Publicacións (19) Publicacións de Eva Ramos Luis

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

2020

  1. The place of metropolitan France in the European genomic landscape

    Human Genetics, Vol. 139, Núm. 8, pp. 1091-1105

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. Y-chromosomal DNA analysis in French male lineages

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

2012

  1. Evidence of pre-roman tribal genetic structure in basques from uniparentally inherited markers

    Molecular Biology and Evolution, Vol. 29, Núm. 9, pp. 2211-2222

  2. The peopling of Europe and the cautionary tale of Y chromosome lineage R-M269

    Proceedings of the Royal Society B: Biological Sciences, Vol. 279, Núm. 1730, pp. 884-892

2010

  1. Análisis de genomas completos en genética de poblaciones humanas

    Memorias de la Real Sociedad Española de Historia Natural, Tomo 8, pp. 169-201

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