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Paula Rofes

6PUBLICATIONS

36CO-AUTHORS

Cancer geneticsGene expression (incl. microarray and other genome-wide approaches)Liquid biopsiesMedical biotechnology not elsewhere classified

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Publications (6)

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|Apr 16, 2026

Genome Sequencing of Undiagnosed European Patients Suspected of Hereditary Cancer: Diagnostic Yield and Identification of Candidate Causative Variants.

|Mar 17, 2026

Optimizing GRIDSS for clinical use: A targeted NGS filtering strategy for germline structural variant detection.

Elisabet Munté, Paula Rofes, Miriam Millán-Castillo

|Apr 01, 2024

Tumor analysis of MMR genes in Lynch-like syndrome: Challenges associated with results interpretation.

Paula Rofes, Núria Dueñas, Jesús Del Valle

|Feb 01, 2022

Mosaicism in PTEN-new case and comment on the literature.

Paula Rofes, Álex Teulé, Lídia Feliubadaló

|Jan 27, 2021

<i>BARD1</i> Pathogenic Variants are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer Cohort.

Paula Rofes, Jesús Del Valle, Sara Torres-Esquius

|Apr 03, 2020

Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients.

Jesús Del Valle, Paula Rofes, José Marcos Moreno-Cabrera

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Frequent Collaborators

4 joint publications

Jesús Del Valle

3 joint publications

Gabriel Capellá

3 joint publications

Lídia Feliubadaló

3 joint publications

Joan Brunet

3 joint publications

Conxi Lázaro

2 joint publications

José Marcos Moreno-Cabrera

2 joint publications

Marta Pineda

2 joint publications

Elisabet Munté

1 joint publications

Sami Belhadj

1 joint publications

Núria Dueñas

Frequent Collaborators

4 joint publications

Jesús Del Valle

3 joint publications

Gabriel Capellá

3 joint publications

Lídia Feliubadaló

3 joint publications

Joan Brunet

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