Antiphospholipid autoantibodies as blood biomarkers for detection of early stage Alzheimer’s disease
Authors
J. A. McIntyre, C. J. Ramsey, B. D. Gitter, A. J. Saykin, D. R. Wagenknecht and P. A. Hyslop
Journal
Autoimmunity
Year
2015
Volume
0
Issue
0
Pages
42012
Malik, M., et al., Genetics of CD33 in Alzheimer's Disease and Acute Myeloid Leukemia. Hum Mol Genet, 2015.
Download
Title
Genetics of CD33 in Alzheimer's Disease and Acute Myeloid Leukemia
Authors
M. Malik, J. Chiles, 3rd, H. S. Xi, C. Medway, J. Simpson, S. Potluri, D. Howard, Y. Liang, C. M. Paumi, S. Mukherjee, P. Crane, S. Younkin, D. W. Fardo and S. Estus
Journal
Hum Mol Genet
Year
2015
Volume
Issue
Pages
Jun, G., et al., A novel Alzheimer disease locus located near the gene encoding tau protein. Mol Psychiatry, 2015. 17(10): p. 23.
Download
Title
A novel Alzheimer disease locus located near the gene encoding tau protein
Authors
G. Jun, C. A. Ibrahim-Verbaas, M. Vronskaya, J. C. Lambert, J. Chung, A. C. Naj, B. W. Kunkle, L. S. Wang, J. C. Bis, C. Bellenguez, D. Harold, K. L. Lunetta, A. L. Destefano, B. Grenier-Boley, R. Sims, G. W. Beecham, A. V. Smith, V. Chouraki, K. L. Hamilton-Nelson, M. A. Ikram, N. Fievet, N. Denning, E. R. Martin, H. Schmidt, Y. Kamatani, M. L. Dunstan, O. Valladares, A. R. Laza, D. Zelenika, A. Ramirez, T. M. Foroud, S. H. Choi, A. Boland, T. Becker, W. A. Kukull, S. J. van der Lee, F. Pasquier, C. Cruchaga, D. Beekly, A. L. Fitzpatrick, O. Hanon, M. Gill, R. Barber, V. Gudnason, D. Campion, S. Love, D. A. Bennett, N. Amin, C. Berr, M. Tsolaki, J. D. Buxbaum, O. L. Lopez, V. Deramecourt, N. C. Fox, L. B. Cantwell, L. Tarraga, C. Dufouil, J. Hardy, P. K. Crane, G. Eiriksdottir, D. Hannequin, R. Clarke, D. Evans, T. H. Mosley, Jr., L. Letenneur, C. Brayne, W. Maier, P. De Jager, V. Emilsson, J. F. Dartigues, H. Hampel, M. I. Kamboh, R. F. de Bruijn, C. Tzourio, P. Pastor, E. B. Larson, J. I. Rotter, M. C. O'Donovan, T. J. Montine, M. A. Nalls, S. Mead, E. M. Reiman, P. V. Jonsson, C. Holmes, P. H. St George-Hyslop, M. Boada, P. Passmore, J. R. Wendland, R. Schmidt, K. Morgan, A. R. Winslow, J. F. Powell, M. Carasquillo, S. G. Younkin, J. Jakobsdottir, J. S. Kauwe, K. C. Wilhelmsen, D. Rujescu, M. M. Nothen, A. Hofman, L. Jones, J. L. Haines, B. M. Psaty, C. Van Broeckhoven, P. Holmans, L. J. Launer, R. Mayeux, M. Lathrop, A. M. Goate, V. Escott-Price, S. Seshadri, M. A. Pericak-Vance, P. Amouyel, J. Williams, C. M. van Duijn, G. D. Schellenberg and L. A. Farrer
Journal
Mol Psychiatry
Year
2015
Volume
17
Issue
10
Pages
23
Hua, W.Y., T.E. Nichols, and D. Ghosh, Multiple comparison procedures for neuroimaging genomewide association studies. Biostatistics, 2015. 16(1): p. 17-30.
Download
Title
Multiple comparison procedures for neuroimaging genomewide association studies
Authors
W. Y. Hua, T. E. Nichols and D. Ghosh
Journal
Biostatistics
Year
2015
Volume
16
Issue
1
Pages
17-30
Hibar, D.P., et al., Common genetic variants influence human subcortical brain structures. Nature, 2015. advance online publication.
Download
Title
Common genetic variants influence human subcortical brain structures
Authors
D. P. Hibar, J. L. Stein, M. E. Renteria, A. Arias-Vasquez, S. Desrivieres, N. Jahanshad, R. Toro, K. Wittfeld, L. Abramovic, M. Andersson, B. S. Aribisala, N. J. Armstrong, M. Bernard, M. M. Bohlken, M. P. Boks, J. Bralten, A. A. Brown, M. Mallar Chakravarty, Q. Chen, C. R. K. Ching, G. Cuellar-Partida, A. den Braber, S. Giddaluru, A. L. Goldman, O. Grimm, T. Guadalupe, J. Hass, G. Woldehawariat, A. J. Holmes, M. Hoogman, D. Janowitz, T. Jia, S. Kim, M. Klein, B. Kraemer, P. H. Lee, L. M. Olde Loohuis, M. Luciano, C. Macare, K. A. Mather, M. Mattheisen, Y. Milaneschi, K. Nho, M. Papmeyer, A. Ramasamy, S. L. Risacher, R. Roiz-Santianez, E. J. Rose, A. Salami, P. G. Samann, L. Schmaal, A. J. Schork, J. Shin, L. T. Strike, A. Teumer, M. M. J. van Donkelaar, K. R. van Eijk, R. K. Walters, L. T. Westlye, C. D. Whelan, A. M. Winkler, M. P. Zwiers, S. Alhusaini, L. Athanasiu, S. Ehrlich, M. M. H. Hakobjan, C. B. Hartberg, U. K. Haukvik, A. J. G. A. M. Heister, D. Hoehn, D. Kasperaviciute, D. C. M. Liewald, L. M. Lopez, R. R. R. Makkinje, M. Matarin, M. A. M. Naber, D. Reese McKay, M. Needham, A. C. Nugent, B. Putz, N. A. Royle, L. Shen, E. Sprooten, D. Trabzuni, S. S. L. van der Marel, K. J. E. van Hulzen, E. Walton, C. Wolf, L. Almasy, D. Ames, S. Arepalli, A. A. Assareh, M. E. Bastin, H. Brodaty, K. B. Bulayeva, M. A. Carless, S. Cichon, A. Corvin, J. E. Curran, M. Czisch, G. I. de Zubicaray, A. Dillman, R. Duggirala, T. D. Dyer, S. Erk, I. O. Fedko, L. Ferrucci, T. M. Foroud, P. T. Fox, M. Fukunaga, J. Raphael Gibbs, H. H. H. Goring, R. C. Green, S. Guelfi, N. K. Hansell, C. A. Hartman, K. Hegenscheid, A. Heinz, D. G. Hernandez, D. J. Heslenfeld, P. J. Hoekstra, F. Holsboer, G. Homuth, J.-J. Hottenga, M. Ikeda, C. R. Jack Jr, M. Jenkinson, R. Johnson, R. Kanai, M. Keil, J. W. Kent Jr, P. Kochunov, J. B. Kwok, S. M. Lawrie, X. Liu, D. L. Longo, K. L. McMahon, E. Meisenzahl, I. Melle, S. Mohnke, G. W. Montgomery, J. C. Mostert, T. W. Muhleisen, M. A. Nalls, T. E. Nichols, L. G. Nilsson, M. M. Nothen, K. Ohi, R. L. Olvera, R. Perez-Iglesias, G. Bruce Pike, S. G. Potkin, I. Reinvang, S. Reppermund, M. Rietschel, N. Romanczuk-Seiferth, G. D. Rosen, D. Rujescu, K. Schnell, P. R. Schofield, C. Smith, V. M. Steen, J. E. Sussmann, A. Thalamuthu, A. W. Toga, B. J. Traynor, J. Troncoso, J. A. Turner, M. C. Valdes Hernandez, D. van 't Ent, M. van der Brug, N. J. A. van der Wee, M.-J. van Tol, D. J. Veltman, T. H. Wassink, E. Westman, R. H. Zielke, A. B. Zonderman, D. G. Ashbrook, R. Hager, L. Lu, F. J. McMahon, D. W. Morris, R. W. Williams, H. G. Brunner, R. L. Buckner, J. K. Buitelaar, W. Cahn, V. D. Calhoun, G. L. Cavalleri, B. Crespo-Facorro, A. M. Dale, G. E. Davies, N. Delanty, C. Depondt, S. Djurovic, W. C. Drevets, T. Espeseth, R. L. Gollub, B.-C. Ho, W. Hoffmann, N. Hosten, R. S. Kahn, S. Le Hellard, A. Meyer-Lindenberg, B. Muller-Myhsok, M. Nauck, L. Nyberg, M. Pandolfo, B. W. J. H. Penninx, J. L. Roffman, S. M. Sisodiya, J. W. Smoller, H. van Bokhoven, N. E. M. van Haren, H. Volzke, H. Walter, M. W. Weiner, W. Wen, T. White, I. Agartz, O. A. Andreassen, J. Blangero, D. I. Boomsma, R. M. Brouwer, D. M. Cannon, M. R. Cookson, E. J. C. de Geus, I. J. Deary, G. Donohoe, G. Fernandez, S. E. Fisher, C. Francks, D. C. Glahn, H. J. Grabe, O. Gruber, J. Hardy, R. Hashimoto, H. E. Hulshoff Pol, E. G. Jonsson, I. Kloszewska, S. Lovestone, V. S. Mattay, P. Mecocci, C. McDonald, A. M. McIntosh, R. A. Ophoff, T. Paus, Z. Pausova, M. Ryten, P. S. Sachdev, A. J. Saykin, A. Simmons, A. Singleton, H. Soininen, J. M. Wardlaw, M. E. Weale, D. R. Weinberger, H. H. H. Adams, L. J. Launer, S. Seiler, R. Schmidt, G. Chauhan, C. L. Satizabal, J. T. Becker, L. Yanek, S. J. van der Lee, M. Ebling, B. Fischl, W. T. Longstreth Jr, D. Greve, H. Schmidt, P. Nyquist, L. N. Vinke, C. M. van Duijn, L. Xue, B. Mazoyer, J. C. Bis, V. Gudnason, S. Seshadri, M. Arfan Ikram, I. The Alzheimer/'s Disease Neuroimaging, C. C. The, Epigen, Imagen, Sys, N. G. Martin, M. J. Wright, G. Schumann, B. Franke, P. M. Thompson and S. E. Medland
Journal
Nature
Year
2015
Volume
advance online publication
Issue
Pages
Hibar, D.P., et al., Genome-wide interaction analysis reveals replicated epistatic effects on brain structure. Neurobiology of Aging, 2015. 36, Supplement 1(0): p. S151-S158.
Download
Title
Genome-wide interaction analysis reveals replicated epistatic effects on brain structure
Authors
D. P. Hibar, J. L. Stein, N. Jahanshad, O. Kohannim, X. Hua, A. W. Toga, K. L. McMahon, G. I. de Zubicaray, N. G. Martin, M. J. Wright, M. W. Weiner and P. M. Thompson
Journal
Neurobiology of Aging
Year
2015
Volume
36, Supplement 1
Issue
0
Pages
S151-S158
Ghetti, B., et al., Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging. Neuropathology and Applied Neurobiology, 2015. 41(1): p. 24-46.
Download
Title
Invited review: Frontotemporal dementia caused by microtubule-associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging
Authors
B. Ghetti, A. L. Oblak, B. F. Boeve, K. A. Johnson, B. C. Dickerson and M. Goedert
Journal
Neuropathology and Applied Neurobiology
Year
2015
Volume
41
Issue
1
Pages
24-46
Desikan, R.S., et al., Genetic overlap between Alzheimer/'s disease and Parkinson/'s disease at the MAPT locus. Mol Psychiatry, 2015.
Download
Title
Genetic overlap between Alzheimer/'s disease and Parkinson/'s disease at the MAPT locus
Authors
R. S. Desikan, A. J. Schork, Y. Wang, A. Witoelar, M. Sharma, L. K. McEvoy, D. Holland, J. B. Brewer, C. H. Chen, W. K. Thompson, D. Harold, J. Williams, M. J. Owen, M. C. O'Donovan, M. A. Pericak-Vance, R. Mayeux, J. L. Haines, L. A. Farrer, G. D. Schellenberg, P. Heutink, A. B. Singleton, A. Brice, N. W. Wood, J. Hardy, M. Martinez, S. H. Choi, A. DeStefano, M. A. Ikram, J. C. Bis, A. Smith, A. L. Fitzpatrick, L. Launer, C. van Duijn, S. Seshadri, I. D. Ulstein, D. Aarsland, T. Fladby, S. Djurovic, B. T. Hyman, J. Snaedal, H. Stefansson, K. Stefansson, T. Gasser, O. A. Andreassen and A. M. Dale
Journal
Mol Psychiatry
Year
2015
Volume
Issue
Pages
Chen, J.A., et al., A multiancestral genome-wide exome array study of alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy. JAMA Neurology, 2015.
Download
Title
A multiancestral genome-wide exome array study of alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy
Authors
J. A. Chen, Q. Wang, J. Davis-Turak and et al.
Journal
JAMA Neurology
Year
2015
Volume
Issue
Pages
Caroli, A., et al., Mild cognitive impairment with suspected nonamyloid pathology (SNAP): Prediction of progression. Neurology, 2015. 84(5): p. 508-15.
Download
Title
Mild cognitive impairment with suspected nonamyloid pathology (SNAP): Prediction of progression
Authors
A. Caroli, A. Prestia, S. Galluzzi, C. Ferrari, W. M. van der Flier, R. Ossenkoppele, B. Van Berckel, F. Barkhof, C. Teunissen, A. E. Wall, S. F. Carter, M. Scholl, I. H. Choo, T. Grimmer, A. Redolfi, A. Nordberg, P. Scheltens, A. Drzezga and G. B. Frisoni
Journal
Neurology
Year
2015
Volume
84
Issue
5
Pages
508-15
Bertram, L. and C. Klein, PRobing the exome in alzheimer disease and other neurodegenerative disorders. JAMA Neurology, 2015.
Download
Title
PRobing the exome in alzheimer disease and other neurodegenerative disorders
Authors
L. Bertram and C. Klein
Journal
JAMA Neurology
Year
2015
Volume
Issue
Pages
Beecham, G.W., et al., PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease. Neurology, 2015.
Download
Title
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease
Authors
G. W. Beecham, D. W. Dickson, W. K. Scott, E. R. Martin, G. Schellenberg, K. Nuytemans, E. B. Larson, J. D. Buxbaum, J. Q. Trojanowski, V. M. Van Deerlin, H. I. Hurtig, D. C. Mash, T. G. Beach, J. C. Troncoso, O. Pletnikova, M. P. Frosch, B. Ghetti, T. M. Foroud, L. S. Honig, K. Marder, J. P. Vonsattel, S. M. Goldman, H. V. Vinters, O. A. Ross, Z. K. Wszolek, L. Wang, D. M. Dykxhoorn, M. A. Pericak-Vance, T. J. Montine, J. B. Leverenz, T. M. Dawson and J. M. Vance
Journal
Neurology
Year
2015
Volume
Issue
Pages
Zhu, H., et al., Bayesian Generalized Low Rank Regression Models for Neuroimaging Phenotypes and Genetic Markers. Journal of the American Statistical Association, 2014. 109(507): p. 997-990.
Download
Title
Bayesian Generalized Low Rank Regression Models for Neuroimaging Phenotypes and Genetic Markers
Authors
H. Zhu, Z. Khondker, Z. Lu, J. G. Ibrahim and I. Alzheimer's Disease Neuroimaging
Journal
Journal of the American Statistical Association
Year
2014
Volume
109
Issue
507
Pages
997-990
Zhong, Y., et al., Altered effective connectivity patterns of the default mode network in Alzheimer's disease: an fMRI study. Neurosci Lett, 2014. 578: p. 171-5.
Download
Title
Altered effective connectivity patterns of the default mode network in Alzheimer's disease: an fMRI study
Authors
Y. Zhong, L. Huang, S. Cai, Y. Zhang, K. M. von Deneen, A. Ren and J. Ren
Journal
Neurosci Lett
Year
2014
Volume
578
Issue
Pages
171-5
Zhang, Z., H. Huang, and D. Shen, Integrative analysis of multi-dimensional imaging genomics data for Alzheimer's disease prediction. Front Aging Neurosci, 2014. 6(260).
Download
Title
Integrative analysis of multi-dimensional imaging genomics data for Alzheimer's disease prediction
Authors
Z. Zhang, H. Huang and D. Shen
Journal
Front Aging Neurosci
Year
2014
Volume
6
Issue
260
Pages
Zhang, Y., et al., Testing for association with multiple traits in generalized estimation equations, with application to neuroimaging data. Neuroimage, 2014. 96(0): p. 309-325.
Download
Title
Testing for association with multiple traits in generalized estimation equations, with application to neuroimaging data
Authors
Y. Zhang, Z. Xu, X. Shen and W. Pan
Journal
Neuroimage
Year
2014
Volume
96
Issue
0
Pages
309-325
Young, A.L., et al., A data-driven model of biomarker changes in sporadic Alzheimer's disease. Brain, 2014. 137(9): p. 2564-2577.
Download
Title
A data-driven model of biomarker changes in sporadic Alzheimer's disease
Authors
A. L. Young, N. P. Oxtoby, P. Daga, D. M. Cash, I. on behalf of the Alzheimer’s Disease Neuroimaging, N. C. Fox, S. Ourselin, J. M. Schott and D. C. Alexander
Journal
Brain
Year
2014
Volume
137
Issue
9
Pages
2564-2577
Yan, J., et al., Transcriptome-guided amyloid imaging genetic analysis via a novel structured sparse learning algorithm. Bioinformatics, 2014. 30(17).
Download
Title
Transcriptome-guided amyloid imaging genetic analysis via a novel structured sparse learning algorithm
Authors
J. Yan, L. Du, S. Kim, S. L. Risacher, H. Huang, J. H. Moore, A. J. Saykin and L. Shen
Journal
Bioinformatics
Year
2014
Volume
30
Issue
17
Pages
Xu, Z., et al., Longitudinal Analysis Is More Powerful than Cross-Sectional Analysis in Detecting Genetic Association with Neuroimaging Phenotypes. PLoS One, 2014. 9(8): p. e102312.
Download
Title
Longitudinal Analysis Is More Powerful than Cross-Sectional Analysis in Detecting Genetic Association with Neuroimaging Phenotypes
Authors
Z. Xu, X. Shen, W. Pan and I. for the Alzheimer's Disease Neuroimaging
Journal
PLoS One
Year
2014
Volume
9
Issue
8
Pages
e102312
Wetzel-Smith, M.K., et al., A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death. Nat Med, 2014. 20(12): p. 1452-1457.
Download
Title
A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death
Authors
M. K. Wetzel-Smith, J. Hunkapiller, T. R. Bhangale, K. Srinivasan, J. A. Maloney, J. K. Atwal, S. M. Sa, M. B Yaylaoglu, O. Foreman, W. Ortmann, N. Rathore, D. V. Hansen, M. Tessier-Lavigne, C. Alzheimer's Disease Genetics, R. Mayeux, M. Pericak-Vance, J. Haines, L. A. Farrer, G. D. Schellenberg, A. Goate, T. W. Behrens, C. Cruchaga, R. J. Watts and R. R. Graham
Journal
Nat Med
Year
2014
Volume
20
Issue
12
Pages
1452-1457
Weiner, M.W., et al., Effects of traumatic brain injury and posttraumatic stress disorder on Alzheimer's disease in veterans, using the Alzheimer's Disease Neuroimaging Initiative. Alzheimer's & Dementia, 2014. 10(3, Supplement): p. S226-S235.
Download
Title
Effects of traumatic brain injury and posttraumatic stress disorder on Alzheimer's disease in veterans, using the Alzheimer's Disease Neuroimaging Initiative
Authors
M. W. Weiner, D. P. Veitch, J. Hayes, T. Neylan, J. Grafman, P. S. Aisen, R. C. Petersen, C. Jack, W. Jagust, J. Q. Trojanowski, L. M. Shaw, A. J. Saykin, R. C. Green, D. Harvey, A. W. Toga, K. E. Friedl, A. Pacifico, Y. Sheline, K. Yaffe and B. Mohlenoff
Journal
Alzheimer's & Dementia
Year
2014
Volume
10
Issue
3, Supplement
Pages
S226-S235
Warstadt, N.M., et al., Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure. Neurobiology of Aging, 2014. 35(11): p. 2504-2513.
Download
Title
Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure
Authors
N. M. Warstadt, E. L. Dennis, N. Jahanshad, O. Kohannim, T. M. Nir, K. L. McMahon, G. I. de Zubicaray, G. W. Montgomery, A. K. Henders, N. G. Martin, J. B. Whitfield, C. R. Jack Jr, M. A. Bernstein, M. W. Weiner, A. W. Toga, M. J. Wright and P. M. Thompson
Journal
Neurobiology of Aging
Year
2014
Volume
35
Issue
11
Pages
2504-2513
Vardarajan, B.N., et al., Inbreeding among Caribbean Hispanics from the Dominican Republic and its effects on risk of Alzheimer disease. Genet Med, 2014.
Download
Title
Inbreeding among Caribbean Hispanics from the Dominican Republic and its effects on risk of Alzheimer disease
Authors
B. N. Vardarajan, D. J. Schaid, C. Reitz, R. Lantigua, M. Medrano, I. Z. Jimenez-Velazquez, J. H. Lee, M. Ghani, E. Rogaeva, P. St George-Hyslop and R. P. Mayeux
Journal
Genet Med
Year
2014
Volume
Issue
Pages
Vardarajan, B.N., et al., Age-specific incidence rates for dementia and alzheimer disease in nia-load/ncrad and efiga families: National institute on aging genetics initiative for late-onset alzheimer disease/national cell repository for alzheimer disease (nia-load/ncrad) and estudio familiar de influencia genetica en alzheimer (efiga). JAMA Neurology, 2014.
Download
Title
Age-specific incidence rates for dementia and alzheimer disease in nia-load/ncrad and efiga families: National institute on aging genetics initiative for late-onset alzheimer disease/national cell repository for alzheimer disease (nia-load/ncrad) and estudio familiar de influencia genetica en alzheimer (efiga)
Authors
B. N. Vardarajan, K. M. Faber, T. D. Bird and et al.
Journal
JAMA Neurology
Year
2014
Volume
Issue
Pages
Thompson, P.M., et al., The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 2014. 8(2): p. 153-182.
Download
Title
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
Authors
P. M. Thompson, J. L. Stein, S. E. Medland, D. P. Hibar, A. A. Vasquez, M. E. Renteria, R. Toro, N. Jahanshad, G. Schumann, B. Franke, M. J. Wright, N. G. Martin, I. Agartz, M. Alda, S. Alhusaini, L. Almasy, J. Almeida, K. Alpert, N. C. Andreasen, O. A. Andreassen, L. G. Apostolova, K. Appel, N. J. Armstrong, B. Aribisala, M. E. Bastin, M. Bauer, C. E. Bearden, Ø. Bergmann, E. B. Binder, J. Blangero, H. J. Bockholt, E. Bøen, C. Bois, D. I. Boomsma, T. Booth, I. J. Bowman, J. Bralten, R. M. Brouwer, H. G. Brunner, D. G. Brohawn, R. L. Buckner, J. Buitelaar, K. Bulayeva, J. R. Bustillo, V. D. Calhoun, D. M. Cannon, R. M. Cantor, M. A. Carless, X. Caseras, G. L. Cavalleri, M. M. Chakravarty, K. D. Chang, C. R. K. Ching, A. Christoforou, S. Cichon, V. P. Clark, P. Conrod, G. Coppola, B. Crespo-Facorro, J. E. Curran, M. Czisch, I. J. Deary, E. J. C. de Geus, A. den Braber, G. Delvecchio, C. Depondt, L. de Haan, G. I. de Zubicaray, D. Dima, R. Dimitrova, S. Djurovic, H. Dong, G. Donohoe, R. Duggirala, T. D. Dyer, S. Ehrlich, C. J. Ekman, T. Elvsåshagen, L. Emsell, S. Erk, T. Espeseth, J. Fagerness, S. Fears, I. Fedko, G. Fernández, S. E. Fisher, T. Foroud, P. T. Fox, C. Francks, S. Frangou, E. M. Frey, T. Frodl, V. Frouin, H. Garavan, S. Giddaluru, D. C. Glahn, B. Godlewska, R. Z. Goldstein, R. L. Gollub, H. J. Grabe, O. Grimm, O. Gruber, T. Guadalupe, R. E. Gur, R. C. Gur, H. H. H. Göring, S. Hagenaars, T. Hajek, G. B. Hall, J. Hall, J. Hardy, C. A. Hartman, J. Hass, S. N. Hatton, U. K. Haukvik, K. Hegenscheid, A. Heinz, I. B. Hickie, B.-C. Ho, D. Hoehn, P. J. Hoekstra, M. Hollinshead, A. J. Holmes, G. Homuth, M. Hoogman, L. E. Hong, N. Hosten, J.-J. Hottenga, H. E. Hulshoff Pol, K. S. Hwang, C. R. Jack, M. Jenkinson, C. Johnston, E. G. Jönsson, R. S. Kahn, D. Kasperaviciute, S. Kelly, S. Kim, P. Kochunov, L. Koenders, B. Krämer, J. B. J. Kwok, J. Lagopoulos, G. Laje, M. Landen, B. A. Landman, J. Lauriello, S. M. Lawrie, P. H. Lee, S. Le Hellard, H. Lemaître, C. D. Leonardo, C.-s. Li, B. Liberg, D. C. Liewald, X. Liu, L. M. Lopez, E. Loth, A. Lourdusamy, M. Luciano, F. Macciardi, M. W. J. Machielsen, G. M. MacQueen, U. F. Malt, R. Mandl, D. S. Manoach, J.-L. Martinot, M. Matarin, K. A. Mather, M. Mattheisen, M. Mattingsdal, A. Meyer-Lindenberg, C. McDonald, A. M. McIntosh, F. J. McMahon, K. L. McMahon, E. Meisenzahl, I. Melle, Y. Milaneschi, S. Mohnke, G. W. Montgomery, D. W. Morris, E. K. Moses, B. A. Mueller, S. Muñoz Maniega, T. W. Mühleisen, B. Müller-Myhsok, B. Mwangi, M. Nauck, K. Nho, T. E. Nichols, L.-G. Nilsson, A. C. Nugent, L. Nyberg, R. L. Olvera, J. Oosterlaan, R. A. Ophoff, M. Pandolfo, M. Papalampropoulou-Tsiridou, M. Papmeyer, T. Paus, Z. Pausova, G. D. Pearlson, B. W. Penninx, C. P. Peterson, A. Pfennig, M. Phillips, G. B. Pike, J.-B. Poline, S. G. Potkin, B. Pütz, A. Ramasamy, J. Rasmussen, M. Rietschel, M. Rijpkema, S. L. Risacher, J. L. Roffman, R. Roiz-Santiañez, N. Romanczuk-Seiferth, E. J. Rose, N. A. Royle, D. Rujescu, M. Ryten, P. S. Sachdev, A. Salami, T. D. Satterthwaite, J. Savitz, A. J. Saykin, C. Scanlon, L. Schmaal, H. G. Schnack, A. J. Schork, S. C. Schulz, R. Schür, L. Seidman, L. Shen, J. M. Shoemaker, A. Simmons, S. M. Sisodiya, C. Smith, J. W. Smoller, J. C. Soares, S. R. Sponheim, E. Sprooten, J. M. Starr, V. M. Steen, S. Strakowski, L. Strike, J. Sussmann, P. G. Sämann, A. Teumer, A. W. Toga, D. Tordesillas-Gutierrez, D. Trabzuni, S. Trost, J. Turner, M. Van den Heuvel, N. J. van der Wee, K. van Eijk, T. G. M. van Erp, N. E. M. van Haren, D. van ‘t Ent, M.-J. van Tol, M. C. Valdés Hernández, D. J. Veltman, A. Versace, H. Völzke, R. Walker, H. Walter, L. Wang, J. M. Wardlaw, M. E. Weale, M. W. Weiner, W. Wen, L. T. Westlye, H. C. Whalley, C. D. Whelan, T. White, A. M. Winkler, K. Wittfeld, G. Woldehawariat, C. Wolf, D. Zilles, M. P. Zwiers, A. Thalamuthu, P. R. Schofield, N. B. Freimer, N. S. Lawrence, W. Drevets and E. C. I. C. S. Y. S. G. the Alzheimer’s Disease Neuroimaging Initiative
Journal
Brain Imaging and Behavior
Year
2014
Volume
8
Issue
2
Pages
153-182
Szigeti, K., et al., Ordered Subset Analysis of Copy Number Variation Association with Age at Onset of Alzheimer's Disease. Journal of Alzheimer's Disease, 2014. 41(4): p. 1063-1071.
Download
Title
Ordered Subset Analysis of Copy Number Variation Association with Age at Onset of Alzheimer's Disease
Authors
K. Szigeti, B. Kellermayer, J. M. Lentini, B. Trummer, D. Lal, R. S. Doody, L. Yan, S. Liu and C. Ma
Journal
Journal of Alzheimer's Disease
Year
2014
Volume
41
Issue
4
Pages
1063-1071
Swaminathan, S., et al., Association of plasma and cortical amyloid beta is modulated by APOE ε4 status. Alzheimer's & dementia : the journal of the Alzheimer's Association, 2014. 10(1): p. e9-e18.
Download
Title
Association of plasma and cortical amyloid beta is modulated by APOE ε4 status
Authors
S. Swaminathan, S. L. Risacher, K. K. Yoder, J. D. West, L. Shen, S. Kim, M. Inlow, T. Foroud, W. J. Jagust, R. A. Koeppe, C. A. Mathis, L. M. Shaw, J. Q. Trojanowski, H. Soares, P. S. Aisen, R. C. Petersen, M. W. Weiner and A. J. Saykin
Journal
Alzheimer's & dementia : the journal of the Alzheimer's Association
Year
2014
Volume
10
Issue
1
Pages
e9-e18
Shpanskaya, K.S., et al., Educational attainment and hippocampal atrophy in the Alzheimer's disease neuroimaging initiative cohort. J Neuroradiol, 2014. 41(5): p. 350-7.
Download
Title
Educational attainment and hippocampal atrophy in the Alzheimer's disease neuroimaging initiative cohort
Authors
K. S. Shpanskaya, K. R. Choudhury, C. Hostage, Jr., K. R. Murphy, J. R. Petrella and P. M. Doraiswamy
Journal
J Neuroradiol
Year
2014
Volume
41
Issue
5
Pages
350-7
Shi, J., et al., Genetic influence of apolipoprotein E4 genotype on hippocampal morphometry: An N = 725 surface-based Alzheimer's disease neuroimaging initiative study. Hum Brain Mapp, 2014. 35(8): p. 3903-18.
Download
Title
Genetic influence of apolipoprotein E4 genotype on hippocampal morphometry: An N = 725 surface-based Alzheimer's disease neuroimaging initiative study
Authors
J. Shi, N. Lepore, B. A. Gutman, P. M. Thompson, L. C. Baxter, R. J. Caselli and Y. Wang
Journal
Hum Brain Mapp
Year
2014
Volume
35
Issue
8
Pages
3903-18
Sherva, R., et al., Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. Alzheimer's & Dementia, 2014. 10(1): p. 45-52.
Download
Title
Genome-wide association study of the rate of cognitive decline in Alzheimer's disease
Authors
R. Sherva, Y. Tripodis, D. A. Bennett, L. B. Chibnik, P. K. Crane, P. L. de Jager, L. A. Farrer, A. J. Saykin, J. M. Shulman, A. Naj and R. C. Green
Journal
Alzheimer's & Dementia
Year
2014
Volume
10
Issue
1
Pages
45-52
Shen, L., et al., Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers. Brain Imaging and Behavior, 2014. 8(2): p. 183-207.
Download
Title
Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers
Authors
L. Shen, P. M. Thompson, S. G. Potkin, L. Bertram, L. A. Farrer, T. M. Foroud, R. C. Green, X. Hu, M. J. Huentelman, S. Kim, J. S. K. Kauwe, Q. Li, E. Liu, F. Macciardi, J. H. Moore, L. Munsie, K. Nho, V. K. Ramanan, S. L. Risacher, D. J. Stone, S. Swaminathan, A. W. Toga, M. W. Weiner, A. J. Saykin and I. for the Alzheimer’s Disease Neuroimaging
Journal
Brain Imaging and Behavior
Year
2014
Volume
8
Issue
2
Pages
183-207
Sharp, A.R., et al., Population substructure in Cache County, Utah: the Cache County study. BMC Bioinformatics, 2014. 15(7): p. 1471-2105.
Download
Title
Population substructure in Cache County, Utah: the Cache County study
Authors
A. R. Sharp, P. G. Ridge, M. H. Bailey, K. L. Boehme, M. C. Norton, J. T. Tschanz, R. G. Munger, C. D. Corcoran and J. S. Kauwe
Journal
BMC Bioinformatics
Year
2014
Volume
15
Issue
7
Pages
1471-2105
Ruiz, A., et al., Follow-up of loci from the International Genomics of Alzheimer/'s Disease Project identifies TRIP4 as a novel susceptibility gene. Transl Psychiatry, 2014. 4: p. e358.
Download
Title
Follow-up of loci from the International Genomics of Alzheimer/'s Disease Project identifies TRIP4 as a novel susceptibility gene
Authors
A. Ruiz, S. Heilmann, T. Becker, I. Hernandez, H. Wagner, M. Thelen, A. Mauleon, M. Rosende-Roca, C. Bellenguez, J. C. Bis, D. Harold, A. Gerrish, R. Sims, O. Sotolongo-Grau, A. Espinosa, M. Alegret, J. L. Arrieta, A. Lacour, M. Leber, J. Becker, A. Lafuente, S. Ruiz, L. Vargas, O. Rodriguez, G. Ortega, M. A. Dominguez, R. Mayeux, J. L. Haines, M. A. Pericak-Vance, L. A. Farrer, G. D. Schellenberg, V. Chouraki, L. J. Launer, C. van Duijn, S. Seshadri, C. Antunez, M. M. Breteler, M. Serrano-Rios, F. Jessen, L. Tarraga, M. M. Nothen, W. Maier, M. Boada and A. Ramirez
Journal
Transl Psychiatry
Year
2014
Volume
4
Issue
Pages
e358
Roussotte, F.F., et al., Altered regional brain volumes in elderly carriers of a risk variant for drug abuse in the dopamine D2 receptor gene (DRD2). Brain Imaging Behav, 2014. 16: p. 16.
Download
Title
Altered regional brain volumes in elderly carriers of a risk variant for drug abuse in the dopamine D2 receptor gene (DRD2)
Authors
F. F. Roussotte, N. Jahanshad, D. P. Hibar and P. M. Thompson
Journal
Brain Imaging Behav
Year
2014
Volume
16
Issue
Pages
16
Roussotte, F.F., et al., A Commonly Carried Genetic Variant in the Delta Opioid Receptor Gene, OPRD1, is Associated with Smaller Regional Brain Volumes: Replication in Elderly and Young Populations. Human brain mapping, 2014. 35(4): p. 1226-1236.
Download
Title
A Commonly Carried Genetic Variant in the Delta Opioid Receptor Gene, OPRD1, is Associated with Smaller Regional Brain Volumes: Replication in Elderly and Young Populations
Authors
F. F. Roussotte, N. Jahanshad, D. P. Hibar, E. R. Sowell, O. Kohannim, M. Barysheva, N. K. Hansell, K. L. McMahon, G. I. de Zubicaray, G. W. Montgomery, N. G. Martin, M. J. Wright, A. W. Toga, C. R. Jack, M. W. Weiner, P. M. Thompson and A. the
Journal
Human brain mapping
Year
2014
Volume
35
Issue
4
Pages
1226-1236
Roussotte, F.F., et al., Combined effects of Alzheimer risk variants in the CLU and ApoE genes on ventricular expansion patterns in the elderly. J Neurosci, 2014. 34(19): p. 6537-45.
Download
Title
Combined effects of Alzheimer risk variants in the CLU and ApoE genes on ventricular expansion patterns in the elderly
Authors
F. F. Roussotte, B. A. Gutman, S. K. Madsen, J. B. Colby and P. M. Thompson
Journal
J Neurosci
Year
2014
Volume
34
Issue
19
Pages
6537-45
Roussotte, F.F., et al., The apolipoprotein E epsilon 4 allele is associated with ventricular expansion rate and surface morphology in dementia and normal aging. Neurobiology of Aging, 2014. 35(6): p. 1309-1317.
Download
Title
The apolipoprotein E epsilon 4 allele is associated with ventricular expansion rate and surface morphology in dementia and normal aging
Authors
F. F. Roussotte, B. A. Gutman, S. K. Madsen, J. B. Colby, K. L. Narr and P. M. Thompson
Journal
Neurobiology of Aging
Year
2014
Volume
35
Issue
6
Pages
1309-1317
Ridge, P.G., et al., Mitochondrial genomic variation associated with higher mitochondrial copy number: the Cache County Study on Memory Health and Aging. BMC Bioinformatics, 2014. 15 Suppl 7: p. S6.
Download
Title
Mitochondrial genomic variation associated with higher mitochondrial copy number: the Cache County Study on Memory Health and Aging
Authors
P. G. Ridge, T. J. Maxwell, S. J. Foutz, M. H. Bailey, C. D. Corcoran, J. T. Tschanz, M. C. Norton, R. G. Munger, E. O'Brien, R. A. Kerber, R. M. Cawthon and J. S. Kauwe
Journal
BMC Bioinformatics
Year
2014
Volume
15 Suppl 7
Issue
Pages
S6
Reitz, C. and R. Mayeux, Alzheimer disease: Epidemiology, diagnostic criteria, risk factors and biomarkers. Biochemical Pharmacology, 2014. 88(4): p. 640-651.
Download
Title
Alzheimer disease: Epidemiology, diagnostic criteria, risk factors and biomarkers
Authors
C. Reitz and R. Mayeux
Journal
Biochemical Pharmacology
Year
2014
Volume
88
Issue
4
Pages
640-651
Reitz, C. and R. Mayeux, Genetics of Alzheimer’s Disease in Caribbean Hispanic and African American Populations. Biological Psychiatry, 2014(0).
Download
Title
Genetics of Alzheimer’s Disease in Caribbean Hispanic and African American Populations
Authors
C. Reitz and R. Mayeux
Journal
Biological Psychiatry
Year
2014
Volume
Issue
0
Pages
Ramirez, A., et al., SUCLG2 identified as both a determinator of CSF Abeta1-42 levels and an attenuator of cognitive decline in Alzheimer's disease. Hum Mol Genet, 2014. 23(24): p. 6644-58.
Download
Title
SUCLG2 identified as both a determinator of CSF Abeta1-42 levels and an attenuator of cognitive decline in Alzheimer's disease
Authors
A. Ramirez, W. M. van der Flier, C. Herold, D. Ramonet, S. Heilmann, P. Lewczuk, J. Popp, A. Lacour, D. Drichel, E. Louwersheimer, M. P. Kummer, C. Cruchaga, P. Hoffmann, C. Teunissen, H. Holstege, J. Kornhuber, O. Peters, A. C. Naj, V. Chouraki, C. Bellenguez, A. Gerrish, R. Heun, L. Frolich, M. Hull, L. Buscemi, S. Herms, H. Kolsch, P. Scheltens, M. M. Breteler, E. Ruther, J. Wiltfang, A. Goate, F. Jessen, W. Maier, M. T. Heneka, T. Becker and M. M. Nothen
Journal
Hum Mol Genet
Year
2014
Volume
23
Issue
24
Pages
6644-58
Ramanan, V.K., et al., APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study. Mol Psychiatry, 2014.
Download
Title
APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study
Authors
V. K. Ramanan, S. L. Risacher, K. Nho, S. Kim, S. Swaminathan, L. Shen, T. M. Foroud, H. Hakonarson, M. J. Huentelman, P. S. Aisen, R. C. Petersen, R. C. Green, C. R. Jack, R. A. Koeppe, W. J. Jagust, M. W. Weiner and A. J. Saykin
Journal
Mol Psychiatry
Year
2014
Volume
Issue
Pages
Radmanesh, F., et al., Accuracy of imputation to infer unobserved APOE epsilon alleles in genome-wide genotyping data. Eur J Hum Genet, 2014. 22(10): p. 1239-42.
Download
Title
Accuracy of imputation to infer unobserved APOE epsilon alleles in genome-wide genotyping data
Authors
F. Radmanesh, W. J. Devan, C. D. Anderson, J. Rosand and G. J. Falcone
Journal
Eur J Hum Genet
Year
2014
Volume
22
Issue
10
Pages
1239-42
Proitsi, P., et al., Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a mendelian randomization analysis. PLoS Med, 2014. 11(9).
Download
Title
Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a mendelian randomization analysis
Authors
P. Proitsi, M. K. Lupton, L. Velayudhan, S. Newhouse, I. Fogh, M. Tsolaki, M. Daniilidou, M. Pritchard, I. Kloszewska, H. Soininen, P. Mecocci, B. Vellas, J. Williams, R. Stewart, P. Sham, S. Lovestone and J. F. Powell
Journal
PLoS Med
Year
2014
Volume
11
Issue
9
Pages
Proitsi, P., et al., Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease. Neurobiology of Aging, 2014. 35(12): p. 2883.e3-2883.e10.
Download
Title
Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease
Authors
P. Proitsi, M. K. Lupton, L. Velayudhan, G. Hunter, S. Newhouse, K. Lin, I. Fogh, M. Tsolaki, M. Daniilidou, M. Pritchard, D. Craig, S. Todd, J. A. Johnston, B. McGuinness, I. Kloszewska, H. Soininen, P. Mecocci, B. Vellas, P. A. Passmore, R. Sims, J. Williams, C. Brayne, R. Stewart, P. Sham, S. Lovestone and J. F. Powell
Journal
Neurobiology of Aging
Year
2014
Volume
35
Issue
12
Pages
2883.e3-2883.e10
Printy, B.P., et al., Effects of genetic variation on the dynamics of neurodegeneration in Alzheimer's disease. Conf Proc IEEE Eng Med Biol Soc, 2014. 7(10): p. 6944121.
Download
Title
Effects of genetic variation on the dynamics of neurodegeneration in Alzheimer's disease
Authors
B. P. Printy, N. Verma, M. C. Cowperthwaite and M. K. Markey
Journal
Conf Proc IEEE Eng Med Biol Soc
Year
2014
Volume
7
Issue
10
Pages
6944121
Peterson, D., et al., Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: The Cache County Dementia Progression Study. Alzheimer's & Dementia, 2014(0).
Download
Title
Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: The Cache County Dementia Progression Study
Authors
D. Peterson, C. Munger, J. Crowley, C. Corcoran, C. Cruchaga, A. M. Goate, M. C. Norton, R. C. Green, R. G. Munger, J. C. S. Breitner, K. A. Welsh-Bohmer, C. Lyketsos, J. Tschanz and J. S. K. Kauwe
Journal
Alzheimer's & Dementia
Year
2014
Volume
Issue
0
Pages
Pérez-Palma, E., et al., Overrepresentation of Glutamate Signaling in Alzheimer's Disease: Network-Based Pathway Enrichment Using Meta-Analysis of Genome-Wide Association Studies. PLoS ONE, 2014. 9(4): p. e95413.
Download
Title
Overrepresentation of Glutamate Signaling in Alzheimer's Disease: Network-Based Pathway Enrichment Using Meta-Analysis of Genome-Wide Association Studies
Authors
E. Pérez-Palma, B. I. Bustos, C. F. Villamán, M. A. Alarcón, M. E. Avila, G. D. Ugarte, A. E. Reyes, C. Opazo, G. V. De Ferrari, I. the Alzheimer's Disease Neuroimaging and N. I. A. L. N. F. S. G. the
Journal
PLoS ONE
Year
2014
Volume
9
Issue
4
Pages
e95413
Paterson, R.W., et al., Cerebrospinal fluid markers including trefoil factor 3 are associated with neurodegeneration in amyloid-positive individuals. Transl Psychiatry, 2014. 29(4): p. 58.
Download
Title
Cerebrospinal fluid markers including trefoil factor 3 are associated with neurodegeneration in amyloid-positive individuals
Authors
R. W. Paterson, J. W. Bartlett, K. Blennow, N. C. Fox, L. M. Shaw, J. Q. Trojanowski, H. Zetterberg and J. M. Schott
Journal
Transl Psychiatry
Year
2014
Volume
29
Issue
4
Pages
58
Parsaik, A.K., et al., Hypothyroidism and risk of mild cognitive impairment in elderly persons: A population-based study. JAMA Neurology, 2014. 71(2): p. 201-207.
Download
Title
Hypothyroidism and risk of mild cognitive impairment in elderly persons: A population-based study
Authors
A. K. Parsaik, B. Singh, R. O. Roberts and et al.
Journal
JAMA Neurology
Year
2014
Volume
71
Issue
2
Pages
201-207
Nuytemans, K., et al., Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease. Movement Disorders, 2014: p. n/a-n/a.
Download
Title
Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease
Authors
K. Nuytemans, V. Inchausti, G. W. Beecham, L. Wang, D. W. Dickson, J. Q. Trojanowski, V. M. Y. Lee, D. C. Mash, M. P. Frosch, T. M. Foroud, L. S. Honig, T. J. Montine, T. M. Dawson, E. R. Martin, W. K. Scott and J. M. Vance
Journal
Movement Disorders
Year
2014
Volume
Issue
Pages
Nelson, P., et al., ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. Acta Neuropathologica, 2014. 127(6): p. 825-843.
Download
Title
ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology
Authors
P. Nelson, S. Estus, E. Abner, I. Parikh, M. Malik, J. Neltner, E. Ighodaro, W.-X. Wang, B. Wilfred, L.-S. Wang, W. Kukull, K. Nandakumar, M. Farman, W. Poon, M. Corrada, C. Kawas, D. Cribbs, D. Bennett, J. Schneider, E. Larson, P. Crane, O. Valladares, F. Schmitt, R. Kryscio, G. Jicha, C. Smith, S. Scheff, J. Sonnen, J. Haines, M. Pericak-Vance, R. Mayeux, L. Farrer, L. Van Eldik, C. Horbinski, R. Green, M. Gearing, L. Poon, P. Kramer, R. Woltjer, T. Montine, A. Partch, A. Rajic, K. Richmire, S. Monsell, G. Schellenberg and D. Fardo
Journal
Acta Neuropathologica
Year
2014
Volume
127
Issue
6
Pages
825-843
Nalls, M.A., et al., Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nat Genet, 2014. 46(9): p. 989-993.
Download
Title
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Authors
M. A. Nalls, N. Pankratz, C. M. Lill, C. B. Do, D. G. Hernandez, M. Saad, A. L. DeStefano, E. Kara, J. Bras, M. Sharma, C. Schulte, M. F. Keller, S. Arepalli, C. Letson, C. Edsall, H. Stefansson, X. Liu, H. Pliner, J. H. Lee, R. Cheng, C. International Parkinson's Disease Genomics, G. I. Parkinson's Study Group Parkinson's Research: The Organized, andMe, GenePd, C. NeuroGenetics Research, G. Hussman Institute of Human, I. The Ashkenazi Jewish Dataset, H. Cohorts for, E. Aging Research in Genetic, C. North American Brain Expression, C. United Kingdom Brain Expression, C. Greek Parkinson's Disease, G. Alzheimer Genetic Analysis, M. A. Ikram, J. P. A. Ioannidis, G. M. Hadjigeorgiou, J. C. Bis, M. Martinez, J. S. Perlmutter, A. Goate, K. Marder, B. Fiske, M. Sutherland, G. Xiromerisiou, R. H. Myers, L. N. Clark, K. Stefansson, J. A. Hardy, P. Heutink, H. Chen, N. W. Wood, H. Houlden, H. Payami, A. Brice, W. K. Scott, T. Gasser, L. Bertram, N. Eriksson, T. Foroud and A. B. Singleton
Journal
Nat Genet
Year
2014
Volume
46
Issue
9
Pages
989-993
Naj, A.C., et al., Effects of multiple genetic loci on age at onset in late-onset alzheimer disease: A genome-wide association study. JAMA Neurology, 2014. 71(11): p. 1394-1404.
Download
Title
Effects of multiple genetic loci on age at onset in late-onset alzheimer disease: A genome-wide association study
Authors
A. C. Naj, G. Jun, C. Reitz and et al.
Journal
JAMA Neurology
Year
2014
Volume
71
Issue
11
Pages
1394-1404
Mukherjee, S., et al., Gene-based GWAS and biological pathway analysis of the resilience of executive functioning. Brain Imaging and Behavior, 2014: p. 1-9.
Download
Title
Gene-based GWAS and biological pathway analysis of the resilience of executive functioning
Authors
S. Mukherjee, S. Kim, V. Ramanan, L. Gibbons, K. Nho, M. M. Glymour, N. Ertekin-Taner, T. Montine, A. Saykin and P. Crane
Journal
Brain Imaging and Behavior
Year
2014
Volume
Issue
Pages
42013
Medway, C.W., et al., ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer’s disease. Molecular Neurodegeneration, 2014. 9: p. 11-11.
Download
Title
ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer’s disease
Authors
C. W. Medway, S. Abdul-Hay, T. Mims, L. Ma, G. Bisceglio, F. Zou, S. Pankratz, S. B. Sando, J. O. Aasly, M. Barcikowska, J. Siuda, Z. K. Wszolek, O. A. Ross, M. Carrasquillo, D. W. Dickson, N. Graff-Radford, R. C. Petersen, N. Ertekin-Taner, K. Morgan, G. Bu and S. G. Younkin
Journal
Molecular Neurodegeneration
Year
2014
Volume
9
Issue
Pages
42319
McCarter, S.J., et al., Factors associated with injury in REM sleep behavior disorder. Sleep Medicine, 2014. 15(11): p. 1332-1338.
Download
Title
Factors associated with injury in REM sleep behavior disorder
Authors
S. J. McCarter, E. K. St. Louis, C. L. Boswell, L. G. Dueffert, N. Slocumb, B. F. Boeve, M. H. Silber, E. J. Olson, T. I. Morgenthaler and M. Tippmann-Peikert
Journal
Sleep Medicine
Year
2014
Volume
15
Issue
11
Pages
1332-1338
Mattsson, N., et al., Association of brain amyloid-β with cerebral perfusion and structure in Alzheimer’s disease and mild cognitive impairment. Vol. 137. 2014. 1550-1561.
Download
Title
Association of brain amyloid-β with cerebral perfusion and structure in Alzheimer’s disease and mild cognitive impairment
Authors
N. Mattsson, D. Tosun, P. S. Insel, A. Simonson, C. R. Jack, L. A. Beckett, M. Donohue, W. Jagust, N. Schuff and M. W. Weiner
Journal
Brain
Year
2014
Volume
137
Issue
Pages
1550-1561
Manning, E.N., et al., APOE ε4 Is Associated with Disproportionate Progressive Hippocampal Atrophy in AD. PLoS ONE, 2014. 9(5): p. e97608.
Download
Title
APOE ε4 Is Associated with Disproportionate Progressive Hippocampal Atrophy in AD
Authors
E. N. Manning, J. Barnes, D. M. Cash, J. W. Bartlett, K. K. Leung, S. Ourselin, N. C. Fox and I. for the Alzheimer's Disease NeuroImaging
Journal
PLoS ONE
Year
2014
Volume
9
Issue
5
Pages
e97608
Luis, E.O., et al., Frontobasal gray matter loss is associated with the TREM2 p.R47H variant. Neurobiology of Aging, 2014. 35(12): p. 2681-2690.
Download
Title
Frontobasal gray matter loss is associated with the TREM2 p.R47H variant
Authors
E. O. Luis, S. Ortega-Cubero, I. Lamet, C. Razquin, C. Cruchaga, B. A. Benitez, E. Lorenzo, J. Irigoyen, M. A. Pastor and P. Pastor
Journal
Neurobiology of Aging
Year
2014
Volume
35
Issue
12
Pages
2681-2690
Logue, M.W., et al., Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans. Alzheimer's & Dementia, 2014. 10(6): p. 609-618.e11.
Download
Title
Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans
Authors
M. W. Logue, M. Schu, B. N. Vardarajan, J. Farrell, D. A. Bennett, J. D. Buxbaum, G. S. Byrd, N. Ertekin-Taner, D. Evans, T. Foroud, A. Goate, N. R. Graff-Radford, M. I. Kamboh, W. A. Kukull and J. J. Manly
Journal
Alzheimer's & Dementia
Year
2014
Volume
10
Issue
6
Pages
609-618.e11
Liu, Y., et al., Association between NME8 Locus Polymorphism and Cognitive Decline, Cerebrospinal Fluid and Neuroimaging Biomarkers in Alzheimer's Disease. PLoS ONE, 2014. 9(12): p. e114777.
Download
Title
Association between NME8 Locus Polymorphism and Cognitive Decline, Cerebrospinal Fluid and Neuroimaging Biomarkers in Alzheimer's Disease
Authors
Y. Liu, J.-T. Yu, H.-F. Wang, X.-K. Hao, Y.-F. Yang, T. Jiang, X.-C. Zhu, L. Cao, D.-Q. Zhang and L. Tan
Journal
PLoS ONE
Year
2014
Volume
9
Issue
12
Pages
e114777
Li, M., et al., Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Mol Psychiatry, 2014.
Download
Title
Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility
Authors
M. Li, X. j. Luo, M. Rietschel, C. M. Lewis, M. Mattheisen, B. Muller-Myhsok, S. Jamain, M. Leboyer, M. Landen, P. M. Thompson, S. Cichon, M. M. Nothen, T. G. Schulze, P. F. Sullivan, S. E. Bergen, G. Donohoe, D. W. Morris, A. Hargreaves, M. Gill, A. Corvin, C. Hultman, A. W. Toga, L. Shi, Q. Lin, H. Shi, L. Gan, A. Meyer-Lindenberg, D. Czamara, C. Henry, B. Etain, J. C. Bis, M. A. Ikram, M. Fornage, S. Debette, L. J. Launer, S. Seshadri, S. Erk, H. Walter, A. Heinz, F. Bellivier, J. L. Stein, S. E. Medland, A. Arias Vasquez, D. P. Hibar, B. Franke, N. G. Martin, M. J. Wright and B. Su
Journal
Mol Psychiatry
Year
2014
Volume
Issue
Pages
Leduc, V., et al., HMGCR is a genetic modifier for risk, age of onset and MCI conversion to Alzheimer/'s disease in a three cohorts study. Mol Psychiatry, 2014.
Download
Title
HMGCR is a genetic modifier for risk, age of onset and MCI conversion to Alzheimer/'s disease in a three cohorts study
Authors
V. Leduc, L. De Beaumont, L. Theroux, D. Dea, P. Aisen, R. C. Petersen, I. the Alzheimer's Disease Neuroimaging, R. Dufour and J. Poirier
Journal
Mol Psychiatry
Year
2014
Volume
Issue
Pages
Lebedev, A.V., et al., Random Forest ensembles for detection and prediction of Alzheimer's disease with a good between-cohort robustness(). NeuroImage : Clinical, 2014. 6: p. 115-125.
Download
Title
Random Forest ensembles for detection and prediction of Alzheimer's disease with a good between-cohort robustness()
Authors
A. V. Lebedev, E. Westman, G. J. P. Van Westen, M. G. Kramberger, A. Lundervold, D. Aarsland, H. Soininen, I. Kłoszewska, P. Mecocci, M. Tsolaki, B. Vellas, S. Lovestone, A. Simmons, I. for the Alzheimer's Disease Neuroimaging and c. the AddNeuroMed
Journal
NeuroImage : Clinical
Year
2014
Volume
6
Issue
Pages
115-125
Koran, M.E.I., et al., Genetic Interactions within Inositol-Related Pathways are Associated with Longitudinal Changes in Ventricle Size. Journal of Alzheimer's Disease, 2014. 38(1): p. 145-154.
Download
Title
Genetic Interactions within Inositol-Related Pathways are Associated with Longitudinal Changes in Ventricle Size
Authors
M. E. I. Koran, T. J. Hohman, S. A. Meda and T. A. Thornton-Wells
Journal
Journal of Alzheimer's Disease
Year
2014
Volume
38
Issue
1
Pages
145-154
Koran, M., T. Hohman, and T. Thornton-Wells, Genetic interactions found between calcium channel genes modulate amyloid load measured by positron emission tomography. Human Genetics, 2014. 133(1): p. 85-93.
Download
Title
Genetic interactions found between calcium channel genes modulate amyloid load measured by positron emission tomography
Authors
M. Koran, T. Hohman and T. Thornton-Wells
Journal
Human Genetics
Year
2014
Volume
133
Issue
1
Pages
85-93
Kim, J.H., et al., Gene-Based Rare Allele Analysis Identified a Risk Gene of Alzheimer’s Disease. PLoS ONE, 2014. 9(10): p. e107983.
Download
Title
Gene-Based Rare Allele Analysis Identified a Risk Gene of Alzheimer’s Disease
Authors
J. H. Kim, P. Song, H. Lim, J.-H. Lee, J. H. Lee, S. A. Park and I. for the Alzheimer’s Disease Neuroimaging
Journal
PLoS ONE
Year
2014
Volume
9
Issue
10
Pages
e107983
Kennedy, R.E., G.R. Cutter, and L.S. Schneider, Effect of APOE genotype status on targeted clinical trials outcomes and efficiency in dementia and mild cognitive impairment resulting from Alzheimer's disease. Alzheimer's & Dementia, 2014. 10(3): p. 349-359.
Download
Title
Effect of APOE genotype status on targeted clinical trials outcomes and efficiency in dementia and mild cognitive impairment resulting from Alzheimer's disease
Authors
R. E. Kennedy, G. R. Cutter and L. S. Schneider
Journal
Alzheimer's & Dementia
Year
2014
Volume
10
Issue
3
Pages
349-359
Kauwe, J.S.K., et al., Genome-Wide Association Study of CSF Levels of 59 Alzheimer's Disease Candidate Proteins: Significant Associations with Proteins Involved in Amyloid Processing and Inflammation. PLoS Genet, 2014. 10(10): p. e1004758.
Download
Title
Genome-Wide Association Study of CSF Levels of 59 Alzheimer's Disease Candidate Proteins: Significant Associations with Proteins Involved in Amyloid Processing and Inflammation
Authors
J. S. K. Kauwe, M. H. Bailey, P. G. Ridge, R. Perry, M. E. Wadsworth, K. L. Hoyt, L. A. Staley, C. M. Karch, O. Harari, C. Cruchaga, B. J. Ainscough, K. Bales, E. H. Pickering, S. Bertelsen, A. M. Fagan, D. M. Holtzman, J. C. Morris, A. M. Goate and I. the Alzheimer's Disease Neuroimaging
Journal
PLoS Genet
Year
2014
Volume
10
Issue
10
Pages
e1004758
Jun, G., et al., PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation. Annals of Neurology, 2014. 76(3): p. 379-392.
Download
Title
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation
Authors
G. Jun, H. Asai, E. Zeldich, E. Drapeau, C. Chen, J. Chung, J.-H. Park, S. Kim, V. Haroutunian, T. Foroud, R. Kuwano, J. L. Haines, M. A. Pericak-Vance, G. D. Schellenberg, K. L. Lunetta, J.-W. Kim, J. D. Buxbaum, R. Mayeux, T. Ikezu, C. R. Abraham and L. A. Farrer
Journal
Annals of Neurology
Year
2014
Volume
76
Issue
3
Pages
379-392
Jin, S.C., et al., Coding variants in TREM2 increase risk for Alzheimer's disease. Human Molecular Genetics, 2014. 23(21): p. 5838-5846.
Download
Title
Coding variants in TREM2 increase risk for Alzheimer's disease
Authors
S. C. Jin, B. A. Benitez, C. M. Karch, B. Cooper, T. Skorupa, D. Carrell, J. B. Norton, S. Hsu, O. Harari, Y. Cai, S. Bertelsen, A. M. Goate and C. Cruchaga
Journal
Human Molecular Genetics
Year
2014
Volume
23
Issue
21
Pages
5838-5846
Janicki, S.C., et al., Estrogen Receptor β Variants Modify Risk for Alzheimer's Disease in a Multiethnic Female Cohort. Journal of Alzheimer's Disease, 2014. 40(1): p. 83-93.
Download
Title
Estrogen Receptor β Variants Modify Risk for Alzheimer's Disease in a Multiethnic Female Cohort
Authors
S. C. Janicki, N. Park, R. Cheng, J. H. Lee, N. Schupf and L. N. Clark
Journal
Journal of Alzheimer's Disease
Year
2014
Volume
40
Issue
1
Pages
83-93
Hooli, B.V., et al., The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk. Neurology, 2014. 83(15): p. 1353-8.
Download
Title
The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk
Authors
B. V. Hooli, A. R. Parrado, K. Mullin, W. K. Yip, T. Liu, J. T. Roehr, D. Qiao, F. Jessen, O. Peters, T. Becker, A. Ramirez, C. Lange, L. Bertram and R. E. Tanzi
Journal
Neurology
Year
2014
Volume
83
Issue
15
Pages
1353-8
Hohman, T.J., et al., Genetic variation modifies risk for neurodegeneration based on biomarker status. Frontiers in Aging Neuroscience, 2014. 6: p. 183.
Download
Title
Genetic variation modifies risk for neurodegeneration based on biomarker status
Authors
T. J. Hohman, M. E. I. Koran, T. A. Thornton-Wells and I. for the Alzheimer's Neuroimaging
Journal
Frontiers in Aging Neuroscience
Year
2014
Volume
6
Issue
Pages
183
Hohman, T.J., M.E.I. Koran, and T.A. Thornton-Wells, Genetic modification of the relationship between phosphorylated tau and neurodegeneration. Alzheimer's & Dementia, 2014. 10(6): p. 637-645.e1.
Download
Title
Genetic modification of the relationship between phosphorylated tau and neurodegeneration
Authors
T. J. Hohman, M. E. I. Koran and T. A. Thornton-Wells
Journal
Alzheimer's & Dementia
Year
2014
Volume
10
Issue
6
Pages
637-645.e1
Hohman, T.J., M.E.I. Koran, and T.A. Thornton-Wells, Interactions between GSK3β and amyloid genes explain variance in amyloid burden. Neurobiology of Aging, 2014. 35(3): p. 460-465.
Download
Title
Interactions between GSK3β and amyloid genes explain variance in amyloid burden
Authors
T. J. Hohman, M. E. I. Koran and T. A. Thornton-Wells
Journal
Neurobiology of Aging
Year
2014
Volume
35
Issue
3
Pages
460-465
Green, A.E., et al., A combined effect of two Alzheimer's risk genes on medial temporal activity during executive attention in young adults. Neuropsychologia, 2014. 56(0): p. 1-8.
Download
Title
A combined effect of two Alzheimer's risk genes on medial temporal activity during executive attention in young adults
Authors
A. E. Green, J. R. Gray, C. G. DeYoung, T. R. Mhyre, R. Padilla, A. M. DiBattista and G. William Rebeck
Journal
Neuropsychologia
Year
2014
Volume
56
Issue
0
Pages
42012
Graff-Radford, J., et al., Dementia with Lewy bodies: basis of cingulate island sign. Neurology, 2014. 83(9): p. 801-9.
Download
Title
Dementia with Lewy bodies: basis of cingulate island sign
Authors
J. Graff-Radford, M. E. Murray, V. J. Lowe, B. F. Boeve, T. J. Ferman, S. A. Przybelski, T. G. Lesnick, M. L. Senjem, J. L. Gunter, G. E. Smith, D. S. Knopman, C. R. Jack, Jr., D. W. Dickson, R. C. Petersen and K. Kantarci
Journal
Neurology
Year
2014
Volume
83
Issue
9
Pages
801-9
Gomar, J.J., et al., Extension and refinement of the predictive value of different classes of markers in ADNI: Four-year follow-up data. Alzheimer's & Dementia, 2014. 10(6): p. 704-712.
Download
Title
Extension and refinement of the predictive value of different classes of markers in ADNI: Four-year follow-up data
Authors
J. J. Gomar, C. Conejero-Goldberg, P. Davies and T. E. Goldberg
Journal
Alzheimer's & Dementia
Year
2014
Volume
10
Issue
6
Pages
704-712
Geda, Y.E., et al., Baseline Neuropsychiatric Symptoms and the Risk of Incident Mild Cognitive Impairment: A Population-Based Study. American Journal of Psychiatry, 2014. 171(5): p. 572-581.
Download
Title
Baseline Neuropsychiatric Symptoms and the Risk of Incident Mild Cognitive Impairment: A Population-Based Study
Authors
Y. E. Geda, R. O. Roberts, M. M. Mielke, D. S. Knopman, T. J. H. Christianson, V. S. Pankratz, B. F. Boeve, O. Sochor, E. G. Tangalos, R. C. Petersen and W. A. Rocca
Journal
American Journal of Psychiatry
Year
2014
Volume
171
Issue
5
Pages
572-581
Gao, S., et al., Mild Cognitive Impairment, Incidence, Progression, and Reversion: Findings from a Community-Based Cohort of Elderly African Americans. The American Journal of Geriatric Psychiatry, 2014. 22(7): p. 670-681.
Download
Title
Mild Cognitive Impairment, Incidence, Progression, and Reversion: Findings from a Community-Based Cohort of Elderly African Americans
Authors
S. Gao, F. W. Unverzagt, K. S. Hall, K. A. Lane, J. R. Murrell, A. M. Hake, V. Smith-Gamble and H. C. Hendrie
Journal
The American Journal of Geriatric Psychiatry
Year
2014
Volume
22
Issue
7
Pages
670-681
Fujioka, S., et al., A familial form of parkinsonism, dementia, and motor neuron disease: A longitudinal study. Parkinsonism & Related Disorders, 2014. 20(11): p. 1129-1134.
Download
Title
A familial form of parkinsonism, dementia, and motor neuron disease: A longitudinal study
Authors
S. Fujioka, B. F. Boeve, J. E. Parisi, P. Tacik, N. Aoki, A. J. Strongosky, M. Baker, M. Sanchez-Contreras, O. A. Ross, R. Rademakers, V. Sossi, D. W. Dickson, A. J. Stoessl and Z. K. Wszolek
Journal
Parkinsonism & Related Disorders
Year
2014
Volume
20
Issue
11
Pages
1129-1134
Fagan, A.M., et al., Longitudinal change in CSF biomarkers in autosomal-dominant Alzheimer disease. Science translational medicine, 2014. 6(226): p. 226ra30-226ra30.
Download
Title
Longitudinal change in CSF biomarkers in autosomal-dominant Alzheimer disease
Authors
A. M. Fagan, C. Xiong, M. S. Jasielec, R. J. Bateman, A. M. Goate, T. L. S. Benzinger, B. Ghetti, R. N. Martins, C. L. Masters, R. Mayeux, J. M. Ringman, M. N. Rossor, S. Salloway, P. R. Schofield, R. A. Sperling, D. Marcus, N. J. Cairns, V. D. Buckles, J. H. Ladenson, J. C. Morris, D. M. Holtzman and N. the Dominantly Inherited Alzheimer
Journal
Science translational medicine
Year
2014
Volume
6
Issue
226
Pages
226ra30-226ra30
Escott-Price, V., et al., Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease. PLoS One, 2014. 9(6): p. e94661.
Download
Title
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease
Authors
V. Escott-Price, C. Bellenguez, L.-S. Wang, S.-H. Choi, D. Harold, L. Jones, P. Holmans, A. Gerrish, A. Vedernikov, A. Richards, A. L. DeStefano, J.-C. Lambert, C. A. Ibrahim-Verbaas, A. C. Naj, R. Sims, G. Jun, J. C. Bis, G. W. Beecham, B. Grenier-Boley, G. Russo, T. A. Thornton-Wells, N. Denning, A. V. Smith, V. Chouraki, C. Thomas, M. A. Ikram, D. Zelenika, B. N. Vardarajan, Y. Kamatani, C.-F. Lin, H. Schmidt, B. Kunkle, M. L. Dunstan, M. Vronskaya, A. D. Johnson, A. Ruiz, M.-T. Bihoreau, C. Reitz, F. Pasquier, P. Hollingworth, O. Hanon, A. L. Fitzpatrick, J. D. Buxbaum, D. Campion, P. K. Crane, C. Baldwin, T. Becker, V. Gudnason, C. Cruchaga, D. Craig, N. Amin, C. Berr, O. L. Lopez, P. L. De Jager, V. Deramecourt, J. A. Johnston, D. Evans, S. Lovestone, L. Letenneur, I. Hernández, D. C. Rubinsztein, G. Eiriksdottir, K. Sleegers, A. M. Goate, N. Fiévet, M. J. Huentelman, M. Gill, K. Brown, M. I. Kamboh, L. Keller, P. Barberger-Gateau, B. McGuinness, E. B. Larson, A. J. Myers, C. Dufouil, S. Todd, D. Wallon, S. Love, E. Rogaeva, J. Gallacher, P. S. George-Hyslop, J. Clarimon, A. Lleo, A. Bayer, D. W. Tsuang, L. Yu, M. Tsolaki, P. Bossù, G. Spalletta, P. Proitsi, J. Collinge, S. Sorbi, F. S. Garcia, N. C. Fox, J. Hardy, M. C. D. Naranjo, P. Bosco, R. Clarke, C. Brayne, D. Galimberti, E. Scarpini, U. Bonuccelli, M. Mancuso, G. Siciliano, S. Moebus, P. Mecocci, M. D. Zompo, W. Maier, H. Hampel, A. Pilotto, A. Frank-García, F. Panza, V. Solfrizzi, P. Caffarra, B. Nacmias, W. Perry, M. Mayhaus, L. Lannfelt, H. Hakonarson, S. Pichler, M. M. Carrasquillo, M. Ingelsson, D. Beekly, V. Alvarez, F. Zou, O. Valladares, S. G. Younkin, E. Coto, K. L. Hamilton-Nelson, W. Gu, C. Razquin, P. Pastor, I. Mateo, M. J. Owen, K. M. Faber, P. V. Jonsson, O. Combarros, M. C. O'Donovan, L. B. Cantwell, H. Soininen, D. Blacker, S. Mead, T. H. Mosley, Jr., D. A. Bennett, T. B. Harris, L. Fratiglioni, C. Holmes, R. F. A. G. de Bruijn, P. Passmore, T. J. Montine, K. Bettens, J. I. Rotter, A. Brice, K. Morgan, T. M. Foroud, W. A. Kukull, D. Hannequin, J. F. Powell, M. A. Nalls, K. Ritchie, K. L. Lunetta, J. S. K. Kauwe, E. Boerwinkle, M. Riemenschneider, M. Boada, M. Hiltunen, E. R. Martin, R. Schmidt, D. Rujescu, J.-F. Dartigues, R. Mayeux, C. Tzourio, A. Hofman, M. M. Nöthen, C. Graff, B. M. Psaty, J. L. Haines, M. Lathrop, M. A. Pericak-Vance, L. J. Launer, C. Van Broeckhoven, L. A. Farrer, C. M. van Duijn, A. Ramirez, S. Seshadri, G. D. Schellenberg, P. Amouyel, J. Williams and C. the United Kingdom Brain Expression
Journal
PLoS One
Year
2014
Volume
9
Issue
6
Pages
e94661
Edmonds, E.C., et al., Subjective cognitive complaints contribute to misdiagnosis of mild cognitive impairment. J Int Neuropsychol Soc, 2014. 20(8): p. 836-47.
Download
Title
Subjective cognitive complaints contribute to misdiagnosis of mild cognitive impairment
Authors
E. C. Edmonds, L. Delano-Wood, D. R. Galasko, D. P. Salmon and M. W. Bondi
Journal
J Int Neuropsychol Soc
Year
2014
Volume
20
Issue
8
Pages
836-47
DeFerrari, G.V., et al., Overrepresentation of Glutamate Signaling in Alzheimer's Disease: Network-Based Pathway Enrichment using Meta-analysis of Genome-Wide Association Studies. PLoS One, 2014.
Download
Title
Overrepresentation of Glutamate Signaling in Alzheimer's Disease: Network-Based Pathway Enrichment Using Meta-Analysis of Genome-Wide Association Studies
Authors
G. V. DeFerrari, E. Pérez-Palma, B. I. Bustos, C. Villamán, M. A. Alarcón, M. E. Avila, G. D. Ugarte, A. E. Reyes and C. Opazo
Journal
Year
2014
Volume
Issue
Pages
Cruchaga, C., et al., Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer/'s disease. Nature, 2014. advance online publication.
Download
Title
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer/'s disease
Authors
C. Cruchaga, C. M. Karch, S. C. Jin, B. A. Benitez, Y. Cai, R. Guerreiro, O. Harari, J. Norton, J. Budde, S. Bertelsen, A. T. Jeng, B. Cooper, T. Skorupa, D. Carrell, D. Levitch, S. Hsu, J. Choi, M. Ryten, U. K. B. E. Consortium, C. Sassi, J. Bras, J. R. Gibbs, D. G. Hernandez, M. K. Lupton, J. Powell, P. Forabosco, P. G. Ridge, C. D. Corcoran, J. T. Tschanz, M. C. Norton, R. G. Munger, C. Schmutz, M. Leary, F. Y. Demirci, M. N. Bamne, X. Wang, O. L. Lopez, M. Ganguli, C. Medway, J. Turton, J. Lord, A. Braae, I. Barber, K. Brown, U. K. C. The Alzheimer/'s Research, P. Pastor, O. Lorenzo-Betancor, Z. Brkanac, E. Scott, E. Topol, K. Morgan, E. Rogaeva, A. B. Singleton, J. Hardy, M. I. Kamboh, P. St George-Hyslop, N. Cairns, J. C. Morris, J. S. K. Kauwe and A. M. Goate
Journal
Nature
Year
2014
Volume
advance online publication
Issue
Pages
Chouraki, V., et al., A genome-wide association meta-analysis of plasma A[beta] peptides concentrations in the elderly. Mol Psychiatry, 2014. 19(12): p. 1326-1335.
Download
Title
A genome-wide association meta-analysis of plasma A[beta] peptides concentrations in the elderly
Authors
V. Chouraki, R. F. A. G. De Bruijn, J. Chapuis, J. C. Bis, C. Reitz, S. Schraen, C. A. Ibrahim-Verbaas, B. Grenier-Boley, C. Delay, R. Rogers, F. Demiautte, A. Mounier, A. L. Fitzpatrick, C. Berr, J. F. Dartigues, A. G. Uitterlinden, A. Hofman, M. Breteler, J. T. Becker, M. Lathrop, N. Schupf, A. Alperovitch, R. Mayeux, C. M. van Duijn, L. Buee, P. Amouyel, O. L. Lopez, M. A. Ikram, C. Tzourio and J. C. Lambert
Journal
Mol Psychiatry
Year
2014
Volume
19
Issue
12
Pages
1326-1335
Chang, Y.-L., et al., APOE interacts with age to modify rate of decline in cognitive and brain changes in Alzheimer's disease. Alzheimer's & Dementia, 2014. 10(3): p. 336-348.
Download
Title
APOE interacts with age to modify rate of decline in cognitive and brain changes in Alzheimer's disease
Authors
Y.-L. Chang, C. Fennema-Notestine, D. Holland, L. K. McEvoy, N. H. Stricker, D. P. Salmon, A. M. Dale and M. W. Bondi
Journal
Alzheimer's & Dementia
Year
2014
Volume
10
Issue
3
Pages
336-348
Cao, Y., et al., A Versatile Omnibus Test for Detecting Mean and Variance Heterogeneity. Genetic epidemiology, 2014. 38(1): p. 51-59.
Download
Title
A Versatile Omnibus Test for Detecting Mean and Variance Heterogeneity
Authors
Y. Cao, P. Wei, M. Bailey, J. S. K. Kauwe and T. J. Maxwell
Journal
Genetic epidemiology
Year
2014
Volume
38
Issue
1
Pages
51-59
Benitez, B.A., et al., Missense variant in TREML2 protects against Alzheimer’s Disease. Neurobiology of Aging, 2014.
Download
Title
Missense variant in TREML2 protects against Alzheimer’s Disease
Authors
B. A. Benitez, S. C. Jin, R. Guerreiro, R. Graham, J. Lord, D. Harold, R. Sims, J.-C. Lambert, J. R. Gibbs, J. Bras, C. Sassi, O. Harari, S. Bertelsen, M. K. Lupton, J. Powell, C. Bellenguez, K. Brown, C. Medway, P. C. G. Haddick, M. P. van der Brug, T. Bhangale, W. Ortmann, T. Behrens, R. Mayeux, M. A. Pericak-Vance, L. A. Farrer, G. D. Schellenberg, J. L. Haines, J. Turton, A. Braae, I. Barber, A. M. Fagan, D. M. Holtzman, J. C. Morris, J. Williams, J. Kauwe, P. Amouyel, K. Morgan, A. Singleton, J. Hardy, A. M. Goate and C. Cruchaga
Journal
Neurobiology of Aging
Year
2014
Volume
Issue
Pages
Beecham, G.W., et al., Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias. PLoS Genet, 2014. 10(9): p. e1004606.
Download
Title
Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias
Authors
G. W. Beecham, K. Hamilton, A. C. Naj, E. R. Martin, M. Huentelman, A. J. Myers, J. J. Corneveaux, J. Hardy, J.-P. Vonsattel, S. G. Younkin, D. A. Bennett, P. L. De Jager, E. B. Larson, P. K. Crane, M. I. Kamboh, J. K. Kofler, D. C. Mash, L. Duque, J. R. Gilbert, H. Gwirtsman, J. D. Buxbaum, P. Kramer, D. W. Dickson, L. A. Farrer, M. P. Frosch, B. Ghetti, J. L. Haines, B. T. Hyman, W. A. Kukull, R. P. Mayeux, M. A. Pericak-Vance, J. A. Schneider, J. Q. Trojanowski, E. M. Reiman, G. D. Schellenberg, T. J. Montine and C. the Alzheimer's Disease Genetics
Journal
PLoS Genet
Year
2014
Volume
10
Issue
9
Pages
e1004606
Barral, S., et al., Genetic variants in a ‘cAMP element binding protein’ (CREB)-dependent histone acetylation pathway influence memory performance in cognitively healthy elderly individuals. Neurobiology of Aging, 2014. 35(12): p. 2881.e7-2881.e10.
Download
Title
Genetic variants in a ‘cAMP element binding protein’ (CREB)-dependent histone acetylation pathway influence memory performance in cognitively healthy elderly individuals
Authors
S. Barral, C. Reitz, S. A. Small and R. Mayeux
Journal
Neurobiology of Aging
Year
2014
Volume
35
Issue
12
Pages
2881.e7-2881.e10
Barral, S., et al., COmmon genetic variants on 6q24 associated with exceptional episodic memory performance in the elderly. JAMA Neurology, 2014. 71(12): p. 1514-1519.
Download
Title
COmmon genetic variants on 6q24 associated with exceptional episodic memory performance in the elderly
Authors
S. Barral, S. Cosentino, K. Christensen and et al.
Journal
JAMA Neurology
Year
2014
Volume
71
Issue
12
Pages
1514-1519
Allen, M., et al., Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels. Alzheimer's Research & Therapy, 2014. 6(4): p. 39.
Download
Title
Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels
Authors
M. Allen, M. Kachadoorian, Z. Quicksall, F. Zou, H. Chai, C. Younkin, J. Crook, V. Pankratz, M. Carrasquillo, S. Krishnan, T. Nguyen, L. Ma, K. Malphrus, S. Lincoln, G. Bisceglio, C. Kolbert, J. Jen, S. Mukherjee, J. Kauwe, P. Crane, J. Haines, R. Mayeux, M. Pericak-Vance, L. Farrer, G. Schellenberg, J. Parisi, R. Petersen, N. Graff-Radford, D. Dickson, S. Younkin and N. Ertekin-Taner
Journal
Alzheimer's Research & Therapy
Year
2014
Volume
6
Issue
4
Pages
39
(IGAP), I.G.o.A.s.D.C., Convergent genetic and expression data implicate immunity in Alzheimer's disease. Alzheimer's & Dementia, 2014(0).
Download
Title
Convergent genetic and expression data implicate immunity in Alzheimer's disease
Authors
I. G. o. A. s. D. C. (IGAP)
Journal
Alzheimer's & Dementia
Year
2014
Volume
Issue
0
Pages
Whitwell, J.L., et al., Frontal asymmetry in behavioral variant FTD: clinicoimaging & pathogenetic correlates. Neurobiology of Aging, 2013. 34(2): p. 636-639.
Download
Title
Frontal asymmetry in behavioral variant FTD: clinicoimaging & pathogenetic correlates
Authors
J. L. Whitwell, J. Xu, J. Mandrekar, B. F. Boeve, D. S. Knopman, J. E. Parisi, M. L. Senjem, D. W. Dickson, R. C. Petersen, R. Rademakers, C. R. Jack and K. A. Josephs
Journal
Neurobiology of Aging
Year
2013
Volume
34
Issue
2
Pages
636-639
Weiner, M.W., et al., The Alzheimer's Disease Neuroimaging Initiative: a review of papers published since its inception. Alzheimers Dement, 2013. 8(1 Suppl): p. S1-68.
Download
Title
The Alzheimer's Disease Neuroimaging Initiative: a review of papers published since its inception
Authors
M. W. Weiner, D. P. Veitch, P. S. Aisen, L. A. Beckett, N. J. Cairns, R. C. Green, D. Harvey, C. R. Jack, W. Jagust, E. Liu, J. C. Morris, R. C. Petersen, A. J. Saykin, M. E. Schmidt, L. Shaw, J. A. Siuciak, H. Soares, A. W. Toga and J. Q. Trojanowski
Journal
Alzheimers Dement
Year
2013
Volume
8
Issue
1 Suppl
Pages
S1-68
Thambisetty, M., et al., Effect of Complement CR1 on Brain Amyloid Burden During Aging and Its Modification by APOE Genotype. Biological Psychiatry, 2013. 73(5): p. 422-428.
Download
Title
Effect of Complement CR1 on Brain Amyloid Burden During Aging and Its Modification by APOE Genotype
Authors
M. Thambisetty, Y. An, M. Nalls, J. Sojkova, S. Swaminathan, Y. Zhou, A. B. Singleton, D. F. Wong, L. Ferrucci, A. J. Saykin and S. M. Resnick
Journal
Biological Psychiatry
Year
2013
Volume
73
Issue
5
Pages
422-428
Spina, S., et al., Phenotypic variability in three families with valosin-containing protein mutation. Eur J Neurol, 2013. 20(2): p. 251-8.
Download
Title
Phenotypic variability in three families with valosin-containing protein mutation
Authors
S. Spina, A. D. Van Laar, J. R. Murrell, R. L. Hamilton, J. K. Kofler, F. Epperson, M. R. Farlow, O. L. Lopez, J. Quinlan, S. T. DeKosky and B. Ghetti
Journal
Eur J Neurol
Year
2013
Volume
20
Issue
2
Pages
251-8
Shulman, J.M., et al., Genetic susceptibility for alzheimer disease neuritic plaque pathology. JAMA Neurology, 2013. 70(9): p. 1150-1157.
Download
Title
Genetic susceptibility for alzheimer disease neuritic plaque pathology
Authors
J. M. Shulman, K. Chen, B. T. Keenan and et al.
Journal
JAMA Neurology
Year
2013
Volume
70
Issue
9
Pages
1150-1157
Shen, L., et al., Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers. Brain Imaging and Behavior, 2013: p. 1-25.
Download
Title
Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers
Authors
L. Shen, P. Thompson, S. Potkin, L. Bertram, L. Farrer, T. Foroud, R. Green, X. Hu, M. Huentelman, S. Kim, J. K. Kauwe, Q. Li, E. Liu, F. Macciardi, J. Moore, L. Munsie, K. Nho, V. Ramanan, S. Risacher, D. Stone, S. Swaminathan, A. Toga, M. Weiner and A. Saykin
Journal
Brain Imaging and Behavior
Year
2013
Volume
Issue
Pages
42029
Ridge, P.G., et al., Alzheimer's Disease: Analyzing the Missing Heritability PLOS One, 2013.
Download
Title
Alzheimer's Disease: Analyzing the Missing Heritability
Authors
P. G. Ridge, S. Mukherjee, P. Crane, J. S. Kauwe and A. s. D. Consortium
Journal
PLOS One
Year
2013
Volume
Issue
Pages
Ridge, P.G., et al., Mitochondrial Haplotypes Associated with Biomarkers for Alzheimer’s Disease. PLoS One, 2013. 8(9): p. e74158.
Download
Title
Mitochondrial Haplotypes Associated with Biomarkers for Alzheimer’s Disease
Authors
P. G. Ridge, A. Koop, T. J. Maxwell, M. H. Bailey, R. H. Swerdlow, J. S. K. Kauwe, R. A. Honea and I. for the Alzheimer’s Disease Neuroimaging
Journal
PLoS One
Year
2013
Volume
8
Issue
9
Pages
e74158
Reitz, C.M.D.P., et al., Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E [epsilon]4,and the Risk of Late-Onset Alzheimer Disease in African Americans. JAMA, 2013. 309(14): p. 1483-1492.
Download
Title
Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E [epsilon]4,and the Risk of Late-Onset Alzheimer Disease in African Americans
Authors
C. M. D. P. Reitz, G. P. Jun, A. P. Naj, R. M. P. H. Rajbhandary, B. N. P. Vardarajan, L.-S. P. Wang, O. M. S. Valladares, C.-F. P. Lin, E. B. M. D. M. P. H. Larson, N. R. M. D. Graff-Radford, D. M. D. Evans, P. L. M. D. P. De Jager, P. K. M. D. M. P. H. Crane, J. D. P. Buxbaum, J. R. P. Murrell, T. P. Raj, N. M. D. P. Ertekin-Taner, M. P. Logue, C. T. P. Baldwin, R. C. M. D. M. P. H. Green, L. L. P. Barnes, L. B. M. P. H. Cantwell, M. D. P. Fallin, R. C. P. Go, P. M. D. Griffith, T. O. M. D. Obisesan, J. J. P. Manly, K. L. P. Lunetta, M. I. P. Kamboh, O. L. M. D. Lopez, D. A. M. D. Bennett, H. M. B. C. D. Hendrie, K. S. P. Hall, A. M. P. Goate, G. S. P. Byrd, W. A. P. Kukull, T. M. P. Foroud, J. L. P. Haines, L. A. P. Farrer, M. A. P. Pericak-Vance, G. D. P. Schellenberg, R. M. D. M. Mayeux and C. for the Alzheimer Disease Genetics
Journal
JAMA
Year
2013
Volume
309
Issue
14
Pages
1483-1492
Reitz, C., et al., Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Transl Psychiatry Psychiatry, 2013. 3: p. e256.
Download
Title
Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)
Authors
C. Reitz, G. Tosto, B. Vardarajan, E. Rogaeva, M. Ghani, R. S. Rogers, C. Conrad, J. L. Haines, M. A. Pericak-Vance, M. D. Fallin, T. Foroud, L. A. Farrer, G. D. Schellenberg, P. S. George-Hyslop, R. Mayeux and C. Alzheimer's Disease Genetics
Journal
Transl Psychiatry Psychiatry
Year
2013
Volume
3
Issue
Pages
e256
Reitz, C., R. Mayeux, and C. Alzheimer's Disease Genetics, TREM2 and Neurodegenerative Disease. New England Journal of Medicine, 2013. 369(16): p. 1564-1570.
Download
Title
TREM2 and Neurodegenerative Disease
Authors
C. Reitz, R. Mayeux and C. Alzheimer's Disease Genetics
Journal
New England Journal of Medicine
Year
2013
Volume
369
Issue
16
Pages
1564-1570
Potter, R., et al., Increased in Vivo Amyloid-β42 Production, Exchange, and Loss in Presenilin Mutation Carriers. Science Translational Medicine, 2013. 5(189): p. 189ra77.
Download
Title
Increased in Vivo Amyloid-β42 Production, Exchange, and Loss in Presenilin Mutation Carriers
Authors
R. Potter, B. W. Patterson, D. L. Elbert, V. Ovod, T. Kasten, W. Sigurdson, K. Mawuenyega, T. Blazey, A. Goate, R. Chott, K. E. Yarasheski, D. M. Holtzman, J. C. Morris, T. L. S. Benzinger and R. J. Bateman
Journal
Science Translational Medicine
Year
2013
Volume
5
Issue
189
Pages
189ra77
Nho, K., et al., Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics. Mol Psychiatry, 2013. 18(7): p. 739-739.
Download
Title
Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics
Authors
K. Nho, J. J. Corneveaux, S. Kim, H. Lin, S. L. Risacher, L. Shen, S. Swaminathan, V. K. Ramanan, Y. Liu, T. Foroud, M. H. Inlow, A. L. Siniard, R. A. Reiman, P. S. Aisen, R. C. Petersen, R. C. Green, C. R. Jack, M. W. Weiner, C. T. Baldwin, K. Lunetta, L. A. Farrer, S. J. Furney, S. Lovestone, A. Simmons, P. Mecocci, B. Vellas, M. Tsolaki, I. Kloszewska, H. Soininen, B. C. McDonald, M. R. Farlow, B. Ghetti, M. J. Huentelman and A. J. Saykin
Journal
Mol Psychiatry
Year
2013
Volume
18
Issue
7
Pages
739-739
Nho, K., et al., Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment. Mol Psychiatry, 2013. 18(7): p. 781-787.
Download
Title
Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment
Authors
K. Nho, J. J. Corneveaux, S. Kim, H. Lin, S. L. Risacher, L. Shen, S. Swaminathan, V. K. Ramanan, Y. Liu, T. Foroud, M. H. Inlow, A. L. Siniard, R. A. Reiman, P. S. Aisen, R. C. Petersen, R. C. Green, C. R. Jack, M. W. Weiner, C. T. Baldwin, K. Lunetta, L. A. Farrer, S. J. Furney, S. Lovestone, A. Simmons, P. Mecocci, B. Vellas, M. Tsolaki, I. Kloszewska, H. Soininen, B. C. McDonald, M. R. Farlow, B. Ghetti, M. J. Huentelman and A. J. Saykin
Journal
Mol Psychiatry
Year
2013
Volume
18
Issue
7
Pages
781-787
Miyashita, A., et al., SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians. PLoS One, 2013. 8(4): p. e58618.
Download
Title
SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians
Authors
A. Miyashita, A. Koike, G. Jun, L.-S. Wang, S. Takahashi, E. Matsubara, T. Kawarabayashi, M. Shoji, N. Tomita, H. Arai, T. Asada, Y. Harigaya, M. Ikeda, M. Amari, H. Hanyu, S. Higuchi, T. Ikeuchi, M. Nishizawa, M. Suga, Y. Kawase, H. Akatsu, K. Kosaka, T. Yamamoto, M. Imagawa, T. Hamaguchi, M. Yamada, T. Moriaha, M. Takeda, T. Takao, K. Nakata, Y. Fujisawa, K. Sasaki, K. Watanabe, K. Nakashima, K. Urakami, T. Ooya, M. Takahashi, T. Yuzuriha, K. Serikawa, S. Yoshimoto, R. Nakagawa, J.-W. Kim, C.-S. Ki, H.-H. Won, D. L. Na, S. W. Seo, I. Mook-Jung, P. St. George-Hyslop, R. Mayeux, J. L. Haines, M. A. Pericak-Vance, M. Yoshida, N. Nishida, K. Tokunaga, K. Yamamoto, S. Tsuji, I. Kanazawa, Y. Ihara, G. D. Schellenberg, L. A. Farrer, R. Kuwano and C. The Alzheimer Disease Genetics
Journal
PLoS One
Year
2013
Volume
8
Issue
4
Pages
e58618
Meda, S.A., et al., Genetic interactions associated with 12-month atrophy in hippocampus and entorhinal cortex in Alzheimer's Disease Neuroimaging Initiative. Neurobiology of Aging, 2013. 34(5): p. 1518.e9-1518.e18.
Download
Title
Genetic interactions associated with 12-month atrophy in hippocampus and entorhinal cortex in Alzheimer's Disease Neuroimaging Initiative
Authors
S. A. Meda, M. E. I. Koran, J. R. Pryweller, J. N. Vega and T. A. Thornton-Wells
Journal
Neurobiology of Aging
Year
2013
Volume
34
Issue
5
Pages
1518.e9-1518.e18
Mattsson, N., et al., Effects of baseline CSF alpha-synuclein on regional brain atrophy rates in healthy elders, mild cognitive impairment and Alzheimer's disease. PLoS One, 2013. 8(12).
Download
Title
Effects of baseline CSF alpha-synuclein on regional brain atrophy rates in healthy elders, mild cognitive impairment and Alzheimer's disease
Authors
N. Mattsson, P. Insel, D. Tosun, J. Zhang, C. R. Jack, Jr., D. Galasko and M. Weiner
Journal
PLoS One
Year
2013
Volume
8
Issue
12
Pages
Lin, C.-F., et al., DRAW+SneakPeek: Analysis Workflow and Quality Metric Management for DNA-Seq Experiments. Bioinformatics, 2013.
Download
Title
DRAW+SneakPeek: Analysis Workflow and Quality Metric Management for DNA-Seq Experiments
Authors
C.-F. Lin, O. Valladares, D. M. Childress, E. Klevak, E. T. Geller, Y.-C. Hwang, E. A. Tsai, G. D. Schellenberg and L.-S. Wang
Journal
Bioinformatics
Year
2013
Volume
Issue
Pages
Lambert, J.C., et al., Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nature Genetics, 2013. Advanced Online Publication p. 1-9.
Download
Title
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Authors
J. C. Lambert, C. A. Ibrahim, D. Harold, A. C. Naj, R. Sims, C. Bellenguez, A. L. DeStefano, J. C. Bis, G. W. Beecham, B. Grenier-Boley, G. Russo, T. A. Thornton-Wells, N. Jones and E. al.
Journal
Nature Genetics
Year
2013
Volume
Advanced Online Publication
Issue
Pages
42013
Kohli, M.A., et al., Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians. Neurobiology of Aging, 2013. 34(5): p. 1519.e5-1519.e12.
Download
Title
Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians
Authors
M. A. Kohli, K. John-Williams, R. Rajbhandary, A. Naj, P. Whitehead, K. Hamilton, R. M. Carney, C. Wright, E. Crocco, H. E. Gwirtzman, R. Lang, G. Beecham, E. R. Martin, J. Gilbert, M. Benatar, G. W. Small, D. Mash, G. Byrd, J. L. Haines, M. A. Pericak-Vance and S. Züchner
Journal
Neurobiology of Aging
Year
2013
Volume
34
Issue
5
Pages
1519.e5-1519.e12
Kohannim, O., et al., Multilocus genetic profiling to empower drug trials and predict brain atrophy. NeuroImage: Clinical, 2013. 2(0): p. 827-835.
Download
Title
Multilocus genetic profiling to empower drug trials and predict brain atrophy
Authors
O. Kohannim, X. Hua, P. Rajagopalan, D. P. Hibar, N. Jahanshad, J. D. Grill, L. G. Apostolova, A. W. Toga, C. R. Jack Jr, M. W. Weiner and P. M. Thompson
Journal
NeuroImage: Clinical
Year
2013
Volume
2
Issue
0
Pages
827-835
Kim, S., et al., Influence of Genetic Variation on Plasma Protein Levels in Older Adults Using a Multi-Analyte Panel. PLoS One, 2013. 8(7): p. e70269.
Download
Title
Influence of Genetic Variation on Plasma Protein Levels in Older Adults Using a Multi-Analyte Panel
Authors
S. Kim, S. Swaminathan, M. Inlow, S. L. Risacher, K. Nho, L. Shen, T. M. Foroud, R. C. Petersen, P. S. Aisen, H. Soares, J. B. Toledo, L. M. Shaw, J. Q. Trojanowski, M. W. Weiner, B. C. McDonald, M. R. Farlow, B. Ghetti, A. J. Saykin and I. for the Alzheimer’s Disease Neuroimaging
Journal
PLoS One
Year
2013
Volume
8
Issue
7
Pages
e70269
Karch, C.M., et al., Novel progranulin variants do not disrupt progranulin secretion and cleavage. Neurobiology of Aging, 2013. 34(11): p. 2538-2540.
Download
Title
Novel progranulin variants do not disrupt progranulin secretion and cleavage
Authors
C. M. Karch, A. T. Jeng, T. Skorupa, C. Cruchaga and A. M. Goate
Journal
Neurobiology of Aging
Year
2013
Volume
34
Issue
11
Pages
2538-2540
Jonsson, T., et al., Variant of TREM2 associated with the risk of Alzheimer's disease. N Engl J Med, 2013. 368(2): p. 107-16.
Download
Title
Variant of TREM2 associated with the risk of Alzheimer's disease
Authors
T. Jonsson, H. Stefansson, S. Steinberg, I. Jonsdottir, P. V. Jonsson, J. Snaedal, S. Bjornsson, J. Huttenlocher, A. I. Levey, J. J. Lah, D. Rujescu, H. Hampel, I. Giegling, O. A. Andreassen, K. Engedal, I. Ulstein, S. Djurovic, C. Ibrahim-Verbaas, A. Hofman, M. A. Ikram, C. M. van Duijn, U. Thorsteinsdottir, A. Kong and K. Stefansson
Journal
N Engl J Med
Year
2013
Volume
368
Issue
2
Pages
107-16
Janicki, S.C., et al., Aromatase Variants Modify Risk for Alzheimer’s Disease in a Multiethnic Female Cohort. Dementia and geriatric cognitive disorders, 2013. 35(0): p. 340-346.
Download
Title
Aromatase Variants Modify Risk for Alzheimer’s Disease in a Multiethnic Female Cohort
Authors
S. C. Janicki, N. Park, R. Cheng, N. Schupf, L. N. Clark and J. H. Lee
Journal
Dementia and geriatric cognitive disorders
Year
2013
Volume
35
Issue
0
Pages
340-346
Jahanshad, N., et al., Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity. Proceedings of the National Academy of Sciences, 2013. 110(12): p. 4768-4773.
Download
Title
Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity
Authors
N. Jahanshad, P. Rajagopalan, X. Hua, D. P. Hibar, T. M. Nir, A. W. Toga, C. R. Jack, A. J. Saykin, R. C. Green, M. W. Weiner, S. E. Medland, G. W. Montgomery, N. K. Hansell, K. L. McMahon, G. I. de Zubicaray, N. G. Martin, M. J. Wright, P. M. Thompson and t. A. s. D. N. Initiative
Journal
Proceedings of the National Academy of Sciences
Year
2013
Volume
110
Issue
12
Pages
4768-4773
Iakoubov, L., et al., A Common Copy Number Variation (CNV) Polymorphism in the <italic>CNTNAP4</italic> Gene: Association with Aging in Females. PLoS One, 2013. 8(11): p. e79790.
Download
Title
A Common Copy Number Variation (CNV) Polymorphism in the &#60;italic&#62;CNTNAP4&#60;/italic&#62; Gene: Association with Aging in Females
Authors
L. Iakoubov, M. Mossakowska, M. Szwed, Z. Duan, F. Sesti and M. Puzianowska-Kuznicka
Journal
PLoS One
Year
2013
Volume
8
Issue
11
Pages
e79790
Hooli, B.V., et al., Rare autosomal copy number variations in early-onset familial Alzheimer/'s disease. Mol Psychiatry, 2013.
Download
Title
Rare autosomal copy number variations in early-onset familial Alzheimer/'s disease
Authors
B. V. Hooli, Z. M. Kovacs-Vajna, K. Mullin, M. A. Blumenthal, M. Mattheisen, C. Zhang, C. Lange, G. Mohapatra, L. Bertram and R. E. Tanzi
Journal
Mol Psychiatry
Year
2013
Volume
Issue
Pages
Honea, R.A., et al., Characterizing the Role of Brain Derived Neurotrophic Factor Genetic Variation in Alzheimer’s Disease Neurodegeneration. PLoS One, 2013. 8(9): p. e76001.
Download
Title
Characterizing the Role of Brain Derived Neurotrophic Factor Genetic Variation in Alzheimer’s Disease Neurodegeneration
Authors
R. A. Honea, C. Cruchaga, R. D. Perea, A. J. Saykin, J. M. Burns, D. R. Weinberger, A. M. Goate and I. For the Alzheimer’s Disease Neuroimaging
Journal
PLoS One
Year
2013
Volume
8
Issue
9
Pages
e76001
Holton, P., et al., Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci. Annals of Human Genetics, 2013. 77(2): p. 85-105.
Download
Title
Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci
Authors
P. Holton, M. Ryten, M. Nalls, D. Trabzuni, M. E. Weale, D. Hernandez, H. Crehan, R. J. Gibbs, R. Mayeux, J. L. Haines, L. A. Farrer, M. A. Pericak-Vance, G. D. Schellenberg, C. The Alzheimer's Disease Genetics, M. Ramirez-Restrepo, A. Engel, A. J. Myers, J. J. Corneveaux, M. J. Huentelman, A. Dillman, M. R. Cookson, E. M. Reiman, A. Singleton, J. Hardy and R. Guerreiro
Journal
Annals of Human Genetics
Year
2013
Volume
77
Issue
2
Pages
85-105
Hibar, D., et al., Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects. Brain Imaging and Behavior, 2013. 7(2): p. 102-115.
Download
Title
Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects
Authors
D. Hibar, J. Stein, A. Ryles, O. Kohannim, N. Jahanshad, S. Medland, N. Hansell, K. McMahon, G. Zubicaray, G. Montgomery, N. Martin, M. Wright, A. Saykin, C. Jack, Jr., M. Weiner, A. Toga and P. Thompson
Journal
Brain Imaging and Behavior
Year
2013
Volume
7
Issue
2
Pages
102-115
Harms, M.M.D., et al., C9orf72 Hexanucleotide Repeat Expansions in Clinical Alzheimer Disease. JAMA Neurology, 2013. 70(6): p. 736-741.
Download
Title
C9orf72 Hexanucleotide Repeat Expansions in Clinical Alzheimer Disease
Authors
M. M. D. Harms, B. A. M. D. Benitez, N. P. Cairns, B. B. S. Cooper, P. B. S. Cooper, K. B. A. Mayo, D. B. S. Carrell, K. M. S. Faber, J. M. S. Williamson, T. M. D. Bird, R. M. D. Diaz-Arrastia, T. M. P. Foroud, B. F. M. D. Boeve, N. R. M. Graff-Radford, R. M. D. M. S. Mayeux, S. M. S. Chakraverty, A. M. P. Goate, C. P. Cruchaga and N. I. A. L. F. S. C. for the
Journal
JAMA Neurology
Year
2013
Volume
70
Issue
6
Pages
736-741
Guffanti, G., et al., Increased CNV-Region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sample. Genomics, 2013. 102(2): p. 112-122.
Download
Title
Increased CNV-Region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sample
Authors
G. Guffanti, F. Torri, J. Rasmussen, A. P. Clark, A. Lakatos, J. A. Turner, J. H. Fallon, A. J. Saykin, M. Weiner, M. P. Vawter, J. A. Knowles, S. G. Potkin and F. Macciardi
Journal
Genomics
Year
2013
Volume
102
Issue
2
Pages
112-122
Guerreiro, R., A. Wojtas, and J. Bras, Supplement to: TREM2 variants in Alzheimer's disease. New England Journal of Medicine January, 2013. 368: p. 2.
Download
Title
Supplement to: TREM2 variants in Alzheimer's disease
Authors
R. Guerreiro, A. Wojtas and J. Bras
Journal
New England Journal of Medicine January
Year
2013
Volume
368
Issue
Pages
2
Giraldo, M., et al., Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease. Neurobiology of Aging, 2013. 34(8): p. 2077.e11-2077.e18.
Download
Title
Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease
Authors
M. Giraldo, F. Lopera, A. L. Siniard, J. J. Corneveaux, I. Schrauwen, J. Carvajal, C. Muñoz, M. Ramirez-Restrepo, C. Gaiteri, A. J. Myers, R. J. Caselli, K. S. Kosik, E. M. Reiman and M. J. Huentelman
Journal
Neurobiology of Aging
Year
2013
Volume
34
Issue
8
Pages
2077.e11-2077.e18
Fjell, A.M., et al., Brain changes in older adults at very low risk for Alzheimer's disease. J Neurosci, 2013. 33(19): p. 8237-42.
Download
Title
Brain changes in older adults at very low risk for Alzheimer's disease
Authors
A. M. Fjell, L. McEvoy, D. Holland, A. M. Dale and K. B. Walhovd
Journal
J Neurosci
Year
2013
Volume
33
Issue
19
Pages
8237-42
Farlow, J. and T. Foroud, The Genetics of Dementia Seminars in Neurology 2013. 33: p. 417-422.
Download
Title
The Genetics of Dementia
Authors
J. Farlow and T. Foroud
Journal
Seminars in Neurology
Year
2013
Volume
33
Issue
Pages
417-422
Cruchaga, C., et al., GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer s Disease. Neuron, 2013. 78(2): p. 256-268.
Download
Title
GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer s Disease
Authors
C. Cruchaga, John S. K. Kauwe, O. Harari, Sheng C. Jin, Y. Cai, Celeste M. Karch, Bruno A. Benitez, Amanda T. Jeng, T. Skorupa, D. Carrell, S. Bertelsen, M. Bailey, D. McKean, Joshua M. Shulman, Philip L. De Jager, L. Chibnik, David A. Bennett, Steve E. Arnold, D. Harold, R. Sims, A. Gerrish, J. Williams, Vivianna M. Van Deerlin, Virginia M. Y. Lee, Leslie M. Shaw, John Q. Trojanowski, Jonathan L. Haines, R. Mayeux, Margaret A. Pericak-Vance, Lindsay A. Farrer, Gerard D. Schellenberg, Elaine R. Peskind, D. Galasko, Anne M. Fagan, David M. Holtzman, John C. Morris and Alison M. Goate
Journal
Neuron
Year
2013
Volume
78
Issue
2
Pages
256-268
Chhatwal, J.P.M.D.P., et al., Impaired default network functional connectivity in autosomal dominant Alzheimer disease. Neurology, 2013. 81(8): p. 736-744.
Download
Title
Impaired default network functional connectivity in autosomal dominant Alzheimer disease
Authors
J. P. M. D. P. Chhatwal, A. P. P. Schultz, K. M. D. Johnson, T. L. S. M. D. P. Benzinger, C. J. M. D. Jack, B. M. M. D. P. Ances, C. A. B. A. Sullivan, S. P. M. D. Salloway, J. M. M. D. Ringman, R. A. P. Koeppe, D. S. P. Marcus, P. P. Thompson, A. J. P. Saykin, S. P. Correia, P. R. P. D. Schofield, C. C. M. D. Rowe, N. C. M. D. Fox, A. M. P. Brickman, R. M. D. Mayeux, E. D. O. McDade, R. M. D. Bateman, A. M. P. Fagan, A. M. D. Goate, C. P. Xiong, V. D. P. Buckles, J. C. M. D. Morris and R. A. M. D. Sperling
Journal
Neurology
Year
2013
Volume
81
Issue
8
Pages
736-744
Chapman, J., et al., A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics, 2013. 22(4): p. 816-824.
Download
Title
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk
Authors
J. Chapman, E. Rees, D. Harold, D. Ivanov, A. Gerrish, R. Sims, P. Hollingworth, A. Stretton, P. Holmans, M. J. Owen, M. C. O'Donovan, J. Williams and G. Kirov
Journal
Human Molecular Genetics
Year
2013
Volume
22
Issue
4
Pages
816-824
Bryant, C., et al., Mapping the Genetic Variation of Regional Brain Volumes as Explained by All Common SNPs from the ADNI Study. PLoS One, 2013. 8(8): p. e71723.
Download
Title
Mapping the Genetic Variation of Regional Brain Volumes as Explained by All Common SNPs from the ADNI Study
Authors
C. Bryant, K. S. Giovanello, J. G. Ibrahim, J. Chang, D. Shen, B. S. Peterson, H. Zhu and I. for The Alzheimer's Disease Neuroimaging
Journal
PLoS One
Year
2013
Volume
8
Issue
8
Pages
e71723
Bradshaw, E.M., et al., CD33 Alzheimer’s disease locus: Altered monocyte function and amyloid biology. Nature neuroscience, 2013. 16(7): p. 10.1038/nn.3435.
Download
Title
CD33 Alzheimer’s disease locus: Altered monocyte function and amyloid biology
Authors
E. M. Bradshaw, L. B. Chibnik, B. T. Keenan, L. Ottoboni, T. Raj, A. Tang, L. L. Rosenkrantz, S. Imboywa, M. Lee, A. Von Korff, I. The Alzheimer’s Disease Neuroimaging, M. C. Morris, D. A. Evans, K. Johnson, R. A. Sperling, J. A. Schneider, D. A. Bennett and P. L. De Jager
Journal
Nature neuroscience
Year
2013
Volume
16
Issue
7
Pages
10.1038/nn.3435
Boada, M., et al., ATP5H/KCTD2 locus is associated with Alzheimer's disease risk. Mol Psychiatry, 2013.
Download
Title
ATP5H/KCTD2 locus is associated with Alzheimer's disease risk
Authors
M. Boada, C. Antunez, R. Ramirez-Lorca, A. L. DeStefano, A. Gonzalez-Perez, J. Gayan, J. Lopez-Arrieta, M. A. Ikram, I. Hernandez, J. Marin, J. J. Galan, J. C. Bis, A. Mauleon, M. Rosende-Roca, C. Moreno-Rey, V. Gudnasson, F. J. Moron, J. Velasco, J. M. Carrasco, M. Alegret, A. Espinosa, G. Vinyes, A. Lafuente, L. Vargas, A. L. Fitzpatrick, L. J. Launer, M. E. Saez, E. Vazquez, J. T. Becker, O. L. Lopez, M. Serrano-Rios, L. Tarraga, C. M. van Duijn, L. M. Real, S. Seshadri and A. Ruiz
Journal
Mol Psychiatry
Year
2013
Volume
Issue
Pages
Benzinger, T.L.S., et al., Regional variability of imaging biomarkers in autosomal dominant Alzheimer’s disease. Proceedings of the National Academy of Sciences, 2013. 110(47): p. E4502-E4509.
Download
Title
Regional variability of imaging biomarkers in autosomal dominant Alzheimer’s disease
Authors
T. L. S. Benzinger, T. Blazey, C. R. Jack, R. A. Koeppe, Y. Su, C. Xiong, M. E. Raichle, A. Z. Snyder, B. M. Ances, R. J. Bateman, N. J. Cairns, A. M. Fagan, A. Goate, D. S. Marcus, P. S. Aisen, J. J. Christensen, L. Ercole, R. C. Hornbeck, A. M. Farrar, P. Aldea, M. S. Jasielec, C. J. Owen, X. Xie, R. Mayeux, A. Brickman, E. McDade, W. Klunk, C. A. Mathis, J. Ringman, P. M. Thompson, B. Ghetti, A. J. Saykin, R. A. Sperling, K. A. Johnson, S. Salloway, S. Correia, P. R. Schofield, C. L. Masters, C. Rowe, V. L. Villemagne, R. Martins, S. Ourselin, M. N. Rossor, N. C. Fox, D. M. Cash, M. W. Weiner, D. M. Holtzman, V. D. Buckles, K. Moulder and J. C. Morris
Journal
Proceedings of the National Academy of Sciences
Year
2013
Volume
110
Issue
47
Pages
E4502-E4509
Benitez, B.A., et al., The PSEN1, p.E318G Variant Increases the Risk of Alzheimer's Disease in APOE-ε4 Carriers. PLoS Genet, 2013. 9(8): p. e1003685.
Download
Title
The PSEN1, p.E318G Variant Increases the Risk of Alzheimer's Disease in APOE-ε4 Carriers
Authors
B. A. Benitez, C. M. Karch, Y. Cai, S. C. Jin, B. Cooper, D. Carrell, S. Bertelsen, L. Chibnik, J. A. Schneider, D. A. Bennett, A. M. Fagan, D. Holtzman, J. C. Morris, A. M. Goate, C. Cruchaga, I. Alzheimer's Disease Neuroimaging, Genetic and C. Environmental Risk for Alzheimer's Disease
Journal
PLoS Genet
Year
2013
Volume
9
Issue
8
Pages
e1003685
Barral, S., et al., Exceptional memory performance in the Long Life Family Study (LLFS). Neurobiology of aging, 2013. 34(11): p. 2445-2448.
Download
Title
Exceptional memory performance in the Long Life Family Study (LLFS)
Authors
S. Barral, S. Cosentino, R. Costa, S. L. Andersen, K. Christensen, J. H. Eckfeldt, A. N. Newman, T. T. Perls, M. A. Province, E. C. Hadley, W. K. Rossi and R. Mayeux
Journal
Neurobiology of aging
Year
2013
Volume
34
Issue
11
Pages
2445-2448
Zou, F., et al., Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants. PLoS Genet, 2012. 8(6): p. e1002707.
Download
Title
Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants
Authors
F. Zou, H. S. Chai, C. S. Younkin, M. Allen, J. Crook, V. S. Pankratz, M. M. Carrasquillo, C. N. Rowley, A. A. Nair, S. Middha, S. Maharjan, T. Nguyen, L. Ma, K. G. Malphrus, R. Palusak, S. Lincoln, G. Bisceglio, C. Georgescu, N. Kouri, C. P. Kolbert, J. Jen, J. L. Haines, R. Mayeux, M. A. Pericak-Vance, L. A. Farrer, G. D. Schellenberg, R. C. Petersen, N. R. Graff-Radford, D. W. Dickson, S. G. Younkin and N. Ertekin-Taner
Journal
PLoS Genet
Year
2012
Volume
8
Issue
6
Pages
e1002707
Xi, Z., et al., Investigation of C9orf72 in 4 Neurodegenerative Disorders. Archives of Neurology, 2012. 69(12): p. 1583-1590.
Download
Title
Investigation of C9orf72 in 4 Neurodegenerative Disorders
Authors
Z. Xi, L. Zinman, Y. Grinberg, D. Moreno, C. Sato, J. M. Bilbao, M. Ghani, I. Hernández, A. Ruiz, M. Boada, F. J. Morón, A. E. Lang, C. Marras, A. Bruni, R. Colao, R. G. Maletta, G. Puccio, I. Rainero, L. Pinessi, D. Galimberti, K. E. Morrison, C. Moorby, J. D. Stockton, M. Masellis, S. E. Black, L.-N. Hazrati, Y. Liang, J. van Haersma de With, L. Fornazzari, R. Villagra, R. Rojas-Garcia, J. Clarimón, R. Mayeux, J. Robertson, P. St George-Hyslop and E. Rogaeva
Journal
Archives of Neurology
Year
2012
Volume
69
Issue
12
Pages
1583-1590
Whitcomb, D.C., et al., Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Nat Genet, 2012. 44(12): p. 1349-54.
Download
Title
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis
Authors
D. C. Whitcomb, J. Larusch, A. M. Krasinskas, L. Klei, J. P. Smith, R. E. Brand, J. P. Neoptolemos, M. M. Lerch, M. Tector, B. S. Sandhu, N. M. Guda, L. Orlichenko, M. S. Albert, R. L. Albin, L. G. Apostolova, S. E. Arnold, C. T. Baldwin, R. Barber, L. L. Barnes, T. G. Beach, G. W. Beecham, D. Beekly, D. A. Bennett, E. H. Bigio, T. D. Bird, D. Blacker, A. Boxer, J. R. Burke, J. D. Buxbaum, N. J. Cairns, L. B. Cantwell, C. Cao, R. M. Carney, S. L. Carroll, H. C. Chui, D. G. Clark, D. H. Cribbs, E. A. Crocco, C. Cruchaga, C. Decarli, F. Y. Demirci, M. Dick, D. W. Dickson, R. Duara, N. Ertekin-Taner, K. M. Faber, K. B. Fallon, M. R. Farlow, S. Ferris, T. M. Foroud, M. P. Frosch, D. R. Galasko, M. Ganguli, M. Gearing, D. H. Geschwind, B. Ghetti, J. R. Gilbert, S. Gilman, J. D. Glass, A. M. Goate, N. R. Graff-Radford, R. C. Green, J. H. Growdon, H. Hakonarson, K. L. Hamilton-Nelson, R. L. Hamilton, L. E. Harrell, E. Head, L. S. Honig, C. M. Hulette, B. T. Hyman, G. A. Jicha, L. W. Jin, G. Jun, M. I. Kamboh, A. Karydas, J. A. Kaye, R. Kim, E. H. Koo, N. W. Kowall, J. H. Kramer, P. Kramer, W. A. Kukull, F. M. Laferla, J. J. Lah, J. B. Leverenz, A. I. Levey, G. Li, C. F. Lin, A. P. Lieberman, O. L. Lopez, K. L. Lunetta, C. G. Lyketsos, W. J. Mack, D. C. Marson, E. R. Martin, F. Martiniuk, D. C. Mash, E. Masliah, A. C. McKee, M. Mesulam, B. L. Miller, C. A. Miller, J. W. Miller, T. J. Montine, J. C. Morris, J. R. Murrell, A. C. Naj, J. M. Olichney, J. E. Parisi, E. Peskind, R. C. Petersen, A. Pierce, W. W. Poon, H. Potter, J. F. Quinn, A. Raj, M. Raskind, E. M. Reiman, B. Reisberg, C. Reitz, J. M. Ringman, E. D. Roberson, H. J. Rosen, R. N. Rosenberg, M. Sano, A. J. Saykin, J. A. Schneider, L. S. Schneider, W. W. Seeley, A. G. Smith, J. A. Sonnen, S. Spina, R. A. Stern, R. E. Tanzi, J. Q. Trojanowski, J. C. Troncoso, D. W. Tsuang, O. Valladares, V. M. Van Deerlin, L. J. Van Eldik, B. N. Vardarajan, H. V. Vinters, J. P. Vonsattel, L. S. Wang, S. Weintraub, K. A. Welsh-Bohmer, J. Williamson, R. L. Woltjer, C. B. Wright, S. G. Younkin, C. E. Yu, L. Yu, S. Alkaade, S. T. Amann, M. A. Anderson, J. Baillie, P. A. Banks, D. Conwell, G. A. Cote, P. B. Cotton, J. Disario, L. A. Farrer, C. E. Forsmark, M. Johnstone, T. B. Gardner, A. Gelrud, W. Greenhalf, J. L. Haines, D. J. Hartman, R. A. Hawes, C. Lawrence, M. Lewis, J. Mayerle, R. Mayeux, N. M. Melhem, M. E. Money, T. Muniraj, G. I. Papachristou, M. A. Pericak-Vance, J. Romagnuolo, G. D. Schellenberg, S. Sherman, P. Simon, V. P. Singh, A. Slivka, D. Stolz, R. Sutton, F. U. Weiss, C. M. Wilcox, N. O. Zarnescu, S. R. Wisniewski, M. R. O'Connell, M. L. Kienholz, K. Roeder, M. M. Barmada, D. Yadav and B. Devlin
Journal
Nat Genet
Year
2012
Volume
44
Issue
12
Pages
1349-54
Swaminathan, S., et al., Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. Brain Imaging Behav, 2012. 6 (1): p. 1-15.
Download
Title
Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort
Authors
S. Swaminathan, L. Shen, S. L. Risacher, K. K. Yoder, J. D. West, S. Kim, K. Nho, T. Foroud, M. Inlow, S. G. Potkin, M. J. Huentelman, D. W. Craig, W. J. Jagust, R. A. Koeppe, C. A. Mathis, C. R. Jack, Jr., M. W. Weiner and A. J. Saykin
Journal
Brain Imaging Behav
Year
2012
Volume
6 (1)
Issue
Pages
42019
Swaminathan, S., et al., Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study. Curr Alzheimer Res, 2012. 9(7): p. 801-14.
Download
Title
Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study
Authors
S. Swaminathan, L. Shen, S. Kim, M. Inlow, J. D. West, K. M. Faber, T. Foroud, R. Mayeux and A. J. Saykin
Journal
Curr Alzheimer Res
Year
2012
Volume
9
Issue
7
Pages
801-14
Swaminathan, S., et al., Analysis of Copy Number Variation in Alzheimer’s Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals. PLoS One, 2012. 7(12): p. e50640.
Download
Title
Analysis of Copy Number Variation in Alzheimer’s Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals
Authors
S. Swaminathan, M. J. Huentelman, J. J. Corneveaux, A. J. Myers, K. M. Faber, T. Foroud, R. Mayeux, L. Shen, S. Kim, M. Turk, J. Hardy, E. M. Reiman, A. J. Saykin, I. the Alzheimer's Disease Neuroimaging and N. I. A. L. N. F. S. G. the
Journal
PLoS One
Year
2012
Volume
7
Issue
12
Pages
e50640
Stein, J.L., et al., Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet, 2012. 44(5): p. 552-61.
Download
Title
Identification of common variants associated with human hippocampal and intracranial volumes
Authors
J. L. Stein, S. E. Medland, A. A. Vasquez, D. P. Hibar, R. E. Senstad, A. M. Winkler, R. Toro, K. Appel, R. Bartecek, O. Bergmann, M. Bernard, A. A. Brown, D. M. Cannon, M. M. Chakravarty, A. Christoforou, M. Domin, O. Grimm, M. Hollinshead, A. J. Holmes, G. Homuth, J. J. Hottenga, C. Langan, L. M. Lopez, N. K. Hansell, K. S. Hwang, S. Kim, G. Laje, P. H. Lee, X. Liu, E. Loth, A. Lourdusamy, M. Mattingsdal, S. Mohnke, S. M. Maniega, K. Nho, A. C. Nugent, C. O'Brien, M. Papmeyer, B. Putz, A. Ramasamy, J. Rasmussen, M. Rijpkema, S. L. Risacher, J. C. Roddey, E. J. Rose, M. Ryten, L. Shen, E. Sprooten, E. Strengman, A. Teumer, D. Trabzuni, J. Turner, K. van Eijk, T. G. van Erp, M. J. van Tol, K. Wittfeld, C. Wolf, S. Woudstra, A. Aleman, S. Alhusaini, L. Almasy, E. B. Binder, D. G. Brohawn, R. M. Cantor, M. A. Carless, A. Corvin, M. Czisch, J. E. Curran, G. Davies, M. A. de Almeida, N. Delanty, C. Depondt, R. Duggirala, T. D. Dyer, S. Erk, J. Fagerness, P. T. Fox, N. B. Freimer, M. Gill, H. H. Goring, D. J. Hagler, D. Hoehn, F. Holsboer, M. Hoogman, N. Hosten, N. Jahanshad, M. P. Johnson, D. Kasperaviciute, J. W. Kent, Jr., P. Kochunov, J. L. Lancaster, S. M. Lawrie, D. C. Liewald, R. Mandl, M. Matarin, M. Mattheisen, E. Meisenzahl, I. Melle, E. K. Moses, T. W. Muhleisen, M. Nauck, M. M. Nothen, R. L. Olvera, M. Pandolfo, G. B. Pike, R. Puls, I. Reinvang, M. E. Renteria, M. Rietschel, J. L. Roffman, N. A. Royle, D. Rujescu, J. Savitz, H. G. Schnack, K. Schnell, N. Seiferth, C. Smith, V. M. Steen, M. C. Valdes Hernandez, M. Van den Heuvel, N. J. van der Wee, N. E. Van Haren, J. A. Veltman, H. Volzke, R. Walker, L. T. Westlye, C. D. Whelan, I. Agartz, D. I. Boomsma, G. L. Cavalleri, A. M. Dale, S. Djurovic, W. C. Drevets, P. Hagoort, J. Hall, A. Heinz, C. R. Jack, Jr., T. M. Foroud, S. Le Hellard, F. Macciardi, G. W. Montgomery, J. B. Poline, D. J. Porteous, S. M. Sisodiya, J. M. Starr, J. Sussmann, A. W. Toga, D. J. Veltman, H. Walter, M. W. Weiner, J. C. Bis, M. A. Ikram, A. V. Smith, V. Gudnason, C. Tzourio, M. W. Vernooij, L. J. Launer, C. DeCarli, S. Seshadri, O. A. Andreassen, L. G. Apostolova, M. E. Bastin, J. Blangero, H. G. Brunner, R. L. Buckner, S. Cichon, G. Coppola, G. I. de Zubicaray, I. J. Deary, G. Donohoe, E. J. de Geus, T. Espeseth, G. Fernandez, D. C. Glahn, H. J. Grabe, J. Hardy, H. E. Hulshoff Pol, M. Jenkinson, R. S. Kahn, C. McDonald, A. M. McIntosh, F. J. McMahon, K. L. McMahon, A. Meyer-Lindenberg, D. W. Morris, B. Muller-Myhsok, T. E. Nichols, R. A. Ophoff, T. Paus, Z. Pausova, B. W. Penninx, S. G. Potkin, P. G. Samann, A. J. Saykin, G. Schumann, J. W. Smoller, J. M. Wardlaw, M. E. Weale, N. G. Martin, B. Franke, M. J. Wright and P. M. Thompson
Journal
Nat Genet
Year
2012
Volume
44
Issue
5
Pages
552-61
Shi, H., et al., Genetic variants influencing human aging from late-onset Alzheimer’s disease (LOAD) genome-wide association studies (GWAS). Neurobiology of Aging, 2012. 33(8): p. 1849.e5-1849.18.
Download
Title
Genetic variants influencing human aging from late-onset Alzheimer’s disease (LOAD) genome-wide association studies (GWAS)
Authors
H. Shi, O. Belbin, C. Medway, K. Brown, N. Kalsheker, M. Carrasquillo, P. Proitsi, J. Powell, S. Lovestone, A. Goate, S. Younkin, P. Passmore, G. the, C. Environmental Risk for Alzheimer’s Disease and K. Morgan
Journal
Neurobiology of Aging
Year
2012
Volume
33
Issue
8
Pages
1849.e5-1849.18
Schellenberg, G.D. and T.J. Montine, The Genetics and Neuropathology of Alzheimer’s Disease. Acta neuropathologica, 2012. 124(3): p. 305-323.
Download
Title
The Genetics and Neuropathology of Alzheimer’s Disease
Authors
G. D. Schellenberg and T. J. Montine
Journal
Acta neuropathologica
Year
2012
Volume
124
Issue
3
Pages
305-323
Reitz, C.T., G; Mayeux, R; NIA-LOAD/NCRAD Family Study Group, Association of the CETP C629A polymorphism with Alzheimer’s disease. 2012.
Download
Title
Association of the CETP C629A polymorphism with Alzheimer’s disease
Authors
C. T. Reitz, G; Mayeux, R; NIA-LOAD/NCRAD Family Study Group
Journal
Year
2012
Volume
Issue
Pages
Reitz, C., et al., Genetic variants in the Fat and Obesity Associated (FTO) gene and risk of Alzheimer's disease. PLoS One, 2012. 7(12): p. e50354.
Download
Title
Genetic variants in the Fat and Obesity Associated (FTO) gene and risk of Alzheimer's disease
Authors
C. Reitz, G. Tosto, R. Mayeux and J. A. Luchsinger
Journal
PLoS One
Year
2012
Volume
7
Issue
12
Pages
e50354
Reitz, C., et al., Effect of Genetic Variation in LRRTM3 on Risk of Alzheimer Disease. Archives of Neurology, 2012. 69(7): p. 894-900.
Download
Title
Effect of Genetic Variation in LRRTM3 on Risk of Alzheimer Disease
Authors
C. Reitz, C. Conrad, K. Roszkowski, R. S. Rogers and R. Mayeux
Journal
Archives of Neurology
Year
2012
Volume
69
Issue
7
Pages
894-900
Pankratz, N., et al., Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Ann Neurol, 2012. 71(3): p. 370-84.
Download
Title
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2
Authors
N. Pankratz, G. W. Beecham, A. L. DeStefano, T. M. Dawson, K. F. Doheny, S. A. Factor, T. H. Hamza, A. Y. Hung, B. T. Hyman, A. J. Ivinson, D. Krainc, J. C. Latourelle, L. N. Clark, K. Marder, E. R. Martin, R. Mayeux, O. A. Ross, C. R. Scherzer, D. K. Simon, C. Tanner, J. M. Vance, Z. K. Wszolek, C. P. Zabetian, R. H. Myers, H. Payami, W. K. Scott and T. Foroud
Journal
Ann Neurol
Year
2012
Volume
71
Issue
3
Pages
370-84
Melville, S.A., et al., Multiple loci influencing hippocampal degeneration identified by genome scan. Ann Neurol, 2012. 72(1): p. 65-75.
Download
Title
Multiple loci influencing hippocampal degeneration identified by genome scan
Authors
S. A. Melville, J. Buros, A. R. Parrado, B. Vardarajan, M. W. Logue, L. Shen, S. L. Risacher, S. Kim, G. Jun, C. DeCarli, K. L. Lunetta, C. T. Baldwin, A. J. Saykin and L. A. Farrer
Journal
Ann Neurol
Year
2012
Volume
72
Issue
1
Pages
65-75
Mayeux, R. and Y. Stern, Epidemiology of Alzheimer Disease. Cold Spring Harb Perspect Med, 2012. 2(8): p. a006239.
Download
Title
Epidemiology of Alzheimer Disease
Authors
R. Mayeux and Y. Stern
Journal
Cold Spring Harb Perspect Med
Year
2012
Volume
2
Issue
8
Pages
a006239
Li, Y., et al., Integrated copy number and gene expression analysis detects a CREB1 association with Alzheimer's disease. Transl Psychiatry Psychiatry, 2012. 2: p. e192.
Download
Title
Integrated copy number and gene expression analysis detects a CREB1 association with Alzheimer's disease
Authors
Y. Li, C. A. Shaw, I. Sheffer, N. Sule, S. Z. Powell, B. Dawson, S. N. Zaidi, K. L. Bucasas, J. R. Lupski, K. C. Wilhelmsen, R. Doody and K. Szigeti
Journal
Transl Psychiatry Psychiatry
Year
2012
Volume
2
Issue
Pages
e192
Kohannim, O., et al., Discovery and Replication of Gene Influences on Brain Structure Using LASSO Regression. Front Neurosci, 2012. 6: p. 115.
Download
Title
Discovery and Replication of Gene Influences on Brain Structure Using LASSO Regression
Authors
O. Kohannim, D. P. Hibar, J. L. Stein, N. Jahanshad, X. Hua, P. Rajagopalan, A. W. Toga, C. R. Jack, Jr., M. W. Weiner, G. I. de Zubicaray, K. L. McMahon, N. K. Hansell, N. G. Martin, M. J. Wright and P. M. Thompson
Journal
Front Neurosci
Year
2012
Volume
6
Issue
Pages
115
Kamboh, M.I., et al., Genome-wide association study of Alzheimer's disease. Transl Psychiatry, 2012. 2: p. e117.
Download
Title
Genome-wide association study of Alzheimer's disease
Authors
M. I. Kamboh, F. Y. Demirci, X. Wang, R. L. Minster, M. M. Carrasquillo, V. S. Pankratz, S. G. Younkin, A. J. Saykin, G. Jun, C. Baldwin, M. W. Logue, J. Buros, L. Farrer, M. A. Pericak-Vance, J. L. Haines, R. A. Sweet, M. Ganguli, E. Feingold, S. T. Dekosky, O. L. Lopez and M. M. Barmada
Journal
Transl Psychiatry
Year
2012
Volume
2
Issue
Pages
e117
Kamboh, M.I., et al., Genome-wide association analysis of age-at-onset in Alzheimer's disease. Mol Psychiatry, 2012.
Download
Title
Genome-wide association analysis of age-at-onset in Alzheimer's disease
Authors
M. I. Kamboh, M. M. Barmada, F. Y. Demirci, R. L. Minster, M. M. Carrasquillo, V. S. Pankratz, S. G. Younkin, A. J. Saykin, R. A. Sweet, E. Feingold, S. T. Dekosky and O. L. Lopez
Journal
Mol Psychiatry
Year
2012
Volume
Issue
Pages
Jun, G., et al., Comprehensive search for Alzheimer disease susceptibility loci in the APOE region. Arch Neurol, 2012. 69(10): p. 1270-9.
Download
Title
Comprehensive search for Alzheimer disease susceptibility loci in the APOE region
Authors
G. Jun, B. N. Vardarajan, J. Buros, C. E. Yu, M. V. Hawk, B. A. Dombroski, P. K. Crane, E. B. Larson, R. Mayeux, J. L. Haines, K. L. Lunetta, M. A. Pericak-Vance, G. D. Schellenberg and L. A. Farrer
Journal
Arch Neurol
Year
2012
Volume
69
Issue
10
Pages
1270-9
Howell, C.D., et al., Single nucleotide polymorphism upstream of interleukin 28B associated with phase 1 and phase 2 of early viral kinetics in patients infected with HCV genotype 1. Journal of hepatology, 2012. 56(3): p. 10.1016/j.jhep.2011.10.004.
Download
Title
Single nucleotide polymorphism upstream of interleukin 28B associated with phase 1 and phase 2 of early viral kinetics in patients infected with HCV genotype 1
Authors
C. D. Howell, A. Gorden, K. A. Ryan, A. J. Thompson, C. Ibrahim, M. Fried, N. H. Afdhal, J. G. McHutchison, K. V. Shianna, D. B. Goldstein, A. R. Shuldiner and B. D. Mitchell
Journal
Journal of hepatology
Year
2012
Volume
56
Issue
3
Pages
10.1016/j.jhep.2011.10.004
Hooli, B.V., et al., Role of common and rare APP DNA sequence variants in Alzheimer disease. Neurology, 2012. 78(16): p. 1250-7.
Download
Title
Role of common and rare APP DNA sequence variants in Alzheimer disease
Authors
B. V. Hooli, G. Mohapatra, M. Mattheisen, A. R. Parrado, J. T. Roehr, Y. Shen, J. F. Gusella, R. Moir, A. J. Saunders, C. Lange, R. E. Tanzi and L. Bertram
Journal
Neurology
Year
2012
Volume
78
Issue
16
Pages
1250-7
Hollingworth, P., et al., Genome-wide association study of Alzheimer's disease with psychotic symptoms. Mol Psychiatry, 2012. 17(12): p. 1316-27.
Download
Title
Genome-wide association study of Alzheimer's disease with psychotic symptoms
Authors
P. Hollingworth, R. Sweet, R. Sims, D. Harold, G. Russo, R. Abraham, A. Stretton, N. Jones, A. Gerrish, J. Chapman, D. Ivanov, V. Moskvina, S. Lovestone, P. Priotsi, M. Lupton, C. Brayne, M. Gill, B. Lawlor, A. Lynch, D. Craig, B. McGuinness, J. Johnston, C. Holmes, G. Livingston, N. J. Bass, H. Gurling, A. McQuillin, P. Holmans, L. Jones, B. Devlin, L. Klei, M. M. Barmada, F. Y. Demirci, S. T. DeKosky, O. L. Lopez, P. Passmore, M. J. Owen, M. C. O'Donovan, R. Mayeux, M. I. Kamboh and J. Williams
Journal
Mol Psychiatry
Year
2012
Volume
17
Issue
12
Pages
1316-27
Hamilton, G., et al., Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. Neurobiol Aging, 2012. 33(8): p. 1848 e1-13.
Download
Title
Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus
Authors
G. Hamilton, R. Killick, J. C. Lambert, P. Amouyel, M. M. Carrasquillo, V. S. Pankratz, N. R. Graff-Radford, D. W. Dickson, R. C. Petersen, S. G. Younkin, J. F. Powell and R. Wade-Martins
Journal
Neurobiol Aging
Year
2012
Volume
33
Issue
8
Pages
1848 e1-13
Guerreiro, R.J., et al., Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease. Neurobiol Aging, 2012. 33(5): p. 1008 e17-23.
Download
Title
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease
Authors
R. J. Guerreiro, E. Lohmann, E. Kinsella, J. M. Bras, N. Luu, N. Gurunlian, B. Dursun, B. Bilgic, I. Santana, H. Hanagasi, H. Gurvit, J. R. Gibbs, C. Oliveira, M. Emre and A. Singleton
Journal
Neurobiol Aging
Year
2012
Volume
33
Issue
5
Pages
1008 e17-23
Cruchaga, C., et al., Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families. PLoS ONE [Electronic Resource], 2012. 7(2): p. e31039.
Download
Title
Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families
Authors
C. Cruchaga, G. Haller, S. Chakraverty, K. Mayo, F. L. Vallania, R. D. Mitra, K. Faber, J. Williamson, T. Bird, R. Diaz-Arrastia, T. M. Foroud, B. F. Boeve, N. R. Graff-Radford, P. St Jean, M. Lawson, M. G. Ehm, R. Mayeux, A. M. Goate and N.-L. N. F. S. Consortium
Journal
PLoS ONE [Electronic Resource]
Year
2012
Volume
7
Issue
2
Pages
e31039
Couthouis, J., et al., Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis. Hum Mol Genet, 2012. 21(13): p. 2899-911.
Download
Title
Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis
Authors
J. Couthouis, M. P. Hart, R. Erion, O. D. King, Z. Diaz, T. Nakaya, F. Ibrahim, H. J. Kim, J. Mojsilovic-Petrovic, S. Panossian, C. E. Kim, E. C. Frackelton, J. A. Solski, K. L. Williams, D. Clay-Falcone, L. Elman, L. McCluskey, R. Greene, H. Hakonarson, R. G. Kalb, V. M. Lee, J. Q. Trojanowski, G. A. Nicholson, I. P. Blair, N. M. Bonini, V. M. Van Deerlin, Z. Mourelatos, J. Shorter and A. D. Gitler
Journal
Hum Mol Genet
Year
2012
Volume
21
Issue
13
Pages
2899-911
Coppola, G., et al., Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases. Hum Mol Genet, 2012. 21(15): p. 3500-12.
Download
Title
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Authors
G. Coppola, S. Chinnathambi, J. J. Lee, B. A. Dombroski, M. C. Baker, A. I. Soto-Ortolaza, S. E. Lee, E. Klein, A. Y. Huang, R. Sears, J. R. Lane, A. M. Karydas, R. O. Kenet, J. Biernat, L. S. Wang, C. W. Cotman, C. S. Decarli, A. I. Levey, J. M. Ringman, M. F. Mendez, H. C. Chui, I. Le Ber, A. Brice, M. K. Lupton, E. Preza, S. Lovestone, J. Powell, N. Graff-Radford, R. C. Petersen, B. F. Boeve, C. F. Lippa, E. H. Bigio, I. Mackenzie, E. Finger, A. Kertesz, R. J. Caselli, M. Gearing, J. L. Juncos, B. Ghetti, S. Spina, Y. M. Bordelon, W. W. Tourtellotte, M. P. Frosch, J. P. Vonsattel, C. Zarow, T. G. Beach, R. L. Albin, A. P. Lieberman, V. M. Lee, J. Q. Trojanowski, V. M. Van Deerlin, T. D. Bird, D. R. Galasko, E. Masliah, C. L. White, J. C. Troncoso, D. Hannequin, A. L. Boxer, M. D. Geschwind, S. Kumar, E. M. Mandelkow, Z. K. Wszolek, R. J. Uitti, D. W. Dickson, J. L. Haines, R. Mayeux, M. A. Pericak-Vance, L. A. Farrer, O. A. Ross, R. Rademakers, G. D. Schellenberg, B. L. Miller, E. Mandelkow and D. H. Geschwind
Journal
Hum Mol Genet
Year
2012
Volume
21
Issue
15
Pages
3500-12
Bonnin, J.M., JR; Farlow, MR, Glazier, B; Foroud, T; Ghetti, B. Early-Onset Alzheimer Disease with the G209E PSEN1 Mutation: A Neuropathologic Study. in American Association of Neuropathologists, Inc. Abstracts of the 88th Annual Meeting. 2012. Chicago, IL: Journal of Neuropathology and Experimental Neurology.
Download
Title
Early-Onset Alzheimer Disease with the G209E PSEN1 Mutation: A Neuropathologic Study
Authors
J. M. Bonnin, JR; Farlow, MR, Glazier, B; Foroud, T; Ghetti, B
Journal
AANP
Year
2012
Volume
Issue
Pages
Barral, S., et al., Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory. Neurology, 2012. 78(19): p. 1464-71.
Download
Title
Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory
Authors
S. Barral, T. Bird, A. Goate, M. R. Farlow, R. Diaz-Arrastia, D. A. Bennett, N. Graff-Radford, B. F. Boeve, R. A. Sweet, Y. Stern, R. S. Wilson, T. Foroud, J. Ott and R. Mayeux
Journal
Neurology
Year
2012
Volume
78
Issue
19
Pages
1464-71
Allen, M., et al., Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications. Mol Neurodegener, 2012. 7: p. 13.
Download
Title
Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications
Authors
M. Allen, F. Zou, H. S. Chai, C. S. Younkin, R. Miles, A. A. Nair, J. E. Crook, V. S. Pankratz, M. M. Carrasquillo, C. N. Rowley, T. Nguyen, L. Ma, K. G. Malphrus, G. Bisceglio, A. I. Ortolaza, R. Palusak, S. Middha, S. Maharjan, C. Georgescu, D. Schultz, F. Rakhshan, C. P. Kolbert, J. Jen, S. B. Sando, J. O. Aasly, M. Barcikowska, R. J. Uitti, Z. K. Wszolek, O. A. Ross, R. C. Petersen, N. R. Graff-Radford, D. W. Dickson, S. G. Younkin and N. Ertekin-Taner
Journal
Mol Neurodegener
Year
2012
Volume
7
Issue
Pages
13
Allen, M., et al., Novel late-onset Alzheimer disease loci variants associate with brain gene expression. Neurology, 2012. 79(3): p. 221-8.
Download
Title
Novel late-onset Alzheimer disease loci variants associate with brain gene expression
Authors
M. Allen, F. Zou, H. S. Chai, C. S. Younkin, J. Crook, V. S. Pankratz, M. M. Carrasquillo, C. N. Rowley, A. A. Nair, S. Middha, S. Maharjan, T. Nguyen, L. Ma, K. G. Malphrus, R. Palusak, S. Lincoln, G. Bisceglio, C. Georgescu, D. Schultz, F. Rakhshan, C. P. Kolbert, J. Jen, J. L. Haines, R. Mayeux, M. A. Pericak-Vance, L. A. Farrer, G. D. Schellenberg, R. C. Petersen, N. R. Graff-Radford, D. W. Dickson, S. G. Younkin and N. Ertekin-Taner
Journal
Neurology
Year
2012
Volume
79
Issue
3
Pages
221-8
Wilson, R.S., et al., Heritability of different forms of memory in the Late Onset Alzheimer's Disease Family Study. J Alzheimers Dis, 2011. 23(2): p. 249-55.
Download
Title
Heritability of different forms of memory in the Late Onset Alzheimer's Disease Family Study
Authors
R. S. Wilson, S. Barral, J. H. Lee, S. E. Leurgans, T. M. Foroud, R. A. Sweet, N. Graff-Radford, T. D. Bird, R. Mayeux and D. A. Bennett
Journal
J Alzheimers Dis
Year
2011
Volume
23
Issue
2
Pages
249-55
Wijsman, E.M., et al., Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. PLoS Genet, 2011. 7(2): p. e1001308.
Download
Title
Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE
Authors
E. M. Wijsman, N. D. Pankratz, Y. Choi, J. H. Rothstein, K. M. Faber, R. Cheng, J. H. Lee, T. D. Bird, D. A. Bennett, R. Diaz-Arrastia, A. M. Goate, M. Farlow, B. Ghetti, R. A. Sweet, T. M. Foroud and R. Mayeux
Journal
PLoS Genet
Year
2011
Volume
7
Issue
2
Pages
e1001308
Swaminathan, S., et al. Analysis of Copy Number Variation in Alzheimer's Disease: The NIA-LOAD/NCRAD Family Study. in The 12th International Congress of Human Genetics (ICHG) The 61st American Society of Human Genetics (ASHG) Annual Meeting. 2011. Montreal, Quebec, Canada.
Download
Title
Analysis of Copy Number Variation in Alzheimer's Disease: The NIA-LOAD/NCRAD Family Study
Authors
S. Swaminathan, L. Shen, S. Kim, M. Inlow, J. D. West, K. Faber, T. Foroud, R. Mayeux, A. J. Saykin, T. A. s. D. N. I. (ADNI) and T. N.-L. N. F. S. Group
Journal
Year
2011
Volume
Issue
Pages
Swaminathan, S., et al., Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. Int J Alzheimers Dis, 2011. 2011: p. 729478.
Download
Title
Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study
Authors
S. Swaminathan, S. Kim, L. Shen, S. L. Risacher, T. Foroud, N. Pankratz, S. G. Potkin, M. J. Huentelman, D. W. Craig, M. W. Weiner, A. J. Saykin and A. The Alzheimer's Disease Neuroimaging Initiative
Journal
Int J Alzheimers Dis
Year
2011
Volume
2011
Issue
Pages
729478
Silver, M., G. Montana, and T.E. Nichols, False positives in neuroimaging genetics using voxel-based morphometry data. Neuroimage, 2011. 54(2): p. 992-1000.
Download
Title
False positives in neuroimaging genetics using voxel-based morphometry data
Authors
M. Silver, G. Montana and T. E. Nichols
Journal
Neuroimage
Year
2011
Volume
54
Issue
2
Pages
992-1000
Schjeide, B.M., et al., The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels. Arch Gen Psychiatry, 2011. 68(2): p. 207-13.
Download
Title
The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels
Authors
B. M. Schjeide, C. Schnack, J. C. Lambert, C. M. Lill, J. Kirchheiner, H. Tumani, M. Otto, R. E. Tanzi, H. Lehrach, P. Amouyel, C. A. von Arnim and L. Bertram
Journal
Arch Gen Psychiatry
Year
2011
Volume
68
Issue
2
Pages
207-13
Renton, A.E., et al., A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron, 2011. 72(2): p. 257-68.
Download
Title
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Authors
A. E. Renton, E. Majounie, A. Waite, J. Simon-Sanchez, S. Rollinson, J. R. Gibbs, J. C. Schymick, H. Laaksovirta, J. C. van Swieten, L. Myllykangas, H. Kalimo, A. Paetau, Y. Abramzon, A. M. Remes, A. Kaganovich, S. W. Scholz, J. Duckworth, J. Ding, D. W. Harmer, D. G. Hernandez, J. O. Johnson, K. Mok, M. Ryten, D. Trabzuni, R. J. Guerreiro, R. W. Orrell, J. Neal, A. Murray, J. Pearson, I. E. Jansen, D. Sondervan, H. Seelaar, D. Blake, K. Young, N. Halliwell, J. B. Callister, G. Toulson, A. Richardson, A. Gerhard, J. Snowden, D. Mann, D. Neary, M. A. Nalls, T. Peuralinna, L. Jansson, V. M. Isoviita, A. L. Kaivorinne, M. Holtta-Vuori, E. Ikonen, R. Sulkava, M. Benatar, J. Wuu, A. Chio, G. Restagno, G. Borghero, M. Sabatelli, D. Heckerman, E. Rogaeva, L. Zinman, J. D. Rothstein, M. Sendtner, C. Drepper, E. E. Eichler, C. Alkan, Z. Abdullaev, S. D. Pack, A. Dutra, E. Pak, J. Hardy, A. Singleton, N. M. Williams, P. Heutink, S. Pickering-Brown, H. R. Morris, P. J. Tienari and B. J. Traynor
Journal
Neuron
Year
2011
Volume
72
Issue
2
Pages
257-68
Reitz, C., et al., SORCS1 alters amyloid precursor protein processing and variants may increase Alzheimer's disease risk. Ann Neurol, 2011. 69(1): p. 47-64.
Download
Title
SORCS1 alters amyloid precursor protein processing and variants may increase Alzheimer's disease risk
Authors
C. Reitz, S. Tokuhiro, L. N. Clark, C. Conrad, J. P. Vonsattel, L. N. Hazrati, A. Palotas, R. Lantigua, M. Medrano, Z. J.-V. I, B. Vardarajan, I. Simkin, J. L. Haines, M. A. Pericak-Vance, L. A. Farrer, J. H. Lee, E. Rogaeva, P. S. George-Hyslop and R. Mayeux
Journal
Ann Neurol
Year
2011
Volume
69
Issue
1
Pages
47-64
Reitz, C., et al., Impact of genetic variation in SORCS1 on memory retention. PLoS One, 2011. 6(10): p. e24588.
Download
Title
Impact of genetic variation in SORCS1 on memory retention
Authors
C. Reitz, J. H. Lee, R. S. Rogers and R. Mayeux
Journal
PLoS One
Year
2011
Volume
6
Issue
10
Pages
e24588
Reitz, C., et al., Meta-analysis of the Association Between Variants in SORL1 and Alzheimer Disease. Archives of Neurology, 2011. 68(1): p. 99-106.
Download
Title
Meta-analysis of the Association Between Variants in SORL1 and Alzheimer Disease
Authors
C. Reitz, R. Cheng, E. Rogaeva, J. H. Lee, S. Tokuhiro, F. Zou, K. Bettens, K. Sleegers, E. K. Tan, R. Kimura, N. Shibata, H. Arai, M. I. Kamboh, J. A. Prince, W. Maier, M. Riemenschneider, M. Owen, D. Harold, P. Hollingworth, E. Cellini, S. Sorbi, B. Nacmias, M. Takeda, M. A. Pericak-Vance, J. L. Haines, S. Younkin, J. Williams, C. van Broeckhoven, L. A. Farrer, P. H. St George–Hyslop and R. Mayeux
Journal
Archives of Neurology
Year
2011
Volume
68
Issue
1
Pages
99-106
Rademakers, R., et al., Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids. Nat Genet, 2011. 44(2): p. 200-5.
Download
Title
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids
Authors
R. Rademakers, M. Baker, A. M. Nicholson, N. J. Rutherford, N. Finch, A. Soto-Ortolaza, J. Lash, C. Wider, A. Wojtas, M. DeJesus-Hernandez, J. Adamson, N. Kouri, C. Sundal, E. A. Shuster, J. Aasly, J. MacKenzie, S. Roeber, H. A. Kretzschmar, B. F. Boeve, D. S. Knopman, R. C. Petersen, N. J. Cairns, B. Ghetti, S. Spina, J. Garbern, A. C. Tselis, R. Uitti, P. Das, J. A. Van Gerpen, J. F. Meschia, S. Levy, D. F. Broderick, N. Graff-Radford, O. A. Ross, B. B. Miller, R. H. Swerdlow, D. W. Dickson and Z. K. Wszolek
Journal
Nat Genet
Year
2011
Volume
44
Issue
2
Pages
200-5
Perry, R.W., H; Go, R. Results from sense SNP genotyping of the 9Q22-Q31CRI in the NIMH and NCRAD AD cohorts. in Alzheimer's Association International Conference. 2011. Paris France: Alzheimer's Association.
Download
Title
Results from sense SNP genotyping of the 9Q22-Q31CRI in the NIMH and NCRAD AD cohorts
Authors
R. W. Perry, H; Go, R
Journal
Year
2011
Volume
Issue
Pages
Nicholson, G., et al., Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P(2) phosphatase FIG4. Brain, 2011. 134(Pt 7): p. 1959-71.
Download
Title
Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P(2) phosphatase FIG4
Authors
G. Nicholson, G. M. Lenk, S. W. Reddel, A. E. Grant, C. F. Towne, C. J. Ferguson, E. Simpson, A. Scheuerle, M. Yasick, S. Hoffman, R. Blouin, C. Brandt, G. Coppola, L. G. Biesecker, S. D. Batish and M. H. Meisler
Journal
Brain
Year
2011
Volume
134
Issue
Pt 7
Pages
1959-71
Nho, K., et al., The effect of reference panels and software tools on genotype imputation. AMIA Annu Symp Proc, 2011. 2011: p. 1013-8.
Download
Title
The effect of reference panels and software tools on genotype imputation
Authors
K. Nho, L. Shen, S. Kim, S. Swaminathan, S. L. Risacher and A. J. Saykin
Journal
AMIA Annu Symp Proc
Year
2011
Volume
2011
Issue
Pages
1013-8
Naj, A.C., et al., Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet, 2011. 43(5): p. 436-41.
Download
Title
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Authors
A. C. Naj, G. Jun, G. W. Beecham, L. S. Wang, B. N. Vardarajan, J. Buros, P. J. Gallins, J. D. Buxbaum, G. P. Jarvik, P. K. Crane, E. B. Larson, T. D. Bird, B. F. Boeve, N. R. Graff-Radford, P. L. De Jager, D. Evans, J. A. Schneider, M. M. Carrasquillo, N. Ertekin-Taner, S. G. Younkin, C. Cruchaga, J. S. Kauwe, P. Nowotny, P. Kramer, J. Hardy, M. J. Huentelman, A. J. Myers, M. M. Barmada, F. Y. Demirci, C. T. Baldwin, R. C. Green, E. Rogaeva, P. S. George-Hyslop, S. E. Arnold, R. Barber, T. Beach, E. H. Bigio, J. D. Bowen, A. Boxer, J. R. Burke, N. J. Cairns, C. S. Carlson, R. M. Carney, S. L. Carroll, H. C. Chui, D. G. Clark, J. Corneveaux, C. W. Cotman, J. L. Cummings, C. Decarli, S. T. Dekosky, R. Diaz-Arrastia, M. Dick, D. W. Dickson, W. G. Ellis, K. M. Faber, K. B. Fallon, M. R. Farlow, S. Ferris, M. P. Frosch, D. R. Galasko, M. Ganguli, M. Gearing, D. H. Geschwind, B. Ghetti, J. R. Gilbert, S. Gilman, B. Giordani, J. D. Glass, J. H. Growdon, R. L. Hamilton, L. E. Harrell, E. Head, L. S. Honig, C. M. Hulette, B. T. Hyman, G. A. Jicha, L. W. Jin, N. Johnson, J. Karlawish, A. Karydas, J. A. Kaye, R. Kim, E. H. Koo, N. W. Kowall, J. J. Lah, A. I. Levey, A. P. Lieberman, O. L. Lopez, W. J. Mack, D. C. Marson, F. Martiniuk, D. C. Mash, E. Masliah, W. C. McCormick, S. M. McCurry, A. N. McDavid, A. C. McKee, M. Mesulam, B. L. Miller, C. A. Miller, J. W. Miller, J. E. Parisi, D. P. Perl, E. Peskind, R. C. Petersen, W. W. Poon, J. F. Quinn, R. A. Rajbhandary, M. Raskind, B. Reisberg, J. M. Ringman, E. D. Roberson, R. N. Rosenberg, M. Sano, L. S. Schneider, W. Seeley, M. L. Shelanski, M. A. Slifer, C. D. Smith, J. A. Sonnen, S. Spina, R. A. Stern, R. E. Tanzi, J. Q. Trojanowski, J. C. Troncoso, V. M. Van Deerlin, H. V. Vinters, J. P. Vonsattel, S. Weintraub, K. A. Welsh-Bohmer, J. Williamson, R. L. Woltjer, L. B. Cantwell, B. A. Dombroski, D. Beekly, K. L. Lunetta, E. R. Martin, M. I. Kamboh, A. J. Saykin, E. M. Reiman, D. A. Bennett, J. C. Morris, T. J. Montine, A. M. Goate, D. Blacker, D. W. Tsuang, H. Hakonarson, W. A. Kukull, T. M. Foroud, J. L. Haines, R. Mayeux, M. A. Pericak-Vance, L. A. Farrer and G. D. Schellenberg
Journal
Nat Genet
Year
2011
Volume
43
Issue
5
Pages
436-41
Lee, J.H., et al., Identification of novel loci for Alzheimer disease and replication of CLU, PICALM, and BIN1 in Caribbean Hispanic individuals. Arch Neurol, 2011. 68(3): p. 320-8.
Download
Title
Identification of novel loci for Alzheimer disease and replication of CLU, PICALM, and BIN1 in Caribbean Hispanic individuals
Authors
J. H. Lee, R. Cheng, S. Barral, C. Reitz, M. Medrano, R. Lantigua, I. Z. Jimenez-Velazquez, E. Rogaeva, P. H. St George-Hyslop and R. Mayeux
Journal
Arch Neurol
Year
2011
Volume
68
Issue
3
Pages
320-8
Lee, J.C., R; Pankratz, N; Wijsman, E; Bird, T; Foroud, T; Mayeux, R; NIA-LOAD Family Study Group. A Genome-wide study of familial Alzheiner's Disease supports additional candidate genes:The NIA-LOAD/NCRAD family study. in AAIC International Conference. 2011. Paris France: Alzheimer's Association.
Download
Title
A Genome-wide study of familial Alzheiner's Disease supports additional candidate genes:The NIA-LOAD/NCRAD family study
Authors
J. C. Lee, R; Pankratz, N; Wijsman, E; Bird, T; Foroud, T; Mayeux, R; NIA-LOAD Family Study Group
Journal
Year
2011
Volume
Issue
Pages
Kim, S., et al., Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort. Neurology, 2011. 76(1): p. 69-79.
Download
Title
Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort
Authors
S. Kim, S. Swaminathan, L. Shen, S. L. Risacher, K. Nho, T. Foroud, L. M. Shaw, J. Q. Trojanowski, S. G. Potkin, M. J. Huentelman, D. W. Craig, B. M. DeChairo, P. S. Aisen, R. C. Petersen, M. W. Weiner and A. J. Saykin
Journal
Neurology
Year
2011
Volume
76
Issue
1
Pages
69-79
Hollingworth, P., et al., Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat Genet, 2011. 43(5): p. 429-435.
Download
Title
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
Authors
P. Hollingworth, D. Harold, R. Sims, A. Gerrish, J. C. Lambert, M. M. Carrasquillo, R. Abraham, M. L. Hamshere, J. S. Pahwa, V. Moskvina, K. Dowzell, N. Jones, A. Stretton, C. Thomas, A. Richards, D. Ivanov, C. Widdowson, J. Chapman, S. Lovestone, J. Powell, P. Proitsi, M. K. Lupton, C. Brayne, D. C. Rubinsztein, M. Gill, B. Lawlor, A. Lynch, K. S. Brown, P. A. Passmore, D. Craig, B. McGuinness, S. Todd, C. Holmes, D. Mann, A. D. Smith, H. Beaumont, D. Warden, G. Wilcock, S. Love, P. G. Kehoe, N. M. Hooper, E. R. Vardy, J. Hardy, S. Mead, N. C. Fox, M. Rossor, J. Collinge, W. Maier, F. Jessen, E. Ruther, B. Schurmann, R. Heun, H. Kolsch, H. van den Bussche, I. Heuser, J. Kornhuber, J. Wiltfang, M. Dichgans, L. Frolich, H. Hampel, J. Gallacher, M. Hull, D. Rujescu, I. Giegling, A. M. Goate, J. S. Kauwe, C. Cruchaga, P. Nowotny, J. C. Morris, K. Mayo, K. Sleegers, K. Bettens, S. Engelborghs, P. P. De Deyn, C. Van Broeckhoven, G. Livingston, N. J. Bass, H. Gurling, A. McQuillin, R. Gwilliam, P. Deloukas, A. Al-Chalabi, C. E. Shaw, M. Tsolaki, A. B. Singleton, R. Guerreiro, T. W. Muhleisen, M. M. Nothen, S. Moebus, K. H. Jockel, N. Klopp, H. E. Wichmann, V. S. Pankratz, S. B. Sando, J. O. Aasly, M. Barcikowska, Z. K. Wszolek, D. W. Dickson, N. R. Graff-Radford, R. C. Petersen, C. M. van Duijn, M. M. Breteler, M. A. Ikram, A. L. Destefano, A. L. Fitzpatrick, O. Lopez, L. J. Launer, S. Seshadri, C. Berr, D. Campion, J. Epelbaum, J. F. Dartigues, C. Tzourio, A. Alperovitch, M. Lathrop, T. M. Feulner, P. Friedrich, C. Riehle, M. Krawczak, S. Schreiber, M. Mayhaus, S. Nicolhaus, S. Wagenpfeil, S. Steinberg, H. Stefansson, K. Stefansson, J. Snaedal, S. Bjornsson, P. V. Jonsson, V. Chouraki, B. Genier-Boley, M. Hiltunen, H. Soininen, O. Combarros, D. Zelenika, M. Delepine, M. J. Bullido, F. Pasquier, I. Mateo, A. Frank-Garcia, E. Porcellini, O. Hanon, E. Coto, V. Alvarez, P. Bosco, G. Siciliano, M. Mancuso, F. Panza, V. Solfrizzi, B. Nacmias, S. Sorbi, P. Bossu, P. Piccardi, B. Arosio, G. Annoni, D. Seripa, A. Pilotto, E. Scarpini, D. Galimberti, A. Brice, D. Hannequin, F. Licastro, L. Jones, P. A. Holmans, T. Jonsson, M. Riemenschneider, K. Morgan, S. G. Younkin, M. J. Owen, M. O'Donovan, P. Amouyel and J. Williams
Journal
Nat Genet
Year
2011
Volume
43
Issue
5
Pages
429-435
Hibar, D.P., et al., Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects. Neuroimage, 2011. 56(4): p. 1875-91.
Download
Title
Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects
Authors
D. P. Hibar, J. L. Stein, O. Kohannim, N. Jahanshad, A. J. Saykin, L. Shen, S. Kim, N. Pankratz, T. Foroud, M. J. Huentelman, S. G. Potkin, C. R. Jack, Jr., M. W. Weiner, A. W. Toga and P. M. Thompson
Journal
Neuroimage
Year
2011
Volume
56
Issue
4
Pages
1875-91
Cruchaga, C., et al., Association and expression analyses with single-nucleotide polymorphisms in TOMM40 in Alzheimer disease. Arch Neurol, 2011. 68(8): p. 1013-9.
Download
Title
Association and expression analyses with single-nucleotide polymorphisms in TOMM40 in Alzheimer disease
Authors
C. Cruchaga, P. Nowotny, J. S. Kauwe, P. G. Ridge, K. Mayo, S. Bertelsen, A. Hinrichs, A. M. Fagan, D. M. Holtzman, J. C. Morris and A. M. Goate
Journal
Arch Neurol
Year
2011
Volume
68
Issue
8
Pages
1013-9
Cruchaga, C., et al., Pathogenic mutations in APP, PSEN1, GRN and MAPT in families with late onset Alzheimer disease. Submitted, 2011.
Download
Title
Pathogenic mutations in APP, PSEN1, GRN and MAPT in families with late onset Alzheimer disease.
Authors
C. Cruchaga, G. Haller, S. Chakraventy, K. Mayo, F. L. Vallania, R. D. Mitra, K. Faber, J. Williamson, T. Bird, R. Diaz-Arrastia, T. Foroud, B. Boeve, N. Graff-Radford, R. Mayeux and A. Goate
Journal
Year
2011
Volume
Issue
Pages
Cruchaga, C., et al., Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels. Arch Neurol, 2011. 68(5): p. 581-6.
Download
Title
Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels
Authors
C. Cruchaga, C. Graff, H. H. Chiang, J. Wang, A. L. Hinrichs, N. Spiegel, S. Bertelsen, K. Mayo, J. B. Norton, J. C. Morris and A. Goate
Journal
Arch Neurol
Year
2011
Volume
68
Issue
5
Pages
581-6
Couthouis, J., et al., A yeast functional screen predicts new candidate ALS disease genes. Proc Natl Acad Sci U S A, 2011. 108(52): p. 20881-90.
Download
Title
A yeast functional screen predicts new candidate ALS disease genes
Authors
J. Couthouis, M. P. Hart, J. Shorter, M. DeJesus-Hernandez, R. Erion, R. Oristano, A. X. Liu, D. Ramos, N. Jethava, D. Hosangadi, J. Epstein, A. Chiang, Z. Diaz, T. Nakaya, F. Ibrahim, H. J. Kim, J. A. Solski, K. L. Williams, J. Mojsilovic-Petrovic, C. Ingre, K. Boylan, N. R. Graff-Radford, D. W. Dickson, D. Clay-Falcone, L. Elman, L. McCluskey, R. Greene, R. G. Kalb, V. M. Lee, J. Q. Trojanowski, A. Ludolph, W. Robberecht, P. M. Andersen, G. A. Nicholson, I. P. Blair, O. D. King, N. M. Bonini, V. Van Deerlin, R. Rademakers, Z. Mourelatos and A. D. Gitler
Journal
Proc Natl Acad Sci U S A
Year
2011
Volume
108
Issue
52
Pages
20881-90
Cenik, B., et al., Suberoylanilide hydroxamic acid (vorinostat) up-regulates progranulin transcription: rational therapeutic approach to frontotemporal dementia. J Biol Chem, 2011. 286(18): p. 16101-8.
Download
Title
Suberoylanilide hydroxamic acid (vorinostat) up-regulates progranulin transcription: rational therapeutic approach to frontotemporal dementia
Authors
B. Cenik, C. F. Sephton, C. M. Dewey, X. Xian, S. Wei, K. Yu, W. Niu, G. Coppola, S. E. Coughlin, S. E. Lee, D. R. Dries, S. Almeida, D. H. Geschwind, F. B. Gao, B. L. Miller, R. V. Farese, Jr., B. A. Posner, G. Yu and J. Herz
Journal
J Biol Chem
Year
2011
Volume
286
Issue
18
Pages
16101-8
Castellano, J.M., et al., Human apoE isoforms differentially regulate brain amyloid-beta peptide clearance. Sci Transl Med, 2011. 3(89): p. 89ra57.
Download
Title
Human apoE isoforms differentially regulate brain amyloid-beta peptide clearance
Authors
J. M. Castellano, J. Kim, F. R. Stewart, H. Jiang, R. B. DeMattos, B. W. Patterson, A. M. Fagan, J. C. Morris, K. G. Mawuenyega, C. Cruchaga, A. M. Goate, K. R. Bales, S. M. Paul, R. J. Bateman and D. M. Holtzman
Journal
Sci Transl Med
Year
2011
Volume
3
Issue
89
Pages
89ra57
Carrasquillo, M.M., et al., Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions. J Alzheimers Dis, 2011. 24(4): p. 751-8.
Download
Title
Replication of BIN1 association with Alzheimer's disease and evaluation of genetic interactions
Authors
M. M. Carrasquillo, O. Belbin, T. A. Hunter, L. Ma, G. D. Bisceglio, F. Zou, J. E. Crook, V. S. Pankratz, S. B. Sando, J. O. Aasly, M. Barcikowska, Z. K. Wszolek, D. W. Dickson, N. R. Graff-Radford, R. C. Petersen, K. Morgan and S. G. Younkin
Journal
J Alzheimers Dis
Year
2011
Volume
24
Issue
4
Pages
751-8
Bennet, D.B., T; Boeve, B; Dias-Arrastia, R; Farlow, M; Foroud, T; Goate, A; Graff-Radford, N; Sweet, R; Wilson, R; Mayeux; R. Multilocus genotype pattern at PICALM, CLU and APOE genes is associated with episodic memory in the NIA-LOAD/NCRAD study. in Alzheimer's Association International Confernece. 2011. Paris France.
Download
Title
Multilocus genotype pattern at PICALM, CLU and APOE genes is associated with episodic memory in the NIA-LOAD/NCRAD study
Authors
D. B. Bennet, T; Boeve, B; Dias-Arrastia, R; Farlow, M; Foroud, T; Goate, A; Graff-Radford, N; Sweet, R; Wilson, R; Mayeux; R
Journal
Year
2011
Volume
Issue
Pages
Belbin, O., et al., Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease. Hum Genet, 2011. 129(3): p. 273-82.
Download
Title
Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease
Authors
O. Belbin, M. M. Carrasquillo, M. Crump, O. J. Culley, T. A. Hunter, L. Ma, G. Bisceglio, F. Zou, M. Allen, D. W. Dickson, N. R. Graff-Radford, R. C. Petersen, K. Morgan and S. G. Younkin
Journal
Hum Genet
Year
2011
Volume
129
Issue
3
Pages
273-82
Belbin, O., et al., A multi-center study of ACE and the risk of late-onset Alzheimer's disease. J Alzheimers Dis, 2011. 24(3): p. 587-97.
Download
Title
A multi-center study of ACE and the risk of late-onset Alzheimer's disease
Authors
O. Belbin, K. Brown, H. Shi, C. Medway, R. Abraham, P. Passmore, D. Mann, A. D. Smith, C. Holmes, B. McGuinness, D. Craig, D. Warden, R. Heun, H. Kolsch, S. Love, N. Kalsheker, J. Williams, M. J. Owen, M. Carrasquillo, S. Younkin, K. Morgan and P. G. Kehoe
Journal
J Alzheimers Dis
Year
2011
Volume
24
Issue
3
Pages
587-97
Zhou, W., et al., BACE1 gene promoter single-nucleotide polymorphisms in Alzheimer's disease. J Mol Neurosci, 2010. 42(1): p. 127-33.
Download
Title
BACE1 gene promoter single-nucleotide polymorphisms in Alzheimer's disease
Authors
W. Zhou, F. Cai, Y. Li, G. S. Yang, K. D. O'Connor, R. A. Holt and W. Song
Journal
J Mol Neurosci
Year
2010
Volume
42
Issue
1
Pages
127-33
Wilson, R.S., et al., Telephone assessment of cognitive function in the late-onset Alzheimer's disease family study. Arch Neurol, 2010. 67(7): p. 855-61.
Download
Title
Telephone assessment of cognitive function in the late-onset Alzheimer's disease family study
Authors
R. S. Wilson, S. E. Leurgans, T. M. Foroud, R. A. Sweet, N. Graff-Radford, R. Mayeux and D. A. Bennett
Journal
Arch Neurol
Year
2010
Volume
67
Issue
7
Pages
855-61
Wilson, R.S., et al., Temporal course of depressive symptoms during the development of Alzheimer disease. Neurology, 2010. 75(1): p. 21-26.
Download
Title
Temporal course of depressive symptoms during the development of Alzheimer disease
Authors
R. S. Wilson, G. M. Hoganson, K. B. Rajan, L. L. Barnes, C. F. Mendes de Leon and D. A. Evans
Journal
Neurology
Year
2010
Volume
75
Issue
1
Pages
21-26
Wilhelmsen, K.C., SA; Gizer, IR; Cameron, NG; Ellis, JW; Diaz-Arrastia, R; Barber, RC; O'Bryant, SE; Doody, R; Fairchild, T; Brodaty, H; Smythe, GA. Genome-Wide Assocation Scan for Biomarker Endophenotypes of Alzheimer's Disease. in ICAD. 2010. Honolulu, HI.
Download
Title
Genome-Wide Assocation Scan for Biomarker Endophenotypes of Alzheimer's Disease
Authors
K. C. Wilhelmsen, SA; Gizer, IR; Cameron, NG; Ellis, JW; Diaz-Arrastia, R; Barber, RC; O'Bryant, SE; Doody, R; Fairchild, T; Brodaty, H; Smythe, GA
Journal
Year
2010
Volume
Issue
Pages
Szymanski, M., et al., Neuroglobin and Alzheimer's dementia: genetic association and gene expression changes. Neurobiol Aging, 2010. 31(11): p. 1835-42.
Download
Title
Neuroglobin and Alzheimer's dementia: genetic association and gene expression changes
Authors
M. Szymanski, R. Wang, M. D. Fallin, S. S. Bassett and D. Avramopoulos
Journal
Neurobiol Aging
Year
2010
Volume
31
Issue
11
Pages
1835-42
Sweet, R.A., et al., Assessment and familial aggregation of psychosis in Alzheimer's disease from the National Institute on Aging Late Onset Alzheimer's Disease Family Study. Brain, 2010. 133(Pt 4): p. 1155-62.
Download
Title
Assessment and familial aggregation of psychosis in Alzheimer's disease from the National Institute on Aging Late Onset Alzheimer's Disease Family Study
Authors
R. A. Sweet, D. A. Bennett, N. R. Graff-Radford and R. Mayeux
Journal
Brain
Year
2010
Volume
133
Issue
Pt 4
Pages
1155-62
Stein, J.L., et al., Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Neuroimage, 2010. 51(2): p. 542-54.
Download
Title
Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease
Authors
J. L. Stein, X. Hua, J. H. Morra, S. Lee, D. P. Hibar, A. J. Ho, A. D. Leow, A. W. Toga, J. H. Sul, H. M. Kang, E. Eskin, A. J. Saykin, L. Shen, T. Foroud, N. Pankratz, M. J. Huentelman, D. W. Craig, J. D. Gerber, A. N. Allen, J. J. Corneveaux, D. A. Stephan, J. Webster, B. M. DeChairo, S. G. Potkin, C. R. Jack, Jr., M. W. Weiner and P. M. Thompson
Journal
Neuroimage
Year
2010
Volume
51
Issue
2
Pages
542-54
Stein, J.L., et al., Voxelwise genome-wide association study (vGWAS). Neuroimage, 2010. 53(3): p. 1160-74.
Download
Title
Voxelwise genome-wide association study (vGWAS)
Authors
J. L. Stein, X. Hua, S. Lee, A. J. Ho, A. D. Leow, A. W. Toga, A. J. Saykin, L. Shen, T. Foroud, N. Pankratz, M. J. Huentelman, D. W. Craig, J. D. Gerber, A. N. Allen, J. J. Corneveaux, B. M. Dechairo, S. G. Potkin, M. W. Weiner and P. Thompson
Journal
Neuroimage
Year
2010
Volume
53
Issue
3
Pages
1160-74
Shen, L., et al., Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. Neuroimage, 2010. 53(3): p. 1051-63.
Download
Title
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort
Authors
L. Shen, S. Kim, S. L. Risacher, K. Nho, S. Swaminathan, J. D. West, T. Foroud, N. Pankratz, J. H. Moore, C. D. Sloan, M. J. Huentelman, D. W. Craig, B. M. Dechairo, S. G. Potkin, C. R. Jack, Jr., M. W. Weiner and A. J. Saykin
Journal
Neuroimage
Year
2010
Volume
53
Issue
3
Pages
1051-63
Seshadri, S., et al., Genome-wide analysis of genetic loci associated with Alzheimer disease. JAMA, 2010. 303(18): p. 1832-40.
Download
Title
Genome-wide analysis of genetic loci associated with Alzheimer disease
Authors
S. Seshadri, A. L. Fitzpatrick, M. A. Ikram, A. L. DeStefano, V. Gudnason, M. Boada, J. C. Bis, A. V. Smith, M. M. Carassquillo, J. C. Lambert, D. Harold, E. M. Schrijvers, R. Ramirez-Lorca, S. Debette, W. T. Longstreth, Jr., A. C. Janssens, V. S. Pankratz, J. F. Dartigues, P. Hollingworth, T. Aspelund, I. Hernandez, A. Beiser, L. H. Kuller, P. J. Koudstaal, D. W. Dickson, C. Tzourio, R. Abraham, C. Antunez, Y. Du, J. I. Rotter, Y. S. Aulchenko, T. B. Harris, R. C. Petersen, C. Berr, M. J. Owen, J. Lopez-Arrieta, B. N. Varadarajan, J. T. Becker, F. Rivadeneira, M. A. Nalls, N. R. Graff-Radford, D. Campion, S. Auerbach, K. Rice, A. Hofman, P. V. Jonsson, H. Schmidt, M. Lathrop, T. H. Mosley, R. Au, B. M. Psaty, A. G. Uitterlinden, L. A. Farrer, T. Lumley, A. Ruiz, J. Williams, P. Amouyel, S. G. Younkin, P. A. Wolf, L. J. Launer, O. L. Lopez, C. M. van Duijn and M. M. Breteler
Journal
JAMA
Year
2010
Volume
303
Issue
18
Pages
1832-40
Saykin, A.J., et al., Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans. Alzheimers Dement, 2010. 6(3): p. 265-73.
Download
Title
Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans
Authors
A. J. Saykin, L. Shen, T. M. Foroud, S. G. Potkin, S. Swaminathan, S. Kim, S. L. Risacher, K. Nho, M. J. Huentelman, D. W. Craig, P. M. Thompson, J. L. Stein, J. H. Moore, L. A. Farrer, R. C. Green, L. Bertram, C. R. Jack, Jr. and M. W. Weiner
Journal
Alzheimers Dement
Year
2010
Volume
6
Issue
3
Pages
265-73
Risacher, S.L., et al., Longitudinal MRI atrophy biomarkers: relationship to conversion in the ADNI cohort. Neurobiol Aging, 2010. 31(8): p. 1401-18.
Download
Title
Longitudinal MRI atrophy biomarkers: relationship to conversion in the ADNI cohort
Authors
S. L. Risacher, L. Shen, J. D. West, S. Kim, B. C. McDonald, L. A. Beckett, D. J. Harvey, C. R. Jack, Jr., M. W. Weiner and A. J. Saykin
Journal
Neurobiol Aging
Year
2010
Volume
31
Issue
8
Pages
1401-18
Rimol, L.M., et al., Sex-dependent association of common variants of microcephaly genes with brain structure. Proc Natl Acad Sci U S A, 2010. 107(1): p. 384-8.
Download
Title
Sex-dependent association of common variants of microcephaly genes with brain structure
Authors
L. M. Rimol, I. Agartz, S. Djurovic, A. A. Brown, J. C. Roddey, A. K. Kahler, M. Mattingsdal, L. Athanasiu, A. H. Joyner, N. J. Schork, E. Halgren, K. Sundet, I. Melle, A. M. Dale and O. A. Andreassen
Journal
Proc Natl Acad Sci U S A
Year
2010
Volume
107
Issue
1
Pages
384-8
Poduslo, S.E., R. Huang, and A. Spiro, 3rd, A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis. Am J Med Genet B Neuropsychiatr Genet, 2010. 153B(1): p. 114-9.
Download
Title
A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis
Authors
S. E. Poduslo, R. Huang and A. Spiro, 3rd
Journal
Am J Med Genet B Neuropsychiatr Genet
Year
2010
Volume
153B
Issue
1
Pages
114-9
Perry, R.T., H. Wiener, and R. Go, Follow-up Dense SNP Genotyping in NTRK2 Continues to Show Significant Association to LOAD in NIMH and NCRAD cohorts. Submitted, 2010.
Download
Title
Follow-up Dense SNP Genotyping in NTRK2 Continues to Show Significant Association to LOAD in NIMH and NCRAD cohorts.
Authors
R. T. Perry, H. Wiener and R. Go
Journal
Submitted
Year
2010
Volume
Issue
Pages
Payami, H., et al., Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease. Genet Epidemiol, 2010. 34(1): p. 92-9.
Download
Title
Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease
Authors
H. Payami, D. M. Kay, C. P. Zabetian, G. D. Schellenberg, S. A. Factor and C. C. McCulloch
Journal
Genet Epidemiol
Year
2010
Volume
34
Issue
1
Pages
92-9
Nelson, O., et al., Familial Alzheimer's disease mutations in presenilins: effects on endoplasmic reticulum calcium homeostasis and correlation with clinical phenotypes. J Alzheimers Dis, 2010. 21(3): p. 781-93.
Download
Title
Familial Alzheimer's disease mutations in presenilins: effects on endoplasmic reticulum calcium homeostasis and correlation with clinical phenotypes
Authors
O. Nelson, C. Supnet, H. Liu and I. Bezprozvanny
Journal
J Alzheimers Dis
Year
2010
Volume
21
Issue
3
Pages
781-93
Naj, A.C., et al., Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. PLoS Genet, 2010. 6(9).
Download
Title
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities
Authors
A. C. Naj, G. W. Beecham, E. R. Martin, P. J. Gallins, E. H. Powell, I. Konidari, P. L. Whitehead, G. Cai, V. Haroutunian, W. K. Scott, J. M. Vance, M. A. Slifer, H. E. Gwirtsman, J. R. Gilbert, J. L. Haines, J. D. Buxbaum and M. A. Pericak-Vance
Journal
PLoS Genet
Year
2010
Volume
6
Issue
9
Pages
Lakatos, A., et al., Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort. Neurobiol Aging, 2010. 31(8): p. 1355-63.
Download
Title
Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort
Authors
A. Lakatos, O. Derbeneva, D. Younes, D. Keator, T. Bakken, M. Lvova, M. Brandon, G. Guffanti, D. Reglodi, A. Saykin, M. Weiner, F. Macciardi, N. Schork, D. C. Wallace and S. G. Potkin
Journal
Neurobiol Aging
Year
2010
Volume
31
Issue
8
Pages
1355-63
Kauwe, J.S., et al., Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels. J Alzheimers Dis, 2010. 21(3): p. 833-42.
Download
Title
Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels
Authors
J. S. Kauwe, C. Cruchaga, S. Bertelsen, K. Mayo, W. Latu, P. Nowotny, A. L. Hinrichs, A. M. Fagan, D. M. Holtzman and A. M. Goate
Journal
J Alzheimers Dis
Year
2010
Volume
21
Issue
3
Pages
833-42
Kauwe, J.S., et al., Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet, 2010. 153B(4): p. 955-9.
Download
Title
Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease
Authors
J. S. Kauwe, S. Bertelsen, K. Mayo, C. Cruchaga, R. Abraham, P. Hollingworth, D. Harold, M. J. Owen, J. Williams, S. Lovestone, J. C. Morris and A. M. Goate
Journal
Am J Med Genet B Neuropsychiatr Genet
Year
2010
Volume
153B
Issue
4
Pages
955-9
Jun, G., et al., Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. Arch Neurol, 2010. 67(12): p. 1473-84.
Download
Title
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes
Authors
G. Jun, A. C. Naj, G. W. Beecham, L. S. Wang, J. Buros, P. J. Gallins, J. D. Buxbaum, N. Ertekin-Taner, M. D. Fallin, R. Friedland, R. Inzelberg, P. Kramer, E. Rogaeva, P. St George-Hyslop, L. B. Cantwell, B. A. Dombroski, A. J. Saykin, E. M. Reiman, D. A. Bennett, J. C. Morris, K. L. Lunetta, E. R. Martin, T. J. Montine, A. M. Goate, D. Blacker, D. W. Tsuang, D. Beekly, L. A. Cupples, H. Hakonarson, W. Kukull, T. M. Foroud, J. Haines, R. Mayeux, L. A. Farrer, M. A. Pericak-Vance and G. D. Schellenberg
Journal
Arch Neurol
Year
2010
Volume
67
Issue
12
Pages
1473-84
Ho, A.J., et al., A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly. Proc Natl Acad Sci U S A, 2010. 107(18): p. 8404-9.
Download
Title
A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly
Authors
A. J. Ho, J. L. Stein, X. Hua, S. Lee, D. P. Hibar, A. D. Leow, I. D. Dinov, A. W. Toga, A. J. Saykin, L. Shen, T. Foroud, N. Pankratz, M. J. Huentelman, D. W. Craig, J. D. Gerber, A. N. Allen, J. J. Corneveaux, D. A. Stephan, C. S. DeCarli, B. M. DeChairo, S. G. Potkin, C. R. Jack, Jr., M. W. Weiner, C. A. Raji, O. L. Lopez, J. T. Becker, O. T. Carmichael and P. M. Thompson
Journal
Proc Natl Acad Sci U S A
Year
2010
Volume
107
Issue
18
Pages
8404-9
Han, M.R., G.D. Schellenberg, and L.S. Wang, Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study. BMC Neurol, 2010. 10: p. 90.
Download
Title
Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study
Authors
M. R. Han, G. D. Schellenberg and L. S. Wang
Journal
BMC Neurol
Year
2010
Volume
10
Issue
Pages
90
Ghetti, B., et al. Clinicopathologic Characterization of Frontotemporal Dementia Associated with the IVS10-10G>T MAPT Gene Mutation. in American Association of Neuropathologists Annual Meeting. 2010.
Download
Title
Clinicopathologic Characterization of Frontotemporal Dementia Associated with the IVS10-10G&#62;T MAPT Gene Mutation
Authors
B. Ghetti, J. Murrell, M. Hagen, D. Geldmacher, T. Foroud, M. Goedert and S. Spina
Journal
Year
2010
Volume
Issue
Pages
Fallin, M.D., et al., Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls. Neurogenetics, 2010. 11(3): p. 335-48.
Download
Title
Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls
Authors
M. D. Fallin, M. Szymanski, R. Wang, A. Gherman, S. S. Bassett and D. Avramopoulos
Journal
Neurogenetics
Year
2010
Volume
11
Issue
3
Pages
335-48
Edwards, T.L., et al., Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Ann Hum Genet, 2010. 74(2): p. 97-109.
Download
Title
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease
Authors
T. L. Edwards, W. K. Scott, C. Almonte, A. Burt, E. H. Powell, G. W. Beecham, L. Wang, S. Zuchner, I. Konidari, G. Wang, C. Singer, F. Nahab, B. Scott, J. M. Stajich, M. Pericak-Vance, J. Haines, J. M. Vance and E. R. Martin
Journal
Ann Hum Genet
Year
2010
Volume
74
Issue
2
Pages
97-109
Carrasquillo, M.M., et al., Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease. PLoS One, 2010. 5(1): p. e8764.
Download
Title
Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease
Authors
M. M. Carrasquillo, O. Belbin, F. Zou, M. Allen, N. Ertekin-Taner, M. Ansari, S. L. Wilcox, M. R. Kashino, L. Ma, L. H. Younkin, S. G. Younkin, C. S. Younkin, T. A. Dincman, M. E. Howard, C. C. Howell, C. M. Stanton, C. M. Watson, M. Crump, V. Vitart, C. Hayward, N. D. Hastie, I. Rudan, H. Campbell, O. Polasek, K. Brown, P. Passmore, D. Craig, B. McGuinness, S. Todd, P. G. Kehoe, D. M. Mann, A. D. Smith, H. Beaumont, D. Warden, C. Holmes, R. Heun, H. Kolsch, N. Kalsheker, V. S. Pankratz, D. W. Dickson, N. R. Graff-Radford, R. C. Petersen, A. F. Wright and K. Morgan
Journal
PLoS One
Year
2010
Volume
5
Issue
1
Pages
e8764
Carrasquillo, M.M., et al., Replication of CLU, CR1, and PICALM associations with alzheimer disease. Arch Neurol, 2010. 67(8): p. 961-4.
Download
Title
Replication of CLU, CR1, and PICALM associations with alzheimer disease
Authors
M. M. Carrasquillo, O. Belbin, T. A. Hunter, L. Ma, G. D. Bisceglio, F. Zou, J. E. Crook, V. S. Pankratz, D. W. Dickson, N. R. Graff-Radford, R. C. Petersen, K. Morgan and S. G. Younkin
Journal
Arch Neurol
Year
2010
Volume
67
Issue
8
Pages
961-4
Campbell, N.L., et al., Use of anticholinergics and the risk of cognitive impairment in an African American population. Neurology, 2010. 75(2): p. 152-9.
Download
Title
Use of anticholinergics and the risk of cognitive impairment in an African American population
Authors
N. L. Campbell, M. A. Boustani, K. A. Lane, S. Gao, H. Hendrie, B. A. Khan, J. R. Murrell, F. W. Unverzagt, A. Hake, V. Smith-Gamble and K. Hall
Journal
Neurology
Year
2010
Volume
75
Issue
2
Pages
152-9
Biffi, A., et al., Genetic variation and neuroimaging measures in Alzheimer disease. Arch Neurol, 2010. 67(6): p. 677-85.
Download
Title
Genetic variation and neuroimaging measures in Alzheimer disease
Authors
A. Biffi, C. D. Anderson, R. S. Desikan, M. Sabuncu, L. Cortellini, N. Schmansky, D. Salat and J. Rosand
Journal
Arch Neurol
Year
2010
Volume
67
Issue
6
Pages
677-85
Beecham, G.W., et al., PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility. Psychiatr Genet, 2010. 20(6): p. 321-4.
Download
Title
PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility
Authors
G. W. Beecham, A. C. Naj, J. R. Gilbert, J. L. Haines, J. D. Buxbaum and M. A. Pericak-Vance
Journal
Psychiatr Genet
Year
2010
Volume
20
Issue
6
Pages
321-4
Schjeide, B.M., et al., Assessment of Alzheimer's disease case-control associations using family-based methods. Neurogenetics, 2009. 10(1): p. 19-25.
Download
Title
Assessment of Alzheimer's disease case-control associations using family-based methods
Authors
B. M. Schjeide, M. B. McQueen, K. Mullin, J. DiVito, M. F. Hogan, M. Parkinson, B. Hooli, C. Lange, D. Blacker, R. E. Tanzi and L. Bertram
Journal
Neurogenetics
Year
2009
Volume
10
Issue
1
Pages
19-25
Schjeide, B.M., et al., GAB2 as an Alzheimer disease susceptibility gene: follow-up of genomewide association results. Arch Neurol, 2009. 66(2): p. 250-4.
Download
Title
GAB2 as an Alzheimer disease susceptibility gene: follow-up of genomewide association results
Authors
B. M. Schjeide, B. Hooli, M. Parkinson, M. F. Hogan, J. DiVito, K. Mullin, D. Blacker, R. E. Tanzi and L. Bertram
Journal
Arch Neurol
Year
2009
Volume
66
Issue
2
Pages
250-4
Potkin, S.G., et al., Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. PLoS One, 2009. 4(8): p. e6501.
Download
Title
Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
Authors
S. G. Potkin, G. Guffanti, A. Lakatos, J. A. Turner, F. Kruggel, J. H. Fallon, A. J. Saykin, A. Orro, S. Lupoli, E. Salvi, M. Weiner and F. Macciardi
Journal
PLoS One
Year
2009
Volume
4
Issue
8
Pages
e6501
Poduslo, S.E., et al., Genome screen of late-onset Alzheimer's extended pedigrees identifies TRPC4AP by haplotype analysis. Am J Med Genet B Neuropsychiatr Genet, 2009. 150B(1): p. 50-5.
Download
Title
Genome screen of late-onset Alzheimer's extended pedigrees identifies TRPC4AP by haplotype analysis
Authors
S. E. Poduslo, R. Huang, J. Huang and S. Smith
Journal
Am J Med Genet B Neuropsychiatr Genet
Year
2009
Volume
150B
Issue
1
Pages
50-5
Poduslo, S.E., R. Huang, and J. Huang, The frequency of the TRPC4AP haplotype in Alzheimer's patients. Neurosci Lett, 2009. 450(3): p. 344-6.
Download
Title
The frequency of the TRPC4AP haplotype in Alzheimer's patients
Authors
S. E. Poduslo, R. Huang and J. Huang
Journal
Neurosci Lett
Year
2009
Volume
450
Issue
3
Pages
344-6
Pankratz, N., et al., Alpha-synuclein and familial Parkinson's disease. Mov Disord, 2009. 24(8): p. 1125-31.
Download
Title
Alpha-synuclein and familial Parkinson's disease
Authors
N. Pankratz, W. C. Nichols, V. E. Elsaesser, M. W. Pauciulo, D. K. Marek, C. A. Halter, J. Wojcieszek, A. Rudolph, R. F. Pfeiffer and T. Foroud
Journal
Mov Disord
Year
2009
Volume
24
Issue
8
Pages
1125-31
Nichols, W.C., et al., Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset. Neurology, 2009. 72(4): p. 310-6.
Download
Title
Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset
Authors
W. C. Nichols, N. Pankratz, D. K. Marek, M. W. Pauciulo, V. E. Elsaesser, C. A. Halter, A. Rudolph, J. Wojcieszek, R. F. Pfeiffer and T. Foroud
Journal
Neurology
Year
2009
Volume
72
Issue
4
Pages
310-6
Nichols, W.C., et al., Variation in GIGYF2 is not associated with Parkinson disease. Neurology, 2009. 72(22): p. 1886-92.
Download
Title
Variation in GIGYF2 is not associated with Parkinson disease
Authors
W. C. Nichols, D. K. Kissell, N. Pankratz, M. W. Pauciulo, V. E. Elsaesser, K. A. Clark, C. A. Halter, A. Rudolph, J. Wojcieszek, R. F. Pfeiffer and T. Foroud
Journal
Neurology
Year
2009
Volume
72
Issue
22
Pages
1886-92
Liang, X., et al., Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10. Hum Mutat, 2009. 30(3): p. 463-71.
Download
Title
Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10
Authors
X. Liang, M. Slifer, E. R. Martin, N. Schnetz-Boutaud, J. Bartlett, B. Anderson, S. Zuchner, H. Gwirtsman, J. R. Gilbert, M. A. Pericak-Vance and J. L. Haines
Journal
Hum Mutat
Year
2009
Volume
30
Issue
3
Pages
463-71
Kovacs, G.G., et al., TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Mov Disord, 2009. 24(12): p. 1843-7.
Download
Title
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
Authors
G. G. Kovacs, J. R. Murrell, S. Horvath, L. Haraszti, K. Majtenyi, M. J. Molnar, H. Budka, B. Ghetti and S. Spina
Journal
Mov Disord
Year
2009
Volume
24
Issue
12
Pages
1843-7
Kim, M., et al., Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate α-secretase activity. Human Molecular Genetics, 2009. 18(20): p. 3987-3996.
Download
Title
Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate α-secretase activity
Authors
M. Kim, J. Suh, D. Romano, M. H. Truong, K. Mullin, B. Hooli, D. Norton, G. Tesco, K. Elliott, S. L. Wagner, R. D. Moir, K. D. Becker and R. E. Tanzi
Journal
Human Molecular Genetics
Year
2009
Volume
18
Issue
20
Pages
3987-3996
Carrasquillo, M.M., et al., Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. Nat Genet, 2009. 41(2): p. 192-8.
Download
Title
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease
Authors
M. M. Carrasquillo, F. Zou, V. S. Pankratz, S. L. Wilcox, L. Ma, L. P. Walker, S. G. Younkin, C. S. Younkin, L. H. Younkin, G. D. Bisceglio, N. Ertekin-Taner, J. E. Crook, D. W. Dickson, R. C. Petersen and N. R. Graff-Radford
Journal
Nat Genet
Year
2009
Volume
41
Issue
2
Pages
192-8
Blom, E.S., et al., Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs. BMC.Med.Genet., 2009. 10: p. 122.
Download
Title
Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs
Authors
E. S. Blom, V. Giedraitis, S. Arepalli, M. L. Hamshere, O. Adighibe, A. Goate, J. Williams, L. Lannfelt, J. Hardy, F. W. Vrieze and A. Glaser
Journal
BMC.Med.Genet.
Year
2009
Volume
10
Issue
Pages
122
Beecham, G.W., et al., Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. Am J Hum Genet, 2009. 84(1): p. 35-43.
Download
Title
Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease
Authors
G. W. Beecham, E. R. Martin, Y. J. Li, M. A. Slifer, J. R. Gilbert, J. L. Haines and M. A. Pericak-Vance
Journal
Am J Hum Genet
Year
2009
Volume
84
Issue
1
Pages
35-43
Spina, S., et al., The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family. Brain, 2008. 131(Pt 1): p. 72-89.
Download
Title
The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family
Authors
S. Spina, M. R. Farlow, F. W. Unverzagt, D. A. Kareken, J. R. Murrell, G. Fraser, F. Epperson, R. A. Crowther, M. G. Spillantini, M. Goedert and B. Ghetti
Journal
Brain
Year
2008
Volume
131
Issue
Pt 1
Pages
72-89
Perry, R.T., et al., Hemoglobin binding to A beta and HBG2 SNP association suggest a role in Alzheimer's disease. Neurobiol.Aging, 2008. 29(2): p. 185-193.
Download
Title
Hemoglobin binding to A beta and HBG2 SNP association suggest a role in Alzheimer's disease
Authors
R. T. Perry, D. A. Gearhart, H. W. Wiener, L. E. Harrell, J. C. Barton, A. Kutlar, F. Kutlar, O. Ozcan, R. C. Go and W. D. Hill
Journal
Neurobiol.Aging
Year
2008
Volume
29
Issue
2
Pages
185-193
Murrell, J., et al. Two Novel Mutations in Progranulin Associated with Frontotemporal Lobar Degeneration. in 9th European Congress of Neuropathology. 2008.
Download
Title
Two Novel Mutations in Progranulin Associated with Frontotemporal Lobar Degeneration
Authors
J. Murrell, S. Spina, K. Yamaguchi, T. Foroud, M. Farlow and B. Ghetti
Journal
Year
2008
Volume
Issue
Pages
Lee, J.H., et al., Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: implication of additional loci. Arch.Neurol., 2008. 65(11): p. 1518-1526.
Download
Title
Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: implication of additional loci
Authors
J. H. Lee, R. Cheng, N. Graff-Radford, T. Foroud and R. Mayeux
Journal
Arch.Neurol.
Year
2008
Volume
65
Issue
11
Pages
1518-1526
Kay, D.M., et al., Genetic association between alpha-synuclein and idiopathic Parkinson's disease. Am.J.Med.Genet.B Neuropsychiatr.Genet., 2008. 147B(7): p. 1222-1230.
Download
Title
Genetic association between alpha-synuclein and idiopathic Parkinson's disease
Authors
D. M. Kay, S. A. Factor, A. Samii, D. S. Higgins, A. Griffith, J. W. Roberts, B. C. Leis, J. G. Nutt, J. S. Montimurro, R. G. Keefe, A. J. Atkins, D. Yearout, C. P. Zabetian and H. Payami
Journal
Am.J.Med.Genet.B Neuropsychiatr.Genet.
Year
2008
Volume
147B
Issue
7
Pages
1222-1230
Haasl, R.J., et al., A luteinizing hormone receptor intronic variant is significantly associated with decreased risk of Alzheimer's disease in males carrying an apolipoprotein E epsilon4 allele. BMC.Med.Genet., 2008. 9: p. 37.
Download
Title
A luteinizing hormone receptor intronic variant is significantly associated with decreased risk of Alzheimer's disease in males carrying an apolipoprotein E epsilon4 allele
Authors
R. J. Haasl, M. R. Ahmadi, S. V. Meethal, C. E. Gleason, S. C. Johnson, S. Asthana, R. L. Bowen and C. S. Atwood
Journal
BMC.Med.Genet.
Year
2008
Volume
9
Issue
Pages
37
Coppola, G., et al., Gene expression study on peripheral blood identifies progranulin mutations. Ann.Neurol., 2008. 64(1): p. 92-96.
Download
Title
Gene expression study on peripheral blood identifies progranulin mutations
Authors
G. Coppola, A. Karydas, R. Rademakers, Q. Wang, M. Baker, M. Hutton, B. L. Miller and D. H. Geschwind
Journal
Ann.Neurol.
Year
2008
Volume
64
Issue
1
Pages
92-96
Blom, E.S., et al., Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? Am.J.Med.Genet.B Neuropsychiatr.Genet., 2008. 147B(6): p. 778-783.
Download
Title
Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13?
Authors
E. S. Blom, P. Holmans, S. Arepalli, O. Adighibe, M. L. Hamshere, M. Gatz, N. L. Pedersen, A. L. Bergem, M. J. Owen, P. Hollingworth, A. Goate, J. Williams, L. Lannfelt, J. Hardy, V. F. Wavrant-De and A. Glaser
Journal
Am.J.Med.Genet.B Neuropsychiatr.Genet.
Year
2008
Volume
147B
Issue
6
Pages
778-783
Bertram, L., et al., No association between CALHM1 and Alzheimer's disease risk. Cell, 2008. 135(6): p. 993-994.
Download
Title
No association between CALHM1 and Alzheimer's disease risk
Authors
L. Bertram, B. M. Schjeide, B. Hooli, K. Mullin, M. Hiltunen, H. Soininen, M. Ingelsson, L. Lannfelt, D. Blacker and R. E. Tanzi
Journal
Cell
Year
2008
Volume
135
Issue
6
Pages
993-994
Bertram, L., et al., Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE. Am.J.Hum.Genet., 2008. 83(5): p. 623-632.
Download
Title
Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE
Authors
L. Bertram, C. Lange, K. Mullin, M. Parkinson, M. Hsiao, M. F. Hogan, B. M. Schjeide, B. Hooli, J. Divito, I. Ionita, H. Jiang, N. Laird, T. Moscarillo, K. L. Ohlsen, K. Elliott, X. Wang, D. Hu-Lince, M. Ryder, A. Murphy, S. L. Wagner, D. Blacker, K. D. Becker and R. E. Tanzi
Journal
Am.J.Hum.Genet.
Year
2008
Volume
83
Issue
5
Pages
623-632
Baye, T.M., et al., Candidate gene discovery procedure after follow-up confirmatory analyses of candidate regions of interests for Alzheimer's disease in the NIMH sibling dataset. Dis.Markers, 2008. 24(6): p. 293-309.
Download
Title
Candidate gene discovery procedure after follow-up confirmatory analyses of candidate regions of interests for Alzheimer's disease in the NIMH sibling dataset
Authors
T. M. Baye, R. T. Perry, H. W. Wiener, Z. Chen, L. E. Harrell and R. C. Go
Journal
Dis.Markers
Year
2008
Volume
24
Issue
6
Pages
293-309
Yu, C.E., et al., Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association. Genomics, 2007. 89(6): p. 655-665.
Download
Title
Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association
Authors
C. E. Yu, H. Seltman, E. R. Peskind, N. Galloway, P. X. Zhou, E. Rosenthal, E. M. Wijsman, D. W. Tsuang, B. Devlin and G. D. Schellenberg
Journal
Genomics
Year
2007
Volume
89
Issue
6
Pages
655-665
Wiener, H.W., et al., A polymorphism in SOD2 is associated with development of Alzheimer's disease. Genes Brain Behav., 2007. 6(8): p. 770-775.
Download
Title
A polymorphism in SOD2 is associated with development of Alzheimer's disease
Authors
H. W. Wiener, R. T. Perry, Z. Chen, L. E. Harrell and R. C. Go
Journal
Genes Brain Behav.
Year
2007
Volume
6
Issue
8
Pages
770-775
Wavrant De-Vrieze, F., et al., ABCA1 polymorphisms and Alzheimer's disease. Neurosci.Lett., 2007. 416(2): p. 180-183.
Download
Title
ABCA1 polymorphisms and Alzheimer's disease
Authors
F. Wavrant De-Vrieze, D. Compton, M. Womick, S. Arepalli, O. Adighibe, L. Li, J. Perez-Tur and J. Hardy
Journal
Neurosci.Lett.
Year
2007
Volume
416
Issue
2
Pages
180-183
Sieh, W., et al., Accounting for linkage disequilibrium among markers in linkage analysis: impact of haplotype frequency estimation and molecular haplotypes for a gene in a candidate region for Alzheimer's disease. Hum.Hered., 2007. 63(1): p. 26-34.
Download
Title
Accounting for linkage disequilibrium among markers in linkage analysis: impact of haplotype frequency estimation and molecular haplotypes for a gene in a candidate region for Alzheimer's disease
Authors
W. Sieh, C. E. Yu, T. D. Bird, G. D. Schellenberg and E. M. Wijsman
Journal
Hum.Hered.
Year
2007
Volume
63
Issue
1
Pages
26-34
Perry, R.T., et al., Follow-up mapping supports the evidence for linkage in the candidate region at 9q22 in the NIMH Alzheimer's disease Genetics Initiative cohort. Am.J.Med.Genet.B Neuropsychiatr.Genet., 2007. 144B(2): p. 220-227.
Download
Title
Follow-up mapping supports the evidence for linkage in the candidate region at 9q22 in the NIMH Alzheimer's disease Genetics Initiative cohort
Authors
R. T. Perry, H. Wiener, L. E. Harrell, D. Blacker, R. E. Tanzi, L. Bertram, S. S. Bassett and R. C. Go
Journal
Am.J.Med.Genet.B Neuropsychiatr.Genet.
Year
2007
Volume
144B
Issue
2
Pages
220-227
Nichols, W.C., et al., R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation. Mov Disord, 2007. 22(2): p. 254-7.
Download
Title
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation
Authors
W. C. Nichols, D. K. Marek, M. W. Pauciulo, N. Pankratz, C. A. Halter, A. Rudolph, C. W. Shults, J. Wojcieszek and T. Foroud
Journal
Mov Disord
Year
2007
Volume
22
Issue
2
Pages
254-7
Nichols, W.C., et al., LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8. Neurology, 2007. 69(18): p. 1737-44.
Download
Title
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
Authors
W. C. Nichols, V. E. Elsaesser, N. Pankratz, M. W. Pauciulo, D. K. Marek, C. A. Halter, A. Rudolph, C. W. Shults and T. Foroud
Journal
Neurology
Year
2007
Volume
69
Issue
18
Pages
1737-44
Liang, X., et al., Association analysis of genetic polymorphisms in the CDC2 gene with late-onset Alzheimer disease. Dement Geriatr Cogn Disord, 2007. 23(2): p. 126-32.
Download
Title
Association analysis of genetic polymorphisms in the CDC2 gene with late-onset Alzheimer disease
Authors
X. Liang, N. Schnetz-Boutaud, J. Bartlett, B. M. Anderson, H. Gwirtsman, D. Schmechel, R. Carney, J. R. Gilbert, M. A. Pericak-Vance and J. L. Haines
Journal
Dement Geriatr Cogn Disord
Year
2007
Volume
23
Issue
2
Pages
126-32
Liang, X., et al., Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease. Hum Mutat, 2007. 28(11): p. 1065-73.
Download
Title
Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease
Authors
X. Liang, E. R. Martin, N. Schnetz-Boutaud, J. Bartlett, B. Anderson, S. Zuchner, H. Gwirtsman, D. Schmechel, R. Carney, J. R. Gilbert, M. A. Pericak-Vance and J. L. Haines
Journal
Hum Mutat
Year
2007
Volume
28
Issue
11
Pages
1065-73
Kay, D.M., et al., Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients. Ann.Neurol., 2007. 61(1): p. 47-54.
Download
Title
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients
Authors
D. M. Kay, D. Moran, L. Moses, P. Poorkaj, C. P. Zabetian, J. Nutt, S. A. Factor, C. E. Yu, J. S. Montimurro, R. G. Keefe, G. D. Schellenberg and H. Payami
Journal
Ann.Neurol.
Year
2007
Volume
61
Issue
1
Pages
47-54
Kauwe, J.S., et al., Extreme cerebrospinal fluid amyloid beta levels identify family with late-onset Alzheimer's disease presenilin 1 mutation. Ann Neurol, 2007. 61(5): p. 446-53.
Download
Title
Extreme cerebrospinal fluid amyloid beta levels identify family with late-onset Alzheimer's disease presenilin 1 mutation
Authors
J. S. Kauwe, S. Jacquart, S. Chakraverty, J. Wang, K. Mayo, A. M. Fagan, D. M. Holtzman, J. C. Morris and A. M. Goate
Journal
Ann Neurol
Year
2007
Volume
61
Issue
5
Pages
446-53
Huang, R., et al., Genetic variants in brain-derived neurotrophic factor associated with Alzheimer's disease. J.Med.Genet., 2007. 44(2): p. e66.
Download
Title
Genetic variants in brain-derived neurotrophic factor associated with Alzheimer's disease
Authors
R. Huang, J. Huang, H. Cathcart, S. Smith and S. E. Poduslo
Journal
J.Med.Genet.
Year
2007
Volume
44
Issue
2
Pages
e66
Hamshere, M.L., et al., Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Hum.Mol.Genet., 2007. 16(22): p. 2703-2712.
Download
Title
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease
Authors
M. L. Hamshere, P. A. Holmans, D. Avramopoulos, S. S. Bassett, D. Blacker, L. Bertram, H. Wiener, N. Rochberg, R. E. Tanzi, A. Myers, V. F. Wavrant-De, R. Go, D. Fallin, S. Lovestone, J. Hardy, A. Goate, M. O'Donovan, J. Williams and M. J. Owen
Journal
Hum.Mol.Genet.
Year
2007
Volume
16
Issue
22
Pages
2703-2712
De Ferrari, G.V., et al., Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease. Proc.Natl.Acad.Sci.U.S.A, 2007. 104(22): p. 9434-9439.
Download
Title
Common genetic variation within the low-density lipoprotein receptor-related protein 6 and late-onset Alzheimer's disease
Authors
G. V. De Ferrari, A. Papassotiropoulos, T. Biechele, F. Wavrant De-Vrieze, M. E. Avila, M. B. Major, A. Myers, K. Saez, J. P. Henriquez, A. Zhao, M. A. Wollmer, R. M. Nitsch, C. Hock, C. M. Morris, J. Hardy and R. T. Moon
Journal
Proc.Natl.Acad.Sci.U.S.A
Year
2007
Volume
104
Issue
22
Pages
9434-9439
Coppola, G., et al. Genetic Investigation in Frontotemporal Dementia and Alzheimer's Disease: The GIFT study. in ANA Meeting. 2007.
Download
Title
Genetic Investigation in Frontotemporal Dementia and Alzheimer's Disease: The GIFT study
Authors
G. Coppola, B. Miller, H. Chui, A. Varpetian, A. I. Levey, C. Cotman, C. S. DeCarli, G. Bartzokis, W. A. Kukull, T. Foroud and D. H. Geschwind
Journal
Year
2007
Volume
Issue
Pages
Chun, L.S., et al., DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease. Ann.Neurol., 2007. 62(1): p. 99-101.
Download
Title
DBH -1021C--&#62;T does not modify risk or age at onset in Parkinson's disease
Authors
L. S. Chun, A. Samii, C. M. Hutter, A. Griffith, J. W. Roberts, B. C. Leis, A. D. Mosley, P. L. Wander, K. L. Edwards, H. Payami and C. P. Zabetian
Journal
Ann.Neurol.
Year
2007
Volume
62
Issue
1
Pages
99-101
Brown, A.M., et al., Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations. Neurochem.Res., 2007. 32(4-5): p. 857-869.
Download
Title
Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations
Authors
A. M. Brown, D. Gordon, H. Lee, V. F. Wavrant-De, E. Cellini, S. Bagnoli, B. Nacmias, S. Sorbi, J. Hardy and J. P. Blass
Journal
Neurochem.Res.
Year
2007
Volume
32
Issue
42099
Pages
857-869
Zabetian, C.P., et al., Analysis of the LRRK2 G2019S mutation in Alzheimer Disease. Arch.Neurol., 2006. 63(1): p. 156-157.
Download
Title
Analysis of the LRRK2 G2019S mutation in Alzheimer Disease
Authors
C. P. Zabetian, C. J. Lauricella, D. W. Tsuang, J. B. Leverenz, G. D. Schellenberg and H. Payami
Journal
Arch.Neurol.
Year
2006
Volume
63
Issue
1
Pages
156-157
Pankratz, N., et al., Mutations in DJ-1 are rare in familial Parkinson disease. Neurosci.Lett., 2006. 408(3): p. 209-213.
Download
Title
Mutations in DJ-1 are rare in familial Parkinson disease
Authors
N. Pankratz, M. W. Pauciulo, V. E. Elsaesser, D. K. Marek, C. A. Halter, J. Wojcieszek, A. Rudolph, C. W. Shults, T. Foroud and W. C. Nichols
Journal
Neurosci.Lett.
Year
2006
Volume
408
Issue
3
Pages
209-213
Murrell, J., et al., The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen families. Neurogenetics., 2006. 7(4): p. 277-279.
Download
Title
The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen families
Authors
J. Murrell, B. Ghetti, E. Cochran, M. A. ias-Islas, L. Medina, A. Varpetian, J. L. Cummings, M. F. Mendez, C. Kawas, H. Chui and J. M. Ringman
Journal
Neurogenetics.
Year
2006
Volume
7
Issue
4
Pages
277-279
Liang, X., et al., Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus. Mol.Psychiatry, 2006. 11(3): p. 280-285.
Download
Title
Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus
Authors
X. Liang, N. Schnetz-Boutaud, S. J. Kenealy, L. Jiang, J. Bartlett, B. Lynch, P. C. Gaskell, H. Gwirtsman, L. McFarland, M. L. Bembe, P. Bronson, J. R. Gilbert, E. R. Martin, M. A. Pericak-Vance and J. L. Haines
Journal
Mol.Psychiatry
Year
2006
Volume
11
Issue
3
Pages
280-285
Li, Y.J., et al., Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases. Neurobiol.Aging, 2006. 27(8): p. 1087-1093.
Download
Title
Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases
Authors
Y. J. Li, W. K. Scott, L. Zhang, P. I. Lin, S. A. Oliveira, T. Skelly, M. P. Doraiswamy, K. A. Welsh-Bohmer, E. R. Martin, J. L. Haines, M. A. Pericak-Vance and J. M. Vance
Journal
Neurobiol.Aging
Year
2006
Volume
27
Issue
8
Pages
1087-1093
Kay, D.M., et al., Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's disease. Genet.Test., 2006. 10(3): p. 221-227.
Download
Title
Validity and utility of a LRRK2 G2019S mutation test for the diagnosis of Parkinson's disease
Authors
D. M. Kay, T. D. Bird, C. P. Zabetian, S. A. Factor, A. Samii, D. S. Higgins, J. Nutt, J. W. Roberts, A. Griffith, B. C. Leis, J. S. Montimurro, S. Philpott and H. Payami
Journal
Genet.Test.
Year
2006
Volume
10
Issue
3
Pages
221-227
Huang, R. and S.E. Poduslo, CYP19 haplotypes increase risk for Alzheimer's disease. J Med Genet, 2006. 43(8): p. e42.
Download
Title
CYP19 haplotypes increase risk for Alzheimer's disease
Authors
R. Huang and S. E. Poduslo
Journal
J Med Genet
Year
2006
Volume
43
Issue
8
Pages
e42
Grupe, A., et al., A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. Am.J.Hum.Genet., 2006. 78(1): p. 78-88.
Download
Title
A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease
Authors
A. Grupe, Y. Li, C. Rowland, P. Nowotny, A. L. Hinrichs, S. Smemo, J. S. Kauwe, T. J. Maxwell, S. Cherny, L. Doil, K. Tacey, L. R. van, A. Myers, V. F. Wavrant-De, M. Kaleem, P. Hollingworth, L. Jehu, C. Foy, N. Archer, G. Hamilton, P. Holmans, C. M. Morris, J. Catanese, J. Sninsky, T. J. White, J. Powell, J. Hardy, M. O'Donovan, S. Lovestone, L. Jones, J. C. Morris, L. Thal, M. Owen, J. Williams and A. Goate
Journal
Am.J.Hum.Genet.
Year
2006
Volume
78
Issue
1
Pages
78-88
Elbaz, A., et al., Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study. Lancet Neurol., 2006. 5(11): p. 917-923.
Download
Title
Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study
Authors
A. Elbaz, L. M. Nelson, H. Payami, J. P. Ioannidis, B. K. Fiske, G. Annesi, B. A. Carmine, S. A. Factor, C. Ferrarese, G. M. Hadjigeorgiou, D. S. Higgins, H. Kawakami, R. Kruger, K. S. Marder, R. P. Mayeux, G. D. Mellick, J. G. Nutt, B. Ritz, A. Samii, C. M. Tanner, B. C. Van, S. K. Van Den Eeden, K. Wirdefeldt, C. P. Zabetian, M. Dehem, J. S. Montimurro, A. Southwick, R. M. Myers and T. A. Trikalinos
Journal
Lancet Neurol.
Year
2006
Volume
5
Issue
11
Pages
917-923
Corder, E.H., et al., Membership in genetic groups predicts Alzheimer disease. Rejuvenation.Res., 2006. 9(1): p. 89-93.
Download
Title
Membership in genetic groups predicts Alzheimer disease
Authors
E. H. Corder, R. Huang, H. M. Cathcart, I. S. Lanham, G. R. Parker, D. Cheng, S. Smith and S. E. Poduslo
Journal
Rejuvenation.Res.
Year
2006
Volume
9
Issue
1
Pages
89-93
Baba, Y., et al., Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred. Acta Neuropathol., 2006. 111(4): p. 300-311.
Download
Title
Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred
Authors
Y. Baba, B. Ghetti, M. C. Baker, R. J. Uitti, M. L. Hutton, K. Yamaguchi, T. Bird, W. Lin, M. W. DeLucia, D. W. Dickson and Z. K. Wszolek
Journal
Acta Neuropathol.
Year
2006
Volume
111
Issue
4
Pages
300-311
Adighibe, O., et al., Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease. Neurobiol.Aging, 2006. 27(10): p. 1431-1434.
Download
Title
Genetic variability at the LXR gene (NR1H2) may contribute to the risk of Alzheimer's disease
Authors
O. Adighibe, S. Arepalli, J. Duckworth, J. Hardy and V. F. Wavrant-De
Journal
Neurobiol.Aging
Year
2006
Volume
27
Issue
10
Pages
1431-1434
Wijsman, E.M., et al., APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation. Am.J.Med.Genet.B Neuropsychiatr.Genet., 2005. 132B(1): p. 14-20.
Download
Title
APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation
Authors
E. M. Wijsman, E. W. Daw, X. Yu, E. J. Steinbart, D. Nochlin, T. D. Bird and G. D. Schellenberg
Journal
Am.J.Med.Genet.B Neuropsychiatr.Genet.
Year
2005
Volume
132B
Issue
1
Pages
14-20
van der Walt, J.M., et al., Maternal lineages and Alzheimer disease risk in the Old Order Amish. Hum.Genet., 2005. 118(1): p. 115-122.
Download
Title
Maternal lineages and Alzheimer disease risk in the Old Order Amish
Authors
J. M. van der Walt, W. K. Scott, S. Slifer, P. C. Gaskell, E. R. Martin, K. Welsh-Bohmer, M. Creason, A. Crunk, D. Fuzzell, L. McFarland, C. C. Kroner, C. E. Jackson, J. L. Haines and M. A. Pericak-Vance
Journal
Hum.Genet.
Year
2005
Volume
118
Issue
1
Pages
115-122
Slifer, M.A., et al., The ubiquilin 1 gene and Alzheimer's disease. N Engl J Med, 2005. 352(26): p. 2752-3; author reply 2752-3.
Download
Title
The ubiquilin 1 gene and Alzheimer's disease
Authors
M. A. Slifer, E. R. Martin, J. L. Haines and M. A. Pericak-Vance
Journal
N Engl J Med
Year
2005
Volume
352
Issue
26
Pages
2752-3; author reply 2752-3
Pittman, A.M., et al., Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration. J.Med.Genet., 2005. 42(11): p. 837-846.
Download
Title
Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration
Authors
A. M. Pittman, A. J. Myers, P. bou-Sleiman, H. C. Fung, M. Kaleem, L. Marlowe, J. Duckworth, D. Leung, D. Williams, L. Kilford, N. Thomas, C. M. Morris, D. Dickson, N. W. Wood, J. Hardy, A. J. Lees and S. R. de
Journal
J.Med.Genet.
Year
2005
Volume
42
Issue
11
Pages
837-846
Parker, G.R., et al., Apolipoprotein gene E4 allele promoter polymorphisms as risk factors for Alzheimer's disease. Psychiatr Genet, 2005. 15(4): p. 271-5.
Download
Title
Apolipoprotein gene E4 allele promoter polymorphisms as risk factors for Alzheimer's disease
Authors
G. R. Parker, H. M. Cathcart, R. Huang, I. S. Lanham, E. H. Corder and S. E. Poduslo
Journal
Psychiatr Genet
Year
2005
Volume
15
Issue
4
Pages
271-5
Nowotny, P., et al., Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. Am.J.Med.Genet.B Neuropsychiatr.Genet., 2005. 136B(1): p. 62-68.
Download
Title
Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme
Authors
P. Nowotny, A. L. Hinrichs, S. Smemo, J. S. Kauwe, T. Maxwell, P. Holmans, M. Hamshere, D. Turic, L. Jehu, P. Hollingworth, P. Moore, L. Bryden, A. Myers, L. M. Doil, K. M. Tacey, A. M. Gibson, I. G. McKeith, R. H. Perry, C. M. Morris, L. Thal, J. C. Morris, M. C. O'Donovan, S. Lovestone, A. Grupe, J. Hardy, M. J. Owen, J. Williams and A. Goate
Journal
Am.J.Med.Genet.B Neuropsychiatr.Genet.
Year
2005
Volume
136B
Issue
1
Pages
62-68
Myllykangas, L., et al., Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: a two-stage study. J.Neurol.Sci., 2005. 236(1-2): p. 17-24.
Download
Title
Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: a two-stage study
Authors
L. Myllykangas, V. F. Wavrant-De, T. Polvikoski, I. L. Notkola, R. Sulkava, L. Niinisto, S. D. Edland, S. Arepalli, O. Adighibe, D. Compton, J. Hardy, M. Haltia and P. J. Tienari
Journal
J.Neurol.Sci.
Year
2005
Volume
236
Issue
42006
Pages
17-24
Martin, E.R., et al., Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease. J.Med.Genet., 2005. 42(10): p. 787-792.
Download
Title
Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease
Authors
E. R. Martin, P. G. Bronson, Y. J. Li, N. Wall, R. H. Chung, D. E. Schmechel, G. Small, P. T. Xu, J. Bartlett, N. Schnetz-Boutaud, J. L. Haines, J. R. Gilbert and M. A. Pericak-Vance
Journal
J.Med.Genet.
Year
2005
Volume
42
Issue
10
Pages
787-792
Li, Y., et al., The BDNF Val66Met polymorphism is not associated with late onset Alzheimer's disease in three case-control samples. Mol.Psychiatry, 2005. 10(9): p. 809-810.
Download
Title
The BDNF Val66Met polymorphism is not associated with late onset Alzheimer's disease in three case-control samples
Authors
Y. Li, C. Rowland, K. Tacey, J. Catanese, J. Sninsky, J. Hardy, J. Powell, S. Lovestone, J. C. Morris, L. Thal, A. Goate, M. Owen, J. Williams and A. Grupe
Journal
Mol.Psychiatry
Year
2005
Volume
10
Issue
9
Pages
809-810
Li, Y., et al., Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Hum.Mutat., 2005. 25(3): p. 270-277.
Download
Title
Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease
Authors
Y. Li, P. Hollingworth, P. Moore, C. Foy, N. Archer, J. Powell, P. Nowotny, P. Holmans, M. O'Donovan, K. Tacey, L. Doil, L. R. van, V. Garcia, C. Rowland, K. Lau, J. Cantanese, J. Sninsky, J. Hardy, L. Thal, J. C. Morris, A. Goate, S. Lovestone, M. Owen, J. Williams and A. Grupe
Journal
Hum.Mutat.
Year
2005
Volume
25
Issue
3
Pages
270-277
Holmans, P., et al., Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. Am.J.Med.Genet.B Neuropsychiatr.Genet., 2005. 135B(1): p. 24-32.
Download
Title
Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease
Authors
P. Holmans, M. Hamshere, P. Hollingworth, F. Rice, N. Tunstall, S. Jones, P. Moore, D. F. Wavrant, A. Myers, R. Crook, D. Compton, H. Marshall, D. Meyer, S. Shears, J. Booth, D. Ramic, N. Williams, N. Norton, R. Abraham, P. Kehoe, H. Williams, V. Rudrasingham, M. O'Donovan, L. Jones, J. Hardy, A. Goate, S. Lovestone, M. Owen and J. Williams
Journal
Am.J.Med.Genet.B Neuropsychiatr.Genet.
Year
2005
Volume
135B
Issue
1
Pages
24-32
Go, R.C., et al., Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses. Am.J.Med.Genet.B Neuropsychiatr.Genet., 2005. 139B(1): p. 28-32.
Download
Title
Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses
Authors
R. C. Go, R. T. Perry, H. Wiener, S. S. Bassett, D. Blacker, B. Devlin and R. A. Sweet
Journal
Am.J.Med.Genet.B Neuropsychiatr.Genet.
Year
2005
Volume
139B
Issue
1
Pages
28-32
Dickson, M.R., et al., Association studies of transforming growth factor-beta 1 and Alzheimer's disease. Am.J.Med.Genet.B Neuropsychiatr.Genet., 2005. 139B(1): p. 38-41.
Download
Title
Association studies of transforming growth factor-beta 1 and Alzheimer's disease
Authors
M. R. Dickson, R. T. Perry, H. Wiener and R. C. Go
Journal
Am.J.Med.Genet.B Neuropsychiatr.Genet.
Year
2005
Volume
139B
Issue
1
Pages
38-41
Cheng, D., et al., Functional interaction between APOE4 and LDL receptor isoforms in Alzheimer's disease. J.Med.Genet., 2005. 42(2): p. 129-131.
Download
Title
Functional interaction between APOE4 and LDL receptor isoforms in Alzheimer's disease
Authors
D. Cheng, R. Huang, I. S. Lanham, H. M. Cathcart, M. Howard, E. H. Corder and S. E. Poduslo
Journal
J.Med.Genet.
Year
2005
Volume
42
Issue
2
Pages
129-131
Cathcart, H.M., et al., Cystatin C as a risk factor for Alzheimer disease. Neurology, 2005. 64(4): p. 755-757.
Download
Title
Cystatin C as a risk factor for Alzheimer disease
Authors
H. M. Cathcart, R. Huang, I. S. Lanham, E. H. Corder and S. E. Poduslo
Journal
Neurology
Year
2005
Volume
64
Issue
4
Pages
755-757
Bodner, S.M., et al., Genetic variation in the brain derived neurotrophic factor gene in Alzheimer's disease. Am.J.Med.Genet.B Neuropsychiatr.Genet., 2005. 134B(1): p. 1-5.
Download
Title
Genetic variation in the brain derived neurotrophic factor gene in Alzheimer's disease
Authors
S. M. Bodner, W. Berrettini, D. V. van, D. A. Bennett, R. S. Wilson, J. Q. Trojanowski and S. E. Arnold
Journal
Am.J.Med.Genet.B Neuropsychiatr.Genet.
Year
2005
Volume
134B
Issue
1
Pages
42009
Wijsman, E.M., et al., Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2. Am.J.Hum.Genet., 2004. 75(3): p. 398-409.
Download
Title
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2
Authors
E. M. Wijsman, E. W. Daw, C. E. Yu, H. Payami, E. J. Steinbart, D. Nochlin, E. M. Conlon, T. D. Bird and G. D. Schellenberg
Journal
Am.J.Hum.Genet.
Year
2004
Volume
75
Issue
3
Pages
398-409