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Journal of Human Genetics|August 19, 2011
Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodesDanhua Zhao, Daojun Hong, Wei Zhang, et al.Journal of Human Genetics|August 12, 2011
Mitochondrial DNA and Y-chromosome microstructure in TunisiaHajer Ennafaa, Rosa Fregel, Houssein Khodjet-El-Khil, et al.Journal of Human Genetics|September 9, 2011
Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levelsHaiqing Shen, Coleen Damcott, Scott R Shuldiner, et al.Journal of Human Genetics|September 9, 2011
Identification of independent risk loci for Graves' disease within the MHC in the Japanese populationKazuhiko Nakabayashi, Atsushi Tajima, Ken Yamamoto, et al.Journal of Human Genetics|June 3, 2011
A population-based study of copy number variants and regions of homozygosity in healthy Swedish individualsShu-Mei Teo, Chee-Seng Ku, Nasheen Naidoo, et al.Journal of Human Genetics|June 3, 2011
Molecular and clinical studies of X-linked deafness among Pakistani familiesAli M Waryah, Zubair M Ahmed, Munir A Bhinder, et al.Journal of Human Genetics|April 29, 2011
A single nucleotide polymorphism in the 3'-untranslated region of MyD88 gene is associated with Buerger disease but not with Takayasu arteritis in JapaneseZhiyong Chen, Toshiaki Nakajima, Yoshinori Inoue, et al.Journal of Human Genetics|March 18, 2011
HLA-C, CSTA and DS12346 susceptibility alleles confer over 100-fold increased risk of developing psoriasis: evidence of gene interactionYiannis Vasilopoulos, Gurdeep S Sagoo, Michael J Cork, et al.Journal of Human Genetics|March 18, 2011
Fabry-database.org: database of the clinical phenotypes, genotypes and mutant α-galactosidase A structures in Fabry diseaseSeiji Saito, Kazuki Ohno, Hitoshi SakurabaJournal of Human Genetics|April 8, 2011
Gene-gene interactions contribute to eye colour variation in humansEwelina Pośpiech, Jolanta Draus-Barini, Tomasz Kupiec, et al.Pageof 353