RAFAEL
JIMÉNEZ MEDINA
CATEDRÁTICO DE UNIVERSIDAD
ANA
CLAVERO GILABERT
PROFESORA ASOCIADA LABORAL
ANA CLAVERO GILABERT-rekin lankidetzan egindako argitalpenak (7)
2022
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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
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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
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Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia
Frontiers in Cell and Developmental Biology, Vol. 10
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Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility
Communications Biology, Vol. 5, Núm. 1
2021
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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
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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
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Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment
Fertility and Sterility, Vol. 114, Núm. 2, pp. 398-406