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Journal of Human Genetics|October 21, 2011
A genome-wide CNV association study on panic disorder in a Japanese populationYoshiya Kawamura, Takeshi Otowa, Asako Koike, et al.Journal of Human Genetics|December 2, 2011
Functional single-nucleotide polymorphism of epidermal growth factor is associated with the development of Barrett's esophagus and esophageal adenocarcinomaVivianda Menke, Raymond G J Pot, Leon M G Moons, et al.Journal of Human Genetics|September 23, 2011
Single-nucleotide polymorphisms at five loci are associated with C-reactive protein levels in a cohort of Filipino young adultsGhenadie Curocichin, Ying Wu, Thomas W McDade, et al.Journal of Human Genetics|September 23, 2011
A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13Muhammad Ansar, Kwanghyuk Lee, Syed Kamran-Ul-Hassan Naqvi, et al.Journal of Human Genetics|September 23, 2011
High prevalence of an anti-hypertriglyceridemic variant of the MLXIPL gene in Central AsiaKazuhiro Nakayama, Yoshiko Yanagisawa, Ayumi Ogawa, et al.Journal of Human Genetics|November 18, 2011
Functional analysis of APOE locus genetic variation implicates regional enhancers in the regulation of both TOMM40 and APOELynn M Bekris, Franziska Lutz, Chang-En YuJournal of Human Genetics|November 18, 2011
Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type IIIAmira Mili, Ilhem Ben Charfeddine, Ons Mamaï, et al.Journal of Human Genetics|June 27, 2009
MTHFR polymorphisms, dietary folate intake and breast cancer risk in Chinese womenChang-Ming Gao, Jin-Hai Tang, Hai-Xia Cao, et al.Journal of Human Genetics|May 23, 2009
Novel OTOF mutations in Brazilian patients with auditory neuropathyJihane Romanos, Lilian Kimura, Mariana Lopes Fávero, et al.Journal of Human Genetics|February 21, 2009
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3Muhammad Salman Chishti, Kwanghyuk Lee, Merry-Lynn McDonald, et al.Pageof 351