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Verónica Palma‐Barqueros

Observed names: Palma Barqueros, Verónica, Palma-Barqueros V, Palma-Barqueros, V., Palma-Barqueros, Veronica, Palma-Barqueros, Verónica, V. Palma-Barqueros, Veronica Palma Barqueros, Veronica Palma-Barqueros, Verónica Palma-Barquero, Verónica Palma-Barqueros
ORCID: 0000-0002-5699-0053
Observed ORCID: 0000-0002-5699-0053
OpenAlex ID: A5015970395
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
2017 · José M. Bastida, María L. Lozano, et al. · Haematologica · 138
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Inherited Platelet Disorders: An Updated Overview
2021 · Verónica Palma-Barqueros, Nuria Revilla, et al. · International Journal of Molecular Sciences · 126
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Molecular Diagnosis of Inherited Coagulation and Bleeding Disorders
2019 · José María Bastida, Rocío Benito, et al. · Seminars in Thrombosis and Hemostasis · 55
Comprehensive comparison of neonate and adult human platelet transcriptomes
2017 · Eva Caparrós-Pérez, Raúl Teruel-Montoya, et al. · PLoS ONE · 53
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Expanding the genetic spectrum of TUBB1 -related thrombocytopenia
2021 · Verónica Palma-Barqueros, Loredana Bury, et al. · Blood Advances · 47
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Significant Hypo-Responsiveness to GPVI and CLEC-2 Agonists in Pre-Term and Full-Term Neonatal Platelets and following Immune Thrombocytopenia
2018 · Alexander Hardy, Verónica Palma-Barqueros, et al. · Thrombosis and Haemostasis · 44
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Identification of two novel mutations in RASGRP2 affecting platelet CalDAG-GEFI expression and function in patients with bleeding diathesis
2017 · Teresa Sevivas, José María Bastida, et al. · Platelets · 31
Impaired hemostatic activity of healthy transfused platelets in inherited and acquired platelet disorders: Mechanisms and implications
2019 · Robert H. Lee, Raymond Piatt, et al. · Science Translational Medicine · 24
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Down Regulation of the Munc18b-syntaxin-11 Complex and β1-tubulin Impairs Secretion and Spreading in Neonatal Platelets
2017 · Eva Caparrós-Pérez, Raúl Teruel-Montoya, et al. · Thrombosis and Haemostasis · 24
Platelet transcriptome analysis in patients with germline RUNX1 mutations
2023 · Verónica Palma-Barqueros, José María Bastida, et al. · Journal of Thrombosis and Haemostasis · 23
Developmental Differences in Platelet Inhibition Response to Prostaglandin E1
2019 · Verónica Palma-Barqueros, José Miguel Torregrosa, et al. · Neonatology · 19
RASGRP2 gene variations associated with platelet dysfunction and bleeding
2019 · Verónica Palma-Barqueros, Juan Ruiz-Pividal, et al. · Platelets · 19
Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencing
2019 · Jose María Bastida, Sara Morais, et al. · Annals of Medicine · 18
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Src-related thrombocytopenia: a fine line between a megakaryocyte dysfunction and an immune-mediated disease
2022 · Verónica Palma-Barqueros, Nuria Revilla, et al. · Blood Advances · 17
PTGS1 gene variations associated with bleeding and platelet dysfunction
2020 · Verónica Palma-Barqueros, Natalia Bohdan, et al. · Platelets · 17
A novel nonsense variant in TPM4 caused dominant macrothrombocytopenia, mild bleeding tendency and disrupted cytoskeleton remodeling
2022 · Ana Marín‐Quílez, Elena Vuelta, et al. · Journal of Thrombosis and Haemostasis · 15
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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
2022 · José Bastida, Stefano Malvestiti, et al. · Cells · 14
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Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model
2021 · Ana Marín-Quílez, Ignacio García-Tuñón, et al. · Thrombosis and Haemostasis · 7
A novel genetic variant in PTGS1 affects N‐glycosylation of cyclooxygenase‐1 causing a dominant‐negative effect on platelet function and bleeding diathesis
2020 · Verónica Palma‐Barqueros, Marilena Crescente, et al. · American Journal of Hematology · 5
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A Modern Approach to the Molecular Diagnosis of Inherited Bleeding Disorders
2018 · Jose Maria Bastida, Veronica Palma Barqueros, et al. · Journal of Molecular and Genetic Medicine · 2
Ten New Cases of Hermansky-Pudlak Syndrome in the Iberian Peninsula: Identification of Novel Genetic Variants in HPS3, HPS4, HPS6 and DTNBP1 Associated with Significant Clinical Complications
2018 · Jose Maria Bastida, Sara Morais, et al. · Blood · 1
Identification By Longread Nanopore Sequencing of a Complex Structural Variant in ITGB3 with a Founder Effect Causing Glanzmann's Thrombasthenia in Two Unrelated Patients
2022 · Maria Luisa Lozano, Ana Zamora-Cánovas, et al. · Blood
P1644: Novel Variants in Gale Caused Syndromic Macrothrombocytopenia Disrupting Thrombopoiesis and Glycosylation
2022 · A. Marin Quilez, C. A. Di Buduo, et al. · HemaSphere
Identification By Whole Exome Sequencing of the Molecular Defect in a Novel Gene Related to Glycosylation in Two Unrelated Families with Syndromic Macrothrombocytopenia
2021 · Ana Marín-Quílez, Elena Vuelta, et al. · Blood
Functional and molecular characterization of new genetic variants and development of a new gene therapy approach in Congenital Platelet Disorders
2021 · Palma Barqueros, Verónica · Hispana
Works count: 31
Citation count: 699
H-index: 15
I10-index: 17
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