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Belén de la Morena‐Barrio

Observed names: B. de la Morena-Barrio, B. de la Morena‐Barrio, B. de la morena-Barrio, Belen De La Morena-Barrio, Belen De la Morena-Barrio, Belen de la Morena, Belen de la Morena Barrio, Belen de la Morena-Barrio, Belen de la Morena‐Barrio, Belen de la Morena‐Barrio, Belén De la Morena-Barrio, Belén De la Morena‐Barrio, Belén de la Morena, Belén de la Morena-Barrio, de La Morena-Barrio, B
Institutions: Instituto de Salud Carlos III, Hospital General Universitario Morales Meseguer, Centre for Biomedical Network Research on Rare Diseases, Centro Regional de Hemodonación, Instituto Murciano de Investigación Biosanitaria, Universidad de Murcia
Observed institutions: University of Cambridge, Instituto de Salud Carlos III, Hospital General Universitario Morales Meseguer, Centre for Biomedical Network Research on Rare Diseases, Centro de Investigación Biomédica en Red, Centro Regional de Hemodonación, Instituto Murciano de Investigación Biosanitaria, Universidad de Murcia
ORCID: 0000-0002-6696-7762
Observed ORCID: 0000-0002-6696-7762
OpenAlex ID: A5000123957
Prognostic value of thrombin generation parameters in hospitalized COVID-19 patients
2021 · María Eugenia de la Morena-Barrio, Carlos Bravo-Pérez, et al. · Scientific Reports · 44
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Incidence and features of thrombosis in children with inherited antithrombin deficiency
2019 · Belén de la Morena-Barrio, Christelle Orlando, et al. · Haematologica · 37
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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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
Analysis of AlphaFold and molecular dynamics structure predictions of mutations in serpins
2024 · Pedro Garrido-Rodríguez, Miguel Carmena-Bargueño, et al. · PLoS ONE · 22
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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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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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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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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ALG12‐CDG: An unusual patient without intellectual disability and facial dysmorphism, and with a novel variant
2020 · María Eugenia de la Morena‐Barrio, María Sabater, et al. · Molecular Genetics & Genomic Medicine · 13
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Full-length antithrombin frameshift variant with aberrant C-terminus causes endoplasmic reticulum retention with a dominant-negative effect
2022 · Carlos Bravo-Pérez, Mara Toderici, et al. · JCI Insight · 12
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Antithrombin p.Thr147Ala: The First Founder Mutation in People of African Origin Responsible for Inherited Antithrombin Deficiency
2020 · Belén de la Morena-Barrio, Kristin Jochmans, et al. · Thrombosis and Haemostasis · 12
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Long-read sequencing improves the genetic diagnosis of retinitis pigmentosa by identifying an Alu retrotransposon insertion in the EYS gene
2024 · Elena Fernández-Suárez, María González-del Pozo, et al. · Mobile DNA · 11
Improvement of large copy number variant detection by whole genome nanopore sequencing
2022 · Javier Cuenca-Guardiola, Belén de la Morena-Barrio, et al. · Journal of Advanced Research · 11
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Detection and annotation of transposable element insertions and deletions on the human genome using nanopore sequencing
2023 · Javier Cuenca-Guardiola, Belén de la Morena-Barrio, et al. · iScience · 10
Identification of the first large intronic deletion responsible of type I antithrombin deficiency not detected by routine molecular diagnostic methods
2019 · Belén De la Morena‐Barrio, Nina Borràs, et al. · British Journal of Haematology · 10
Identification of a New Mechanism of Antithrombin Deficiency Hardly Detected by Current Methods: Duplication of SERPINC1 Exon 6
2018 · Belén de la Morena-Barrio, José Padilla, et al. · Thrombosis and Haemostasis · 10
Usefulness and Limitations of Multiple Ligation-Dependent Probe Amplification in Antithrombin Deficiency
2023 · Rosa Cifuentes, José Padilla, et al. · International Journal of Molecular Sciences · 9
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Gynaecological and obstetrical bleeding in Caucasian women with congenital factor XI deficiency: Results from a twenty-year, retrospective, observational study
2019 · Carlos Bravo-Perez, Teresa Ródenas, et al. · Medicina Clínica · 8
Archeogenetics of F11 p.Cys38Arg: a 5400-year-old mutation identified in different southwestern European countries
2019 · María Eugenia de la Morena-Barrio, Salam Salloum-Asfar, et al. · Blood · 7
The whole is greater than the sum of its parts: Long‐read sequencing for solving clinical problems in haematology
2024 · Carlos Bravo‐Perez, Rosa Cifuentes‐Riquelme, et al. · Journal of Cellular and Molecular Medicine · 4
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Functional, biochemical, molecular and clinical characterization of antithrombin c.1157T>C (p.Ile386Thr), a recurrent Polish variant with a founder effect
2023 · Anna Weronska, Belen De la Morena-Barrio, et al. · Haematologica · 4
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Works count: 53
Citation count: 451
H-index: 13
I10-index: 20
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