Fundación Pública Galega de Medicina Xenómica
Research center
Hospital do Meixoeiro
Vigo, EspañaPublications in collaboration with researchers from Hospital do Meixoeiro (19)
2020
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Nature Genetics, Vol. 52, Núm. 1, pp. 56-73
2019
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Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
American Journal of Human Genetics, Vol. 104, Núm. 1, pp. 21-34
2017
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Candidate predisposing germline copy number variants in early onset colorectal cancer patients
Clinical and Translational Oncology, Vol. 19, Núm. 5, pp. 625-632
2015
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Thyroid pathology findings in Cowden syndrome: A clue for the diagnosis of the PTEN hamartoma tumor syndrome
American Journal of Clinical Pathology, Vol. 144, Núm. 2, pp. 322-328
2014
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A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer
Human Genetics, Vol. 133, Núm. 5, pp. 525-534
2013
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A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12
BMC Genomics, Vol. 14, Núm. 1
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BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern european populations
Carcinogenesis, Vol. 34, Núm. 2, pp. 314-318
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Genetic susceptibility variants associated with colorectal cancer prognosis
Carcinogenesis, Vol. 34, Núm. 10, pp. 2286-2291
2012
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COGENT (COlorectal cancer GENeTics) revisited
Mutagenesis, Vol. 27, Núm. 2, pp. 143-151
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Increased clopidogrel response is associated with ABCC3 expression: A pilot study
Clinica Chimica Acta, Vol. 413, Núm. 3-4, pp. 417-421
2011
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A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy
Neuromuscular Disorders, Vol. 21, Núm. 4, pp. 254-262
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Case-control study for colorectal cancer genetic susceptibility in EPICOLON: Previously identified variants and mucins
BMC Cancer, Vol. 11
2010
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CADASIL: Comunicación de una familia con una nueva mutación p.G296C en el exón 6 del gen Notch-3
Revista de Neurologia, Vol. 51, Núm. 12, pp. 729-732
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Colorectal cancer susceptibility quantitative trait loci in mice as a novel approach to detect low-penetrance variants in humans: A two-stage case-control study
Cancer Epidemiology Biomarkers and Prevention, Vol. 19, Núm. 2, pp. 619-623
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Single nucleotide polymorphisms in the wnt and bmp pathways and colorectal cancer risk in a spanish cohort
PLoS ONE, Vol. 5, Núm. 9, pp. 1-9
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Susceptibility genetic variants associated with colorectal cancer risk correlate with cancer phenotype
Gastroenterology, Vol. 139, Núm. 3
2007
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Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy
Journal of Clinical Endocrinology and Metabolism, Vol. 92, Núm. 6, pp. 2370-2373
2004
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A new rare mutation (691delCC/insAAA) in exon 17 of the PYGM gene causing McArdle disease
Archives of Neurology, Vol. 61, Núm. 7, pp. 1108-1110
2003
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Banco de Tejidos Neurológicos en el Laboratorio de Neuropatología. Organización básica
Neurologia, Vol. 18, Núm. 10, pp. 709-715