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Journal of Human Genetics|August 20, 2010
Polymorphisms of the endothelial nitric oxide synthase gene in breast cancer: a genetic association study and meta-analysisElias Zintzaras, Maria Grammatikou, Georgios D Kitsios, et al.Journal of Human Genetics|July 9, 2010
The pattern of natural selection in somatic cancer mutations of human mtDNAPete Stafford, Estella B Chen-QuinJournal of Human Genetics|July 9, 2010
Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysmsKoichi Akiyama, Akira Narita, Hirofumi Nakaoka, et al.Journal of Human Genetics|December 15, 2010
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from ChinaYi Sun, Jing Chen, Hanjun Sun, et al.Journal of Human Genetics|November 26, 2010
Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 geneFarah Ouechtati, Ahlem Merdassi, Yosra Bouyacoub, et al.Journal of Human Genetics|November 5, 2010
A genome-wide association study identifies RNF213 as the first Moyamoya disease geneFumiaki Kamada, Yoko Aoki, Ayumi Narisawa, et al.Journal of Human Genetics|December 17, 2010
Haplotype block structure of the genomic region of the mu opioid receptor geneOrna Levran, Olaoluwakitan Awolesi, Shirley Linzy, et al.Journal of Human Genetics|December 24, 2010
Association of HLA-A*02:06 and HLA-DRB1*04:05 with clinical subtypes of juvenile idiopathic arthritisMasakatsu Yanagimachi, Takako Miyamae, Takuya Naruto, et al.Journal of Human Genetics|December 24, 2010
A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutationJunko Nakayama, Nobuaki Iwasaki, Kenji Shin, et al.Journal of Human Genetics|February 25, 2011
Mutation in PVRL4 gene encoding nectin-4 underlies ectodermal-dysplasia-syndactyly syndrome (EDSS1)Musharraf Jelani, Muhammad Salman Chishti, Wasim AhmadPageof 351