Miho Toyama

Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility

Yanjie Yu, Yingni Lin, Yuto Takasaki et al. · Translational Psychiatry · 2018 · 59 citations · Full text

NUS1 mutation in a family with epilepsy, cerebellar ataxia, and tremor

Kunihiko Araki, Ryoichi Nakamura, Daisuke Ito et al. · Epilepsy Research · 2020 · 30 citations

Mendelian Disorder, Neurological Disorder, Genetic Disorder +11

Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder

Hidekazu Kato, Itaru Kushima, Daisuke Mori et al. · Translational Psychiatry · 2020 · 17 citations · Full text

Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility

Yoshihiro Nawa, Hiroki Kimura, Daisuke Mori et al. · Human Genome Variation · 2020 · 15 citations · Full text

Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes

Hiroki Kimura, Masahiro Nakatochi, Branko Aleksić et al. · Translational Psychiatry · 2022 · 11 citations · Full text