Yu-ichi Goto - Concepedia

Author

Yu-ichi Goto

National Center of Neurology and Psychiatry

Also Known As

Y Goto, Y. Goto, Y.I. Goto, Y.‐I. Goto, Yoshihiro Goto, Yu-Ichi Goto, Yu-ichi Goto

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

National Center of Neurology and Psychiatry Keio University Kyushu University The University of Osaka Teikyo University

About

Yu-ichi Goto is an author at National Center of Neurology and Psychiatry specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	22	2.1K
2	Natural Sciences	6	6	212
3	Social Sciences	1	1	231
4	Biochemistry	1	1	69
5	Biology	1	1	45

Yu-ichi Goto

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice Naotada Ishihara, Masatoshi Nomura, Akihiro Jofuku, Nature Cell Biology Developmental BiologySynapse FormationMitochondrial FunctionGeneticsMitochondrial Dynamics	2009	1K
Mitochondrial Lon protease regulates mitochondrial DNA copy number and transcription by selective degradation of mitochondrial transcription factor A (TFAM) Yuichi Matsushima, Yu-ichi Goto, Laurie S. Kaguni Proceedings of the National Academy of Sciences	2010	291
Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights Itaru Kushima, Branko Aleksić, Masahiro Nakatochi, Cell Reports GeneticsGenetic EpidemiologyDisease Gene IdentificationSocial SciencesAutism Spectrum Disorder	2018	231
Genome-Wide Association Study Identifies HLA-DP as a Susceptibility Gene for Pediatric Asthma in Asian Populations Emiko Noguchi, Hiromi Sakamoto, Tomomitsu Hirota, PLoS Genetics	2011	126
Plasma Metabolites Predict Severity of Depression and Suicidal Ideation in Psychiatric Patients-A Multicenter Pilot Analysis Daiki Setoyama, Takahiro A. Kato, Ryota Hashimoto, PLoS ONE	2016	120
Imprinting of Human GRB10 and Its Mutations in Two Patients with Russell-Silver Syndrome Hiroshi Yoshihashi, Katsuhiro Maeyama, Rika Kosaki, The American Journal of Human Genetics Genetic DisorderMedicineGeneticsRussell-silver SyndromePathology	2000	91
Mitochondrial Complex III Deficiency Caused by a Homozygous<i>UQCRC2</i>Mutation Presenting with Neonatal-Onset Recurrent Metabolic Decompensation Noriko Miyake, Shoji Yano, Chika Sakai, Human Mutation Systems BiologyMitochondrial CiiiMitochondrial BiogenesisMitochondrial FunctionGenetic Disorder	2012	88
ECHS1 Mutations Cause Combined Respiratory Chain Deficiency Resulting in Leigh Syndrome Chika Sakai, Seiji Yamaguchi, Masayuki Sasaki, Human Mutation GeneticsGenetic EpidemiologyPathologyMolecular GeneticsMitochondrial Biology	2014	69
Impaired respiratory function in MELAS‐induced pluripotent stem cells with high heteroplasmy levels Masaki Kodaira, Hideyuki Hatakeyama, Shinsuke Yuasa, FEBS Open Bio Regenerative MedicineInduced Pluripotent Stem CellDevelopmental BiologyMitochondrial FunctionMitochondrial Dysfunction	2015	65
A girl with West syndrome and autistic features harboring a de novo TBL1XR1 mutation Hirotomo Saitsu, Jun Tohyama, Tom Walsh, Journal of Human Genetics Tbl1xr1 MutationSyndromic AutismGenetic DisorderGeneticsWest Syndrome	2014	55

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