Author

Hisayoshi Nakamura

National Center of Neurology and Psychiatry

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetic & Genomic Medicine· 1

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Approach:experimental assay· 1 Organism:mouse· 1

Frequent Co-Authors

Ichizo NishinoiD· 1 shared Ikuya Nonaka· 1 shared Katsuhisa OgataiD· 1 shared Ken‐ichi DewaiD· 1 shared Mariko OkuboiD· 1 shared Megumu Ogawa· 1 shared Mikio HoshinoiD· 1 shared Nobuyuki EuraiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ichizo NishinoORCID

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1 paper

Recent·Most cited

Genetic SNUPN variants cause spinocerebellar atrophy by disrupting global splicing in Purkinje cells

Mariko Okubo, Megumu Ogawa, Nobuyuki Eura, Yukiko Inoue, Ken‐ichi Dewa, Tomohiro Owa, Satoshi Miyashita, Terumi Murakami, Hisayoshi Nakamura, Shinichiro Hayashi, Ikuya Nonaka, Katsuhisa Ogata, Mikio Hoshino, Takayoshi Inoue, Ichizo Nishino, S. Noguchi

The paper identifies SNUPN variants causing spinocerebellar atrophy by disrupting splicing in Purkinje cells through impaired U1 snRNP nuclear transport.

medRxiv · Jul 11, 2024 · PreprintGenetic & Genomic Medicine