Mitsuhiro Kato - Concepedia

Author

Mitsuhiro Kato

Also Known As

Alessandra Boncristiano, Borut Peterlin, Daniela Karall, Emma Vittery, G.-S Ch'ng, H. Kashii, Hajime Ikehara, Jun Tohyama, Kato, Mitsuhiro, M Kato

386

Publications

13.9K

Citations

H-Index

188

Concepts

All Affiliations

Yamagata University Yokohama City University Showa University Hamamatsu University School of Medicine Nishi Niigata Chuo National Hospital

About

Mitsuhiro Kato is an author at Yamagata University specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	40	94	6.5K
2	Health Sciences	6	6	153
3	Public Health	5	5	151
4	Natural Sciences	2	2	189
5	Engineering	1	1	23

Mitsuhiro Kato

191

Publications

12K

Citations

H-Index

Page 1

	Year	Citations
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, Noriyuki Sugiyama, Nature Genetics SpermatogenesisKnockout MouseInfertilityDevelopmental BiologyAbnormal Genitalia	2002	703
De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy Hirotomo Saitsu, Mitsuhiro Kato, Takeshi Mizuguchi, Nature Genetics Neurological DisorderGenetic DisorderGeneticsNeurologyNeuroscience	2008	539
Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome Yoshinori Tsurusaki, Nobuhiko Okamoto, Hirofumi Ohashi, Nature Genetics Mendelian DisorderTranslational BiologyDisease MechanismGenetic DisorderGenetics	2012	515
De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood Hirotomo Saitsu, Taki Nishimura, Kazuhiro Muramatsu, Nature Genetics Cell AutophagyNeurodegenerative DiseasesMitophagyNeurological DisorderGenetics	2013	471
Mutations of <i>ARX</i> are associated with striking pleiotropy and consistent genotype–phenotype correlation Mitsuhiro Kato, Soma Das, Kristin Petras, Human Mutation GeneticsPathologyMolecular GeneticsMendelian DisorderGenotype-phenotype Association	2004	327
Diffusion MRI abnormalities after prolonged febrile seizures with encephalopathy Jun‐ichi Takanashi, Hiroshi Oba, A. James Barkovich, Neurology	2006	240
De Novo Mutations in GNAO1, Encoding a Gαo Subunit of Heterotrimeric G Proteins, Cause Epileptic Encephalopathy Kazuyuki Nakamura, Hirofumi Kodera, Tenpei Akita, The American Journal of Human Genetics G Protein-coupled ReceptorGenetic DisorderGeneticsMolecular GeneticsCause Epileptic Encephalopathy	2013	228
Clinical spectrum of early onset epileptic encephalopathies caused by <scp><i>KCNQ2</i></scp> mutation Mitsuhiro Kato, Takanori Yamagata, Masaya Kubota, Epilepsia	2013	222
Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency Louis‐Daniel Brun, Lock Hock Ngu, Wee Teik Keng, Neurology	2010	219
Somatic Mutations in the <scp><i>MTOR</i></scp> gene cause focal cortical dysplasia type <scp>II</scp>b Mitsuko Nakashima, Hirotomo Saitsu, Nobuyuki Takei, Annals of Neurology	2015	197

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