Xiaoya Ren

28 Fuxing Road
Beijing, 100853, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 16 publications

NR5A1 gene variants: variable phenotypes, new variants, and genotype-phenotype correlations.

NR5A1 gene variants: variable phenotypes, new variants, and genotype-phenotype correlations.

Journal: Frontiers in endocrinology

Published: March 17, 2026

The role of ubiquitin system in ageing-related diseases and potential therapeutic opportunities.

The role of ubiquitin system in ageing-related diseases and potential therapeutic opportunities.

Journal: Molecular biomedicine

Published: June 25, 2025

Investigational Treatment of Congenital Hypogonadotropic Hypogonadism in Infants.

Investigational Treatment of Congenital Hypogonadotropic Hypogonadism in Infants.

Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme

Published: July 09, 2024

Analysis of genetic and clinical characteristics of androgen insensitivity syndrome: a cohort study including 12 families.

Analysis of genetic and clinical characteristics of androgen insensitivity syndrome: a cohort study including 12 families.

Journal: European journal of endocrinology

Published: November 16, 2023

Ubiquitin-specific protease 28: the decipherment of its dual roles in cancer development.

Ubiquitin-specific protease 28: the decipherment of its dual roles in cancer development.

Journal: Experimental hematology & oncology

Published: September 02, 2022

Growth Curves of Chinese Children with Androgen Insensitivity Syndrome: A Multicenter Registry Study.

Growth Curves of Chinese Children with Androgen Insensitivity Syndrome: A Multicenter Registry Study.

Journal: Journal of personalized medicine

Published: March 01, 2022

Hormonal changes throughout puberty in boys: an observational study on the treatment outcome of congenital hypogonadotropic hypogonadism.

Hormonal changes throughout puberty in boys: an observational study on the treatment outcome of congenital hypogonadotropic hypogonadism.

Journal: Chinese medical journal

Published: February 02, 2022

SOX2 heterozygous mutations cause multiple extraocular phenotypes in boys.

SOX2 heterozygous mutations cause multiple extraocular phenotypes in boys.

Journal: Chinese medical journal

Published: November 11, 2021

Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients.

Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients.

Journal: Frontiers in endocrinology

Published: May 19, 2021

Clinical characteristics and genotype-phenotype correlations of 130 Chinese children in a high-homogeneity single-center cohort with 5α-reductase 2 deficiency.

Clinical characteristics and genotype-phenotype correlations of 130 Chinese children in a high-homogeneity single-center cohort with 5α-reductase 2 deficiency.

Journal: Molecular genetics & genomic medicine

Published: February 17, 2020

Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children.

Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children.

Journal: Orphanet journal of rare diseases

Published: August 04, 2019

Persistent Müllerian duct syndrome: A case report and review.

Persistent Müllerian duct syndrome: A case report and review.

Journal: Experimental and therapeutic medicine

Published: April 25, 2017

Showing 1-12 of 16

Last Updated: 09/26/2026