Sugirthan Sivalingam
8PUBLICATIONS
99CO-AUTHORS
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Publications (8)
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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
|Feb 11, 2022
GestaltMatcher facilitates rare disease matching using facial phenotype descriptors.Tzung-Chien Hsieh, Aviram Bar-Haim, Shahida Moosa
|Sep 28, 2021
Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO).Luca M Schierbaum, Sophia Schneider, Stefan Herms
|Jul 02, 2021
TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19.Axel Schmidt, Sophia Peters, Alexej Knaus
|Mar 28, 2020
A high-salt diet compromises antibacterial neutrophil responses through hormonal perturbation.Katarzyna Jobin, Natascha E Stumpf, Sebastian Schwab
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Frequent Collaborators
4 joint publications
Peter M Krawitz
4 joint publications
Markus Nöthen
4 joint publications
Axel Schmidt
3 joint publications
Tzung-Chien Hsieh
3 joint publications
Hannah Klinkhammer
3 joint publications
Stefan Herms
3 joint publications
Jean Tori Pantel
3 joint publications
Alexej Knaus
3 joint publications
Hartmut Engels
3 joint publications
Shahida Moosa
