Julia Hoefele
21PUBLICATIONS
134CO-AUTHORS

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Publications (21)
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|Mar 19, 2026
Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous results.Korbinian M Riedhammer, Patrick Richthammer, Dominik S Westphal
|Mar 12, 2026
'Missing' disease-causing variants in Alport syndrome.Judy Savige, Adam M Bournazos, Tomoko Horinouchi
|May 19, 2025
Genotype-phenotype correlations and clinical outcomes of genetic TRPC6 podocytopathies.Susan M McAnallen, Elhussein A E Elhassan, Sinead Stoneman
|Dec 12, 2024
Further delineation of the SCAF4-associated neurodevelopmental disorder.Cosima M Schmid, Anne Gregor, Anna Ruiz
|Aug 03, 2024
Extrarenal manifestations in inherited kidney diseases.Julia Hoefele, Julian Eble, Tobias Hermle
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Frequent Collaborators
8 joint publications
Korbinian Maria Riedhammer
5 joint publications
Alessandra Renieri
4 joint publications
Constantinos Deltas
3 joint publications
Judy Savige
3 joint publications
Anna Maria Pinto
2 joint publications
Matias Wagner
2 joint publications
Louise Hopkinson
2 joint publications
Pascale Hilbert
2 joint publications
Helen Storey
2 joint publications
Laura Bryant