Sara Munoz-Gonzalez

Granada, AN 18012, Spain

Last Updated: 09/26/2026

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Found 11 publications

Single-Cell TCR Sequencing Uncovers Remodeling of the Immune Repertoire After a Short-Term Gluten-Free Diet in Pediatric Celiac Disease.

Single-Cell TCR Sequencing Uncovers Remodeling of the Immune Repertoire After a Short-Term Gluten-Free Diet in Pediatric Celiac Disease.

Journal: International journal of molecular sciences

Published: July 30, 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

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

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

Journal: Investigative ophthalmology & visual science

Published: October 22, 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

Changes in environmental exposures over decades may influence the genetic architecture of severe spermatogenic failure.

Changes in environmental exposures over decades may influence the genetic architecture of severe spermatogenic failure.

Journal: Human reproduction (Oxford, England)

Published: October 31, 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

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.

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: Journal of dermatological science

Published: October 11, 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

Showing 1-11 of 11

Last Updated: 09/26/2026