JOSÉ ANTONIO CASTILLA ALCALÁ-rekin lankidetzan egindako argitalpenak (6)

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

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