Publications en collaboration avec des chercheurs de Hospital Universitario Virgen de las Nieves (7)

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

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