A. Blanco-Verea

发表

V. Pascali, C. Capelli, Á. Carracedo, 2012, Forensic science international. Genetics.

Á. Carracedo, P. Sánchez-Diz, M. Brión, 2009 .

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

Á. Carracedo, F. Lotufo-Neto, M. Hirata, 2019, Forensic science international. Genetics.

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

Á. Carracedo, N. Morling, D. Syndercombe-Court, 2005, Electrophoresis.

Uniparental Markers of Contemporary Italian Population Reveals Details on Its Pre-Roman Heritage

V. Pascali, C. Capelli, Á. Carracedo, 2012, PloS one.

Sequenom MassArray™ application in the long QT syndrome mutation detection

Á. Carracedo, P. Sánchez-Diz, I. Quintela, 2009 .

The genetic male legacy from El Salvador.

Á. Carracedo, A. Blanco-Verea, M. Brion, 2007, Forensic science international.

Research update for articles published in EJCI in 2016

M. Sánchez-Niño, N. Veronese, M. Burtscher, 2018, European journal of clinical investigation.

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

Á. Carracedo, L. Concheiro, C. Allegue, 2011, International Journal of Legal Medicine.

PRKG1 and genetic diagnosis of early‐onset thoracic aortic disease

M. Gut, I. Gut, Á. Carracedo, 2016, European journal of clinical investigation.

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

Á. Carracedo, W. Parson, N. Morling, 2004, Forensic science international.

Novel Genomic Approach to the Arrhytmogenic Sudden Cardiac Death

Á. Carracedo, B. Sobrino, R. Gil, 2012 .

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

Á. Carracedo, B. Sobrino, A. Blanco-Verea, 2015, Forensic science international. Genetics.

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

J. Amigo, J. González-Juanatey, B. Sobrino, 2022, Molecular Diagnosis & Therapy.

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

Á. Carracedo, A. Braza-Boïls, J. Amigo, 2017, International Journal of Legal Medicine.

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

Á. Carracedo, J. Amigo, B. Sobrino, 2014, Electrophoresis.

Searching for genetic modulators of the phenotypic heterogeneity in Brugada syndrome

R. Cruz, R. Lage, M. Sabater-Molina, 2022, PloS one.

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

R. Brugada, Á. Carracedo, B. Madea, 2012, Forensic science international.

Y-chromosome lineages in native South American population.

Á. Carracedo, J. C. Jaime, A. Blanco-Verea, 2010, Forensic science international. Genetics.

Forensic Population Genetics - Original Research Y-chromosomal DNA analysis in French male lineages

Á. Carracedo, P. Sánchez-Diz, E. Ramos-Luis, 2014 .

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

M. Kettner, B. Beckmann, C. Geisen, 2018, Forensic science international.

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

Á. Carracedo, M. Volpe, S. Rubattu, 2010, Annals of clinical and laboratory science.

Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation.

R. Brugada, Á. Carracedo, R. Gil, 2019, Forensic science international. Genetics.

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

Á. Carracedo, P. Schneider, J. Cortis, 2015, Archives of Disease in Childhood.

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

Á. Carracedo, A. Evangelista, J. Amigo, 2014, Clinica chimica acta; international journal of clinical chemistry.

Hierarchical analysis of 30 Y-chromosome SNPs in European populations

Á. Carracedo, M. Lareu, B. Sobrino, 2004, International Journal of Legal Medicine.

Ancestry Analysis in the 11-M Madrid Bomb Attack Investigation

Ángel Carracedo, Antonio Salas, Christopher Phillips, 2009, PloS one.

Correction: Uniparental Markers of Contemporary Italian Population Reveals Details on Its Pre-Roman Heritage

V. Pascali, C. Capelli, Á. Carracedo, 2014, PloS one.

The relationship between surname frequency and Y chromosome variation in Spain

C. Capelli, Á. Carracedo, A. Salas, 2015, European Journal of Human Genetics.

Phylogenetic evidence for multiple independent duplication events at the DYS19 locus.

V. Pascali, C. Capelli, F. Brisighelli, 2007, Forensic science international. Genetics.

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

Á. Carracedo, J. González-Juanatey, J. García-Seara, 2019, Revista espanola de cardiologia.

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

Á. Carracedo, J. Amigo, P. Molina, 2017, International Journal of Legal Medicine.

Y-chromosomal DNA analysis in French male lineages.

P. Sánchez-Diz, E. Ramos-Luis, A. Blanco-Verea, 2014, Forensic science international. Genetics.