Author

Zakia Abdelhamed

Cincinnati Children's Hospital Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Developmental Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:mouse· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Heymut OmraniD· 1 shared Marshall Lukacs· 1 shared Rolf W. StottmanniD· 1 shared Sandra CindrićiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

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4 top collaborators · 6 mutual co-author links

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1 shared paperDevelopmental Biology

Heymut OmranORCID

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1 paper

Recent·Most cited

A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice

Zakia Abdelhamed, Marshall Lukacs, Sandra Cindrić, Heymut Omran, Rolf W. Stottmann

This study identifies a hypomorphic Spag17 allele in mice that causes PCD-like phenotypes, revealing differential roles of SPAG17 in motile cilia development and hydrocephalus.

Disease Models & Mechanisms · Sep 8, 2020Peer-reviewedDevelopmental Biology