Works matching IS 07410395 AND DT 2019 AND VI 43 AND IP 1

Results: 9

Variance components genetic association test for zero‐inflated count outcomes.

Published in:

Genetic Epidemiology, 2019, v. 43, n. 1, p. 82, doi. 10.1002/gepi.22162

By:

Goodman, Matthew O.;
Chibnik, Lori;
Cai, Tianxi

Publication type:

Article

Relative impact of indels versus SNPs on complex disease.

Published in:

Genetic Epidemiology, 2019, v. 43, n. 1, p. 112, doi. 10.1002/gepi.22175

By:

Gagliano, Sarah A.;
Sengupta, Sebanti;
Sidore, Carlo;
Maschio, Andrea;
Cucca, Francesco;
Schlessinger, David;
Abecasis, Gonçalo R.

Publication type:

Article

Generalized multifactor dimensionality reduction approaches to identification of genetic interactions underlying ordinal traits.

Published in:

Genetic Epidemiology, 2019, v. 43, n. 1, p. 24, doi. 10.1002/gepi.22169

By:

Hou, Ting‐Ting;
Lin, Feng;
Bai, Shasha;
Cleves, Mario A.;
Xu, Hai‐Ming;
Lou, Xiang‐Yang

Publication type:

Article

The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.

Published in:

Genetic Epidemiology, 2019, v. 43, n. 1, p. 63, doi. 10.1002/gepi.22167

By:

Stanaway, Ian B.;
Hall, Taryn O.;
Rosenthal, Elisabeth A.;
Palmer, Melody;
Naranbhai, Vivek;
Knevel, Rachel;
Namjou‐Khales, Bahram;
Carroll, Robert J.;
Kiryluk, Krzysztof;
Gordon, Adam S.;
Linder, Jodell;
Howell, Kayla Marie;
Mapes, Brandy M.;
Lin, Frederick T.J.;
Joo, Yoonjung Yoonie;
Hayes, M. Geoffrey;
Gharavi, Ali G.;
Pendergrass, Sarah A.;
Ritchie, Marylyn D.;
Andrade, Mariza

Publication type:

Article

ComPaSS‐GWAS: A method to reduce type I error in genome‐wide association studies when replication data are not available.

Published in:

Genetic Epidemiology, 2019, v. 43, n. 1, p. 102, doi. 10.1002/gepi.22168

By:

Sabourin, Jeremy A.;
Cropp, Cheryl D.;
Sung, Heejong;
Brody, Lawrence C.;
Bailey‐Wilson, Joan E.;
Wilson, Alexander F.

Publication type:

Article

Generalizing polygenic risk scores from Europeans to Hispanics/Latinos.

Published in:

Genetic Epidemiology, 2019, v. 43, n. 1, p. 50, doi. 10.1002/gepi.22166

By:

Grinde, Kelsey E.;
Qi, Qibin;
Thornton, Timothy A.;
Liu, Simin;
Shadyab, Aladdin H.;
Chan, Kei Hang K.;
Reiner, Alexander P.;
Sofer, Tamar

Publication type:

Article

Multi‐SKAT: General framework to test for rare‐variant association with multiple phenotypes.

Published in:

Genetic Epidemiology, 2019, v. 43, n. 1, p. 4, doi. 10.1002/gepi.22156

By:

Dutta, Diptavo;
Scott, Laura;
Boehnke, Michael;
Lee, Seunggeun

Publication type:

Article

Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.

Published in:

Genetic Epidemiology, 2019, v. 43, n. 1, p. 37, doi. 10.1002/gepi.22155

By:

Bureau, Alexandre;
Begum, Ferdouse;
Taub, Margaret A.;
Hetmanski, Jacqueline B.;
Parker, Margaret M.;
Albacha‐Hejazi, Hasan;
Scott, Alan F.;
Murray, Jeffrey C.;
Marazita, Mary L.;
Bailey‐Wilson, Joan E.;
Beaty, Terri H.;
Ruczinski, Ingo

Publication type:

Article

Issue Information.

Published in:: Genetic Epidemiology, 2019, v. 43, n. 1, p. 1, doi. 10.1002/gepi.22139
Publication type:: Article