Works matching IS 07410395 AND DT 2017 AND VI 41 AND IP 4

Results: 9

Issue Information.

Published in:: Genetic Epidemiology, 2017, v. 41, n. 4, p. 279, doi. 10.1002/gepi.22005
Publication type:: Article

Are rare variants really independent?

Published in:

Genetic Epidemiology, 2017, v. 41, n. 4, p. 363, doi. 10.1002/gepi.22039

By:

Turkmen, Asuman;
Lin, Shili

Publication type:

Article

On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows.

Published in:

Genetic Epidemiology, 2017, v. 41, n. 4, p. 332, doi. 10.1002/gepi.22040

By:

Loehlein Fier, Heide;
Prokopenko, Dmitry;
Hecker, Julian;
Cho, Michael H.;
Silverman, Edwin K.;
Weiss, Scott T.;
Tanzi, Rudolph E.;
Lange, Christoph

Publication type:

Article

Semiparametric methods for estimation of a nonlinear exposure-outcome relationship using instrumental variables with application to Mendelian randomization.

Published in:

Genetic Epidemiology, 2017, v. 41, n. 4, p. 341, doi. 10.1002/gepi.22041

By:

Staley, James R.;
Burgess, Stephen

Publication type:

Article

A genome-wide linkage and association analysis of imputed insertions and deletions with cardiometabolic phenotypes in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study.

Published in:

Genetic Epidemiology, 2017, v. 41, n. 4, p. 353, doi. 10.1002/gepi.22042

By:

Gao, Chuan;
Hsu, Fang‐Chi;
Dimitrov, Latchezar M.;
Okut, Hayrettin;
Chen, Yii‐Der I.;
Taylor, Kent D.;
Rotter, Jerome I.;
Langefeld, Carl D.;
Bowden, Donald W.;
Palmer, Nicholette D.

Publication type:

Article

Genetic risk models: Influence of model size on risk estimates and precision.

Published in:

Genetic Epidemiology, 2017, v. 41, n. 4, p. 282, doi. 10.1002/gepi.22035

By:

Shan, Ying;
Tromp, Gerard;
Kuivaniemi, Helena;
Smelser, Diane T.;
Verma, Shefali S.;
Ritchie, Marylyn D.;
Elmore, James R.;
Carey, David J.;
Conley, Yvette P.;
Gorin, Michael B.;
Weeks, Daniel E.

Publication type:

Article

Gene-based segregation method for identifying rare variants in family-based sequencing studies.

Published in:

Genetic Epidemiology, 2017, v. 41, n. 4, p. 309, doi. 10.1002/gepi.22037

By:

Qiao, Dandi;
Lange, Christoph;
Laird, Nan M.;
Won, Sungho;
Hersh, Craig P.;
Morrow, Jarrett;
Hobbs, Brian D.;
Lutz, Sharon M.;
Ruczinski, Ingo;
Beaty, Terri H.;
Silverman, Edwin K.;
Cho, Michael H.

Publication type:

Article

Inclusion of biological knowledge in a Bayesian shrinkage model for joint estimation of SNP effects.

Published in:

Genetic Epidemiology, 2017, v. 41, n. 4, p. 320, doi. 10.1002/gepi.22038

By:

Pereira, Miguel;
Thompson, John R.;
Weichenberger, Christian X.;
Thomas, Duncan C.;
Minelli, Cosetta

Publication type:

Article

gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels.

Published in:

Genetic Epidemiology, 2017, v. 41, n. 4, p. 297, doi. 10.1002/gepi.22036

By:

Larson, Nicholas B.;
McDonnell, Shannon;
Cannon Albright, Lisa;
Teerlink, Craig;
Stanford, Janet;
Ostrander, Elaine A.;
Isaacs, William B.;
Xu, Jianfeng;
Cooney, Kathleen A.;
Lange, Ethan;
Schleutker, Johanna;
Carpten, John D.;
Powell, Isaac;
Bailey‐Wilson, Joan E.;
Cussenot, Olivier;
Cancel‐Tassin, Geraldine;
Giles, Graham G.;
MacInnis, Robert J.;
Maier, Christiane;
Whittemore, Alice S.

Publication type:

Article