Author

Arisa Igarashi

National Center For Child Health and DevelopmentORCID 0000-0001-7206-3105Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:eQTL / molecular QTL mapping· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:long-read sequencing· 1

Frequent Co-Authors

Tadashi KanameiD· 2 shared Akihiro FujimotoiD· 1 shared Hiroki Kiyose· 1 shared Kenji KurosawaiD· 1 shared Kumiko YanagiiD· 1 shared Masahiko Yamamori· 1 shared Mihoko ShimadaiD· 1 shared Motoko UnokiiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Tadashi KanameORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 27, 2026

CREBBP variants underlying Menke-Hennekam syndrome exhibit histone acetyltransferase hyperactivity with divergent phase behaviors

Taiga Aoki, Yasuyuki Fukuhara, Tetsumin So…·Tadashi Kaname

This study identifies two CREBBP variants causing Menke-Hennekam syndrome that increase HAT activity but disrupt phase separation differently, with HAT inhibition restoring condensate dynamics in one variant.

DOI 10.64898/2026.10.26.26365886

humanDNA methylation

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Genetic & Genomic MedicinemedRxivPreprintFeb 21, 2024

Long-read sequencing reveals novel isoform-specific eQTLs and regulatory mechanisms of isoform expression

Yuya Nagura, Mihoko Shimada, Ryoji Kuribayashi…·Akihiro Fujimoto

This study uses long-read sequencing to identify isoform-specific eQTLs in B cells, revealing new regulatory mechanisms and functional variants not detected by gene-level analysis.

1 citation

humanlong-read sequencing

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