Author

Björn Neubauer

University of FreiburgORCID 0000-0002-2143-5316Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Michael KöttgeniD· 2 shared Alexis HofherriD· 1 shared Anna KöttgeniD· 1 shared Carola HunteiD· 1 shared Christoph SchelliD· 1 shared Christophe WirthiD· 1 shared Felix Schöler· 1 shared Isabel Cascante· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersMolecular Biology

Michael KöttgenORCID

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2 papers

Recent·Most cited

The Role of the Co-Chaperone DNAJB11 in Polycystic Kidney Disease: Molecular Mechanisms and Cellular Origin of Cyst Formation

Tilman Busch, Björn Neubauer, Lars Schmitt, Isabel Cascante, Luise Knoblich, Oliver Wegehaupt, Felix Schöler, Stefan Tholen, Alexis Hofherr, Christoph Schell, Oliver Schilling, Lukas Westermann, Michael Köttgen

This study investigates DNAJB11's role in atypical ADPKD, showing biallelic loss causes cystic kidney disease and identifying impaired PC1 cleavage as a potential mechanism.

The FASEB Journal · Nov 12, 2024Peer-reviewedMolecular Biology

SLC25A48 is a human mitochondrial choline transporter

Suraj Dasharath Patil, Oleg Borisov, Nora Scherer, Christophe Wirth, Pascal Schlosser, Matthias Wuttke, Kai-Uwe Eckardt, Carola Hunte, Björn Neubauer, Anna Köttgen, Michael Köttgen

This study identifies SLC25A48 as a human mitochondrial choline transporter and shows that loss-of-function mutations lead to elevated choline levels in urine and plasma.

Journal of the American Society of Nephrology · Oct 1, 2024Peer-reviewedGenetic & Genomic Medicine