Riccardo Berutti
5PUBLICATIONS
66CO-AUTHORS
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Publications (5)
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|Jun 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.Axel Schmidt, Magdalena Danyel, Kathrin Grundmann
|Jul 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.Axel Schmidt, Magdalena Danyel, Kathrin Grundmann
|Jun 26, 2023
Episignature analysis of moderate effects and mosaics.Konrad Oexle, Michael Zech, Lara G Stühn
|Mar 16, 2023
Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience.Korbinian M Riedhammer, Jasmina Ćomić, Velibor Tasic
|Sep 25, 2021
Clinico-genetic findings in 509 frontotemporal dementia patients.Matias Wagner, Georg Lorenz, Alexander E Volk
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Frequent Collaborators
3 joint publications
Theresa Brunet
3 joint publications
Hartmut Engels
3 joint publications
Korbinian M Riedhammer
2 joint publications
Matias Wagner
2 joint publications
Shahida Moosa
2 joint publications
Tzung-Chien Hsieh
2 joint publications
Tobias Haack
2 joint publications
Jean Tori Pantel
2 joint publications
Hannah Klinkhammer
2 joint publications
Alexej Knaus
