Author

Maximilian Breuer

Institut National de la Recherche ScientifiqueORCID 0000-0002-8830-3684Unclaimed ORCID profile · follow to get notified of new preprints

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 RummleriD· 1 shared Nicolas PiloniD· 1 shared Priyanka Jamadagni· 1 shared Sabrina Maher· 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

GeneticsJournal of Bone and Mineral ResearchPeer-reviewedFeb 4, 2024

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

Maximilian Breuer, Maximilian Rummler, Jaskaran Singh…·Shunmoogum A. Patten

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

7 citations

zebrafishspatial transcriptomics

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