Matthias Rath
6PUBLICATIONS
18CO-AUTHORS
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Publications (6)
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|Jul 10, 2025
Lifetime Risk of First Symptomatic ICH or Seizure in Familial Cerebral Cavernous Malformations: A Multicenter Patient Data Analysis.Philipp Dammann, Alejandro N Santos, Laven Mavarani
|Nov 05, 2024
Novel postzygotic RASA1 mutation in a patient with Parkes Weber syndrome: A case report and literature review.Robin A Pilz, Dariush Skowronek, Tamara Ehresmann
|Jun 06, 2022
Contact-dependent signaling triggers tumor-like proliferation of CCM3 knockout endothelial cells in co-culture with wild-type cells.Matthias Rath, Konrad Schwefel, Matteo Malinverno
|Aug 26, 2019
Postzygotic mosaicism in cerebral cavernous malformation.Matthias Rath, Axel Pagenstecher, Alexander Hoischen
|Dec 18, 2018
Identification of pathogenic YY1AP1 splice variants in siblings with Grange syndrome by whole exome sequencing.Matthias Rath, Stefanie Spiegler, Tim M Strom
|Dec 15, 2018
Biallelic CCM3 mutations cause a clonogenic survival advantage and endothelial cell stiffening.Konrad Schwefel, Stefanie Spiegler, Sabine Ameling
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Frequent Collaborators
1 joint publications
Alejandro N Santos
1 joint publications
Stéphanie Guey
1 joint publications
Hugues Chabriat
1 joint publications
Dominique Herve
1 joint publications
Jun Zhang
1 joint publications
Jian-Cong Weng
1 joint publications
Gary K Steinberg
1 joint publications
David Bervini
1 joint publications
Laurèl Rauschenbach
1 joint publications
Ramazan Jabbarli
