Editor's Choice – VASCUNET Rare Vascular Diseases: Multicentre Genetic Investigation of Patients with Carotid Paraganglioma
Genetic variants, especially in the SDHD gene, were common and associated with worse CPGL outcomes, thus emphasising the benefit of genetic diagnostics and counselling.
Authors
- Christian‐Alexander Behrendt (ORCID: https://orcid.org/0000-0003-0406-3319)
- Philipp Erhart (ORCID: https://orcid.org/0000-0002-4964-2448)
- Gregor Siegl
- Stefano Ancetti (ORCID: https://orcid.org/0000-0001-9634-9490)
- Imke Matthys (ORCID: https://orcid.org/0000-0002-1434-4969)
- C. López Espada (ORCID: https://orcid.org/0000-0002-6157-7829)
- Alicja Szatko (ORCID: https://orcid.org/0000-0003-0297-7344)
- Suzana Anjum (ORCID: https://orcid.org/0000-0001-5483-9002)
- Tina Cohnert (ORCID: https://orcid.org/0000-0001-7451-7588)
- Silvia Romagnoli (ORCID: https://orcid.org/0000-0002-2904-0351)
- María‐Dolores Chiara (ORCID: https://orcid.org/0000-0002-1112-1583)
Institutions
- St Bartholomew's Hospital (GB)
- Universidad de Oviedo (ES)
- Medical University of Graz (AT)
- Heidelberg University (DE)
- Barts Health NHS Trust (GB)
- Ghent University Hospital (BE)
- University Hospital Heidelberg (DE)
- Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico (IT)
- Ospedale Maggiore (IT)
- MSH Medical School Hamburg – University of Applied Sciences and Medical University (DE)
- IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola (IT)
- Hospital Universitario Virgen de las Nieves (ES)
- Postgraduate School of Molecular Medicine (PL)
- Asklepios (DE)
- University of Bologna (IT)
Publication Details
- Journal
- European Journal of Vascular and Endovascular Surgery
- Published
- 2025-07-16
- DOI
- https://doi.org/10.1016/j.ejvs.2025.07.013
- Citations
- 4
- Primary Topic
- Adrenal and Paraganglionic Tumors
- Type
- article
- Field-Weighted Citation Impact
- 8.03
Funders
- Heidelberger Stiftung Chirurgie