Francisco Vidal

15PUBLICATIONS
28CO-AUTHORS
HaematologyGene expression (incl. microarray and other genome-wide approaches)Genetic immunologyEpidemiological modellingHaematological tumours
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Publications (15)

|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

|Jan 25, 2023
Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism.

Laura Martin-Fernandez, Iris Garcia-Martínez, Sonia Lopez

|Jun 28, 2022
Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency.

Belén de la Morena-Barrio, Jonathan Stephens, María Eugenia de la Morena-Barrio

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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