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
8216*2007
A haplotype map of the human genome
International HapMap Consortium
Nature 437 (7063), 1299, 2005
5434*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
18692007
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
16472007
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
14382001
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
13622005
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
10252018
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
8962016
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
7991999
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
7982007
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
7851996
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
7501996
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
7022016
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
6292016
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
5232017
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
4812016
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
4732007
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
4162006
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
3961998
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
3942010
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Articles 1–20