Serwet Demirdas
8PUBLICATIONS
62CO-AUTHORS
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Publications (8)
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|Jul 29, 2025
Clinical utility of DNA-methylation signatures in routine diagnostics for neurodevelopmental disorders.Daphne J Smits, Christophe Debuy, Alice S Brooks
|Jan 14, 2025
Tenascin-X Deficiency Causing Classical-Like Ehlers-Danlos Syndrome Type 1 in Humans is a Significant Risk Factor of Gastrointestinal and Tracheal Ruptures.Jonneke E van Gurp, Rosan L Lechner, Dimitra Micha
|Dec 04, 2024
Genetic diagnosis of the Ehlers-Danlos syndromes.Johannes Zschocke, Serwet Demirdas, Fleur S van Dijk
|Dec 04, 2024
Clinical diagnosis of the monogenic Ehlers-Danlos syndromes.Fleur S van Dijk, Chloe Angwin, Serwet Demirdas
|Oct 04, 2024
Biallelic and monoallelic variants in EFEMP1 can cause a severe and distinct subtype of heritable connective tissue disorder.M O Mol, T J van Ham, N Bannink
|Jul 11, 2024
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition.Jiarna R Zerella, Claire C Homan, Peer Arts
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Frequent Collaborators
3 joint publications
Hennie T Brüggenwirth
2 joint publications
Virginie J M Verhoeven
2 joint publications
Johannes Zschocke
2 joint publications
Fleur S van Dijk
1 joint publications
M O Mol
1 joint publications
R M Verdijk
1 joint publications
J Vlot
1 joint publications
Rosan Lechner
1 joint publications
Tahsin Stefan Barakat
1 joint publications
Suzanne I M Alsters
