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Journal of Human Genetics|December 14, 2012
Mutational analysis of ATP7B in north Chinese patients with Wilson diseaseKui Li, Wei-Min Zhang, Sheng Lin, et al.Journal of Human Genetics|December 14, 2012
Comprehensive DNA methylation analysis of peripheral blood cells derived from patients with first-episode schizophreniaMasaki Nishioka, Miki Bundo, Shinsuke Koike, et al.Journal of Human Genetics|January 18, 2013
Hypertension-susceptibility gene prevalence in the Pacific Islands and associations with hypertension in MelanesiaTakuro Furusawa, Izumi Naka, Taro Yamauchi, et al.Journal of Human Genetics|February 8, 2013
3'-UTR variations and G6PD deficiencyFarahnaz Amini, Endom IsmailJournal of Human Genetics|February 15, 2013
A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathyKentaro Toyota, Taeko Hashimoto, Daisuke Ogino, et al.Journal of Human Genetics|January 11, 2013
Quaternary protein modeling to predict the function of DNA variation found in human mitochondrial cytochrome c oxidaseMartin Patrick Horan, Jon N Rumbley, Richard G Melvin, et al.Journal of Human Genetics|January 11, 2013
The proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in KoreaSung Yoon Cho, Chang-Seok Ki, Young Bae Sohn, et al.Journal of Human Genetics|January 11, 2013
Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: a case-control study in the context of the IMMEnSE consortiumAlessandro Martino, Juan Sainz, Rui Manuel Reis, et al.Journal of Human Genetics|April 19, 2013
A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian familiesMohamed H Al-Hamed, Essam Al-Sabban, Hamad Al-Mojalli, et al.Journal of Human Genetics|May 31, 2013
Tet family of 5-methylcytosine dioxygenases in mammalian developmentHongbo Zhao, Taiping ChenPageof 353