Toshimitsu Suzuki

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Lecturer

Nagoya University

Japan

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About

Toshimitsu Suzuki is a Lecturer at Nagoya City University, Japan. His research focuses on the genetic underpinnings of epilepsy and related neurodevelopmental disorders. Recent articles include studies on exome sequencing and genome-wide analyses that identify genetic risk factors and characterize seizure-associated variations.

Recent Grants

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SCN2A遺伝子変異による社会性行動障害に関わる神経回路の解明

Open Date: 2022-04-01

Close Date: 2025-03-01

Grant: Close

SCN2A遺伝子欠損による皮質－側坐核神経回路の異常を介した社会性行動障害の解明

Open Date: 2022-04-01

Close Date: 2023-03-01

Grant: Close

EFHC1およびICK遺伝子変異によるてんかんに共通する発症メカニズムの解明

Open Date: 2019-04-01

Close Date: 2022-03-31

Grant: Close

EFHC1変異によるてんかん新規発症機序の解明

Open Date: 2016-04-01

Close Date: 2019-03-31

Grant: Close

Characterization of Ehhc1 conditional knockout mouse and understand the pathology of epilepsy

Open Date: 2012-04-01

Close Date: 2015-03-31

Articles (11)

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2024

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2022

Collaborators (20)

Heidi Kirsch

Professor of Clinical Neurology and Radiology & Biomedical Imaging

UCSF Medical Center

UNITED STATES

Toshimitsu Suzuki

Research Interests

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About

Recent Grants

Articles (11)

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Epilepsies of presumed genetic etiology show enrichment of rare variants that occur in the general population

<i>Scn1a</i>-GFP transgenic mouse revealed Nav1.1 expression in neocortical pyramidal tract projection neurons.

Inversed Effects of Nav1.2 Deficiency at Medial Prefrontal Cortex and Ventral Tegmental Area for Prepulse Inhibition in Acoustic Startle Response

A cross-disorder dosage sensitivity map of the human genome

The role of common genetic variation in presumed monogenic epilepsies

CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate

De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations

Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder

Collaborators (20)

Heidi Kirsch

Hidekazu Kato

Tsuyoshi Miyakawa

Sarah Weckhuysen

Lachlan De Hayr

Gianpiero Cavalleri

Tomoyasu Wakuda

Paula Marques

Caroline Cusick

Satoko Hattori

Iori Ohmori

Anna Sophia Kirstein

Yoshihiro Nawa

Ingrid Scheffer

Kazuhiro Yamakawa

Samuel Berkovic

Stefan Wolking

Toshiya Inada

Robert Harvey

Doug Speed

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