A Robust Example of Collider Bias in a Genetic Association Study

被引:75
作者
Day, Felix R. [1 ]
Loh, Po-Ru [2 ,3 ]
Scott, Robert A. [1 ]
Ong, Ken K. [1 ]
Perry, John R. B. [1 ]
机构
[1] Univ Cambridge, Inst Metab Sci, MRC, Epidemiol Unit, Box 285,Hills Rd, Cambridge CB2 0QQ, England
[2] Harvard Univ, TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[3] Broad Inst Harvard & MIT, Program Med & Populat Genet, Cambridge, MA 02142 USA
关键词
D O I
10.1016/j.ajhg.2015.12.019
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:392 / 393
页数:2
相关论文
共 6 条
[1]   Adjusting for Heritable Covariates Can Bias Effect Estimates in Genome-Wide Association Studies [J].
Aschard, Hugues ;
Vilhjalmsson, Bjarni J. ;
Joshi, Amit D. ;
Price, Alkes L. ;
Kraft, Peter .
AMERICAN JOURNAL OF HUMAN GENETICS, 2015, 96 (02) :329-339
[2]   Efficient Bayesian mixed-model analysis increases association power in large cohorts [J].
Loh, Po-Ru ;
Tucker, George ;
Bulik-Sullivan, Brendan K. ;
Vilhjalmsson, Bjarni J. ;
Finucane, Hilary K. ;
Salem, Rany M. ;
Chasman, Daniel I. ;
Ridker, Paul M. ;
Neale, Benjamin M. ;
Berger, Bonnie ;
Patterson, Nick ;
Price, Alkes L. .
NATURE GENETICS, 2015, 47 (03) :284-+
[3]   UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age [J].
Sudlow, Cathie ;
Gallacher, John ;
Allen, Naomi ;
Beral, Valerie ;
Burton, Paul ;
Danesh, John ;
Downey, Paul ;
Elliott, Paul ;
Green, Jane ;
Landray, Martin ;
Liu, Bette ;
Matthews, Paul ;
Ong, Giok ;
Pell, Jill ;
Silman, Alan ;
Young, Alan ;
Sprosen, Tim ;
Peakman, Tim ;
Collins, Rory .
PLOS MEDICINE, 2015, 12 (03)
[4]   Why evidence for the fetal origins of adult disease might be a statistical artifact: The "reversal paradox" for the relation between birth weight and blood pressure in later life [J].
Tu, YK ;
West, R ;
Ellison, GTH ;
Gilthorpe, MS .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2005, 161 (01) :27-32
[5]   Defining the role of common variation in the genomic and biological architecture of adult human height [J].
Wood, Andrew R. ;
Esko, Tonu ;
Yang, Jian ;
Vedantam, Sailaja ;
Pers, Tune H. ;
Gustafsson, Stefan ;
Chun, Audrey Y. ;
Estrada, Karol ;
Luan, Jian'an ;
Kutalik, Zoltan ;
Amin, Najaf ;
Buchkovich, Martin L. ;
Croteau-Chonka, Damien C. ;
Day, Felix R. ;
Duan, Yanan ;
Fall, Tove ;
Fehrmann, Rudolf ;
Ferreira, Teresa ;
Jackson, Anne U. ;
Karjalainen, Juha ;
Lo, Ken Sin ;
Locke, Adam E. ;
Maegi, Reedik ;
Mihailov, Evelin ;
Porcu, Eleonora ;
Randall, Joshua C. ;
Scherag, Andre ;
Vinkhuyzen, Anna A. E. ;
Westra, Harm-Jan ;
Winkler, Thomas W. ;
Workalemahu, Tsegaselassie ;
Zhao, Jing Hua ;
Absher, Devin ;
Albrecht, Eva ;
Anderson, Denise ;
Baron, Jeffrey ;
Beekman, Marian ;
Demirkan, Ayse ;
Ehret, Georg B. ;
Feenstra, Bjarke ;
Feitosa, Mary F. ;
Fischer, Krista ;
Fraser, Ross M. ;
Goel, Anuj ;
Gong, Jian ;
Justice, Anne E. ;
Kanoni, Stavroula ;
Kleber, Marcus E. ;
Kristiansson, Kati ;
Lim, Unhee .
NATURE GENETICS, 2014, 46 (11) :1173-1186
[6]   Association Analysis of 29,956 Individuals Confirms That a Low-Frequency Variant at CCND2 Halves the Risk of Type 2 Diabetes by Enhancing Insulin Secretion [J].
Yaghootkar, Hanieh ;
Stancakova, Alena ;
Freathy, Rachel M. ;
Vangipurapu, Jagadish ;
Weedon, Michael N. ;
Xie, Weijia ;
Wood, Andrew R. ;
Ferrannini, Ele ;
Mari, Andrea ;
Ring, Susan M. ;
Lawlor, Debbie A. ;
Smith, George Davey ;
Jorgensen, Torben ;
Hansen, Torben ;
Pedersen, Oluf ;
Steinthorsdottir, Valgerdur ;
Gudbjartsson, Daniel F. ;
Thorleifsson, Gudmar ;
Thorsteinsdottir, Unnur ;
Stefanssonn, Kari ;
Hattersley, Andrew T. ;
Walker, Mark ;
Morris, Andrew D. ;
McCarthy, Mark I. ;
Palmer, Colin N. A. ;
Laakso, Markku ;
Frayling, Timothy M. .
DIABETES, 2015, 64 (06) :2279-2285