Publicacións (78) Publicacións nas que participase algún/ha investigador/a

2020

  1. A Comparison of Forensic Age Prediction Models Using Data From Four DNA Methylation Technologies

    Frontiers in Genetics, Vol. 11

  2. 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

  3. 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

  4. 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

  5. Acute appendicitis is associated with appendiceal microbiome changes including elevated Campylobacter jejuni levels

    BMJ Open Gastroenterology, Vol. 7, Núm. 1

  6. An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk

    Nature Communications, Vol. 11, Núm. 1

  7. 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

  8. Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis

    Translational Psychiatry, Vol. 10, Núm. 1

  9. 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

  10. Association of single nucleotide polymorphisms with renal cell carcinoma in Algerian population

    African Journal of Urology, Vol. 26, Núm. 1

  11. Blood biomarkers of Uveal Melanoma: Current perspectives

    Clinical Ophthalmology, Vol. 14, pp. 157-169

  12. Broadening the Applicability of a Custom Multi-Platform Panel of Microhaplotypes: Bio-Geographical Ancestry Inference and Expanded Reference Data

    Frontiers in Genetics, Vol. 11

  13. 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

  14. Candidate causal variants at the 8p12 breast cancer risk locus regulate DUSP4

    Cancers, Vol. 12, Núm. 1

  15. 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

  16. Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)

    Cerebellum, Vol. 19, Núm. 4, pp. 501-509

  17. 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

  18. Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36

    Neuron, Vol. 107, Núm. 2, pp. 292-305.e6

  19. Chromatin interactome mapping at 139 independent breast cancer risk signals

    Genome Biology, Vol. 21, Núm. 1

  20. Clinical and neurophysiological response to ephedrine in a patient affected with slow-channel congenital myasthenic syndrome

    Revista de Neurologia, Vol. 71, Núm. 6, pp. 221-224