Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ... Nature genetics 45 (12), 1452-1458, 2013 | 4746 | 2013 |
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease D Harold, R Abraham, P Hollingworth, R Sims, A Gerrish, ML Hamshere, ... Nature genetics 41 (10), 1088-1093, 2009 | 3453 | 2009 |
TREM2 Variants in Alzheimer's Disease R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ... New England Journal of Medicine 368 (2), 117-127, 2013 | 3350 | 2013 |
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ... Nature genetics 51 (3), 414-430, 2019 | 2673 | 2019 |
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease P Hollingworth, D Harold, R Sims, A Gerrish, JC Lambert, ... Nature genetics 43 (5), 429-435, 2011 | 2322 | 2011 |
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease AC Naj, G Jun, GW Beecham, LS Wang, BN Vardarajan, J Buros, ... Nature genetics 43 (5), 436-441, 2011 | 2260 | 2011 |
Genome-wide analysis of genetic loci associated with Alzheimer disease S Seshadri, AL Fitzpatrick, MA Ikram, AL DeStefano, V Gudnason, ... Jama 303 (18), 1832-1840, 2010 | 1513 | 2010 |
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ... Nature genetics 49 (9), 1373-1384, 2017 | 1012 | 2017 |
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease L Jones, PA Holmans, ML Hamshere, D Harold, V Moskvina, D Ivanov, ... PloS one 5 (11), e13950, 2010 | 476 | 2010 |
High-throughput variation detection and genotyping using microarrays DJ Cutler, ME Zwick, MM Carrasquillo, CT Yohn, KP Tobin, C Kashuk, ... Genome research 11 (11), 1913-1925, 2001 | 432 | 2001 |
Human whole genome genotype and transcriptome data for Alzheimer’s and other neurodegenerative diseases M Allen, MM Carrasquillo, C Funk, BD Heavner, F Zou, CS Younkin, ... Scientific data 3 (1), 1-10, 2016 | 406 | 2016 |
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease MM Carrasquillo, F Zou, VS Pankratz, SL Wilcox, L Ma, LP Walker, ... Nature genetics 41 (2), 192-198, 2009 | 379 | 2009 |
Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease MM Carrasquillo, AS McCallion, EG Puffenberger, CS Kashuk, N Nouri, ... Nature genetics 32 (2), 237-244, 2002 | 321 | 2002 |
A novel Alzheimer disease locus located near the gene encoding tau protein G Jun, CA Ibrahim-Verbaas, M Vronskaya, JC Lambert, J Chung, AC Naj, ... Molecular psychiatry 21 (1), 108-117, 2016 | 312 | 2016 |
Genome-wide association study of Alzheimer's disease MI Kamboh, FY Demirci, X Wang, RL Minster, MM Carrasquillo, ... Translational psychiatry 2 (5), e117-e117, 2012 | 301 | 2012 |
Assessment of the genetic variance of late-onset Alzheimer's disease PG Ridge, KB Hoyt, K Boehme, S Mukherjee, PK Crane, JL Haines, ... Neurobiology of aging 41, 200. e13-200. e20, 2016 | 278 | 2016 |
Replication of CLU, CR1, and PICALM associations with alzheimer disease MM Carrasquillo, O Belbin, TA Hunter, L Ma, GD Bisceglio, F Zou, ... Archives of neurology 67 (8), 961-964, 2010 | 275 | 2010 |
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers N Finch, MM Carrasquillo, M Baker, NJ Rutherford, G Coppola, ... Neurology 76 (5), 467-474, 2011 | 274 | 2011 |
Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants F Zou, HS Chai, CS Younkin, M Allen, J Crook, VS Pankratz, ... PLoS genetics 8 (6), e1002707, 2012 | 260 | 2012 |
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations MM Carrasquillo, J Zlotogora, S Barges, A Chakravarti Human molecular genetics 6 (12), 2163-2172, 1997 | 223 | 1997 |