Mitsuhiro Kato
Tokyo Institute of Technology(JP)Showa University(JP)Wakayama Medical University(JP)Showa University Hospital(JP)The University of Tokyo(JP)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Epilepsy research and treatment, Fetal and Pediatric Neurological Disorders
Most-Cited Works
- → Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans(2002)704 cited
- → De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy(2008)541 cited
- → Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome(2012)519 cited
- → De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood(2013)471 cited
- → Lissencephaly and the molecular basis of neuronal migration(2003)328 cited
- → Mutations of ARX are associated with striking pleiotropy and consistent genotype–phenotype correlation(2004)327 cited