Works matching IS 00034800 AND DT 2015 AND VI 79 AND IP 4

Results: 9

Statistical Methods for Association Tests of Multiple Continuous Traits in Genome-Wide Association Studies.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 4, p. 282, doi. 10.1111/ahg.12110

By:

Wu, Baolin;
Pankow, James S.

Publication type:

Article

Classical and Atypical Fibrodysplasia Ossificans Progressiva in India.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 4, p. 245, doi. 10.1111/ahg.12112

By:

Madhuri, Vrisha;
Santhanam, Mona;
Sugumar, Legasri K;
Rajagopal, Karthikeyan;
Chilbule, Sanjay K

Publication type:

Article

Analysis of Human Triallelic SNPs by Next-Generation Sequencing.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 4, p. 275, doi. 10.1111/ahg.12114

By:

Cao, Min;
Shi, Juan;
Wang, Jiqiu;
Hong, Jie;
Cui, Bin;
Ning, Guang

Publication type:

Article

Joint Effect of Unlinked Genotypes: Application to Type 2 Diabetes in the EPIC-Potsdam Case-Cohort Study.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 4, p. 253, doi. 10.1111/ahg.12115

By:

Knüppel, Sven;
Meidtner, Karina;
Arregui, Maria;
Holzhütter, Hermann‐Georg;
Boeing, Heiner

Publication type:

Article

Homozygous Sequence Variants in the NPR2 Gene Underlying Acromesomelic Dysplasia Maroteaux Type (AMDM) in Consanguineous Families.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 4, p. 238, doi. 10.1111/ahg.12116

By:

Irfanullah;
Umair, Muhammad;
Khan, Saadullah;
Ahmad, Wasim

Publication type:

Article

SVSI: Fast and Powerful Set-Valued System Identification Approach to Identifying Rare Variants in Sequencing Studies for Ordered Categorical Traits.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 4, p. 294, doi. 10.1111/ahg.12117

By:

Bi, Wenjian;
Kang, Guolian;
Zhao, Yanlong;
Cui, Yuehua;
Yan, Song;
Li, Yun;
Cheng, Cheng;
Pounds, Stanley B.;
Borowitz, Michael J.;
Relling, Mary V.;
Yang, Jun J.;
Liu, Zhifa;
Pui, Ching‐Hon;
Hunger, Stephen P.;
Hartford, Christine M.;
Leung, Wing;
Zhang, Ji‐Feng

Publication type:

Article

Genetic Association and Altered Gene Expression of Osteoprotegerin in Otosclerosis Patients.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 4, p. 225, doi. 10.1111/ahg.12118

By:

Priyadarshi, Saurabh;
Ray, Chinmay Sundar;
Biswal, Narayan Chandra;
Nayak, Soumya Ranjan;
Panda, Khirod Chandra;
Desai, Ashim;
Ramchander, Puppala Venkat

Publication type:

Article

Trans-Ethnic Meta-Analysis Identifies Common and Rare Variants Associated with Hepatocyte Growth Factor Levels in the Multi-Ethnic Study of Atherosclerosis (MESA).

Published in:

Annals of Human Genetics, 2015, v. 79, n. 4, p. 264, doi. 10.1111/ahg.12119

By:

Larson, Nicholas B.;
Berardi, Cecilia;
Decker, Paul A.;
Wassel, Christina L.;
Kirsch, Phillip S.;
Pankow, James S.;
Sale, Michele M.;
Andrade, Mariza;
Sicotte, Hugues;
Tang, Weihong;
Hanson, Naomi Q.;
Tsai, Michael Y.;
Taylor, Kent D.;
Bielinski, Suzette J.

Publication type:

Article

Novel A219P Mutation of Hydroxymethylbilane Synthase Identified in a Chinese Woman with Acute Intermittent Porphyria and Syndrome of Inappropriate Antidiuretic Hormone.

Published in:

Annals of Human Genetics, 2015, v. 79, n. 4, p. 310, doi. 10.1111/ahg.12107

By:

Li, Yingjie;
Qu, Hua;
Wang, Hang;
Deng, Huacong;
Liu, Ziyan

Publication type:

Article