| Prognostic value of thrombin generation parameters in hospitalized COVID-19 patients ME de la Morena-Barrio, C Bravo-Pérez, A Miñano, B de la Morena-Barrio, ... Scientific reports 11 (1), 7792, 2021 | 41 | 2021 |
| Incidence and features of thrombosis in children with inherited antithrombin deficiency B de la Morena-Barrio, C Orlando, ME de la Morena-Barrio, V Vicente, ... Haematologica 104 (12), 2512, 2019 | 27 | 2019 |
| High levels of latent antithrombin in plasma from patients with antithrombin deficiency M de la Morena-Barrio, E Sandoval, P Llamas, E Wypasek, M Toderici, ... Thrombosis and haemostasis 117 (05), 880-888, 2017 | 27 | 2017 |
| A pilot study on the impact of congenital thrombophilia in COVID‐19 ME de la Morena‐Barrio, C Bravo‐Pérez, B de la Morena‐Barrio, ... European Journal of Clinical Investigation 51 (5), e13546, 2021 | 24 | 2021 |
| ALG12‐CDG: An unusual patient without intellectual disability and facial dysmorphism, and with a novel variant ME de la Morena‐Barrio, M Sabater, B de la Morena‐Barrio, RL Ruhaak, ... Molecular Genetics & Genomic Medicine 8 (8), e1304, 2020 | 14 | 2020 |
| Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays ME de la Morena-Barrio, P Suchon, EM Jacobsen, N Iversen, A Miñano, ... Blood, The Journal of the American Society of Hematology 140 (2), 140-151, 2022 | 13 | 2022 |
| Molecular and clinical characterization of transient antithrombin deficiency: a new concept in congenital thrombophilia C Bravo‐Pérez, ME de la Morena‐Barrio, B de la Morena‐Barrio, ... American Journal of Hematology 97 (2), 216-225, 2022 | 13 | 2022 |
| Long-read sequencing identifies the first retrotransposon insertion and resolves structural variants causing antithrombin deficiency B De La Morena-Barrio, J Stephens, ME de la Morena-Barrio, ... Thrombosis and haemostasis 122 (08), 1369-1378, 2022 | 11 | 2022 |
| Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo C Bravo-Pérez, ME de la Morena-Barrio, A Palomo, L Entrena, ... British journal of haematology 191 (1), e32-e35, 2020 | 9 | 2020 |
| Antithrombin p. Thr147Ala: the first founder mutation in people of African origin responsible for inherited antithrombin deficiency C Orlando, B de la Morena-Barrio, I Pareyn, K Vanhoorelbeke, ... Thrombosis and Haemostasis 121 (02), 182-191, 2021 | 8 | 2021 |
| Gynaecological and obstetrical bleeding in Caucasian women with congenital factor XI deficiency: results from a twenty-year, retrospective, observational study C Bravo-Perez, T Ródenas, J Esteban, ME de la Morena-Barrio, ... Medicina Clinica 153 (10), 373-379, 2019 | 8 | 2019 |
| Molecular dissection of structural variations involved in antithrombin deficiency B de la Morena-Barrio, C Orlando, A Sanchis-Juan, JL García, J Padilla, ... The Journal of Molecular Diagnostics 24 (5), 462-475, 2022 | 7 | 2022 |
| High penetrance of inferior vena cava system atresia in severe thrombophilia caused by homozygous antithrombin Budapest 3 variant: Description of a new syndrome ME de la Morena‐Barrio, R Gindele, C Bravo‐Pérez, P Ilonczai, I Zuazu, ... American Journal of Hematology 96 (11), 1363-1373, 2021 | 7 | 2021 |
| Identification of a new mechanism of antithrombin deficiency hardly detected by current methods: duplication of SERPINC1 exon 6 B de la Morena-Barrio, ME de la Morena-Barrio, J Padilla, ... Thrombosis and Haemostasis 118 (05), 939-941, 2018 | 7 | 2018 |
| Full-length antithrombin frameshift variant with aberrant C-terminus causes endoplasmic reticulum retention with a dominant-negative effect C Bravo-Pérez, M Toderici, JE Chambers, JA Martínez-Menárguez, ... JCI insight 7 (19), 2022 | 6 | 2022 |
| Long-read sequencing resolves structural variants in SERPINC1 causing antithrombin deficiency and identifies a complex rearrangement and a retrotransposon … B de la Morena-Barrio, J Stephens, ME de la Morena-Barrio, L Stefanucci, ... bioRxiv, 2020.08. 28.271932, 2020 | 6 | 2020 |
| Identification of the first large intronic deletion responsible of type I antithrombin deficiency not detected by routine molecular diagnostic methods B De la Morena‐Barrio, N Borràs, A Rodríguez‐Alén, ... British Journal of Haematology 186 (4), e82-e86, 2019 | 6 | 2019 |
| Archeogenetics of F11 p.Cys38Arg: a 5400-year-old mutation identified in different southwestern European countries ME de la Morena-Barrio, S Salloum-Asfar, J Esteban, ... Blood, The Journal of the American Society of Hematology 133 (24), 2618-2622, 2019 | 6 | 2019 |
| Improvement of large copy number variant detection by whole genome nanopore sequencing J Cuenca-Guardiola, B de la Morena-Barrio, JL García, A Sanchis-Juan, ... Journal of Advanced Research 50, 145-158, 2023 | 4 | 2023 |
| New SERPINC1 gene mutations in patients with antithrombin deficiency: antithrombin Lodz I, II, III, and IV W Nowak, J Treliński, E Wypasek, B de la Morena-Barrio, ... Pol Arch Intern Med 132 (1), 16158, 2022 | 3 | 2022 |
