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Journal of Human Genetics|June 8, 2007
Allelic variation in the NPY gene in 14 Indian populationsL V K S Bhaskar, K Thangaraj, Anish M Shah, et al.Journal of Human Genetics|July 7, 2007
Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndromeIn-Suk Kim, Soo-Young Oh, Suk-Joo Choi, et al.Journal of Human Genetics|July 3, 2007
A grid-search algorithm for optimal allocation of sample size in two-stage association studiesS H Wen, C K HsiaoJournal of Human Genetics|July 14, 2007
A comprehensive analysis of microsatellite diversity in Aboriginal AustraliansSimon J Walsh, R John Mitchell, Natalie Watson, et al.Journal of Human Genetics|January 31, 2009
Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairmentNele Hilgert, Kelly Monahan, Kiyoto Kurima, et al.Journal of Human Genetics|January 24, 2009
Role of HCN4 channel in preventing ventricular arrhythmiaKazuo Ueda, Yuji Hirano, Yasushi Higashiuesato, et al.Journal of Human Genetics|January 24, 2009
Genome-wide association study of panic disorder in the Japanese populationTakeshi Otowa, Eiji Yoshida, Nagisa Sugaya, et al.Journal of Human Genetics|April 4, 2009
Structural modeling of mutant alpha-glucosidases resulting in a processing/transport defect in Pompe diseaseKanako Sugawara, Seiji Saito, Masakazu Sekijima, et al.Journal of Human Genetics|April 4, 2009
Novel KCNA5 loss-of-function mutations responsible for atrial fibrillationYiqing Yang, Jun Li, Xiaoping Lin, et al.Journal of Human Genetics|March 27, 2009
Median network analysis of defectively sequenced entire mitochondrial genomes from early and contemporary disease studiesHans-Jürgen Bandelt, Yong-Gang Yao, Claudio M Bravi, et al.Pageof 351