Francisco Vidal

15PUBLICATIONS
28CO-AUTHORS
Gene mappingHaematologyGene expression (incl. microarray and other genome-wide approaches)Genetic immunologyRegenerative medicine (incl. stem cells)
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Publications (15)

|Mar 25, 2026
Co-inheritance of ITGA2B and TUBB1 variants in a family reveals distinct genetic contributions to platelet dysfunction.

Perla Bandini, Nina Borràs, Laura Martin-Fernandez

|Feb 11, 2026
Unveiling the Genetic Landscape of Inherited Primary Hemostasis Disorders by Whole-Exome Sequencing: Insights from a Multicenter Study.

Perla Bandini, Nina Borràs, Laura Martin-Fernandez

|Oct 16, 2025
A High-Throughput Sequencing Strategy for Clinical Repertoire Profiling of T Cell Receptor Beta Chain: Development and Reference Values Across Healthy Adults, Paediatrics, and Cord Blood Units.

Emma Enrich, Mireia Antón-Iborra, Carlos Hobeich

|Dec 02, 2024
Increased Platelet Adhesiveness in Patients with Venous Thromboembolic Disease.

Julia Martinez-Sanchez, Sergi Torramade-Moix, Ana Belén Moreno-Castaño

|Dec 29, 2023
Gaining Insights into Inherited Bleeding Disorders of Complex Etiology in Pediatric Patients: Whole-Exome Sequencing as First-Line Investigation Tool.

Perla Bandini, Nina Borràs, Ruben Berrueco

|Sep 11, 2023
First description of bone marrow failure syndrome in Spain caused by mutations in the ERCC6L2 gene.

Perla Bandini, Nina Borràs, Eugenia Fernandez Mellid

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Frequent Collaborators

4 joint publications

Perla Bandini

4 joint publications

Laura Martin-Fernandez

3 joint publications

Laia Closa

2 joint publications

Irene Corrales