Jordi Surralles

12PUBLICATIONS
68CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Predictive and prognostic markersMolecular targetsCancer geneticsHaematological tumours
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Publications (12)

|Oct 15, 2025
Ending diagnostic odyssey by reanalysis of whole exome sequencing data: reclassification of suspected Fanconi anemia cases to dyskeratosis congenita and Diamond-Blackfan anemia.

Eudald Tejero, María José Ramírez de Haro, Roser Pujol

|Nov 20, 2024
Prognostic significance of mutation type and chromosome fragility in Fanconi anemia.

María José Ramírez, Roser Pujol, Jordi Minguillón

|Nov 30, 2022
Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer.

Andrew L H Webster, Mathijs A Sanders, Krupa Patel

|Jan 21, 2022
CDK5RAP3, a New BRCA2 Partner That Regulates DNA Repair, Is Associated with Breast Cancer Survival.

Jordi Minguillón, María José Ramírez, Llorenç Rovirosa

|Sep 10, 2021
Clinical consequences of BRCA2 hypomorphism.

Laia Castells-Roca, Sara Gutiérrez-Enríquez, Sandra Bonache

|May 13, 2021
Natural gene therapy by reverse mosaicism leads to improved hematology in Fanconi anemia patients.

María José Ramírez, Roser Pujol, Juan Pablo Trujillo-Quintero

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Frequent Collaborators

4 joint publications

María José Ramirez

3 joint publications

Julián Sevilla

2 joint publications

Juan Pablo Trujillo-Quintero

2 joint publications

Cristina Beléndez