Rogelio J. Morales-Palomino
Granada, AN, Spain
Last Updated: 09/26/2026
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Found 29 publications
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.
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.
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.
Journal: Human reproduction open
Published: July 26, 2024
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.
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.
Journal: Journal of dermatological science
Published: October 11, 2022
Different phenotypic outcome due to site-specific phosphorylation in the cancer-associated NQO1 enzyme studied by phosphomimetic mutations.
Journal: Archives of biochemistry and biophysics
Published: August 10, 2022
Allosteric Communication in the Multifunctional and Redox NQO1 Protein Studied by Cavity-Making Mutations.
Journal: Antioxidants (Basel, Switzerland)
Published: April 26, 2022
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
Targeting HIF-1α Function in Cancer through the Chaperone Action of NQO1: Implications of Genetic Diversity of NQO1.
Journal: Journal of personalized medicine
Published: April 05, 2022
Last Updated: 09/26/2026