Shinji Saitoh - Concepedia

Author

Shinji Saitoh

Also Known As

Kumiko Hayashi, S SAITOH, S Saitoh, S. Saitoh, S.-I. Saitoh, S.I. Saitoh, SHINJI SAITOH, Saitoh, Shinji, Shigeyuki Saitoh, Shinji SAITOH

444

Publications

10.1K

Citations

H-Index

222

Concepts

All Affiliations

Nagoya City University Hokkaido University Nagoya University National Center For Child Health and Development Keio University

About

Shinji Saitoh is an author at Nagoya City University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	32	83	4.4K
2	Natural Sciences	8	8	643
3	Engineering	5	5	264
4	Health Sciences	5	5	106
5	Education	2	2	49

Shinji Saitoh

171

Publications

8.4K

Citations

H-Index

Page 1

	Year	Citations
Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15 Karin Buiting, Shinji Saitoh, Bärbel Dittrich, Nature Genetics Developmental BiologyGenetic DisorderDevelopmental GeneticsGeneticsChromosome Biology	1995	598
Imprinting-Mutation Mechanisms in Prader-Willi Syndrome Tohru Ohta, Todd A. Gray, Peter K. Rogan, The American Journal of Human Genetics Developmental BiologyGenetic DisorderGeneticsMolecular GeneticsImprinting-mutation Mechanisms	1999	276
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene Bärbel Dittrich, Karin Buiting, Bernd Korn, Nature Genetics ChromatinTranscriptional RegulationDevelopmental BiologyDevelopmental GeneticsGenetics	1996	257
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy Lucie Gueneau, A. Bertrand, Jean-Philippe Jaı̈s, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsDegenerative DiseaseMolecular Genetics	2009	236
Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene. Christopher C. Glenn, Shinji Saitoh, M T Jong, PubMed	1996	236
A Novel Imprinted Gene, Encoding a RING Zinc-Finger Protein, and Overlapping Antisense Transcript in the Prader-Willi Syndrome Critical Region M T Jong, Todd A. Gray, Yazhong Ji, Human Molecular Genetics	1999	229
An imprinted, mammalian bicistronic transcript encodes two independent proteins Todd A. Gray, Shinji Saitoh, Robert D. Nicholls Proceedings of the National Academy of Sciences	1999	186
Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder Atsushi Takata, Noriko Miyake, Yoshinori Tsurusaki, Cell Reports	2018	179
A Longer Polyalanine Expansion Mutation in the ARX Gene Causes Early Infantile Epileptic Encephalopathy with Suppression-Burst Pattern (Ohtahara Syndrome) Mitsuhiro Kato, Shinji Saitoh, Atsushi Kamei, The American Journal of Human Genetics Clinical DisordersMolecular NeuroscienceGenetic DisorderGeneticsSuppression-burst Pattern	2007	178
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations. Shinji Saitoh, Karin Buiting, Peter K. Rogan, Proceedings of the National Academy of Sciences Imprinting CenterCytogeneticsImprinting MutationGeneticsEpigenetic Change	1996	174

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