Exome sequencing and the genetic basis of complex traits

被引:291
作者
Kiezun, Adam [1 ,2 ]
Garimella, Kiran [2 ]
Do, Ron [2 ,3 ]
Stitziel, Nathan O. [2 ,4 ]
Neale, Benjamin M. [2 ,3 ,5 ]
McLaren, Paul J. [1 ,2 ]
Gupta, Namrata [2 ]
Sklar, Pamela [6 ,7 ]
Sullivan, Patrick F. [8 ]
Moran, Jennifer L. [2 ]
Hultman, Christina M. [9 ]
Lichtenstein, Paul [9 ]
Magnusson, Patrik [9 ]
Lehner, Thomas
Shugart, Yin Yao [10 ]
Price, Alkes L. [2 ,11 ,12 ]
de Bakker, Paul I. W. [1 ,2 ,13 ,14 ]
Purcell, Shaun M. [5 ]
Sunyaev, Shamil R. [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Dept Med, Div Genet,Brigham & Womens Hosp, Boston, MA 02114 USA
[2] Broad Inst MIT & Harvard, Cambridge, MA USA
[3] Massachusetts Gen Hosp, Ctr Human Genet Res, Boston, MA 02114 USA
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Cardiovasc Med, Boston, MA 02115 USA
[5] Massachusetts Gen Hosp, Analyt & Translat Genet Unit, Boston, MA 02114 USA
[6] Mt Sinai Sch Med, Dept Psychiat, Friedman Brain Inst, New York, NY USA
[7] Mt Sinai Sch Med, Inst Genom & Multiscale Biol, New York, NY USA
[8] Univ N Carolina, Sch Med, Dept Genet, Chapel Hill, NC USA
[9] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[10] NIMH, Div Neurosci & Basic Behav Sci, Bethesda, MD 20892 USA
[11] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[12] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[13] Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands
[14] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
GENOME-WIDE ASSOCIATION; SINGLE-NUCLEOTIDE POLYMORPHISMS; ALLELE FREQUENCY-SPECTRUM; RARE VARIANTS; POPULATION-STRUCTURE; PROTEIN FUNCTION; COMMON DISEASES; PLASMA-LEVELS; MUTATIONS; SELECTION;
D O I
10.1038/ng.2303
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:623 / 630
页数:8
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