Publicaciones en colaboración con investigadores/as de Hospital Universitario Virgen de las Nieves (16)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

2022

  1. Novel genes and sex differences in COVID-19 severity

    Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806

  2. PKP1 and MYC create a feedforward loop linking transcription and translation in squamous cell lung cancer

    Cellular Oncology, Vol. 45, Núm. 2, pp. 323-332

2020

  1. Correction: Plakophilin 1 enhances MYC translation, promoting squamous cell lung cancer (Oncogene, (2020), 39, 32, (5479-5493), 10.1038/s41388-019-1129-3)

    Oncogene

  2. Lncrna-mrna co-expression analysis identifies al133346.1/ccn2 as biomarkers in pediatric b-cell acute lymphoblastic leukemia

    Cancers, Vol. 12, Núm. 12, pp. 1-15

  3. Plakophilin 1 enhances MYC translation, promoting squamous cell lung cancer

    Oncogene, Vol. 39, Núm. 32, pp. 5479-5493

  4. The value of transcranial doppler sonography in hyperperfusion syndrome after carotid artery stenting: A nationwide prospective study

    Journal of Stroke

2019

  1. Clinical Predictors of Hyperperfusion Syndrome Following Carotid Stenting: Results From a National Prospective Multicenter Study

    JACC: Cardiovascular Interventions, Vol. 12, Núm. 9, pp. 873-882

  2. Expression of the long non-coding RNA TCL6 is associated with clinical outcome in pediatric B-cell acute lymphoblastic leukemia

    Blood Cancer Journal

2017

  1. GRECOS Project (Genotyping Recurrence Risk of Stroke): The Use of Genetics to Predict the Vascular Recurrence after Stroke

    Stroke, Vol. 48, Núm. 5, pp. 1147-1153

2014

  1. Análisis de recursos asistenciales para el ictus en España en 2012: ¿beneficios de la Estrategia del Ictus del Sistema Nacional de Salud?

    Neurologia, Vol. 29, Núm. 7, pp. 387-396

  2. Clinical management guidelines for subarachnoid haemorrhage. Diagnosis and treatment

    Neurologia

2013

  1. Functional characterization of a novel frameshift mutation in the c-terminus of the nav1.5 channel underlying a brugada syndrome with variable expression in a spanish family

    PLoS ONE, Vol. 8, Núm. 11

2011

  1. Plan de asistencia sanitaria al ICTUS II. 2010

    Neurologia, Vol. 26, Núm. 7, pp. 383-396

  2. Recursos asistenciales en ictus en España 2010: análisis de una encuesta nacional del Grupo de Estudio de Enfermedades Cerebrovasculares

    Neurologia, Vol. 26, Núm. 8, pp. 449-454

2008

  1. Ateromatosis intracraneal

    Medicina Clinica, Vol. 131, Núm. 4, pp. 141-152