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Journal of Human Genetics|May 27, 2011
16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disordersArivudainambi Ramalingam, Xin-Gang Zhou, Stephanie D Fiedler, et al.
Journal of Human Genetics|May 27, 2011
Association of interleukin-1β genetic polymorphisms with cognitive performance in elderly females without dementiaDaimei Sasayama, Hiroaki Hori, Toshiya Teraishi, et al.
Journal of Human Genetics|October 21, 2011
Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysisGanka V Douglas, Joanna Wiszniewska, Mark H Lipson, et al.
Journal of Human Genetics|October 21, 2011
Mutational analysis for biotinidase deficiency of a Greek patients' cohort ascertained through expanded newborn screeningGeorgia Thodi, Elina Molou, Vassiliki Georgiou, et al.
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|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 Yu
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