Filipa M. Carvalho

Porto, 4200319, Portugal

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 28 publications

Dissecting methylation errors at imprinted genes in human spermatozoa: from molecular observations to clinical applications†.

Dissecting methylation errors at imprinted genes in human spermatozoa: from molecular observations to clinical applications†.

Journal: Biology of reproduction

Published: May 08, 2025

Dissecting methylation errors at imprinted genes in human spermatozoa: from molecular observations to clinical applications†.

Dissecting methylation errors at imprinted genes in human spermatozoa: from molecular observations to clinical applications†.

Journal: Biology of reproduction

Published: May 08, 2025

Genetic study on candidates for oocyte donation.

Genetic study on candidates for oocyte donation.

Journal: JBRA assisted reproduction

Published: December 17, 2024

Peptide aggregation-induced immunogenic cell death in a breast cancer spheroid model.

Peptide aggregation-induced immunogenic cell death in a breast cancer spheroid model.

Journal: bioRxiv : the preprint server for biology

Published: November 14, 2023

Tensile and Tearing Properties of a Geocomposite Mechanically Damaged by Repeated Loading and Abrasion.

Tensile and Tearing Properties of a Geocomposite Mechanically Damaged by Repeated Loading and Abrasion.

Journal: Materials (Basel, Switzerland)

Published: October 06, 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

Diverse monogenic subforms of human spermatogenic failure.

Diverse monogenic subforms of human spermatogenic failure.

Journal: Nature communications

Published: March 08, 2022

109 Utilising cell-free DNA for detection of gene editing outcomes in rhesus macaque embryos.

109 Utilising cell-free DNA for detection of gene editing outcomes in rhesus macaque embryos.

Journal: Reproduction, fertility, and development

Published: March 01, 2022

Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient management.

Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient management.

Journal: Human reproduction (Oxford, England)

Published: February 16, 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 1-12 of 28

Last Updated: 09/26/2026