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
8072*2007
A haplotype map of the human genome
International HapMap Consortium
Nature 437 (7063), 1299, 2005
5338*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
18362007
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
15592007
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
14242001
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
13552005
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
8282016
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
8272018
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
7831999
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
7792007
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
7751996
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
7451996
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, 2016
6042016
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
5682016
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
4632007
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
4202016
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, 2017
4192017
Common deletions and SNPs are in linkage disequilibrium in the human genome
DA Hinds, AP Kloek, M Jen, X Chen, KA Frazer
Nature genetics 38 (1), 82-85, 2006
4122006
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus
P Concannon, KJ Gogolin-Ewens, DA Hinds, B Wapelhorst, VA Morrison, ...
Nature genetics 19 (3), 292-296, 1998
3881998
Variant in PNPLA3 is associated with alcoholic liver disease
C Tian, RP Stokowski, D Kershenobich, DG Ballinger, DA Hinds
Nature genetics 42 (1), 21-23, 2010
3752010
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Articles 1–20