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Journal of Human Genetics|June 11, 1998
A polymorphic CA repeat sequence at the human calcitonin locusK Tsukamoto, M EmiJournal of Human Genetics|May 22, 2015
GWA meta-analysis of personality in Korean cohortsBo-Hye Kim, Han-Na Kim, Seung-Ju Roh, et al.Journal of Human Genetics|May 22, 2015
Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations?Katja Stange, Claus-Eric Ott, Mareen Schmidt-von Kegler, et al.Journal of Human Genetics|May 22, 2015
Genetics of atrial fibrillation: from families to genomesIngrid E Christophersen, Patrick T EllinorJournal of Human Genetics|May 22, 2015
Genome-wide signatures of male-mediated migration shaping the Indian gene poolGaneshPrasad ArunKumar, Tatiana V Tatarinova, Jeff Duty, et al.Journal of Human Genetics|May 15, 2015
DMD mutation spectrum analysis in 613 Chinese patients with dystrophinopathyRuolan Guo, Guosheng Zhu, Huimin Zhu, et al.Journal of Human Genetics|September 1, 2025
Identification of two novel pathogenic mutations in the SKOR2 gene linked to cerebellar hypoplasia and a broad spectrum of neurodevelopmental delay in two Iranian familiesMohammad Ali Farazi Fard, Zahra Tabatabaei, Mobarakeh Ajam-Hosseini, et al.Journal of Human Genetics|September 1, 2025
Congenital disorders caused by aberrations in the biosynthesis of chondroitin/dermatan sulfateTadahisa Mikami, Shuji Mizumoto, Hiroshi Kitagawa, et al.Journal of Human Genetics|August 31, 2025
MYH2-associated myopathy caused by novel compound heterozygous mutations: a case report and literature reviewYulai Kang, Tong Yang, Xue Chen, et al.Journal of Human Genetics|May 20, 2020
Phylogenetic analysis of the Y-chromosome haplogroup C2b-F1067, a dominant paternal lineage in Eastern EurasiaQiao Wu, Hui-Zhen Cheng, Na Sun, et al.Pageof 352