Works matching IS 07410395 AND DT 2020 AND VI 44 AND IP 1

Results: 12

Combining sequence data from multiple studies: Impact of analysis strategies on rare variant calling and association results.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. 41, doi. 10.1002/gepi.22261

By:

Chen, Zhongsheng;
Boehnke, Michael;
Fuchsberger, Christian

Publication type:

Article

Population genetic simulation study of power in association testing across genetic architectures and study designs.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. 90, doi. 10.1002/gepi.22264

By:

Tong, Dominic M. H.;
Hernandez, Ryan D.

Publication type:

Article

Joint analysis of multiple phenotypes using a clustering linear combination method based on hierarchical clustering.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. 67, doi. 10.1002/gepi.22263

By:

Li, Xueling;
Zhang, Shuanglin;
Sha, Qiuying

Publication type:

Article

An adaptive test for meta‐analysis of rare variant association studies.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. 104, doi. 10.1002/gepi.22273

By:

Yang, Tianzhong;
Kim, Junghi;
Wu, Chong;
Ma, Yiding;
Wei, Peng;
Pan, Wei

Publication type:

Article

Transethnic meta‐analysis of metabolic syndrome in a multiethnic study.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. 16, doi. 10.1002/gepi.22267

By:

Willems, Emileigh L.;
Wan, Jia Y.;
Norden‐Krichmar, Trina M.;
Edwards, Karen L.;
Santorico, Stephanie A.

Publication type:

Article

Issue Information.

Published in:: Genetic Epidemiology, 2020, v. 44, n. 1, p. 1, doi. 10.1002/gepi.22218
Publication type:: Article

Powerful rare variant association testing in a copula‐based joint analysis of multiple phenotypes.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. 26, doi. 10.1002/gepi.22265

By:

Konigorski, Stefan;
Yilmaz, Yildiz E.;
Janke, Jürgen;
Bergmann, Manuela M.;
Boeing, Heiner;
Pischon, Tobias

Publication type:

Article

Case‐control versus case‐only estimates of gene‐environment interactions with common and misclassified clinical diagnosis.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. 4, doi. 10.1002/gepi.22266

By:

Lobach, Iryna;
Sheng, Ying;
Lobach, Siarhei;
Zablotska, Lydia;
Huang, Chiung‐Yu

Publication type:

Article

Cover Image.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. i, doi. 10.1002/gepi.22219

By:

Png, Grace;
Suveges, Daniel;
Park, Young‐Chan;
Walter, Klaudia;
Kundu, Kousik;
Ntalla, Ioanna;
Tsafantakis, Emmanouil;
Karaleftheri, Maria;
Dedoussis, George;
Zeggini, Eleftheria;
Gilly, Arthur

Publication type:

Article

Embracing study heterogeneity for finding genetic interactions in large‐scale research consortia.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. 52, doi. 10.1002/gepi.22262

By:

Liu, Yulun;
Huang, Jing;
Urbanowicz, Ryan J.;
Chen, Kun;
Manduchi, Elisabetta;
Greene, Casey S.;
Moore, Jason H.;
Scheet, Paul;
Chen, Yong

Publication type:

Article

Back Cover Image.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. ii, doi. 10.1002/gepi.22220

By:

Liu, Yulun;
Huang, Jing;
Urbanowicz, Ryan J.;
Chen, Kun;
Manduchi, Elisabetta;
Greene, Casey S.;
Moore, Jason H.;
Scheet, Paul;
Chen, Yong

Publication type:

Article

Population‐wide copy number variation calling using variant call format files from 6,898 individuals.

Published in:

Genetic Epidemiology, 2020, v. 44, n. 1, p. 79, doi. 10.1002/gepi.22260

By:

Png, Grace;
Suveges, Daniel;
Park, Young‐Chan;
Walter, Klaudia;
Kundu, Kousik;
Ntalla, Ioanna;
Tsafantakis, Emmanouil;
Karaleftheri, Maria;
Dedoussis, George;
Zeggini, Eleftheria;
Gilly, Arthur

Publication type:

Article