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Journal of Human Genetics|August 30, 2013
Single-nucleotide polymorphisms in Toll-like receptor (TLR)-2, TLR4 and heat shock protein 70 genes and susceptibility to scrub typhusJeshina Janardhanan, Sherry Joseph Martin, Elisabeth Astrup, et al.Journal of Human Genetics|August 9, 2013
Association of XRCC3 and XRCC4 gene polymorphisms, family history of cancer and tobacco smoking with non-small-cell lung cancer in a Chinese population: a case-control studyFei He, Shen-Chih Chang, Gina Maria Wallar, et al.Journal of Human Genetics|August 9, 2013
Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern ChineseChing-Lung Cheung, Kam-Shing Lau, Pak-Chung Sham, et al.Journal of Human Genetics|September 20, 2013
Polymorphisms in alcohol-metabolizing enzymes and esophageal carcinoma susceptibility: a Dutch Caucasian case-control studyPolat Dura, Tineke Berkers, Elke M van Veen, et al.Journal of Human Genetics|September 27, 2013
Systematic evaluation of personal genome services for Japanese individualsTakashi Kido, Minae Kawashima, Seiji Nishino, et al.Journal of Human Genetics|September 6, 2013
High-dose enzyme replacement therapy attenuates cerebroventriculomegaly in a mouse model of mucopolysaccharidosis type IISo Yoon Ahn, Yun Sil Chang, Dong Kyung Sung, et al.Journal of Human Genetics|September 6, 2013
A common polymorphism in the tissue kallikrein gene is associated with increased urinary excretions of calcium and sodium in Japanese volunteersTomoe Fujita, Shuichi Yasuda, Mariko Kamata, et al.Journal of Human Genetics|August 16, 2013
Higher-order repeat structure in alpha satellite DNA is an attribute of hominoids rather than hominidsShoko Terada, Yuriko Hirai, Hirohisa Hirai, et al.Journal of Human Genetics|January 15, 2016
Effect of obesity on the association between MYL2 (rs3782889) and high-density lipoprotein cholesterol among Korean menEo Rin Cho, Yon Ho Jee, Sang Won Kim, et al.Journal of Human Genetics|January 15, 2016
Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet-Biedl syndromeElise Schaefer, Corinne Stoetzel, Sophie Scheidecker, et al.Pageof 352