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

Results: 9

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
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
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
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
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
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
Issue Information.
Published in:
Genetic Epidemiology, 2019, v. 43, n. 1, p. 1, doi. 10.1002/gepi.22139
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