Integrating common and rare genetic variation in diverse human populations
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Integrating common and rare genetic variation in diverse human populations

;Altshuler DM;Gibbs RA;Peltonen L;Altshuler DM;Gibbs RA;Peltonen L;Dermitzakis E;Schaffner SF;Yu F;Peltonen L;Dermitzakis E;Bonnen PE;Altshuler DM;Gibbs RA;de Bakker PI;Deloukas P;Gabriel SB;Gwilliam R;Hunt S;Inouye M;Jia X;Palotie A;Parkin M;Whittaker P;Yu F;Chang K;Hawes A;Lewis LR;Ren Y;Wheeler D;Gibbs RA;Muzny DM;Barnes C;Darvishi K;Hurles M;Korn JM;Kristiansson K;Lee C;McCarrol SA;Nemesh J;Dermitzakis E;Keinan A;Montgomery SB;Pollack S;Price AL;Soranzo N;Bonnen PE;Gibbs RA;Gonzaga-Jauregui C;Keinan A;Price AL;Yu F;Anttila V;Brodeur W;Daly MJ;Leslie S;McVean G;Moutsianas L;Nguyen H;Schaffner SF;Zhang Q;Ghori MJ;McGinnis R;McLaren W;Pollack S;Price AL;Schaffner SF;Takeuchi F;Grossman SR;Shlyakhter I;Hostetter EB;Sabeti PC;Adebamowo CA;Foster MW;Gordon DR;Licinio J;Manca MC;Marshall PA;Matsuda I;Ngare D;Wang VO;Reddy D;Rotimi CN;Royal CD;Sharp RR;Zeng C;Brooks LD;McEwen JE;;
Nature 2010 Vol. 467 pp. -
322
2010natureintegrating

Abstract

Despite great progress in identifying genetic variants that influence human disease, most inherited risk remains unexplained. A more complete understanding requires genome-wide studies that fully examine less common alleles in populations with a wide range of ancestry. To inform the design and inter …

Keywords

National Center for Biotechnology Information NCBI NLM MEDLINE humans pubmed abstract nih national institutes of health national library of medicine research support non-u.s. gov't N.I.H. Extramural genome Polymorphism human* single nucleotide* dna copy number variations* investigators=[] pmid:20811451 pmc3173859 doi:10.1038/nature09298 collabauthor(name='international hapmap 3 consortium' affs=[{1: 'broad institute 7 cambridge center cambridge massachusetts 02138 usa. altshuler@molbio.mgh.harvard.edu'}]) david m altshuler jean e mcewen human genome project population groups / genetics*

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