Author

Sabrina Maher

Shriners Hospitals for Children - Canada

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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Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Assay:spatial transcriptomics· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Bettina M. WillieiD· 1 shared Charlotte Zaouter· 1 shared Jaskaran SinghiD· 1 shared Maximilian BreueriD· 1 shared Maximilian RummleriD· 1 shared Nicolas PiloniD· 1 shared Priyanka Jamadagni· 1 shared Shunmoogum A. PatteniD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetics

Bettina M. WillieORCID

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1 paper

Recent·Most cited

Abnormal craniofacial and spinal bone development with col2a1a depletion in a zebrafish model of CHARGE syndrome

Maximilian Breuer, Maximilian Rummler, Jaskaran Singh, Sabrina Maher, Charlotte Zaouter, Priyanka Jamadagni, Nicolas Pilon, Bettina M. Willie, Shunmoogum A. Patten

This study identifies skeletal abnormalities in chd7-/- zebrafish, linking col2a1a depletion to craniofacial and spinal bone development defects in CHARGE syndrome.

Journal of Bone and Mineral Research · Feb 4, 2024Peer-reviewedGenetics