Jordi Surrallés

Universitat Autònoma de Barcelona — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

46h-index8.8kcitations213works4.82yr avg
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Research Topics

DNA Repair Mechanisms(113), CRISPR and Genetic Engineering(45), Carcinogens and Genotoxicity Assessment(39), BRCA gene mutations in cancer(24), Chromosomal and Genetic Variations(20)

Publications200 total

Multi-lineage natural gene therapy mediated by embryonic triploid mosaicism in the context of Fanconi anaemia
2025Open Access
BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes
The American Journal of Human Genetics·2025· 1 citedOpen Access
Ending diagnostic odyssey by reanalysis of whole exome sequencing data: reclassification of suspected Fanconi anemia cases to dyskeratosis congenita and Diamond-Blackfan anemia
Orphanet Journal of Rare Diseases·2025Open Access
Opening of a phase Ib/II study to investigate the safety and efficacy of Afatinib in patients with Fanconi anemia and unresectable locally advanced or metastatic head and neck squamous cell carcinoma
BMC Cancer·2025Open Access
Eltrombopag for Bone Marrow Failure in Fanconi Anemia: Results From the Phase II Clinical Trial FANCREV
European Journal Of Haematology·2025
Analysis of <i>BRCA1</i> , <i>BRCA2</i> and <i>PALB2</i> related Fanconi anemia identifies scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes
2025Open Access
Translating Muscle <scp>RNAseq</scp> Into the Clinic for the Diagnosis of Muscle Diseases
Annals of Clinical and Translational Neurology·2025· 3 citedOpen Access
Strategies for early detection and detailed characterization of oral lesions and head and neck squamous cell carcinoma in Fanconi anemia patients
Cancer Letters·2025· 4 citedOpen Access
Targeting protein-protein interactions in drug discovery: Modulators approved or in clinical trials for cancer treatment
Pharmacological Research·2024· 21 citedOpen Access
Haematopoietic gene therapy of non-conditioned patients with Fanconi anaemia-A: results from open-label phase 1/2 (FANCOLEN-1) and long-term clinical trials
The Lancet·2024· 20 cited
Prognostic significance of mutation type and chromosome fragility in Fanconi anemia
American Journal of Hematology·2024· 12 citedOpen Access
EP.17F.03 An Evidence-Driven Approach to Optimizing Clinical, Operational, And Economic Value in the Lung Cancer Care Pathway
Journal of Thoracic Oncology·2024Open Access
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder
The American Journal of Human Genetics·2024· 1 citedOpen Access
A self-repair history: compensatory effect of a de novo variant on the FANCA c.2778+83C&gt;G splicing mutation
Frontiers in Genetics·2023· 4 citedOpen Access
Diagnóstico citogenético de AF en una cohorte de pacientes con características clínicas de sospecha de anemia de Fanconi
Pediatría·2023Open Access
Gene therapy restores the transcriptional program of hematopoietic stem cells in Fanconi anemia
Haematologica·2023· 13 citedOpen Access
Supplementary Data from Constitutive Activation of Caspase-3 and Poly ADP Ribose Polymerase Cleavage in Fanconi Anemia Cells
2023Open Access
Data from Constitutive Activation of Caspase-3 and Poly ADP Ribose Polymerase Cleavage in Fanconi Anemia Cells
2023Open Access
Supplementary Data from Constitutive Activation of Caspase-3 and Poly ADP Ribose Polymerase Cleavage in Fanconi Anemia Cells
2023Open Access
Data from Constitutive Activation of Caspase-3 and Poly ADP Ribose Polymerase Cleavage in Fanconi Anemia Cells
2023Open Access
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Frequent Co-authors

Juan A. Bueren(14), Ricard Marcos(13), A. Creus(11), Massimo Bogliolo(11), José Antonio Casado(9), Paula Rı́o(8), Marı́a José Ramı́rez(8), Roser Pujol(8), Detlev Schindler(7), Hannu Norppa(6), Susana Navarro(6), María Castellà(6), N. Xamena(6), Javier Benı́tez(6), Julián Sevilla(6), José C. Segovia(5), Juan Pablo Trujillo‐Quintero(4), Jean Soulier(4), Cristina Díaz de Heredia(4), Isabel Badell(4)