Takahito Wada - Concepedia

Author

Takahito Wada

Kanagawa Children's Medical Center ORCID

Also Known As

Shimizu, T Wada, T. Wada, TAKAHITO WADA, Takahito WADA, Takahito Wada, Tomoko Wada

118

Publications

2.3K

Citations

H-Index

108

Concepts

All Affiliations

Kanagawa Children's Medical Center Shinshu University Hokkaido University Kyoto University Yokohama City University

About

Takahito Wada is an author at Kanagawa Children's Medical Center specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	27	974
2	Natural Sciences	5	5	478
3	Public Health	4	4	70
4	Arts	1	1	14
5	Health Sciences	1	1	12

Takahito Wada

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
Clinical spectrum of <i>SCN2A</i> mutations expanding to Ohtahara syndrome Kazuyuki Nakamura, Mitsuhiro Kato, Hitoshi Osaka, Neurology	2013	196
Mutations in the chromatin-associated protein ATRX Richard J. Gibbons, Takahito Wada, Christopher A. Fisher, Human Mutation Constitutional Atrx MutationsGeneticsDna MethylationMolecular GeneticsDisease Gene Identification	2008	184
Phenotypic Spectrum of <i>COL4A1</i> Mutations: Porencephaly to Schizencephaly Yuriko Yoneda, Kazuhiro Haginoya, Mitsuhiro Kato, Annals of Neurology	2012	171
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach Belinda Giardine, Joseph Borg, Douglas R. Higgs, Nature Genetics	2011	160
<i>STXBP1</i> mutations in early infantile epileptic encephalopathy with suppression‐burst pattern Hirotomo Saitsu, Mitsuhiro Kato, Ippei Okada, Epilepsia	2010	155
Targeting G-quadruplex DNA as cognitive function therapy for ATR-X syndrome Norifumi Shioda, Yasushi Yabuki, K Yamaguchi, Nature Medicine Gene TherapiesGenetic DisorderNatural SciencesGeneticsFragile X Spectrum	2018	92
Human HRD1 Promoter Carries a Functional Unfolded Protein Response Element to Which XBP1 but not ATF6 Directly Binds Keisuke Yamamoto, Nobumi Suzuki, Takahito Wada, The Journal of Biochemistry Which Xbp1Molecular RegulationMolecular BiologyTranscriptional RegulationProtein Folding	2008	91
De-novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairment Tomoki Kosho, Satoru Sakazume, Hiroshi Kawame, Clinical Dysmorphology Developmental AnomalyDevelopmental BiologyMendelian DisorderSevere Speech ImpairmentGenetic Disorder	2008	86
Parent-of-Origin Specific Histone Acetylation and Reactivation of a Key Imprinted Gene Locus in Prader-Willi Syndrome Shinji Saitoh, Takahito Wada The American Journal of Human Genetics ChromatinDevelopmental BiologyChromatin StructureGenetic DisorderMedicine	2000	83
Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia Takahito Wada, Norio Kobayashi, Yoshio Takahashi, Pediatric Neurology Hemiplegic MigraineNeurobiology Of DiseaseProgressive AtaxiaNeurological DisorderWide Clinical Variability	2002	65

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