Haplotype Kernel Association Test as a Powerful Method to Identify Chromosomal Regions Harboring Uncommon Causal Variants-Reference-Cited by-同舟云学术

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Haplotype Kernel Association Test as a Powerful Method to Identify Chromosomal Regions Harboring Uncommon Causal Variants

Published:2013-06-05 Issue:6 Volume:37 Page:560-570
ISSN:0741-0395
Container-title:Genetic Epidemiology
language:en
Short-container-title:Genet. Epidemiol.

Author:

Lin Wan-Yu¹,Yi Nengjun²,Lou Xiang-Yang²,Zhi Degui²,Zhang Kui²,Gao Guimin³,Tiwari Hemant K.²,Liu Nianjun²

Affiliation:

1. Institute of Epidemiology and Preventive Medicine; College of Public Health; National Taiwan University; Taipei Taiwan

2. Department of Biostatistics; University of Alabama at Birmingham; Birmingham Alabama

3. Department of Biostatistics; Virginia Commonwealth University; Richmond Virginia

Publisher

Wiley

Subject

Genetics(clinical),Epidemiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/gepi.21740/fullpdf

Reference96 articles.

1. Statistical models for haplotype sharing in case-parent trio data;Allen;Hum Hered,2007

2. A novel haplotype-sharing approach for genome-wide case-control association studies implicates the calpastatin gene in Parkinson's disease;Allen;Genet Epidemiol,2009

3. Activation of downstream signals by the long form of the leptin receptor;Banks;J Biol Chem,2000

4. Evaluating coverage of genome-wide association studies;Barrett;Nat Genet,2006

5. Haploview: analysis and visualization of LD and haplotype maps;Barrett;Bioinformatics,2005

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