Centro de investigación
Fundación Pública Galega de Medicina Xenómica
Publicacións (57) Publicacións nas que participase algún/ha investigador/a
2018
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Agaricus bisporus supplementation reduces high-fat diet-induced body weight gain and fatty liver development
Journal of Physiology and Biochemistry, Vol. 74, Núm. 4, pp. 635-646
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A imparable revolución da Medicina Personalizada
Revista Real Academia Galega de Ciencias, Núm. 37, pp. 24-25
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A transcriptome-wide association study among 97,898 women to identify candidate susceptibility genes for epithelial ovarian cancer risk
Cancer Research, Vol. 78, Núm. 18, pp. 5419-5430
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A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Nature Genetics, Vol. 50, Núm. 7, pp. 968-978
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Ancestry analysis in rural Brazilian populations of African descent
Forensic Science International: Genetics, Vol. 36, pp. 160-166
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Assessment of genotyping tools applied in genetic susceptibility studies of periodontal disease: A systematic review
Archives of Oral Biology, Vol. 92, pp. 38-50
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Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Nature Genetics, Vol. 50, Núm. 7, pp. 928-936
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Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1
American Journal of Kidney Diseases, Vol. 72, Núm. 3, pp. 411-418
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BRCA1 and BRCA2 5′ noncoding region variants identified in breast cancer patients alter promoter activity and protein binding
Human Mutation, Vol. 39, Núm. 12, pp. 2025-2039
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Computational tools for splicing defect prediction in breast/ovarian cancer genes: How efficient are they at predicting RNA alterations?
Frontiers in Genetics, Vol. 9, Núm. SEP
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Congenital hyperinsulinism in two siblings with ABCC8 mutation: Same genotype, different phenotypes
Archives of Endocrinology and Metabolism, Vol. 62, Núm. 5, pp. 560-565
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De novo mutations (DNMs) in autism spectrum disorder (ASD): Pathway and network analysis
Frontiers in Genetics, Vol. 9, Núm. SEP
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Determination and diagnostic value of CA9 mRNA in peripheral blood of patients with oral leukoplakia
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol. 33, Núm. 1, pp. 951-955
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Development of an isotoxic decision support system integrating genetic markers of toxicity for the implantation of a rectum spacer
Acta Oncologica, Vol. 57, Núm. 11, pp. 1499-1505
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FKBP5 polymorphisms and hypothalamic-pituitary-adrenal axis negative feedback in major depression and obsessive-compulsive disorder
Journal of Psychiatric Research, Vol. 104, pp. 227-234
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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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Full in-frame exon 3 skipping of BRCA2 confers high risk of breast and/or ovarian cancer
Oncotarget, Vol. 9, Núm. 25, pp. 17334-17348
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Generation and characterization of the human iPSC line IDISi001-A isolated from blood cells of a CADASIL patient carrying a NOTCH3 mutation
Stem Cell Research, Vol. 28, pp. 16-20
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Genetic testing and clinical management practices for variants in non-BRCA1/2 breast (and breast/ovarian) cancer susceptibility genes: An international survey by the Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) clinical working group
JCO Precision Oncology, Vol. 2
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Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia
Nature Communications, Vol. 9, Núm. 1