Publicaciones en colaboración con investigadores/as de Hospital Universitario Virgen de las Nieves (20)

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

2022

  1. 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

  2. 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

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

    Frontiers in Cell and Developmental Biology, Vol. 10

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

    Communications Biology, Vol. 5, Núm. 1

2021

  1. Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort

    Andrology, Vol. 9, Núm. 4, pp. 1151-1165

  2. Evaluation of male fertility-associated loci in a european population of patients with severe spermatogenic impairment

    Journal of Personalized Medicine, Vol. 11, Núm. 1, pp. 1-19

2020

  1. Genetic landscape of nonobstructive azoospermia and new perspectives for the clinic

    Journal of Clinical Medicine, Vol. 9, Núm. 2

  2. Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment

    Fertility and Sterility, Vol. 114, Núm. 2, pp. 398-406

2016

  1. Interplay between Gemcitabine and Erlotinib over Pancreatic Adenocarcinoma Cells

    Pancreas, Vol. 45, Núm. 2, pp. 269-280

2015

  1. Prognosis Relevance of Serum Cytokines in Pancreatic Cancer

    BioMed Research International, Vol. 2015

  2. The potential role of the glycoprotein osteoactivin/glycoprotein nonmetastatic melanoma protein b in pancreatic cancer

    Pancreas, Vol. 44, Núm. 2, pp. 302-310

2014

  1. Serum cytokine profile in patients with pancreatic cancer

    Pancreas, Vol. 43, Núm. 7, pp. 1042-1049

2011

  1. Analysis of the rel polymorphism rs13031237 in autoimmune diseases

    Annals of the Rheumatic Diseases

2010

  1. Association of FcgR2a, but not FcgR3a, with inflammatory bowel diseases across three Caucasian populations

    Inflammatory Bowel Diseases, Vol. 16, Núm. 12, pp. 2080-2089

  2. Lack of association between IRF5 gene polymorphisms and biopsy-proven giant cell arteritis

    Journal of Rheumatology, Vol. 37, Núm. 1, pp. 136-140

  3. STAT4 gene influences genetic predisposition to ulcerative colitis but not Crohn's disease in the Spanish population: A replication study

    Human Immunology, Vol. 71, Núm. 5, pp. 515-519

2009

  1. Association of ATG16L1 and IRGM genes polymorphisms with inflammatory bowel disease: A meta-analysis approach

    Genes and Immunity, Vol. 10, Núm. 4, pp. 356-364

  2. Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus

    Human Molecular Genetics, Vol. 18, Núm. 19, pp. 3739-3748

  3. Novel association of the interleukin 2-interleukin 21 region with inflammatory bowel disease

    American Journal of Gastroenterology, Vol. 104, Núm. 8, pp. 1968-1975