Fundación Pública Galega de Medicina Xenómica

2021

1. A Collaborative Effort to Define Classification Criteria for ATM Variants in Hereditary Cancer Patients

   Clinical chemistry, Vol. 67, Núm. 3, pp. 518-533

2. A Simple Entropic-Driving Separation Procedure of Low-Size Silver Clusters, Through Interaction with DNA

   ChemistryOpen, Vol. 10, Núm. 8, pp. 760-763

3. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

   Nature Communications, Vol. 12, Núm. 1

4. A data science approach for early-stage prediction of Patient's susceptibility to acute side effects of advanced radiotherapy

   Computers in Biology and Medicine, Vol. 135

5. A polymorphism in the promoter of FRAS1 is a candidate SNP associated with metastatic prostate cancer

   Prostate, Vol. 81, Núm. 10, pp. 683-693

6. A systematic review of augmented reality in health sciences: A guide to decision-making in higher education

   International Journal of Environmental Research and Public Health, Vol. 18, Núm. 8

7. Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer

   Prostate Cancer and Prostatic Diseases, Vol. 24, Núm. 2, pp. 532-541

8. Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants

   Cell Reports Medicine, Vol. 2, Núm. 4

9. Ancestry analysis using autosomal SNPs in northern South America, reveals interpretation differences between an AIM panel and an identification panel

   Forensic Science International, Vol. 326

10. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy

    Forensic Science International: Genetics, Vol. 52

11. Attitudes and knowledge in blood donation among nursing students: A cross-sectional study in Spain and Portugal

    Nurse Education Today, Vol. 106

12. Breast cancer risk genes - Association analysis in more than 113,000 women

    New England Journal of Medicine, Vol. 384, Núm. 5, pp. 428-439

13. CSVS, a crowdsourcing database of the Spanish population genetic variability

    Nucleic acids research, Vol. 49, Núm. D1, pp. D1130-D1137

14. Care tasks and impact of caring in primary family caregivers: A cross-sectional study from a nursing perspective

    Applied Nursing Research, Vol. 62

15. Cognitive functioning throughout adulthood and illness stages in individuals with psychotic disorders and their unaffected siblings

    Molecular Psychiatry, Vol. 26, Núm. 8, pp. 4529-4543

16. Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk

    Journal of the National Cancer Institute, Vol. 113, Núm. 3, pp. 329-337

17. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

    Nature communications, Vol. 12, Núm. 1, pp. 3417

18. Development and evaluation of the ancestry informative marker panel of the visage basic tool

    Genes, Vol. 12, Núm. 8

19. Development of a method for generating SNP interaction-aware polygenic risk scores for radiotherapy toxicity

    Radiotherapy and Oncology, Vol. 159, pp. 241-248

20. Dilated cardiomyopathy and mild limb girdle muscular dystrophy caused by the p.Gly424Ser genetic variant in the fukutin gene

    Revista Espanola de Cardiologia, Vol. 74, Núm. 11, pp. 987-989