Author

Hiromi Kamura

National Research Institute for Child Health and Development

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

Biology Disciplines

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Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Kazuhiko NakabayashiiD· 2 shared Kenichiro HataiD· 2 shared Aaron Bogutz· 1 shared Alice Murigneux· 1 shared Amanda Ha· 1 shared Anne-Charlotte FromagetiD· 1 shared Bertille MontibusiD· 1 shared Catherine Vaurs‐BarrièreiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersMolecular Biology

Kazuhiko NakabayashiORCID

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2 papers

Recent·Most cited

The elongation of Mest transcript into MestXL sustains, but does not initiate, the maternal allele bias of its convergent gene Copg2 during neurogenesis

Sophie Perillous, Anne-Charlotte Fromaget, Céline Gonthier‐Guéret, Ornella Clerici, Marion Espenel, Alice Murigneux, Sophie Phan, Léa Feit, Catherine Vaurs‐Barrière, Floric Slimani, Céline Lemmers, Davide Normanno, Amanda Ha, Nolan Ashworth, Aaron Bogutz, , Philippe Arnaúd

The paper investigates the regulation of maternal allele bias in Copg2 during neurogenesis, showing it involves a two-step mechanism beyond MestXL-mediated interference.

Nature Communications · Sep 23, 2026Peer-reviewedMolecular Biology

DNA methylation signature in NSD2 loss-of-function variants appeared similar to that in Wolf-Hirschhorn syndrome

Tomoko Kawai, Shiori Kinoshita, Yuka Takayama, Eriko Onishi, Hiromi Kamura, Kazuaki Kojima, Hiroki Kikuchi, Miho Terao, Tohru Sugawara, Ohsuke Migita, Masayo Kagami, Tsuyoshi Isojima, Yu Yamaguchi, Keiko Wakui, Hirofumi Ohashi, , Kenichiro Hata

The paper identifies DNA methylation signatures associated with NSD2 loss-of-function variants and shows their similarity to those in Wolf-Hirschhorn syndrome.

bioRxiv · Jan 6, 2023 · PreprintGenetics