Author

Henrike Berns

University Medical Center FreiburgORCID 0009-0002-3578-3271Unclaimed ORCID profile · follow to get notified of new preprints

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Developmental Biology· 1

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Approach:experimental assay· 1 Organism:human· 1

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Magdalena Maria Brislinger-EngelhardtiD· 1 shared Maximilian Haas· 1 shared Miriam SchmidtsiD· 1 shared Peter WalentekiD· 1 shared Zeineb Bakey· 1 shared

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2024-2024 · peak 1/yr

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1 shared paperDevelopmental Biology

Magdalena Maria Brislinger-EngelhardtORCID

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1 paper

Recent·Most cited

A homozygous human WNT11 loss-of-function variant associated with laterality, heart and renal defects

Henrike Berns, Maximilian Haas, Zeineb Bakey, Magdalena Maria Brislinger-Engelhardt, Miriam Schmidts, Peter Walentek

The paper identifies a homozygous WNT11 variant causing laterality, heart, and renal defects in an infant and shows its loss-of-function in Xenopus embryos.

bioRxiv · Nov 14, 2024 · PreprintDevelopmental Biology