Xenética

2020

1. 1p36 is a chromosomal site of genomic instability in cervical intraepithelial neoplasia

   Biotechnic and Histochemistry, Vol. 95, Núm. 2, pp. 137-144

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. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

   Nature Communications, Vol. 11, Núm. 1

6. 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

7. 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

8. Association study of genetic polymorphisms in proteins involved in oseltamivir transport, metabolism, and interactions with adverse reactions in Mexican patients with acute respiratory diseases

   Pharmacogenomics Journal, Vol. 20, Núm. 4, pp. 613-620

9. Baseline predictors for visual acuity loss during observation in diabetic macular oedema with good baseline visual acuity

   Acta Ophthalmologica, Vol. 98, Núm. 7, pp. e801-e806

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

    Frontiers in Genetics, Vol. 11

11. 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

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

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

13. Characterization of disease progression in the initial stages of retinopathy in type 2 diabetes: A 2-year longitudinal study

    Investigative Ophthalmology and Visual Science, Vol. 61, Núm. 3

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

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

15. 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

16. Cumulative Burden of Colorectal Cancer–Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer

    Gastroenterology, Vol. 158, Núm. 5, pp. 1274-1286.e12

17. DNA fragmentation of human spermatozoa: Simple assessment of single- and double-strand DNA breaks and their respective dynamic behavioral response

    Andrology, Vol. 8, Núm. 5, pp. 1287-1303

18. Deciphering adipose tissue extracellular vesicles protein cargo and its role in obesity

    International Journal of Molecular Sciences, Vol. 21, Núm. 24, pp. 1-16

19. Detection of DNA damage in pigeon erythrocytes using a chromatin dispersion assay

    Toxicology Mechanisms and Methods, Vol. 30, Núm. 3, pp. 228-235

20. Efficacy and toxicity of adjuvant chemotherapy on colorectal cancer patients: how much influence from the genetics?

    Journal of Chemotherapy, pp. 1-13