Complexo Hospitalario Universitario de Santiago
Centro de atención
King Abdulaziz University
Jeddah, Arabia SaudíPublicacións en colaboración con investigadores/as de King Abdulaziz University (31)
2022
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Intraparticle Macromolecular Migration Alters the Structure and Function of Proteins Reversibly Immobilized on Porous Microbeads
Advanced Materials Interfaces, Vol. 9, Núm. 18
2021
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Impact of Bacillus Calmette-Gue´rin (BCG) vaccination on postoperative mortality in patients with perioperative SARS-CoV-2 infection
BJS Open
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Machine learning risk prediction of mortality for patients undergoing surgery with perioperative SARS-CoV-2: The COVIDSurg mortality score
British Journal of Surgery, Vol. 19, Núm. 4
2019
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Association of GSTP1 and ERCC1 polymorphisms with toxicity in locally advanced head and neck cancer platinum-based chemoradiotherapy treatment
Head and Neck, Vol. 41, Núm. 8, pp. 2704-2715
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Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1)
Nature Communications
2018
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Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants
Nature Communications, Vol. 9, Núm. 1
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Germline variation at 8q24 and prostate cancer risk in men of European ancestry
Nature Communications, Vol. 9, Núm. 1
2017
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Copy number variation analysis of patients with intellectual disability from North-West Spain
Gene, Vol. 626, pp. 189-199
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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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A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features
American Journal of Medical Genetics, Part A, Vol. 167, Núm. 6, pp. 1315-1322
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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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Caracterización molecular y descripción fenotípica de dos casos con aberraciones cromosómicas recíprocas en la region de los síndromes de microdeleción/microduplicación 3q29
Revista de Neurologia, Vol. 61, Núm. 6, pp. 255-260
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Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome
American Journal of Medical Genetics, Part A, Vol. 167, Núm. 6, pp. 1369-1373
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Deleción en el gen RPS6KA3 en una mujer con un fenotipo clásico del síndrome de Coffin-Lowry incluyendo episodios de caída inducidos por estímulo
Revista de Neurologia, Vol. 61, Núm. 2, pp. 94-96
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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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Interstitial microdeletions including the chromosome band 4q13.2 and the UBA6 gene as possible causes of intellectual disability and behavior disorder
American Journal of Medical Genetics, Part A, Vol. 167, Núm. 12, pp. 3113-3120