Kazuhiro Ogata - Concepedia

Author

Kazuhiro Ogata

Also Known As

K OGATA, K Ogata, K. OGATA, K. Ogata, KAZUHIRO OGATA, Kazuhiro OGATA, Kazuhiro Ogata, Keisuke Hamada, Kikuo OGATA, Koretsugu OGATA

259

Publications

9.3K

Citations

H-Index

143

Concepts

All Affiliations

Yokohama City University Niigata University The University of Tokyo Hamamatsu University School of Medicine Yokohama City University Hospital

About

Kazuhiro Ogata is an author at Yokohama City University specializing in medicine, genetics, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	36	68	6.1K
2	Natural Sciences	20	26	2.3K
3	Public Health	3	3	66
4	Engineering	2	2	39
5	Health Sciences	1	1	86

Kazuhiro Ogata

119

Publications

8.9K

Citations

H-Index

Page 1

	Year	Citations
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
Solution structure of a specific DNA complex of the Myb DNA-binding domain with cooperative recognition helices Kazuhiro Ogata, Souichi Morikawa, Haruki Nakamura, Cell Myb Dna-binding DomainProtein AssemblySpecific Dna ComplexNatural SciencesCooperative Recognition Helices	1994	487
The cavity in the hydrophobic core of Myb DNA-binding domain is reserved for DNA recognition and trans-activation Kazuhiro Ogata, Chie Kanei‐Ishii, Motoko Sasaki, Nature Structural Biology ChromatinHydrophobic CoreMyb Dna-binding DomainNatural SciencesDna Analysis	1996	318
Solution structure of a DNA-binding unit of Myb: a helix-turn-helix-related motif with conserved tryptophans forming a hydrophobic core. Kazuhiro Ogata, Hironobu Hojo, Saburo Aimoto, Proceedings of the National Academy of Sciences Structural BioinformaticsProtein AssemblyBiomolecular Structure PredictionMolecular BiologyImperfect Tandem Repeats	1992	286
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
Cyclin-dependent kinase (CDK) phosphorylation destabilizes somatic Wee1 via multiple pathways Nobumoto Watanabe, Harumi Arai, Jun-ichi Iwasaki, Proceedings of the National Academy of Sciences Somatic Wee1M PhaseSignal TransductionCell RegulationProtein Function	2005	227
Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy Gianina Ravenscroft, Satoko Miyatake, Vilma‐Lotta Lehtokari, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsFrequent CausePathology	2013	220
KDM6A Point Mutations Cause Kabuki Syndrome Noriko Miyake, Seiji Mizuno, Nobuhiko Okamoto, Human Mutation Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderMedicine	2012	210
Proposed uniform nomenclature for mammalian ribosomal proteins Edwin H. McConkey, H Bielka, J. Gordon, Molecular and General Genetics MGG Uniform NomenclatureRna Structure PredictionMolecular BiologyMolecular GeneticsMedicine	1979	200

Page 1