Ana Clavero

Granada, AN, Spain

Last Updated: 09/26/2026

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Found 25 publications

Assessing endometrial microbiota in endometriosis: culturomics and sequencing analysis of receptive-phase tissue.

Assessing endometrial microbiota in endometriosis: culturomics and sequencing analysis of receptive-phase tissue.

Journal: Current research in microbial sciences

Published: April 20, 2026

Optical genome mapping enhances cytogenetic analysis in recurrent miscarriage: confirmation of a suspected (1;10) chromosomal translocation.

Optical genome mapping enhances cytogenetic analysis in recurrent miscarriage: confirmation of a suspected (1;10) chromosomal translocation.

Journal: Molecular cytogenetics

Published: February 23, 2025

A genetic variant in the 3'-UTR of PIWIL4 confers risk for extreme phenotypes of male infertility by altering miR-215 and miR-136 binding affinity.

A genetic variant in the 3'-UTR of PIWIL4 confers risk for extreme phenotypes of male infertility by altering miR-215 and miR-136 binding affinity.

Journal: Human reproduction (Oxford, England)

Published: December 23, 2024

Trans-ethnic GWAS meta-analysis of idiopathic spermatogenic failure highlights the immune-mediated nature of Sertoli cell-only syndrome.

Trans-ethnic GWAS meta-analysis of idiopathic spermatogenic failure highlights the immune-mediated nature of Sertoli cell-only syndrome.

Journal: Communications biology

Published: October 06, 2024

A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure.

A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure.

Journal: Human reproduction open

Published: July 26, 2024

Study of SARS-CoV-2 in semen from asymptomatic donors with the presence of virus in nasopharyngeal swabs.

Study of SARS-CoV-2 in semen from asymptomatic donors with the presence of virus in nasopharyngeal swabs.

Journal: Reproductive biomedicine online

Published: May 08, 2023

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

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

Journal: Frontiers in cell and developmental biology

Published: November 04, 2022

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

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

Journal: Communications biology

Published: June 09, 2022

Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.

Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.

Journal: Journal of personalized medicine

Published: April 20, 2022

Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.

Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.

Journal: Andrology

Published: January 31, 2022

Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort.

Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort.

Journal: Andrology

Published: January 19, 2021

Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment.

Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment.

Journal: Journal of personalized medicine

Published: November 14, 2020

Showing 1-12 of 25

Last Updated: 09/26/2026