Francisco Vidal

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 12

Top Venues

Thrombosis and haemostasis

HLA

PloS one

British journal of haematology

This page only lists publications with an associated author ORCID identifier.

Publications

Laura Martin-Fernandez, Iris Garcia-Martínez, Sonia López, Angel Martinez-Perez, Noelia Vilalta, Melania Plaza, Carla Moret, Ana Viñuela, Andrew A Brown, Nikolaos I Panousis, Alfonso Buil, Emmanouil T Dermitzakis, Irene Corrales, Juan Carlos Souto, Francisco Vidal, Jose Manuel Soria
Multiallelic Copy Number Variation in ORM1 is Associated with Plasma Cell-Free DNA Levels as an Intermediate Phenotype for Venous Thromboembolism. Thrombosis and haemostasis (2023)
Perla Bandini, Nina Borràs, Ruben Berrueco, Susanna Gassiot, Laura Martin-Fernandez, Edurne Sarrate, Natàlia Comes, Lorena Ramírez, Carlos Hobeich, Francisco Vidal, Irene Corrales
Gaining Insights into Inherited Bleeding Disorders of Complex Etiology in Pediatric Patients: Whole-Exome Sequencing as First-Line Investigation Tool. Thrombosis and haemostasis 124 (7) (2023)
Perla Bandini, Nina Borràs, Ruben Berrueco, Susanna Gassiot, Laura Martin-Fernandez, Edurne Sarrate, Natàlia Comes, Lorena Ramírez, Carlos Hobeich, Francisco Vidal, Irene Corrales
Gaining Insights into Inherited Bleeding Disorders of Complex Etiology in Pediatric Patients: Whole-Exome Sequencing as First-Line Investigation Tool. Thrombosis and haemostasis (2023)
Perla Bandini, Nina Borràs, Eugenia Fernandez Mellid, Laura Martin-Fernandez, Paula Melero Valentín, Natalia Comes, Lorena Ramírez, Patricia Cadahia Fernández, Matilde Rodríguez Ruiz, Manuel Mateo Perez Encinas, Francisco Vidal, Irene Corrales
First description of bone marrow failure syndrome in Spain caused by mutations in the ERCC6L2 gene. British journal of haematology (2023)
Belén De la Morena-Barrio, Jonathan Stephens, María Eugenia de la Morena-Barrio, Luca Stefanucci, José Padilla, Antonia Miñano, Nicholas Gleadall, Juan Luis García, María Fernanda López-Fernández, Pierre-Emmanuel Morange, Marja Puurunen, Anetta Undas, Francisco Vidal, Frances Lucy Raymond, Vicente Vicente, Willem H Ouwehand, Javier Corral, Alba Sanchis-Juan, null null
Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency. Thrombosis and haemostasis 122 (8) (2022)
Laia Closa, Blanca Xicoy, Lurdes Zamora, Natalia Estrada, Dolors Colomer, Maria J Herrero, Francisco Vidal, Alberto Alvarez-Larrán, Jose L Caro
Natural killer cell receptors and ligand variants modulate response to tyrosine kinase inhibitors in patients with chronic myeloid leukemia. HLA 99 (2) (2022)
Laia Closa, Francisco Vidal, Maria J Herrero, Jose L Caro
High-throughput genotyping of HLA-G, HLA-F, MICA, and MICB and analysis of frequency distributions in healthy blood donors from Catalonia. HLA 97 (5) (2021)
Laia Closa, Francisco Vidal, Maria J Herrero, Jose L Caro
Distribution of human killer cell immunoglobulin-like receptors and ligands among blood donors of Catalonia. HLA 95 (3) (2019)
Emma Enrich, Eva Campos, Lluís Martorell, María José Herrero, Francisco Vidal, Sergi Querol, Francesc Rudilla Salvador
HLA-A, -B, -C, -DRB1, and -DQB1 allele and haplotype frequencies: An analysis of umbilical cord blood units at the Barcelona Cord Blood Bank. HLA 94 (4) (2019)
María Eugenia de la Morena-Barrio, Salam Salloum-Asfar, Julio Esteban, Belén De la Morena-Barrio, Carmen Altisent, Laura Martin-Fernández, Paul Gueguen, Jose Padilla, Antonia Miñano, Rafael Parra, Vicente Vicente, Francisco Vidal, Frederic Bauduer, Pablo Carbonell, Javier Corral
Archeogenetics of F11 p.Cys38Arg: a 5400-year-old mutation identified in different southwestern European countries. Blood 133 (24) (2019)
Almudena Pérez-Rodríguez, Javier Batlle, Irene Corrales, Nina Borràs, Ángela Rodríguez-Trillo, Esther Lourés, Ana Rosa Cid, Saturnino Haya Guaita, Noelia Cabrera, Andrés Moret, Rafael Parra, Maria-Eva Mingot-Castellano, Nira Navarro, Carmen Altisent, Rocío Pérez-Montes, Shally Marcellini, Ana Moreto, Sonia Herrero, Inmaculada Soto, Nuria Fernández Mosteirín, Víctor Jiménez-Yuste, Nieves Alonso, Aurora de Andrés Jacob, Emilia Fontanes, Rosa Campos, María José Paloma, Nuria Bermejo, Rubén Berrueco, José Mateo, Karmele Arribalzaga, Pascual Marco, Ángeles Palomo, Nerea Castro Quismondo, Belén Iñigo, María Del Mar Nieto, Rosa Vidal, María Paz Martínez, Reyes Aguinaco, Maria Tenorio, María Ferreiro, Javier García-Frade, Ana María Rodríguez-Huerta, Jorge Cuesta, Ramón Rodríguez-González, Faustino García-Candel, Manuela Dobón, Carlos Aguilar, Fernando Batlle, Francisco Vidal, María Fernanda López-Fernández
Role of multimeric analysis of von Willebrand factor (VWF) in von Willebrand disease (VWD) diagnosis: Lessons from the PCM-EVW-ES Spanish project. PloS one 13 (6) (2018)
Javier Del Rey, Francisco Vidal, Lorena Ramírez, Nina Borràs, Irene Corrales, Iris Garcia, Olga Martinez-Pasarell, Silvia F Fernandez, Raquel Garcia-Cruz, Aïda Pujol, Alberto Plaja, Itziar Salaverria, Maria Oliver-Bonet, Jordi Benet, Joaquima Navarro
Novel Double Factor PGT strategy analyzing blastocyst stage embryos in a single NGS procedure. PloS one 13 (10) (2018)

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Publication Activity (10 Years)

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Francisco Vidal