Author

Weise Chang

National Institutes of Health

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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Developmental Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:human· 1 Assay:imaging· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Amal Abu RayyaniD· 1 shared Amihood Singer· 1 shared Amir PelegiD· 1 shared Asgeir Orn ArnthorssoniD· 1 shared Bella DavidoviD· 1 shared Chana VinkleriD· 1 shared Claire A. ScottiD· 1 shared Doaa Ali‐Naffaa· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Amal Abu RayyanORCID

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2 papers

Recent·Most cited

Crosstalk between glucose metabolism and morphogen signalling specifies tonotopic identity in developing hair cells.

James D.B. O’Sullivan, Thomas S. Blacker, Claire A. Scott, Weise Chang, Mohi U. Ahmed, Val Yianni, Zoë F. Mann

The paper shows that glucose metabolism and morphogen signaling interact to establish tonotopic identity in developing hair cells by altering metabolic gradients and morphogen signaling.

eLife · Aug 4, 2023Peer-reviewedDevelopmental Biology

Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1

Zippora Brownstein, Süleyman Gülsüner, Tom Walsh, Fábio Tadeu Arrojo Martins, Shahar Taiber, Ofer Isakov, Ming K. Lee, Mor Bordeynik‐Cohen, Maria Birkan, Weise Chang, Silvia Casadei, Nada Danial‐Farran, Amal Abu Rayyan, Ryan J. Carlson, Lara Kamal, , Karen B. Avraham

The paper identifies genetic causes of inherited hearing loss in the Israeli Jewish population, finding a novel deafness gene ATOH1 and demonstrating the effectiveness of targeted genomic sequencing.

Clinical Genetics · Jul 20, 2020Peer-reviewedGenetics