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Annals of Human Genetics|January 15, 2010
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson diseaseTodd L Edwards, William K Scott, Cherylyn Almonte, et al.Annals of Human Genetics|January 15, 2010
Linkage disequilibrium pattern in asthma candidate genes from 5q31-q33 in the Singapore Chinese populationPallavi N Parate, De Yun Wang, Fook Tim ChewAnnals of Human Genetics|June 17, 2017
Molecular Characterisation of α- and β-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular MalaysiaDanny Xuan Rong Koh, Raja Zahratul Azma Raja Sabudin, Malisa Mohd Yusoff, et al.Annals of Human Genetics|June 17, 2017
Potential Positive Association between Cytochrome P450 1A1 Gene Polymorphisms and Recurrent Pregnancy Loss: a Meta-AnalysisJie Li, Yang Chen, Sien Mo, et al.Annals of Human Genetics|June 1, 2018
Decomposing Pearson's χ2 test: A linear regression and its departure from linearityZhengyang Zhou, Hung-Chih Ku, Guan Xing, et al.Annals of Human Genetics|June 4, 2009
Testing Hardy-Weinberg equilibrium using family data from complex surveysDewei She, Hong Zhang, Zhaohai LiAnnals of Human Genetics|June 4, 2009
Multivariate association test using haplotype trend regressionYu-Fang Pei, Lei Zhang, Jianfeng Liu, et al.Annals of Human Genetics|May 28, 2009
CALHM1 polymorphism is not associated with late-onset Alzheimer diseaseGary W Beecham, Nathalie Schnetz-Boutaud, Jonathan L Haines, et al.Annals of Human Genetics|January 10, 2009
Identifying rarer genetic variants for common complex diseases: diseased versus neutral discovery panelsK Curtin, M M Iles, N J CampAnnals of Human Genetics|January 13, 2009
Distinct clinical characteristics of tuberous sclerosis complex patients with no mutation identifiedS E Camposano, E Greenberg, D J Kwiatkowski, et al.Pageof 231