Author

Tomonobu Hasegawa

Keio UniversityORCID 0000-0002-0143-3989Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Daisuke AriyasuiD· 1 shared Daisuke Higa· 1 shared Emika Kubo· 1 shared Hirofumi OhashiiD· 1 shared K. OkamuraiD· 1 shared Katsuya Aizu· 1 shared Kazunori Imaizumi· 1 shared Kimi ArakiiD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Daisuke AriyasuORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineThe Journal of Clinical Endocrinology & MetabolismPeer-reviewedOct 25, 2023

Single-exon deletions of ZNRF3 exon 2 cause congenital adrenal hypoplasia

Naoko Amano, Satoshi Narumi, Katsuya Aizu…·Tomonobu Hasegawa

The paper identifies single-exon deletions in ZNRF3 exon 2 as a cause of congenital adrenal hypoplasia by disrupting Wnt/β-catenin signaling.

10 citations

humanbulk RNA-seq

GeneticsbioRxivPreprintFeb 8, 2019

Decreased Activity of the Ghrhr and Gh Promoters Causes Dominantly Inherited GH Deficiency

Daisuke Ariyasu, Emika Kubo, Daisuke Higa…·Kimi Araki

The paper establishes an IGHD2 mouse model to study GH deficiency, finding reduced Ghrhr and Gh promoter activities due to decreased nuclear CREB3L2 levels, revealing a novel molecular mechanism.

DOI 10.1101/545384

mouseexperimental assay