Friedhelm Hildebrandt
42PUBLICATIONS
263CO-AUTHORS
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Publications (42)
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|Apr 09, 2026
How variant discovery redefines genetic prevalence: the case of cystine stone disease.Chen-Han Wilfred Wu, Joshua Chang, Katreya Lovrenert
|Mar 05, 2026
N6-adenosine methylation enhances nuclear mRNA export through METTL3 and NUP93.Ji Hoon Lee, Mark Tingey, Zhao Zhang
|Jan 21, 2026
Mechanisms of Podocyte Injury Due to Loss of the Nucleoporin NUP93.Hussein Bachir, Vanessa Krausel, Florian Buerger
|Nov 27, 2025
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment.Florian Buerger, Daanya Salmanullah, Lorrin Liang
|Oct 09, 2025
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena
|Aug 07, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genes.Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena
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Frequent Collaborators
6 joint publications
Maddalena Marasà
6 joint publications
Ali Gharavi
6 joint publications
Simone Sanna-Cherchi
5 joint publications
Miguel Verbitsky
5 joint publications
Sophia Schneider
5 joint publications
Matthew G Sampson
5 joint publications
Heon Yung Gee
4 joint publications
Rik Westland
4 joint publications
Florian Buerger
4 joint publications
Giovanni Montini
