Works matching IS 07410395 AND DT 2018 AND VI 42 AND IP 1

Results: 11

Predictive accuracy of combined genetic and environmental risk scores.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 4, doi. 10.1002/gepi.22092

By:

Dudbridge, Frank;
Pashayan, Nora;
Yang, Jian

Publication type:

Article

Two‐phase designs for joint quantitative‐trait‐dependent and genotype‐dependent sampling in post‐GWAS regional sequencing.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 104, doi. 10.1002/gepi.22099

By:

Espin‐Garcia, Osvaldo;
Craiu, Radu V.;
Bull, Shelley B.

Publication type:

Article

Estimation of a significance threshold for epigenome‐wide association studies.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 20, doi. 10.1002/gepi.22086

By:

Saffari, Ayden;
Silver, Matt J.;
Zavattari, Patrizia;
Moi, Loredana;
Columbano, Amedeo;
Meaburn, Emma L.;
Dudbridge, Frank

Publication type:

Article

On the testing of Hardy‐Weinberg proportions and equality of allele frequencies in males and females at biallelic genetic markers.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 34, doi. 10.1002/gepi.22079

By:

Graffelman, Jan;
Weir, Bruce S.

Publication type:

Article

Gene‐based genetic association test with adaptive optimal weights.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 95, doi. 10.1002/gepi.22098

By:

Chen, Zhongxue;
Lu, Yan;
Lin, Tong;
Liu, Qingzhong;
Wang, Kai

Publication type:

Article

A unified partial likelihood approach for X‐chromosome association on time‐to‐event outcomes.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 80, doi. 10.1002/gepi.22097

By:

Xu, Wei;
Hao, Meiling

Publication type:

Article

Inference on phenotype‐specific effects of genes using multivariate kernel machine regression.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 64, doi. 10.1002/gepi.22096

By:

Maity, Arnab;
Zhao, Jing;
Sullivan, Patrick F.;
Tzeng, Jung‐Ying

Publication type:

Article

Estimating the number of potential family members eligible for <italic>BRCA1</italic> and <italic>BRCA2</italic> mutation testing in a “Traceback” approach.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 117, doi. 10.1002/gepi.22095

By:

Moss, Haley A.;
Samimi, Goli;
Havrilesky, Laura J.;
Sherman, Mark E.;
Myers, Evan R.

Publication type:

Article

Family‐based tests for associating haplotypes with general phenotype data.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 123, doi. 10.1002/gepi.22094

By:

Hecker, Julian;
Xu, Xin;
Townes, F. William;
Loehlein Fier, Heide;
Corcoran, Chris;
Laird, Nan;
Lange, Christoph

Publication type:

Article

An ancestry‐based approach for detecting interactions.

Published in:

Genetic Epidemiology, 2018, v. 42, n. 1, p. 49, doi. 10.1002/gepi.22087

By:

Park, Danny S.;
Eskin, Itamar;
Kang, Eun Yong;
Gamazon, Eric R.;
Eng, Celeste;
Gignoux, Christopher R.;
Galanter, Joshua M.;
Burchard, Esteban;
Ye, Chun J.;
Aschard, Hugues;
Eskin, Eleazar;
Halperin, Eran;
Zaitlen, Noah

Publication type:

Article

Issue Information.

Published in:: Genetic Epidemiology, 2018, v. 42, n. 1, p. 1, doi. 10.1002/gepi.22069
Publication type:: Article