Publicacións nas que colabora con Alejandro José Blanco Verea (15)

2023

  1. Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel Sequencing

    Molecular Diagnosis and Therapy, Vol. 27, Núm. 1, pp. 105-113

2022

  1. Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome

    PLoS ONE, Vol. 17, Núm. 3 March

2019

  1. A Novel Calsequestrin 2 Deletion Causing Catecholaminergic Polymorphic Ventricular Tachycardia and Sudden Cardiac Death

    Revista Espanola de Cardiologia, Vol. 72, Núm. 8, pp. 681-683

  2. Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths

    Forensic Science International: Genetics, Vol. 42, pp. 203-212

2018

  1. Sudden unexpected death in the young — Value of massive parallel sequencing in postmortem genetic analyses

    Forensic Science International, Vol. 293, pp. 70-76

2017

  1. Postmortem genetic testing should be recommended in sudden cardiac death cases due to thoracic aortic dissection

    International Journal of Legal Medicine, Vol. 131, Núm. 5, pp. 1211-1219

2014

  1. Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders

    Electrophoresis, Vol. 35, Núm. 21-22, pp. 3111-3116

  2. Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

    Clinica Chimica Acta, Vol. 437, pp. 88-92

  3. Y-chromosomal DNA analysis in French male lineages

    Forensic Science International: Genetics, Vol. 9, Núm. 1, pp. 162-168

2012

  1. Sarcomeric gene mutations in sudden infant death syndrome (SIDS)

    Forensic Science International, Vol. 219, Núm. 1-3, pp. 278-281

2011

  1. Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases

    International Journal of Legal Medicine, Vol. 125, Núm. 4, pp. 565-572

2010

  1. Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathy

    Annals of Clinical and Laboratory Science, Vol. 40, Núm. 3, pp. 285-289

2009

  1. Phylogeography of French male lineages

    Forensic Science International: Genetics Supplement Series, Vol. 2, Núm. 1, pp. 439-441

  2. Sequenom MassArray™ application in the long QT syndrome mutation detection

    Forensic Science International: Genetics Supplement Series, Vol. 2, Núm. 1, pp. 497-498

2008

  1. Forensic validation and implementation of Y-chromosome SNP multiplexes

    Forensic Science International: Genetics Supplement Series, Vol. 1, Núm. 1, pp. 181-183