Tomonori Hara
Sendai, 9808575, Japan
Last Updated: 09/26/2026
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Found 12 publications
A case of bipolar I disorder with a loss-of-function variant of schizophrenia risk gene SETD1A: possible expansion of the relevant clinical spectrum supported by a meta-analysis.
Journal: Psychiatry and clinical neurosciences
Published: November 29, 2023
Genetics of bipolar disorder: insights into its complex architecture and biology from common and rare variants.
Journal: Journal of human genetics
Published: March 11, 2022
Glyoxalase I disruption and external carbonyl stress impair mitochondrial function in human induced pluripotent stem cells and derived neurons.
Journal: Translational psychiatry
Published: February 22, 2021
Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia.
Journal: Schizophrenia bulletin
Published: February 17, 2021
Fatty Acid Binding Protein 7 is Involved in the Proliferation of Reactive Astrocytes, but not in Cell Migration and Polarity.
Journal: Acta histochemica et cytochemica
Published: January 06, 2020
Excess hydrogen sulfide and polysulfides production underlies a schizophrenia pathophysiology.
Journal: EMBO molecular medicine
Published: April 01, 2019
Five-year history of dysphagia as a sole initial symptom in inclusion body myositis.
Journal: Journal of the neurological sciences
Published: August 06, 2017
D-Shuttle project: measurement and comparison of individual doses of high school students.
Journal: Annals of the ICRP
Published: September 29, 2016
Showing 1-12 of 12
Last Updated: 09/26/2026