Nobuko Moriyama - Concepedia

Author

Nobuko Moriyama

Kanagawa Children's Medical Center

Also Known As

Kazushi Ichikawa, Nobuko MORIYAMA, Nobuko Moriyama

Publications

573

Citations

H-Index

Concepts

All Affiliations

Kanagawa Children's Medical Center Hitachi General Hospital Tokyo Metropolitan Children's Medical Center Shinshu University Fukuoka University

About

Nobuko Moriyama is an author at Kanagawa Children's Medical Center specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	321
2	Health Sciences	1	1	12
3	Biology	1	1	43
4	Hepatology	1	1	43
5	Molecular Biology	1	1	165

Nobuko Moriyama

Publications

418

Citations

H-Index

Page 1

	Year	Citations
Phenotypic spectrum of CHARGE syndrome with CHD7 mutations Michihiko Aramaki, Toru Udaka, Rika Kosaki, The Journal of Pediatrics Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseCharge Syndrome	2006	165
<i>CASK</i> aberrations in male patients with Ohtahara syndrome and cerebellar hypoplasia Hirotomo Saitsu, Mitsuhiro Kato, Hitoshi Osaka, Epilepsia	2012	81
Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies Shoko Komatsuzaki, Yoko Aoki, Tetsuya Niihori, Journal of Human Genetics Noonan-like SyndromeMendelian DisorderGenetic DisorderGeneticsPathology	2010	57
The geographical distribution of common liver flukes (the genus Fasciola) with normal and abnormal spermatogenesis. Kunio Terasaki, Hiroshige Akahane, Shigehisa Habe, The Japanese Journal of Veterinary Science SpermatogenesisBiologyHepatologyGeneticsHistopathology	1982	43
Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population Shweta Singh, Toshimitsu Suzuki, Akira Uchiyama, Journal of Human Genetics Translational BiologyDisease MechanismGenetic DisorderGeneticsPathogenesis	2005	30
The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B Kizuki Watanabe, Shin‐ya Nishio, Shin‐ichi Usami, Scientific Reports	2024	16
Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies Sachiko Miyamoto, Mitsuhiro Kato, Takuya Hiraide, Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsPathogenesis	2021	14
Bardet–Biedl syndrome and related disorders in Japan Makito Hirano, Wataru Satake, Nobuko Moriyama, Journal of Human Genetics Clinical DisordersGenetic DisorderInherited Metabolic DiseaseHematologyPathology	2020	12

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