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Paul I W de Bakker
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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
325042007
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
9385*2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
Management Group Liefer Laura A. 51 Wetterstrand Kris A. 51 Good Peter J. 51 ...
nature 447 (7146), 799-816, 2007
60492007
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
55432003
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
47322015
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
30242007
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
30102011
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
29532016
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
25802012
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
23032008
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
22322007
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
20932014
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
20512005
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), 508-514, 2010
15822010
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
15792009
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
15122008
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
13182007
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, ...
Nature genetics 50 (4), 524-537, 2018
13062018
A haplotype map of the human genome
D Altshuler
Nature 437, 1299-1320, 2005
11992005
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
11512008
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