Centro de investigación
Fundación Pública Galega de Medicina Xenómica
Publicacións (88) Publicacións nas que participase algún/ha investigador/a
2020
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A Comparison of Forensic Age Prediction Models Using Data From Four DNA Methylation Technologies
Frontiers in Genetics, Vol. 11
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A Deep Learning Approach Validates Genetic Risk Factors for Late Toxicity After Prostate Cancer Radiotherapy in a REQUITE Multi-National Cohort
Frontiers in Oncology, Vol. 10
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A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel
Forensic Science International: Genetics, Vol. 46
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A multicentre prospective study evaluating the impact of proton-pump inhibitors omeprazole and pantoprazole on voriconazole plasma concentrations
British Journal of Clinical Pharmacology, Vol. 86, Núm. 8, pp. 1661-1666
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Acute appendicitis is associated with appendiceal microbiome changes including elevated Campylobacter jejuni levels
BMJ Open Gastroenterology, Vol. 7, Núm. 1
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An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk
Nature Communications, Vol. 11, Núm. 1
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Anti-VEGF treatment and response in age-related macular degeneration: Disease’s susceptibility, pharmacogenetics and pharmacokinetics
Current Medicinal Chemistry, Vol. 27, Núm. 4, pp. 549-569
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Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis
Translational Psychiatry, Vol. 10, Núm. 1
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Association of BDNF, HTR2A, TPH1, SLC6A4, and comt polymorphisms with tdcs and escitalopram efficacy: Ancillary analysis of a double-blind, placebo-controlled trial
Brazilian Journal of Psychiatry, Vol. 42, Núm. 2, pp. 128-135
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Association of single nucleotide polymorphisms with renal cell carcinoma in Algerian population
African Journal of Urology, Vol. 26, Núm. 1
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Author Correction: Neutrophil to lymphocyte ratio and breast cancer risk: analysis by subtype and potential interactions (Scientific Reports, (2020), 10, 1, (13203), 10.1038/s41598-020-70077-z)
Scientific Reports
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Blood biomarkers of Uveal Melanoma: Current perspectives
Clinical Ophthalmology, Vol. 14, pp. 157-169
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Broadening the Applicability of a Custom Multi-Platform Panel of Microhaplotypes: Bio-Geographical Ancestry Inference and Expanded Reference Data
Frontiers in Genetics, Vol. 11
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Building a custom large-scale panel of novel microhaplotypes for forensic identification using MiSeq and Ion S5 massively parallel sequencing systems
Forensic Science International: Genetics, Vol. 45
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Candidate causal variants at the 8p12 breast cancer risk locus regulate DUSP4
Cancers, Vol. 12, Núm. 1
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Características del empleo de la vía subcutánea para la administración de medicamentos en pacientes en cuidados paliativos
Index de enfermería: información bibliográfica, investigación y humanidades, Vol. 29, Núm. 1, pp. 37-41
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Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)
Cerebellum, Vol. 19, Núm. 4, pp. 501-509
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Characterization of the Cancer Spectrum in Men with Germline BRCA1 and BRCA2 Pathogenic Variants: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
JAMA Oncology, Vol. 6, Núm. 8, pp. 1218-1230
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Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36
Neuron, Vol. 107, Núm. 2, pp. 292-305.e6
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Chromatin interactome mapping at 139 independent breast cancer risk signals
Genome Biology, Vol. 21, Núm. 1