Paul I W de Bakker
Title
Cited by
Cited by
Year
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
213482007
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
8168*2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
ENCODE Project Consortium
nature 447 (7146), 799, 2007
52322007
Structure validation by Cα geometry: ϕ, ψ and Cβ deviation
SC Lovell, IW Davis, WB Arendall III, PIW De Bakker, JM Word, ...
Proteins: Structure, Function, and Bioinformatics 50 (3), 437-450, 2003
43862003
Genetic studies of body mass index yield new insights for obesity biology
AE Locke, B Kahali, SI Berndt, AE Justice, TH Pers, FR Day, C Powell, ...
Nature 518 (7538), 197-206, 2015
27492015
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
26682007
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
S Sawcer, G Hellenthal, M Pirinen, CCA Spencer, NA Patsopoulos, ...
Nature 476 (7359), 214, 2011
22662011
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
E Zeggini, LJ Scott, R Saxena, BF Voight, JL Marchini, T Hu, ...
Nature genetics 40 (5), 638-645, 2008
20322008
Efficiency and power in genetic association studies
PIW De Bakker, R Yelensky, I Pe'er, SB Gabriel, MJ Daly, D Altshuler
Nature genetics 37 (11), 1217-1223, 2005
19402005
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
18852012
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
16242007
Defining the role of common variation in the genomic and biological architecture of adult human height
AR Wood, T Esko, J Yang, S Vedantam, TH Pers, S Gustafsson, AY Chu, ...
Nature genetics 46 (11), 1173-1186, 2014
14972014
Common variants at 30 loci contribute to polygenic dyslipidemia
S Kathiresan, CJ Willer, GM Peloso, S Demissie, K Musunuru, EE Schadt, ...
Nature genetics 41 (1), 56-65, 2009
13582009
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
AD Johnson, RE Handsaker, SL Pulit, MM Nizzari, CJ O'Donnell, ...
Bioinformatics 24 (24), 2938-2939, 2008
13232008
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
EA Stahl, S Raychaudhuri, EF Remmers, G Xie, S Eyre, BP Thomson, Y Li, ...
Nature genetics 42 (6), 508, 2010
12652010
A reference panel of 64,976 haplotypes for genotype imputation
S McCarthy, S Das, W Kretzschmar, O Delaneau, AR Wood, A Teumer, ...
Nature genetics 48 (10), 1279-1283, 2016
12402016
STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus
EF Remmers, RM Plenge, AT Lee, RR Graham, G Hom, TW Behrens, ...
New England Journal of Medicine 357 (10), 977-986, 2007
11222007
A haplotype map of the human genome
D Altshuler, P Donnelly, International HapMap Consortium
Nature 437 (7063), nature04226, 2005
10852005
Integrated detection and population-genetic analysis of SNPs and copy number variation
SA McCarroll, FG Kuruvilla, JM Korn, S Cawley, J Nemesh, A Wysoker, ...
Nature genetics 40 (10), 1166-1174, 2008
10472008
TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program
JC Florez, KA Jablonski, N Bayley, TI Pollin, PIW de Bakker, AR Shuldiner, ...
New England Journal of Medicine 355 (3), 241-250, 2006
9702006
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Articles 1–20