Author

Noriyuki Katsumata

National Research Institute for Child Health and DevelopmentORCID 0000-0002-9098-7851Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Hirofumi OhashiiD· 1 shared K. OkamuraiD· 1 shared Katsuya Aizu· 1 shared Mari Miyazawa· 1 shared Naoko AmanoiD· 1 shared Satoshi NarumiiD· 1 shared Tomohiro IshiiiD· 1 shared Tomonobu HasegawaiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Hirofumi OhashiORCID

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1 paper

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

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