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Shaun Purcell
Shaun Purcell
Sleep & Neurogenetics Lab, Brigham & Women's Hospital, Boston
Email verificata su bwh.harvard.edu - Home page
Titolo
Citata da
Citata da
Anno
PLINK: a tool set for whole-genome association and population-based linkage analyses
S Purcell, B Neale, K Todd-Brown, L Thomas, MAR Ferreira, D Bender, ...
The American journal of human genetics 81 (3), 559-575, 2007
336572007
Analysis of protein-coding genetic variation in 60,706 humans
M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ...
Nature 536 (7616), 285-291, 2016
105812016
Second-generation PLINK: rising to the challenge of larger and richer datasets
CC Chang, CC Chow, LCAM Tellier, S Vattikuti, SM Purcell, JJ Lee
Gigascience 4 (1), s13742-015-0047-8, 2015
101312015
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
9456*2007
Biological insights from 108 schizophrenia-associated genetic loci
C Pantelis, GN Papadimitriou, S Papiol, E Parkhomenko, MT Pato, ...
Nature 511 (7510), 421-427, 2014
76512014
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
International Schizophrenia Consortium Manuscript preparation Purcell Shaun ...
Nature 460 (7256), 748-752, 2009
53392009
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
EK Speliotes, CJ Willer, SI Berndt, KL Monda, G Thorleifsson, AU Jackson, ...
Nature genetics 42 (11), 937-948, 2010
36072010
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
G Genovese, AK Kähler, RE Handsaker, J Lindberg, SA Rose, ...
New England Journal of Medicine 371 (26), 2477-2487, 2014
35442014
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
R Saxena, BF Voight, V Lyssenko, NP Burtt, PIW de Bakker, H Chen, ...
Science 316 (5829), 1331-1336, 2007
30512007
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
28762014
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ...
Nature genetics 50 (5), 668-681, 2018
27802018
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
BF Voight, GM Peloso, M Orho-Melander, R Frikke-Schmidt, M Barbalic, ...
The Lancet 380 (9841), 572-580, 2012
26372012
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
24032013
Partitioning heritability by functional annotation using genome-wide association summary statistics
HK Finucane, B Bulik-Sullivan, A Gusev, G Trynka, Y Reshef, PR Loh, ...
Nature genetics 47 (11), 1228-1235, 2015
23862015
Hundreds of variants clustered in genomic loci and biological pathways affect human height
H Lango Allen, K Estrada, G Lettre, SI Berndt, MN Weedon, F Rivadeneira, ...
Nature 467 (7317), 832-838, 2010
23382010
Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits
S Purcell, SS Cherny, PC Sham
Bioinformatics 19 (1), 149-150, 2003
23192003
Genome-wide detection and characterization of positive selection in human populations
PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ...
Nature 449 (7164), 913-918, 2007
23002007
Genome-wide association study identifies five new schizophrenia loci
Nature genetics 43 (10), 969-976, 2011
20402011
De novo mutations in schizophrenia implicate synaptic networks
M Fromer, AJ Pocklington, DH Kavanagh, HJ Williams, S Dwyer, ...
Nature 506 (7487), 179-184, 2014
18342014
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
S Ripke, C O'dushlaine, K Chambert, JL Moran, AK Kähler, S Akterin, ...
Nature genetics 45 (10), 1150-1159, 2013
17852013
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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