Centro de investigación
Fundación Pública Gallega de Medicina Genómica
Publicaciones (80) Publicaciones en las que ha participado algún/a investigador/a
2013
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A Generalized Model to Estimate the Statistical Power in Mitochondrial Disease Studies Involving 2×k Tables
PLoS ONE, Vol. 8, Núm. 9
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A Xq21.31 duplication without features of Prader-Willi syndrome
Endocrine
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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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A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy
Investigative Ophthalmology and Visual Science, Vol. 54, Núm. 3, pp. 1665-1678
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A new seipin-associated neurodegenerative syndrome
Journal of Medical Genetics, Vol. 50, Núm. 6, pp. 401-409
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A novel mutation, outside of the candidate region for diagnosis, in the inverted formin 2 gene can cause focal segmental glomerulosclerosis
Kidney International, Vol. 83, Núm. 1, pp. 153-159
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An overview of STRUCTURE: Applications, parameter settings, and supporting software
Frontiers in Genetics, Vol. 4, Núm. MAY
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Analysis of PALB2 Gene in BRCA1/BRCA2 Negative Spanish Hereditary Breast/Ovarian Cancer Families with Pancreatic Cancer Cases
PLoS ONE, Vol. 8, Núm. 7
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Ancestry analysis reveals a predominant Native American component with moderate European admixture in Bolivians
Forensic Science International: Genetics, Vol. 7, Núm. 5, pp. 537-542
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Annular elastolytic giant cell granuloma associated to late-onset X-linked dominant protoporphyria
Dermatology, Vol. 227, Núm. 3, pp. 238-242
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Anti-tumor efficacy of chitosan-g-poly(ethylene glycol) nanocapsules containing docetaxel: Anti-TMEFF-2 functionalized nanocapsules vs. non-functionalized nanocapsules
European Journal of Pharmaceutics and Biopharmaceutics, Vol. 83, Núm. 3, pp. 330-337
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Association of thromboxane A1 synthase (TBXAS1) gene polymorphism with acute urticaria induced by nonsteroidal anti-inflammatory drugs
Journal of Allergy and Clinical Immunology, Vol. 132, Núm. 4, pp. 989-991
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Autosomal recessive congenital ichthyosis
Actas Dermo-Sifiliograficas
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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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BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency
Clinical Genetics
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Breast cancer genes: Beyond BRCA1 and BRCA2
Frontiers in Bioscience, Vol. 18, Núm. 4, pp. 1358-1372
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CHEK2 c.1100delC mutation among non-BRCA1/2 Spanish hereditary breast cancer families
Clinical and Translational Oncology
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Casework application of a stand-alone pentaplex assay of extended-ESS STRs
Legal Medicine, Vol. 15, Núm. 4, pp. 217-221
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Conferencia Inaugural. Perspectivas actuales de la toxicogenómica
Revista de toxicología, Vol. 30, Núm. 1, pp. 22
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Corrigendum
Carcinogenesis