MIRIAM CERVÁN MARTÍN-rekin lankidetzan egindako argitalpenak (11)

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

  2. Comprehensive Evaluation of the Genetic Basis of Keratoconus: New Perspectives for Clinical Translation

    Investigative ophthalmology & visual science, Vol. 65, Núm. 12, pp. 32

2023

  1. Sex-specific association of SELL gene polymorphisms with pattern hair loss in the Thai population: A candidate gene association study and in silico functional characterization

    Journal of Dermatological Science

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