Iris Caetano-Pereira

Instituto Nacional De Saúde Dr. Ricardo Jorge
Lisbon, Portugal

Last Updated: 09/26/2026

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Found 10 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.

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

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

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

Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience.

Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience.

Journal: Genes

Published: March 31, 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

Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment.

Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment.

Journal: Fertility and sterility

Published: December 20, 2019

Showing 1-10 of 10

Last Updated: 09/26/2026