Carla Oliveira

39PUBLICATIONS
167CO-AUTHORS
Cancer geneticsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)VirologyPredictive and prognostic markers
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Publications (39)

|May 13, 2026
Optimising rare tumour risk syndromes care: clinical insights and the PREVENTABLE socioeconomic framework.

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

|Feb 27, 2026
Variant-specific functional effects of CTNNA1 in a humanized Drosophila model.

Silvana Lobo, Ana Maria Pedro, Carla Oliveira

|Sep 25, 2025
Hereditary diffuse gastric cancer spectrum associated with germline CTNNA1 loss of function revealed by clinical and molecular data from 351 carrier families and over 37 000 non-carrier controls.

Silvana Lobo, Alexandre Dias, Ana Maria Pedro

|Jun 19, 2025
Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.

Steven Laurie, Wouter Steyaert, Elke de Boer

|Apr 29, 2025
Decoding migraine disorders: parathyroid hormone-related peptide receptors as key genetic drivers.

Andreia Dias, Marta Ferreira, Mariana Santos

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Frequent Collaborators

9 joint publications

Fatima Carneiro

6 joint publications

Gabriela M Almeida

6 joint publications

Daniel Ferreira

6 joint publications

Irene Gullo