Raffaella Rossetti

Milan, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 18 publications

Global downstream BMP15 pathway analysis in human ovarian granulosa cells reveals novel genetic variations associated with primary ovarian insufficiency.

Global downstream BMP15 pathway analysis in human ovarian granulosa cells reveals novel genetic variations associated with primary ovarian insufficiency.

Journal: Maturitas

Published: December 19, 2025

A TAp63alpha truncating variant associated with primary ovarian insufficiency lowers the cellular apoptotic rate.

A TAp63alpha truncating variant associated with primary ovarian insufficiency lowers the cellular apoptotic rate.

Journal: Journal of ovarian research

Published: May 05, 2025

A Novel Homozygous BMP15 Mutation Causes Ovarian Dysgenesis and Primary Amenorrhea.

A Novel Homozygous BMP15 Mutation Causes Ovarian Dysgenesis and Primary Amenorrhea.

Journal: Journal of the Endocrine Society

Published: September 04, 2024

Primary ovarian insufficiency: update on clinical and genetic findings.

Primary ovarian insufficiency: update on clinical and genetic findings.

Journal: Frontiers in endocrinology

Published: July 15, 2024

The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres.

The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres.

Journal: Endocrine connections

Published: October 06, 2022

Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset.

Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset.

Journal: Frontiers in endocrinology

Published: February 05, 2021

The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report.

The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report.

Journal: Frontiers in endocrinology

Published: March 05, 2020

Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency.

Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency.

Journal: Human mutation

Published: April 10, 2019

High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.

High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.

Journal: Human reproduction (Oxford, England)

Published: September 07, 2018

Mitochondrial DNA copy number in peripheral blood: a potential non-invasive biomarker for female subfertility.

Mitochondrial DNA copy number in peripheral blood: a potential non-invasive biomarker for female subfertility.

Journal: Journal of assisted reproduction and genetics

Published: June 11, 2018

Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.

Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.

Journal: Human molecular genetics

Published: October 08, 2017

Genetics of primary ovarian insufficiency.

Genetics of primary ovarian insufficiency.

Journal: Clinical genetics

Published: October 07, 2016

Showing 1-12 of 18

Last Updated: 09/26/2026