Publicacións nas que colabora con Eva Ramos Luis (13)
2023
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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
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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
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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
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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
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Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders
Electrophoresis, Vol. 35, Núm. 21-22, pp. 3111-3116
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Y-chromosomal DNA analysis in French male lineages
Forensic Science International: Genetics, Vol. 9, Núm. 1, pp. 162-168
2009
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Phylogeography of French male lineages
Forensic Science International: Genetics Supplement Series, Vol. 2, Núm. 1, pp. 439-441
2008
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Forensic validation and implementation of Y-chromosome SNP multiplexes
Forensic Science International: Genetics Supplement Series, Vol. 1, Núm. 1, pp. 181-183
2007
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Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel
Forensic Science International: Genetics, Vol. 1, Núm. 2, pp. 180-185
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Forensic validation of the SNPforID 52-plex assay
Forensic Science International: Genetics, Vol. 1, Núm. 2, pp. 186-190
2006
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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
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Genotyping coding region mtDNA SNPs for Asian and Native American haplogroup assignation
International Congress Series, Vol. 1288, pp. 4-6
2005
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Mutation rates at Y chromosome specific microsatellites
Human Mutation, Vol. 26, Núm. 6, pp. 520-528