Jun Mitsui - Concepedia

Author

Jun Mitsui

The University of Tokyo ORCID

Also Known As

J Mitsui, J. Mitsui, Jun MITSUI, Jun Mitsui, Mitsui, J., The Multiple-System Atrophy Research Collaboration

237

Publications

7.1K

Citations

H-Index

Concepts

All Affiliations

The University of Tokyo National Center of Neurology and Psychiatry International University of Health and Welfare Kagoshima University Mita Hospital

About

Jun Mitsui is an author at The University of Tokyo specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	29	1.6K
2	Engineering	1	1	42
3	Health Sciences	1	1	74
4	Natural Sciences	1	1	21
5	Public Health	1	1	19

Jun Mitsui

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease E. Sidransky, Mike A. Nalls, Jan Aasly, New England Journal of Medicine	2009	2.1K
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease Hiroyuki Ishiura, Shota Shibata, Jun Yoshimura, Nature Genetics Oculopharyngodistal MyopathyAutoimmune DiseaseNeurological DisorderMedicineOverlapping Disease	2019	424
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy Hiroyuki Ishiura, Koichiro Doi, Jun Mitsui, Nature Genetics MedicineNeuroscienceNeuropathologyIntronic TttcaTttta Repeats	2018	323
Human genetic variation database, a reference database of genetic variations in the Japanese population Koichiro Higasa, Noriko Miyake, Jun Yoshimura, Journal of Human Genetics	2016	294
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia Kelly L. Williams, Simon Topp, Shu Yang, Nature Communications	2016	205
Mutations for Gaucher Disease Confer High Susceptibility to Parkinson Disease Jun Mitsui, Ikuko Mizuta, Atsushi Toyoda, Archives of Neurology	2009	202
ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19 Yuji Takahashi, Y. Fukuda, Jun Yoshimura, The American Journal of Human Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisErbb4 MutationsGeneticsNeurology	2013	143
Total deletion and a missense mutation of <i>ITPR1</i> in Japanese SCA15 families Kenju Hara, Atsushi Shiga, Hiroaki Nozaki, Neurology	2008	140
The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement Hiroyuki Ishiura, Wataru Sako, Mari Yoshida, The American Journal of Human Genetics	2012	113
Mutations in<i>MME</i>cause an autosomal‐recessive Charcot–Marie–Tooth disease type 2 Yujiro Higuchi, Akihiro Hashiguchi, Jun‐Hui Yuan, Annals of Neurology	2016	102

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