José Rivera

Spain

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Articles (17)

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2025

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2024

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2022

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2022

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2022

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2021

Collaborators (16)

María Luisa Lozano

Universidad de Murcia

SPAIN

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Jesús María Hernández-Rivas

Universidad de Salamanca

SPAIN

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kathleen freson

Prof

Katholieke Universiteit Leuven

BELGIUM

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Pedro Real

Associate Professor

Universidad de Granada

SPAIN

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Paul Harrison

University of Birmingham

UNITED KINGDOM

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Marie-christine ALESSI

Professor / Director

Aix-Marseille University

FRANCE

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Carsten Deppermann

Assistant Professor (Tenure Track)

Johannes Gutenberg Universität Mainz

GERMANY

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Neil V. Morgan

UNITED KINGDOM

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Steve P. Watson

UNITED KINGDOM

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Ignacio García-Tuñón Llanio

Profesor Ayudante Doctor

Universidad de Alcalá

SPAIN

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Florian Heidel

Professor, Director

Universitätsmedizin Greifswald

GERMANY

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Nicola Pozzi

Associate Professor

Saint Louis University

UNITED STATES

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Ute Modlich

Research Laboratory Head

University of Zurich

SWITZERLAND

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José María Bastida

SPAIN

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M ROCIO BENITO SANCHEZ

Professor

Universidad de Salamanca

SPAIN

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Christian Andrea DI BUDUO

Assistant Professor

University of Pavia

ITALY

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José Rivera

Research Interests

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Articles (17)

Insights into the clinical, platelet and genetic landscape of inherited thrombocytopenia with malignancy risk.

Diagnosis of Inherited Platelet Disorders: Clinical Evaluation and Functional and Molecular Assays

Illustrated State-of-the-Art Capsules of the ISTH 2024 Congress.

The importance of genetic variant cleaners: From patient to wet lab and back to clinical practice

Multi-center evaluation of light transmission platelet aggregation reagents: Communication from the ISTH SSC Subcommittee on Platelet Physiology

Lentiviral gene therapy reverts GPIX expression and phenotype in Bernard-Soulier Syndrome Type C

Inherited Thrombocytopenia Caused by Variants in Crucial Genes for Glycosylation

GALE variants associated with syndromic manifestations, macrothrombocytopenia, bleeding, and platelet dysfunction

Validation of immunofluorescence analysis of blood smears in patients with inherited platelet disorders

Platelet transcriptome analysis in patients with germline RUNX1 mutations.

Aggregates of non-muscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopenia.

Targeted long-read sequencing identifies and characterizes structural variants in cases of inherited platelet disorders

A novel nonsense variant in TPM4 caused dominant macrothrombocytopenia, mild bleeding tendency and disrupted cytoskeleton remodeling.

A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger

Introduction of an ancient founder glycoprotein VI mutation into the Chilean population

Src-related thrombocytopenia: a fine line between a megakaryocyte dysfunction and an immune-mediated disease

Consensus recommendations on flow cytometry for the assessment of inherited and acquired disorders of platelet number and function: Communication from the ISTH SSC Subcommittee on Platelet Physiology

Collaborators (16)

María Luisa Lozano

Jesús María Hernández-Rivas

kathleen freson

Pedro Real

Paul Harrison

Marie-christine ALESSI

Carsten Deppermann

Neil V. Morgan

Steve P. Watson

Ignacio García-Tuñón Llanio

Florian Heidel

Nicola Pozzi

Ute Modlich

José María Bastida

M ROCIO BENITO SANCHEZ

Christian Andrea DI BUDUO

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