Nina Borràs

Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients

Nina Borràs, Javier Batlle, Almudena Pérez‐Rodríguez et al. · Haematologica · 2017 · 60 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Molecular and clinical profile of von Willebrand disease in Spain (PCM–EVW–ES): Proposal for a new diagnostic paradigm

Javier Batlle, Almudena Pérez‐Rodríguez, Irene Corrales et al. · Thrombosis and Haemostasis · 2015 · 45 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Combined study of ADAMTS13 and complement genes in the diagnosis of thrombotic microangiopathies using next‐generation sequencing

Teresa Fidalgo, P. Martinho, Catarina Silva Pinto et al. · Research and Practice in Thrombosis and Haemostasis · 2017 · 28 citations · Full text

Life Sciences, Genetics, Hematology +16

Genotype–phenotype correlation in a cohort of Portuguese patients comprising the entire spectrum of VWD types: impact of NGS

Teresa Fidalgo, Ramón Salvado, Irene Corrales et al. · Thrombosis and Haemostasis · 2016 · 26 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Unraveling the effect of silent, intronic and missense mutations on <i>VWF</i> splicing: contribution of next generation sequencing in the study of mRNA

Nina Borràs, Gerard Orriols, Javier Batlle et al. · Haematologica · 2018 · 24 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17