Chunfang Chu

Beijing, 100006, China

Last Updated: 09/26/2026

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Found 12 publications

Distinct BNC1 variants contribute to premature ovarian insufficiency through different molecular mechanisms.

Distinct BNC1 variants contribute to premature ovarian insufficiency through different molecular mechanisms.

Journal: Gene

Published: November 20, 2025

The Genetic Landscape of Müllerian Duct Anomalies: A Comprehensive Review.

The Genetic Landscape of Müllerian Duct Anomalies: A Comprehensive Review.

Journal: Reproductive medicine and biology

Published: July 19, 2025

HOXD10: A novel gene implicated in human Müllerian duct anomalies.

HOXD10: A novel gene implicated in human Müllerian duct anomalies.

Journal: European journal of obstetrics, gynecology, and reproductive biology

Published: September 14, 2024

Identification and functional characteristics of CHD1L gene variants implicated in human Müllerian duct anomalies.

Identification and functional characteristics of CHD1L gene variants implicated in human Müllerian duct anomalies.

Journal: Biological research

Published: June 11, 2024

Correction: TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2.

Correction: TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2.

Journal: Journal of ovarian research

Published: April 29, 2024

POI-associated EIF4ENIF1 mutations exhibit impaired translation regulation abilities.

POI-associated EIF4ENIF1 mutations exhibit impaired translation regulation abilities.

Journal: Gene

Published: February 12, 2024

Implication of androgen receptor gene dysfunction in human Müllerian duct anomalies.

Implication of androgen receptor gene dysfunction in human Müllerian duct anomalies.

Journal: European journal of obstetrics, gynecology, and reproductive biology

Published: November 09, 2023

TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2.

TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2.

Journal: Journal of ovarian research

Published: August 31, 2023

Variants in genes related to development of the urinary system are associated with Mayer-Rokitansky-Küster-Hauser syndrome.

Variants in genes related to development of the urinary system are associated with Mayer-Rokitansky-Küster-Hauser syndrome.

Journal: Human genomics

Published: January 10, 2022

Renal agenesis-related genes are associated with Herlyn-Werner-Wunderlich syndrome.

Renal agenesis-related genes are associated with Herlyn-Werner-Wunderlich syndrome.

Journal: Fertility and sterility

Published: February 26, 2021

A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing.

A novel EIF4ENIF1 mutation associated with a diminished ovarian reserve and premature ovarian insufficiency identified by whole-exome sequencing.

Journal: Journal of ovarian research

Published: July 24, 2019

Whole-Exome Sequencing Identified a TBX6 Loss of Function Mutation in a Patient with Distal Vaginal Atresia.

Whole-Exome Sequencing Identified a TBX6 Loss of Function Mutation in a Patient with Distal Vaginal Atresia.

Journal: Journal of pediatric and adolescent gynecology

Published: March 01, 2019

Showing 1-12 of 12

Last Updated: 09/26/2026