Gabriel Capellá Munar

23PUBLICATIONS
135CO-AUTHORS
Molecular targetsCancer geneticsMedical infection agents (incl. prions)Haematological tumoursEpigenetics (incl. genome methylation and epigenomics)
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Publications (23)

|Jun 08, 2026
Phase I trial of intravenous VCN-01 oncolytic adenovirus and durvalumab in patients with head and neck metastatic squamous cell carcinoma refractory to immunotherapy.

|Apr 16, 2026
Genome Sequencing of Undiagnosed European Patients Suspected of Hereditary Cancer: Diagnostic Yield and Identification of Candidate Causative Variants.

|Apr 14, 2025
Phenotype Correlations With Pathogenic DNA Variants in the MUTYH Gene: A Review of Over 2000 Cases.

Monica Thet, John-Paul Plazzer, Gabriel Capella

|May 22, 2024
Germline NPAT inactivating variants as cause of hereditary colorectal cancer.

Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti

|Jul 04, 2023
MBD4-associated neoplasia syndrome: screening of cases with suggestive phenotypes.

Mariona Terradas, Noemi Gonzalez-Abuin, Sandra García-Mulero

|Apr 19, 2023
Position statement of the International Society for Gastrointestinal Hereditary Tumours (InSiGHT) on APC I1307K and cancer risk.

Laura Valle, Lior H Katz, Andrew Latchford

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Frequent Collaborators

9 joint publications

Laura Valle

7 joint publications

Joan Brunet

7 joint publications

Marta Pineda

5 joint publications

Maartje Nielsen