Servicio
Genética
Publicaciones (40) Publicaciones en las que ha participado algún/a investigador/a
2014
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A Rb1 promoter variant with reduced activity contributes to osteosarcoma susceptibility in irradiated mice
Molecular Cancer, Vol. 13, Núm. 1
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A collaborative European exercise on mRNA-based body fluid/skin typing and interpretation of DNA and RNA results
Forensic Science International: Genetics, Vol. 10, Núm. 1, pp. 40-48
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A genome-wide study of modern-day Tuscans: Revisiting Herodotus's theory on the origin of the Etruscans
PLoS ONE, Vol. 9, Núm. 9
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A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease
Journal of Medical Genetics, Vol. 51, Núm. 7, pp. 475-478
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Alcohol consumption and survival after a breast cancer diagnosis: A literature-based meta-analysis and collaborative analysis of data for 29,239 cases
Cancer Epidemiology Biomarkers and Prevention, Vol. 23, Núm. 6, pp. 934-945
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Brugada syndrome and p.E61X_RANGRF
Cardiology Journal, Vol. 21, Núm. 2, pp. 121-127
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Characterisation of a subpopulation of sperm with massive nuclear damage, as recognised with the sperm chromatin dispersion test
Andrologia, Vol. 46, Núm. 6, pp. 602-609
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Choroidal thickness in diabetic retinopathy: The influence of antiangiogenic therapy
Retina, Vol. 34, Núm. 6, pp. 1199-1207
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Clinical characteristics of reticular pseudodrusen in the fellow eye of patients with unilateral neovascular age-related macular degeneration
Ophthalmology, Vol. 121, Núm. 9, pp. 1748-1755
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Comprehensive analyses of DNA repair pathways, smoking and bladder cancer risk in Los Angeles and Shanghai
International Journal of Cancer, Vol. 135, Núm. 2, pp. 335-347
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Development of a forensic skin colour predictive test
Forensic Science International: Genetics, Vol. 13, pp. 34-44
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Dietary sources of N-nitroso compounds and bladder cancer risk: Findings from the Los Angeles bladder cancer study
International Journal of Cancer, Vol. 134, Núm. 1, pp. 125-135
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Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia
Clinical Genetics, Vol. 85, Núm. 2, pp. 154-158
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Exploring iris colour prediction and ancestry inference in admixed populations of South America
Forensic Science International: Genetics, Vol. 13, pp. 3-9
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Genome-wide DNA methylation analysis of articular chondrocytes reveals a cluster of osteoarthritic patients
Annals of the Rheumatic Diseases, Vol. 73, Núm. 4, pp. 668-677
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Genome-wide association study identifies multiple loci associated with bladder cancer risk
Human Molecular Genetics, Vol. 23, Núm. 5
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Genome-wide interaction study of smoking and bladder cancer risk
Carcinogenesis, Vol. 35, Núm. 8, pp. 1737-1744
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Genética de la muerte súbita inexplicada
Medicina Clinica, Vol. 142, Núm. 6, pp. 265-269
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Global population variability in Qiagen Investigator HDplex STRs
Forensic Science International: Genetics, Vol. 8, Núm. 1, pp. 36-43
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Identification of genetic alterations, as causative genetic defects in long QT syndrome, using next generation sequencing technology
PLoS ONE, Vol. 9, Núm. 12