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Mitsuhiro Kato | Researchclopedia

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Mitsuhiro Kato

Tokyo Institute of Technology ORCID

391

Works

13,900

Citations

62

h-index

217

i10-index

Research Topics

Genetics and Neurodevelopmental Disorders Genomics and Rare Diseases Genomic variations and chromosomal abnormalities

Affiliations

Dokkyo University1996–1996

Yamagata University1998–2022

Tokyo Institute of Technology2025–2025

Showa University2015–2025

Children's Medical Center2014–2014

Top Works

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

Kunio Kitamura,Masako Yanazawa,et al.

2002704 citations

Epilepsy research and treatment

Fetal and Pediatric Neurological Disorders

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

Hirotomo Saitsu,Mitsuhiro Kato,et al.

2008541 citations

Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome

Yoshinori Tsurusaki,Nobuhiko Okamoto,et al.

2012519 citations

De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood

Hirotomo Saitsu,Taki Nishimura,et al.

2013471 citations

Lissencephaly and the molecular basis of neuronal migration

2003329 citations

Mutations of <i>ARX</i> are associated with striking pleiotropy and consistent genotype–phenotype correlation

Mitsuhiro Kato,Soma Das,et al.

2004327 citations

Diffusion MRI abnormalities after prolonged febrile seizures with encephalopathy

Jun‐ichi Takanashi,Hiroshi Oba,et al.

2006241 citations

De Novo Mutations in GNAO1, Encoding a Gαo Subunit of Heterotrimeric G Proteins, Cause Epileptic Encephalopathy

Kazuyuki Nakamura,Hirofumi Kodera,et al.

2013231 citations

Clinical spectrum of early onset epileptic encephalopathies caused by <scp><i>KCNQ2</i></scp> mutation

Mitsuhiro Kato,Takanori Yamagata,et al.

2013223 citations