David Hinds
David Hinds
Research Fellow, 23andMe, Inc.
Verified email at 23andme.com
Title
Cited by
Cited by
Year
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
8486*2007
A haplotype map of the human genome
International HapMap Consortium
Nature 437 (7063), 1299, 2005
5571*2005
A common allele on chromosome 9 associated with coronary heart disease
R McPherson, A Pertsemlidis, N Kavaslar, A Stewart, R Roberts, DR Cox, ...
Science 316 (5830), 1488-1491, 2007
19282007
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
18062007
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
N Patil, AJ Berno, DA Hinds, WA Barrett, JM Doshi, CR Hacker, ...
Science 294 (5547), 1719-1723, 2001
14772001
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
14192018
Whole-genome patterns of common DNA variation in three human populations
DA Hinds, LL Stuve, GB Nilsen, E Halperin, E Eskin, DG Ballinger, ...
Science 307 (5712), 1072-1079, 2005
14062005
Genome-wide association study identifies 74 loci associated with educational attainment
A Okbay, JP Beauchamp, MA Fontana, JJ Lee, TH Pers, CA Rietveld, ...
Nature 533 (7604), 539-542, 2016
10292016
A genomic screen of autism: evidence for a multilocus etiology
N Risch, D Spiker, L Lotspeich, N Nouri, D Hinds, J Hallmayer, ...
The American Journal of Human Genetics 65 (2), 493-507, 1999
8221999
Detection and interpretation of shared genetic influences on 42 human traits
JK Pickrell, T Berisa, JZ Liu, L Ségurel, JY Tung, DA Hinds
Nature genetics 48 (7), 709-717, 2016
8092016
A full genome search in multiple sclerosis
GC Ebers, K Kukay, DE Bulman, AD Sadovnick, G Rice, C Anderson, ...
Nature genetics 13 (4), 472-476, 1996
8071996
Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana
RM Clark, G Schweikert, C Toomajian, S Ossowski, G Zeller, P Shinn, ...
science 317 (5836), 338-342, 2007
7942007
A genome–wide search for human non–insulin–dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2
CL Hanis, E Boerwinkle, R Chakraborty, DL Ellsworth, P Concannon, ...
Nature genetics 13 (2), 161-166, 1996
7921996
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
A Okbay, BML Baselmans, JE De Neve, P Turley, MG Nivard, MA Fontana, ...
Nature genetics 48 (6), 624-633, 2016
7392016
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
D Chang, MA Nalls, IB Hallgrímsdóttir, J Hunkapiller, M Van Der Brug, ...
Nature genetics 49 (10), 1511-1516, 2017
6802017
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
DM Howard, MJ Adams, TK Clarke, JD Hafferty, J Gibson, M Shirali, ...
Nature neuroscience 22 (3), 343-352, 2019
6372019
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
M Liu, Y Jiang, R Wedow, Y Li, DM Brazel, F Chen, G Datta, ...
Nature genetics 51 (2), 237-244, 2019
5702019
Identification of 15 genetic loci associated with risk of major depression in individuals of European descent
CL Hyde, MW Nagle, C Tian, X Chen, SA Paciga, JR Wendland, JY Tung, ...
Nature genetics 48 (9), 1031-1036, 2016
5602016
A sequence-based variation map of 8.27 million SNPs in inbred mouse strains
KA Frazer, E Eskin, HM Kang, MA Bogue, DA Hinds, EJ Beilharz, ...
Nature 448 (7157), 1050-1053, 2007
4932007
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
4892019
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