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Author

Andrés Moret

Observed names: A. MORET, A. Moret, Moret, A.
ORCID: 0000-0003-2984-7646
Observed ORCID: 0000-0003-2984-7646
OpenAlex ID: A5019192015
Inhibitor development and mortality in non‐severe hemophilia A
2015 · C.L. Eckhardt, J.I. Loomans, et al. · Journal of Thrombosis and Haemostasis · 79
One‐stage and chromogenic FVIII:C assay discrepancy in mild haemophilia A and the relationship with the mutation and bleeding phenotype
2008 · A. R. CID, M. CALABUIG, et al. · Haemophilia · 65
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients
2017 · Nina Borràs, Javier Batlle, et al. · Haematologica · 63
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Molecular and clinical profile of von Willebrand disease in Spain (PCM–EVW–ES): Proposal for a new diagnostic paradigm
2015 · Javier Batlle, Almudena Pérez-Rodríguez, et al. · Thrombosis and Haemostasis · 44
Inhibitors in haemophilia A: current management and open issues
2007 · S. HAYA, A. MORET, et al. · Haemophilia · 37
Comparison of a new chemiluminescent immunoassay for von Willebrand factor activity with the ristocetin cofactor-induced platelet agglutination method
2013 · N. Cabrera, A. Moret, et al. · Haemophilia · 36
Head‐to‐head comparison of the pharmacokinetic profiles of a high‐purity factor IX concentrate (AlphaNine®) and a recombinant factor IX (BeneFIX®) in patients with severe haemophilia B
2013 · T. Lissitchkov, M. Matysiak, et al. · Haemophilia · 28
Is on‐demand treatment effective in patients with severe haemophilia?
2012 · J. A. AZNAR, A. MARCO, et al. · Haemophilia · 27
HLA class II polymorphisms in Spanish melanoma patients: homozygosity for HLA-DQA1 locus can be a potential melanoma risk factor
2005 · D. Planelles, E. Nagore, et al. · British Journal of Dermatology · 26
Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contribution of next generation sequencing in the study of mRNA
2018 · Nina Borràs, Gerard Orriols, et al. · Haematologica · 24
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Home‐delivered ultrasound monitoring for home treatment of haemarthrosis in haemophilia A
2015 · J. A. Aznar, S. Pérez‐Alenda, et al. · Haemophilia · 21
First application of MLPA method in severe von Willebrand disease. Confirmation of a new largeVWFgene deletion and identification of heterozygous carriers
2010 · Noelia Cabrera, Pilar Casaña, et al. · British Journal of Haematology · 19
Secondary prophylaxis vs. on‐demand treatment to improve quality of life in severe adult haemophilia A patients: a prospective study in a single centre
2013 · J. A. Aznar, M. García‐Dasí, et al. · Vox Sanguinis · 17
Clinical and molecular characterization by next generation sequencing of Spanish patients affected by congenital deficiencies of fibrinogen
2019 · Andrés Moret, Ángel Zúñiga, et al. · Thrombosis Research · 13
Inhibitor development after switching of FVIII concentrate in multitransfused patients with severe haemophilia A
2014 · J. A. Aznar, A. Moret, et al. · Haemophilia · 13
Assessment of the thrombin generation assay in haemophilia: Comparative study between fresh and frozen platelet‐rich plasma
2012 · V. Vila, J. A. Aznar, et al. · Haemophilia · 11
Diagnosis and management of von willebrand disease in Spain
2018 · Javier Batlle, Almudena Pérez-Rodríguez, et al. · Annals of Blood · 10
Guía práctica de tratamiento urgente de la microangiopatía trombótica
2018 · Samuel Romero, Amparo Sempere, et al. · Medicina Clínica · 9
Role of multimeric analysis of von Willebrand factor (VWF) in von Willebrand disease (VWD) diagnosis: Lessons from the PCM-EVW-ES Spanish project
2018 · Almudena Pérez-Rodríguez, Javier Batlle, et al. · PLoS ONE · 8
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Unraveling the Influence of Common von Willebrand factor variants on von Willebrand Disease Phenotype: An Exploratory Study on the Molecular and Clinical Profile of von Willebrand Disease in Spain Cohort
2020 · Nina Borràs, Iris Garcia-Martínez, et al. · Thrombosis and Haemostasis · 6
Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management
2020 · Andrés Moret, Ángel Zúñiga, et al. · Journal of Thrombosis and Thrombolysis · 6
Next generation sequencing in bleeding disorders: two novel variants in the F5 gene (Valencia-1 and Valencia-2) associated with mild factor V deficiency
2019 · A. Moret, Ángel Zúñiga, et al. · Journal of Thrombosis and Thrombolysis · 6
Practice guidelines for the emergency treatment of thrombotic microangiopathy
2018 · Samuel Romero, Amparo Sempere, et al. · Medicina Clínica (English Edition) · 6
Kinetics of the interaction between anti‐FVIII antibodies and FVIII from therapeutic concentrates, with and without von Willebrand factor, assessed by surface plasmon resonance
2012 · S. Grancha, A. M. Ortiz, et al. · Haemophilia · 4
Novel missense mutation c.2685G>C (p.Q895H) in VWF gene associated with very low levels of VWF mRNA
2008 · Noelia Cabrera, Pilar Casaña, et al. · Annals of Hematology · 4
Works count: 30
Citation count: 586
H-index: 13
I10-index: 17
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