Artigos (20) Publicacións nas que participase algún/ha investigador/a

2018

  1. A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework

    BMC Genomics, Vol. 19, Núm. 1

  2. Advanced glycation end products (AGEs) estimated by skin autofluorescence are related with cardiovascular risk in renal transplant

    PLoS ONE, Vol. 13, Núm. 8

  3. Age at first birth in women is genetically associated with increased risk of schizophrenia

    Scientific Reports, Vol. 8, Núm. 1

  4. Asleep blood pressure: Significant prognostic marker of vascular risk and therapeutic target for prevention

    European Heart Journal, Vol. 39, Núm. 47, pp. 4159-4171

  5. Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1

    American Journal of Kidney Diseases, Vol. 72, Núm. 3, pp. 411-418

  6. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

    Nature Genetics, Vol. 50, Núm. 3, pp. 381-389

  7. Comprehensive approach to peritoneal dialysis-related peritonitis by enteric microorganisms. Comparison between single organism and polymicrobial infections

    Peritoneal Dialysis International, Vol. 38, Núm. 2, pp. 139-146

  8. Differences in performance in CAMCOG-R domains between old and oldest old patients with alzheimer’s disease

    Aging, Neuropsychology, and Cognition, Vol. 25, Núm. 4, pp. 588-597

  9. Early cardiac abnormalities in obese children and their relationship with adiposity

    Nutrition, Vol. 46, pp. 83-89

  10. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood

    American Journal of Human Genetics, Vol. 102, Núm. 6, pp. 1185-1194

  11. Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

    Cell, Vol. 173, Núm. 7, pp. 1705-1715.e16

  12. Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples

    European Archives of Psychiatry and Clinical Neuroscience, Vol. 268, Núm. 6, pp. 585-592

  13. La espiritualidad en el ámbito de la salud mental y las adicciones

    Labor hospitalaria: organización y pastoral de la salud, Núm. 322, pp. 62-67

  14. Overview of autosomal dominant polycystic kidney disease in the south of Spain

    Nefrologia, Vol. 38, Núm. 2, pp. 220-221

  15. Peritoneal dialysis is an independent factor associated to lower intima media thickness in dialysis patients free from previous cardiovascular disease

    Frontiers in Physiology, Vol. 9

  16. Pkd2 deletion during embryo development does not alter mesonephric programmed cell senescence

    International Journal of Developmental Biology, Vol. 62, Núm. 9-10, pp. 637-640

  17. Rationale and design of DiPPI: A randomized controlled trial to evaluate the safety and effectiveness of progressive hemodialysis in incident patients

    Nefrologia, Vol. 38, Núm. 6, pp. 630-638

  18. Restless legs syndrome: An unresolved uremic disorder after renal transplantation

    Nephron, Vol. 139, Núm. 1, pp. 23-29

  19. Síndrome Guillain-Barré secundario a tacrolimus en paciente con síndrome nefrótico corticorresistente secundario a glomerulonefritis focal y segmentaria y nefropatía IgA

    Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, Vol. 38, Núm. 6, pp. 665-667

  20. The p.Arg118Cys Variant in the GLA Gene Does Not Cause Fabry Disease. More Evidence

    Revista Espanola de Cardiologia, Vol. 71, Núm. 10, pp. 871-873