Publicacións en colaboración con investigadores/as de Universidade de Lisboa (5)

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

    Frontiers in Cell and Developmental Biology, Vol. 10

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

    Communications Biology, Vol. 5, Núm. 1

2021

  1. 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