Genética Cardiovascular
King Abdulaziz University
Jeddah, Arabia SaudíPublicaciones en colaboración con investigadores/as de King Abdulaziz University (11)
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
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The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study
Journal of Molecular and Cellular Cardiology, Vol. 102, pp. 3-9
2016
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PRKG1 and genetic diagnosis of early-onset thoracic aortic disease
European Journal of Clinical Investigation, Vol. 46, Núm. 9, pp. 787-794
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The relationship between surname frequency and Y chromosome variation in Spain
European Journal of Human Genetics, Vol. 24, Núm. 1, pp. 120-128
2015
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Association between SNPs of metalloproteinases and prostaglandin f2α receptor genes and latanoprost response in open-angle glaucoma
Ophthalmology, Vol. 122, Núm. 5, pp. 1040-1048.e4
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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, Vol. 100, Núm. 10, pp. 952-956
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Genetic analysis of arrhythmogenic diseases in the era of NGS: The complexity of clinical decision-making in Brugada Syndrome
PLoS ONE, Vol. 10, Núm. 7
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Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young
Forensic Science International: Genetics, Vol. 18, pp. 160-170
2014
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Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Nature Genetics, Vol. 46, Núm. 8, pp. 826-836
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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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Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease
Clinica Chimica Acta, Vol. 437, pp. 88-92