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Matthias Rath

6PUBLICATIONS
18CO-AUTHORS
Cardiology (incl. cardiovascular diseases)Gene and molecular therapyCancer geneticsPolymerisation mechanismsGene mapping
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Journal

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 <i>RASA1</i> 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

Frequent Collaborators

1 joint publications

Alejandro N Santos

1 joint publications

Stéphanie Guey

1 joint publications

Hugues Chabriat

1 joint publications

Dominique Herve

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