Works matching IS 00034800 AND DT 2013 AND VI 77 AND IP 4

Results: 8

Epistatic Interaction between Genetic Variants in Susceptibility Gene ETS1 Correlates with IL-17 Levels in SLE Patients.

Published in:

Annals of Human Genetics, 2013, v. 77, n. 4, p. 344, doi. 10.1111/ahg.12018

By:

Zhang, Jing;
Zhang, Yan;
Zhang, Lu;
Yang, Jing;
Ying, Dingge;
Zeng, Shuai;
Lee, Tsz Leung;
Lau, Chak Sing;
Chan, Tak Mao;
Leung, Alexander Moon Ho;
Mok, Chi Chiu;
Wong, Sik Nin;
Lee, Ka Wing;
Ho, Marco Hok Kung;
Lee, Pamela Pui Wah;
Hon‐Yin Chung, Brian;
Chong, Chun Yin;
Wong, Raymond Woon Sing;
Mok, Mo Yin;
Wong, Wilfred Hing Sang

Publication type:

Article

A Novel Mutation in FGD4/FRABIN Causes Charcot Marie Tooth Disease Type 4H in Patients from a Consanguineous Tunisian Family.

Published in:

Annals of Human Genetics, 2013, v. 77, n. 4, p. 336, doi. 10.1111/ahg.12017

By:

Boubaker, Chokri;
Hsairi‐Guidara, Inès;
Castro, Christel;
Ayadi, Ines;
Boyer, Amandine;
Kerkeni, Emna;
Courageot, Joël;
Abid, Imen;
Bernard, Rafaëlle;
Bonello‐Palot, Nathalie;
Kamoun, Fatma;
Cheikh, Hassen Ben;
Lévy, Nicolas;
Triki, Chahnez;
Delague, Valérie

Publication type:

Article

A Comparison of the Likelihood Ratio Test and the Variance-Stabilising Transformation-Based Tests for Detecting Association of Rare Variants.

Published in:

Annals of Human Genetics, 2013, v. 77, n. 4, p. 333, doi. 10.1111/ahg.12022

By:

Xing, Guan;
Ku, Hung‐Chih;
Xing, Chao

Publication type:

Article

Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.

Published in:

Annals of Human Genetics, 2013, v. 77, n. 4, p. 321, doi. 10.1111/ahg.12023

By:

Jeff, Janina M.;
Ritchie, Marylyn D.;
Denny, Joshua C.;
Kho, Abel N.;
Ramirez, Andrea H.;
Crosslin, David;
Armstrong, Loren;
Basford, Melissa A.;
Wolf, Wendy A.;
Pacheco, Jennifer A.;
Chisholm, Rex L.;
Roden, Dan M.;
Hayes, M. Geoffrey;
Crawford, Dana C.

Publication type:

Article

The Effect of Genetic Admixture in an Association Study: Genetic Polymorphisms and Chromosome Aberrations in a Colombian Population Exposed to Organic Solvents.

Published in:

Annals of Human Genetics, 2013, v. 77, n. 4, p. 308, doi. 10.1111/ahg.12019

By:

Hoyos‐Giraldo, Luz Stella;
Escobar‐Hoyos, Luisa F.;
Reyes‐Carvajal, Ingrid;
García, Jharley J.;
Córdoba, Liliana;
Gómez, Adalberto Sánchez;
García‐Vallejo, Felipe;
Cajas‐Salazar, Nohelia;
Carvajal, Silvio;
Bedoya, Gabriel

Publication type:

Article

Wilson Disease Mutation Pattern with Genotype-Phenotype Correlations from Western India: Confirmation of p.C271 as a Common Indian Mutation and Identification of 14 Novel Mutations.

Published in:

Annals of Human Genetics, 2013, v. 77, n. 4, p. 299, doi. 10.1111/ahg.12024

By:

Aggarwal, Annu;
Chandhok, Gursimran;
Todorov, Theodor;
Parekh, Saloni;
Tilve, Sharada;
Zibert, Andree;
Bhatt, Mohit;
Schmidt, Hartmut H.‐J.

Publication type:

Article

The Role of Epistasis in the Etiology of Polycystic Ovary Syndrome among Indian Women: SNP-SNP and SNP-Environment Interactions.

Published in:

Annals of Human Genetics, 2013, v. 77, n. 4, p. 288, doi. 10.1111/ahg.12020

By:

Dasgupta, Shilpi;
Reddy, B. Mohan

Publication type:

Article

Genome-Wide Association Study of Pre-Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy-Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort.

Published in:

Annals of Human Genetics, 2013, v. 77, n. 4, p. 277, doi. 10.1111/ahg.12021

By:

Zhao, Linlu;
Bracken, Michael B.;
DeWan, Andrew T.

Publication type:

Article