Irene Corrales

Madrid, MD, Spain

Last Updated: 09/26/2026

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Found 34 publications

Integrating Next-Generation Sequencing into von Willebrand Disease Diagnostics: Insights from the PCM-EVW-ES Multicenter Project.

Integrating Next-Generation Sequencing into von Willebrand Disease Diagnostics: Insights from the PCM-EVW-ES Multicenter Project.

Journal: Seminars in thrombosis and hemostasis

Published: April 15, 2026

Unveiling the genetic landscape of inherited primary hemostasis disorders by whole-exome sequencing: insights from a multi-center study.

Unveiling the genetic landscape of inherited primary hemostasis disorders by whole-exome sequencing: insights from a multi-center study.

Journal: Thrombosis and haemostasis

Published: February 11, 2026

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

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

Journal: Thrombosis and haemostasis

Published: February 11, 2026

Allogeneic hematopoietic stem cell transplantation in ERCC6L2 disease.

Allogeneic hematopoietic stem cell transplantation in ERCC6L2 disease.

Journal: Blood advances

Published: September 09, 2025

Co-inheritance of ITGA2B and TUBB1 variants in a family reveals distinct genetic contributions to platelet dysfunction.

Co-inheritance of ITGA2B and TUBB1 variants in a family reveals distinct genetic contributions to platelet dysfunction.

Journal: British journal of haematology

Published: August 12, 2025

Integrating Next-Generation Sequencing Into Routine Molecular Diagnosis of Inherited Coagulation Factor Deficiencies: Real-World Data From Spanish Patients.

Integrating Next-Generation Sequencing Into Routine Molecular Diagnosis of Inherited Coagulation Factor Deficiencies: Real-World Data From Spanish Patients.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: March 25, 2025

Elucidating the Molecular Basis in a Cohort of Patients With Combined Bleeding Tendencies and Joint Hypermobility Manifestations.

Elucidating the Molecular Basis in a Cohort of Patients With Combined Bleeding Tendencies and Joint Hypermobility Manifestations.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: March 10, 2025

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

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

Journal: Thrombosis and haemostasis

Published: December 29, 2023

Key Genes of the Immune System and Predisposition to Acquired Hemophilia A: Evidence from a Spanish Cohort of 49 Patients Using Next-Generation Sequencing.

Key Genes of the Immune System and Predisposition to Acquired Hemophilia A: Evidence from a Spanish Cohort of 49 Patients Using Next-Generation Sequencing.

Journal: International journal of molecular sciences

Published: October 10, 2023

First description of bone marrow failure syndrome in Spain caused by mutations in the ERCC6L2 gene.

First description of bone marrow failure syndrome in Spain caused by mutations in the ERCC6L2 gene.

Journal: British journal of haematology

Published: June 08, 2023

Comparison of Extracellular Vesicle Isolation Methods for miRNA Sequencing.

Comparison of Extracellular Vesicle Isolation Methods for miRNA Sequencing.

Journal: International journal of molecular sciences

Published: June 02, 2023

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

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

Journal: Thrombosis and haemostasis

Published: January 25, 2023

Showing 1-12 of 34

Last Updated: 09/26/2026