Publicaciones en colaboración con investigadores/as de Hospital Universitario Virgen de las Nieves (108)

2024

  1. Changes in environmental exposures over decades may influence the genetic architecture of severe spermatogenic failure

    Human Reproduction, Vol. 39, Núm. 3, pp. 612-622

  2. Microenvironment of the Lower Reproductive Tract: Focus on the Cervical Mucus Plug

    Seminars in Reproductive Medicine, Vol. 41, Núm. 5, pp. 200-208

2023

  1. A pleiotropic variant in DNAJB4 is associated with multiple myeloma risk

    International Journal of Cancer, Vol. 152, Núm. 2, pp. 239-248

  2. Endometrial whole metabolome profile at the receptive phase: influence of Mediterranean Diet and infertility

    Frontiers in Endocrinology, Vol. 14

  3. From Non-Alcoholic Fatty Liver Disease to Liver Cancer: Microbiota and Inflammation as Key Players

    Pathogens, Vol. 12, Núm. 7

  4. GWAS-Identified Variants for Obesity Do Not Influence the Risk of Developing Multiple Myeloma: A Population-Based Study and Meta-Analysis

    International Journal of Molecular Sciences, Vol. 24, Núm. 7

  5. Identification of novel genetic loci for risk of multiple myeloma by functional annotation

    Leukemia

  6. Microbial composition across body sites in polycystic ovary syndrome: a systematic review and meta-analysis

    Reproductive BioMedicine Online, Vol. 47, Núm. 1, pp. 129-150

  7. Polymorphisms within Autophagy-Related Genes as Susceptibility Biomarkers for Multiple Myeloma: A Meta-Analysis of Three Large Cohorts and Functional Characterization

    International Journal of Molecular Sciences, Vol. 24, Núm. 10

  8. The effects of a 20-week exercise program on blood-circulating biomarkers related to brain health in overweight or obese children: The ActiveBrains project

    Journal of Sport and Health Science, Vol. 12, Núm. 2, pp. 175-185

2022

  1. A polygenic risk score for multiple myeloma risk prediction

    European Journal of Human Genetics, Vol. 30, Núm. 4, pp. 474-479

  2. Acceleration of the DNA methylation clock among lynch syndrome-associated mutation carriers

    BMC medical genomics, Vol. 15, Núm. 1, pp. 45

  3. Autophagy in Hematological Malignancies

    Cancers, Vol. 14, Núm. 20

  4. Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome

    Journal of Personalized Medicine, Vol. 12, Núm. 6

  5. Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility

    Andrology, Vol. 10, Núm. 7, pp. 1339-1350

  6. Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia

    Frontiers in Cell and Developmental Biology, Vol. 10

  7. Corrigendum: Transcriptional and epigenetic response to sedentary behavior and physical activity in children and adolescents: A systematic review, (Front. Pediatr, (2022), 10, (917152), 10.3389/fped.2022.917152)

    Frontiers in Pediatrics

  8. Does a Multiple Myeloma Polygenic Risk Score Predict Overall Survival of Patients with Myeloma?

    Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, Vol. 31, Núm. 9, pp. 1863-1866

  9. Exchange of cellular components between platelets and tumor cells: impact on tumor cells behavior

    Theranostics, Vol. 12, Núm. 5, pp. 2150-2161

  10. Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility

    Communications Biology, Vol. 5, Núm. 1