Author

Michiya Noguchi

Cell Engineering Division, BioResource Research Center, RIKEN, Koyadai, Tsukuba, Ibaraki, 305-0074, Japan.;

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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Cell Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Yukio NakamuraiD· 2 shared Anselmo Jiro KamadaiD· 1 shared Asami F. Gelinas· 1 shared Atsushi Takeda· 1 shared Chikashi C. TeraoiD· 1 shared Daigo Takagi· 1 shared Eijiro NakamuraiD· 1 shared Erica H. Parrish· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCell Biology

Yukio NakamuraORCID

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2 papers

Recent·Most cited

HNRNPC-mediated RNA processing promotes VHL-associated excessive vasculogenesis in von Hippel-Lindau syndrome revealed from patient-derived blood vessel models

Hidenori Ito, Iori Sato, Mami Matsuo-Takasaki, Tomoya Shimizu, Michiya Noguchi, Yukio Nakamura, Naoki Kubo, Daigo Takagi, Masaru Tamura, Megumu K Saito, Shunsaku Takayanagi, Nobuhito Saito, Eijiro Nakamura, Yohei Hayashi

This study uses patient-derived iPSCs to model VHLS-associated excessive vasculogenesis and identifies HNRNPC as a key factor in VHL-driven vascular lesions independent of HIF2A.

bioRxiv · Nov 2, 2026 · PreprintCell Biology

Mobile elements in human population-specific genome and phenotype divergence

Shohei Kojima, Satoshi Koyama, Mirei Ka, Yuka Saito, Erica H. Parrish, Mikiko Endo, Sadaaki Takata, Misaki Mizukoshi, Keiko Hikino, Atsushi Takeda, Asami F. Gelinas, Steven M. Heaton, Rie Koide, Anselmo Jiro Kamada, Michiya Noguchi, , Nicholas F. Parrish

The paper develops a tool to genotype mobile element variants (MEVs) using short-read data and identifies population-specific MEs linked to disease and gene regulation.

bioRxiv · Mar 25, 2022 · PreprintGenetics