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José Padilla

Amelioration of the severity of heparin-binding antithrombin mutations by posttranslational mosaicism
2012 · Irene Martínez-Martínez, José Navarro-Fernández, et al. · Blood · 44
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Expanding the genetic spectrum of TUBB1 -related thrombocytopenia
2021 · Verónica Palma-Barqueros, Loredana Bury, et al. · Blood Advances · 41
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Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study
2014 · Isabel Sánchez-Guiu, Ana I Antón, et al. · Orphanet Journal of Rare Diseases · 40
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Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays
2022 · Maria Eugenia de la Morena-Barrio, Pierre Suchon, et al. · Blood · 35
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Antithrombin Dublin (p.Val30Glu): a relatively common variant with moderate thrombosis risk of causing transient antithrombin deficiency
2016 · José Navarro-Fernández, María Morena-Barrio, et al. · Thrombosis and Haemostasis · 33
High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study
2017 · J. Esteban, M. E. de la Morena‐Barrio, et al. · Haemophilia · 29
Regulatory regions of SERPINC1 gene: Identification of the first mutation associated with antithrombin deficiency
2012 · María de la Morena-Barrio, Ana Antón, et al. · Thrombosis and Haemostasis · 29
High levels of latent antithrombin in plasma from patients with antithrombin deficiency
2017 · María de la Morena-Barrio, Edna Sandoval, et al. · Thrombosis and Haemostasis · 27
Molecular and clinical characterization of transient antithrombin deficiency: A new concept in congenital thrombophilia
2021 · Carlos Bravo‐Pérez, María Eugenia de la Morena‐Barrio, et al. · American Journal of Hematology · 26
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Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency
2022 · Belén de la Morena-Barrio, Jonathan Stephens, et al. · Thrombosis and Haemostasis · 25
Platelet transcriptome analysis in patients with germline RUNX1 mutations
2023 · Verónica Palma-Barqueros, José María Bastida, et al. · Journal of Thrombosis and Haemostasis · 24
A pilot study on the impact of congenital thrombophilia in COVID‐19
2021 · Maria Eugenia de la Morena‐Barrio, Carlos Bravo‐Pérez, et al. · European Journal of Clinical Investigation · 22
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Persistent cytotoxic T lymphocyte expansions after allogeneic haematopoietic stem cell transplantation: kinetics, clinical impact and absence of STAT 3 mutations
2016 · Julia Muñoz‐Ballester, Tzu H. Chen‐Liang, et al. · British Journal of Haematology · 22
Wiskott–Aldrich syndrome in a child presenting with macrothrombocytopenia
2016 · Jose Maria Bastida, Monica Del Rey, et al. · Platelets · 21
Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency
2016 · Mara Toderici, María Eugenia de la Morena-Barrio, et al. · PLoS ONE · 21
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Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation
2017 · María E de la Morena-Barrio, María J Ballesta-Martínez, et al. · Pediatric Research · 20
Molecular Dissection of Structural Variations Involved in Antithrombin Deficiency
2022 · Belén de la Morena-Barrio, Christelle Orlando, et al. · Journal of Molecular Diagnostics · 19
Genotype–phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo
2020 · C. Bravo‐Pérez, M. E. de la Morena‐Barrio, et al. · British Journal of Haematology · 19
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Novel Associations of VKORC1 Variants with Higher Acenocoumarol Requirements
2013 · Ana Isabel Anton, Juan J. Cerezo-Manchado, et al. · PLoS ONE · 19
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High penetrance of inferior vena cava system atresia in severe thrombophilia caused by homozygous antithrombin Budapest 3 variant: Description of a new syndrome
2021 · María E. de la Morena‐Barrio, Réka Gindele, et al. · American Journal of Hematology · 18
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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 · 17
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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 · 16
A correlative biomarker study and integrative prognostic model in chemotherapy‐naïve metastatic castration‐resistant prostate cancer treated with enzalutamide
2022 · María P. Fernandez‐Perez, Enrique Perez‐Navarro, et al. · The Prostate · 14
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Heparin affinity of factor VIIa: Implications on the physiological inhibition by antithrombin and clearance of recombinant factor VIIa
2010 · I. Martínez-Martínez, A. Ordóñez, et al. · Thrombosis Research · 14
Targeted long-read sequencing identifies and characterizes structural variants in cases of inherited platelet disorders
2023 · Ana Zamora-Cánovas, Belén de la Morena-Barrio, et al. · Journal of Thrombosis and Haemostasis · 13
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Works count: 71
Citation count: 759
H-index: 19
I10-index: 31
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