Author

Maximilian Rummler

Max Planck Institute of Colloids and InterfacesORCID 0000-0002-0788-7172Unclaimed ORCID profile · follow to get notified of new preprints

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Maximilian Rummler1 paper · Max Planck Institute of Colloids and Interfaces

Biology Disciplines

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Bioengineering· 1 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Andrea M. BerzlanovichiD· 1 shared Astrid CantamessaiD· 1 shared Bettina M. WillieiD· 1 shared Charlotte Zaouter· 1 shared Davide RuffoniiD· 1 shared Jaskaran SinghiD· 1 shared Markus A. HartmanniD· 1 shared Maximilian BreueriD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperBioengineering

Andrea M. BerzlanovichORCID

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2 papers

Recent·Most cited

The mineralization of osteonal cement line depends on where the osteon is formed

Astrid Cantamessa, Stéphane Blouin, Maximilian Rummler, Andrea M. Berzlanovich, Richard Weinkamer, Markus A. Hartmann, Davide Ruffoni

This study investigates CL mineralization in human femoral samples, finding that CL mineral content correlates with surrounding bone mineral content and increases over time but at a slower rate than the osteon.

JBMR Plus · Jul 2, 2025Peer-reviewedBioengineering

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