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Hierarchical analysis of 30 Y-chromosome SNPs in European populations

International journal of legal medicine, 2005-01, Vol.119 (1), p.10-15

2005

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Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young

Forensic science international : genetics, 2015-09, Vol.18, p.160-170

2015

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

Forensic science international : genetics, 2019-09, Vol.42, p.203-212

2019

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Y-chromosomal DNA analysis in French male lineages

Forensic science international : genetics, 2014-03, Vol.9, p.162-168

2014

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Patterns of Y-STR variation in Italy

Forensic science international : genetics, 2012-12, Vol.6 (6), p.834-839

2012

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Y-chromosome lineages in native South American population

Forensic science international : genetics, 2010-04, Vol.4 (3), p.187-193

2010

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The genetic male legacy from El Salvador

Forensic science international, 2007-09, Vol.171 (2), p.198-203

2007

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Una nueva delección de calsequestrina 2 que causa taquicardia ventricular polimórfica catecolaminérgica y muerte súbita cardiaca

Revista española de cardiologia, 2019-08, Vol.72 (8), p.681-683

2019

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Research update for articles published in EJCI in 2016

European journal of clinical investigation, 2018-10, Vol.48 (10), p.e13016-n/a

2018

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Duplications of the Y-chromosome specific loci P25 and 92R7 and forensic implications

Forensic science international, 2004-03, Vol.140 (2), p.241-250

2004

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Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages

Electrophoresis, 2005-12, Vol.26 (23), p.4411-4420

2005

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Genome-wide association meta-analysis of 5,864 individuals highlights 25 new loci implicated in the pathogenesis of cancer therapy-related cardiac dysfunction

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Meta-analysis of genome-wide association studies for cancer therapy-related cardiovascular dysfunction and functional mapping highlight an intergenic region close to TP63

Scientific reports, 2024-08, Vol.14 (1), p.18413-10, Article 18413

2024

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P5857Study of pharmacodynamic and pharmacokinetic-mediated genetic susceptibility to drug-induced arrhythmia and sudden cardiac death

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

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P5862Catecholaminergic polymorphic ventricular tachycardia and sudden cardiac death in the context of a novel deletion in the CASQ2 gene affecting the last three exons

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

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29 Y-chromosome SNP analysis in European populations

International Congress series, 2004-04, Vol.1261, p.73-75

2004

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Phylogeography of French male lineages

Forensic science international. Genetics supplement series, 2009-12, Vol.2 (1), p.439-441

2009

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Forensic validation and implementation of Y-chromosome SNP multiplexes

Forensic science international. Genetics supplement series, 2008-08, Vol.1 (1), p.181-183

2008

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Sequenom MassArray™ application in the long QT syndrome mutation detection

Forensic science international. Genetics supplement series, 2009-12, Vol.2 (1), p.497-498

2009

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Analysis of Y chromosome lineages in native South American population

International Congress series, 2006-04, Vol.1288, p.222-224

2006

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Analysis of 29 Y-chromosome SNPs in a single multiplex useful to predict the geographic origin of male lineages

International Congress series, 2006-04, Vol.1288, p.13-15

2006

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Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome

PloS one, 2022-03, Vol.17 (3), p.e0263469

2022

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

Electrophoresis, 2014-11, Vol.35 (21-22), p.3111-3116

2014

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PRKG1 and genetic diagnosis of early-onset thoracic aortic disease

European journal of clinical investigation, 2016-09, Vol.46 (9), p.787-794

2016

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Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood

Archives of disease in childhood, 2015-10, Vol.100 (10), p.952-956

2015

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Hierarchical analysis of 30 Y-chromosome SNPs in European populations

Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young

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

Y-chromosomal DNA analysis in French male lineages

Patterns of Y-STR variation in Italy

Y-chromosome lineages in native South American population

The genetic male legacy from El Salvador

Una nueva delección de calsequestrina 2 que causa taquicardia ventricular polimórfica catecolaminérgica y muerte súbita cardiaca

Research update for articles published in EJCI in 2016

Duplications of the Y-chromosome specific loci P25 and 92R7 and forensic implications

Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages

Genome-wide association meta-analysis of 5,864 individuals highlights 25 new loci implicated in the pathogenesis of cancer therapy-related cardiac dysfunction

Meta-analysis of genome-wide association studies for cancer therapy-related cardiovascular dysfunction and functional mapping highlight an intergenic region close to TP63

P5857Study of pharmacodynamic and pharmacokinetic-mediated genetic susceptibility to drug-induced arrhythmia and sudden cardiac death

P5862Catecholaminergic polymorphic ventricular tachycardia and sudden cardiac death in the context of a novel deletion in the CASQ2 gene affecting the last three exons

29 Y-chromosome SNP analysis in European populations

Phylogeography of French male lineages

Forensic validation and implementation of Y-chromosome SNP multiplexes

Sequenom MassArray™ application in the long QT syndrome mutation detection

Analysis of Y chromosome lineages in native South American population

Analysis of 29 Y-chromosome SNPs in a single multiplex useful to predict the geographic origin of male lineages

Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome

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

PRKG1 and genetic diagnosis of early-onset thoracic aortic disease

Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood

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