Daisuke Mori

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Specially Appointed Associate Professor

Nagoya University

Japan

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精神疾患モデル動物の活動休止リズムを長期間モニタリングするシステムの開発

Open Date: 2019-07-01

Close Date: 2020-06-01

Grant: Close

リーリン欠失統合失調症患者モデルマウスを用いた発症メカニズムの解明

Open Date: 2019-04-01

Close Date: 2022-03-01

Grant: Close

精神疾患の特異行動をモニターする機器の開発

Open Date: 2019-01-01

Close Date: 2019-12-01

Grant: Close

Reelin欠失統合失調症患者型モデルマウスによる分子病態解明

Open Date: 2017-12-01

Close Date: 2018-11-01

Grant: Close

（分担）統合失調症と自閉スペクトラム症のゲノム解析結果を活かした診断法・治療法開発

Open Date: 2016-04-01

Close Date:

Articles (13)

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2024

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2022

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JAPAN

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Norio Ozaki

Designated Professor

Nagoya University

JAPAN

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Hidenori Tabata

Institute for Developmental Research, Aichi Developmental Disability Center

JAPAN

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Kazuya Kawabata

Nagoya University Graduate School of Medicine

JAPAN

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Itaru Kushima

Clinical Lecturer

Nagoya University

JAPAN

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Maeri Yamamoto

Nagoya University

JAPAN

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Taku Nagai

Professor

Fujita Health University

JAPAN

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Daisuke Mori

Research Interests

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Recent Grants

Articles (13)

Analysis of human neuronal cells carrying ASTN2 deletion associated with psychiatric disorders

Mice with deficiency in Pcdh15, a gene associated with bipolar disorders, exhibit significantly elevated diurnal amplitudes of locomotion and body temperature

Phenotypes for general behavior, activity, and body temperature in 3q29 deletion model mice

Histological Analysis of a Mouse Model of the 22q11.2 Microdeletion Syndrome

Reserve and Maintenance in the Aging Brain: A Longitudinal Study of Healthy Older Adults

Mice with exonic RELN deletion identified from a patient with schizophrenia have impaired visual discrimination learning and reversal learning in touchscreen operant tasks

Analysis of Reelin signaling and neurodevelopmental trajectory in primary cultured cortical neurons with RELN deletion identified in schizophrenia

ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk

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

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

Identifying the brain's connector hubs at the voxel level using functional connectivity overlap ratio

Generation and analysis of novel Reln‐deleted mouse model corresponding to exonic Reln deletion in schizophrenia

Cell body shape and directional movement stability in human-induced pluripotent stem cell-derived dopaminergic neurons

Collaborators (12)

Koh-ichi Nagata

Hidekazu Kato

Takao Kohno

Branko Aleksic

Hirohisa Watanabe

Yoshihiro Nawa

Norio Ozaki

Hidenori Tabata

Kazuya Kawabata

Itaru Kushima

Maeri Yamamoto

Taku Nagai

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