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Journal of Human Genetics|November 18, 2003
A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetesBorut Peterlin, Mojca Globočnik Petrovič, Jana Makuc, et al.Journal of Human Genetics|September 25, 2003
Log-linear models for assessing gene-age interaction and their application to case-control studies of the apolipoprotein E (apoE) gene in Alzheimer's diseaseNoriko Tanaka, Toru Kinoshita, Takashi Asada, et al.Journal of Human Genetics|September 25, 2003
Interaction effects between estrogen receptor alpha gene, vitamin D receptor gene, age, and sex on bone mineral density in ChineseJirong Long, Pengyuan Liu, Yuanyuan Zhang, et al.Journal of Human Genetics|August 26, 2003
BglII gene polymorphism of the alpha2beta1 integrin gene is a risk factor for diabetic retinopathy in Caucasians with type 2 diabetesMojca Globočnik Petrovič, Marko Hawlina, Borut Peterlin, et al.Journal of Human Genetics|August 26, 2003
Identification of a novel candidate gene in the iron-sulfur pathway implicated in ataxia-susceptibility: human gene encoding HscB, a J-type co-chaperoneGuifeng Sun, J Jay Gargus, Dennis T Ta, et al.Journal of Human Genetics|October 31, 2003
Characterization of six base pair deletion in the putative HNF1-binding site of human PXR promoterYasuhiro Uno, Yoshiko Sakamoto, Kenichi Yoshida, et al.Journal of Human Genetics|June 15, 2007
Origins and genetic features of the Okhotsk people, revealed by ancient mitochondrial DNA analysisTakehiro Sato, Tetsuya Amano, Hiroko Ono, et al.Journal of Human Genetics|June 21, 2007
Identification of seven novel cryptic exons embedded in the dystrophin gene and characterization of 14 cryptic dystrophin exonsZhujun Zhang, Yasuaki Habara, Atsushi Nishiyama, et al.Journal of Human Genetics|November 9, 2007
Clinical and molecular characterization of Italian patients affected by Cohen syndromeEleni Katzaki, Chiara Pescucci, Vera Uliana, et al.Journal of Human Genetics|November 15, 2007
A genome-wide scan in forty large pedigrees with multiple sclerosisCristen J Willer, David A Dyment, Stacey Cherny, et al.Pageof 351