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Perla Bandini

5PUBLICATIONS

5CO-AUTHORS

Gene mappingHaematologyGene expression (incl. microarray and other genome-wide approaches)Genetic immunologyRegenerative medicine (incl. stem cells)

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Publications (5)

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|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

|Jun 27, 2025

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

Nina Borràs, Natàlia Comes, Lorena Ramírez

|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

Francisco Vidal

3 joint publications

Nina Borràs

2 joint publications

Irene Corrales

2 joint publications

Laura Martin-Fernandez

1 joint publications

Iris Garcia-Martínez

Frequent Collaborators

4 joint publications

Francisco Vidal

3 joint publications

Nina Borràs

2 joint publications

Irene Corrales

2 joint publications

Laura Martin-Fernandez

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