Publicacións nas que colabora con Eva Ramos Luis (14)

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

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

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. Estudo de polimorfismos autosómicos e de cromosoma Y humanos con aplicacións en xenética forense e poboacional

    Estudo de polimorfismos autosómicos e de cromosoma Y humanos con aplicacións en xenética forense e poboacional

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

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

  3. Y-chromosomal DNA analysis in French male lineages

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

2009

  1. Phylogeography of French male lineages

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

2008

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

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

2007

  1. Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel

    Forensic Science International: Genetics, Vol. 1, Núm. 2, pp. 180-185

  2. Forensic validation of the SNPforID 52-plex assay

    Forensic Science International: Genetics, Vol. 1, Núm. 2, pp. 186-190

2006

  1. Analysis of artificially degraded DNA using STRs and SNPs-results of a collaborative European (EDNAP) exercise

    Forensic Science International, Vol. 164, Núm. 1, pp. 33-44

  2. Genotyping coding region mtDNA SNPs for Asian and Native American haplogroup assignation

    International Congress Series, Vol. 1288, pp. 4-6

2005

  1. Mutation rates at Y chromosome specific microsatellites

    Human Mutation, Vol. 26, Núm. 6, pp. 520-528