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