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Journal of Human Genetics|September 2, 2016
A partial nuclear genome of the Jomons who lived 3000 years ago in Fukushima, JapanHideaki Kanzawa-Kiriyama, Kirill Kryukov, Timothy A Jinam, et al.Journal of Human Genetics|September 9, 2016
A survey on awareness of genetic counseling for non-invasive prenatal testing: the first year experience in JapanJunko Yotsumoto, Akihiko Sekizawa, Nobuhiro Suzumori, et al.Journal of Human Genetics|April 28, 2017
Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndromeMiwako Nagasaka, Mariko Taniguchi-Ikeda, Hidehito Inagaki, et al.Journal of Human Genetics|May 12, 2017
Effect of genomics-related literacy on non-communicable diseasesSho Nakamura, Hiroto Narimatsu, Kayoko Katayama, et al.Journal of Human Genetics|May 12, 2017
SCA42 mutation analysis in a case series of Japanese patients with spinocerebellar ataxiaMari Kimura, Ichiro Yabe, Yuka Hama, et al.Journal of Human Genetics|October 24, 2009
Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curseHirofumi Nakaoka, Ituro InoueJournal of Human Genetics|November 21, 2009
Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1*1501-DQB1*0602 haplotypeTaku Miyagawa, Makoto Honda, Minae Kawashima, et al.Journal of Human Genetics|November 3, 2009
Human chitotriosidase polymorphism is associated with human longevity in Mediterranean nonagenarians and centenariansLucia Malaguarnera, Luca Nnawuihe Ohazuruike, Christina Tsianaka, et al.Journal of Human Genetics|November 14, 2009
Mutation of ARHGAP9 in patients with coronary spastic anginaMikito Takefuji, Hiroyuki Asano, Kazutaka Mori, et al.Journal of Human Genetics|November 7, 2009
A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2)Katsuya Nakamura, Kunihiro Yoshida, Hideo Makishita, et al.Pageof 351