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Journal of Human Genetics|November 8, 2013
The promise of whole-exome sequencing in medical geneticsBahareh Rabbani, Mustafa Tekin, Nejat MahdiehJournal of Human Genetics|October 4, 2013
Endothelial nitric oxide synthase gene polymorphism is associated with sickle cell disease patients in IndiaSudhansu Sekhar Nishank, Mendi Prema Shyam Sunder Singh, Rajiv Yadav, et al.Journal of Human Genetics|October 11, 2013
Comprehensive analysis of common and rare mitochondrial DNA variants in elite Japanese athletes: a case-control studyEri Mikami, Noriyuki Fuku, Qing-Peng Kong, et al.Journal of Human Genetics|October 4, 2013
Novel FIG4 mutations in Yunis-Varon syndromeJunya Nakajima, Nobuhiko Okamoto, Jun Shiraishi, et al.Journal of Human Genetics|October 4, 2013
Polymorphisms in the UGT1A1 gene predict adverse effects of irinotecan in the treatment of gynecologic cancer in Japanese patientsAkira Hirasawa, Takeru Zama, Tomoko Akahane, et al.Journal of Human Genetics|May 11, 2012
Selective haploinsufficiency of longer isoforms of PTCH1 protein can cause nevoid basal cell carcinoma syndromeMaiko Suzuki, Hiromi Hatsuse, Kazuaki Nagao, et al.Journal of Human Genetics|June 8, 2012
Gender-specific association of TSNAX/DISC1 locus for schizophrenia and bipolar affective disorder in South Indian populationAnjanappa Ram Murthy, Meera Purushottam, Halagur Bhoge Gowda Kiran Kumar, et al.Journal of Human Genetics|August 26, 2016
No common founder for C9orf72 expansion mutation in SwedenHuei-Hsin Chiang, Charlotte Forsell, Anna-Karin Lindström, et al.Journal of Human Genetics|October 19, 2005
A novel expression system for genomic DNA loci using a human artificial chromosome vector with transformation-associated recombination cloningFumiaki Ayabe, Motonobu Katoh, Toshiaki Inoue, et al.Journal of Human Genetics|October 26, 2005
Homocysteine levels are associated with MTHFR A1298C polymorphism in Indian populationJitender Kumar, Swapan K Das, Priyanka Sharma, et al.Pageof 353