undefined Publications

Estrogen deficiency and risk of hearing loss in pediatric Turner syndrome.

Journal: The Journal of clinical investigation

Published: October 08, 2025

TCL1A in naïve B cells as a therapeutic target for type 1 diabetes.

Journal: EBioMedicine

Published: September 11, 2024

Novel ANKRD17 variants implicate synaptic and mitochondrial disruptions in intellectual disability and autism spectrum disorder.

Journal: Journal of neurodevelopmental disorders

Published: August 14, 2024

Long-term efficacy and safety of PEGylated recombinant human growth hormone in treating Chinese children with growth hormone deficiency: a 5-year retrospective study.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: April 19, 2024

Efficacy and safety of leuprorelin 3-month depot (11.25 mg) for idiopathic central precocious puberty treatment of Chinese girls: a single-center retrospective study.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: September 13, 2023

ARID2, a rare cause of Coffin-Siris syndrome: A novel microdeletion at 12q12q13.11 causing severe short stature and literature review.

Journal: American journal of medical genetics. Part A

Published: December 05, 2022

Clinical application of artificial intelligence in longitudinal image analysis of bone age among GHD patients.

Journal: Frontiers in pediatrics

Published: July 05, 2022

Indicators of glucose dysregulation and the relationship with iron overload in Chinese children with beta thalassemia major.

Journal: Pediatric diabetes

Published: January 27, 2021

Gender roles and behavioral problems in children with 21-hydroxylase deficiency in Southern China.

Journal: Steroids

Published: April 16, 2020

Analysis of phenotypes and genotypes in 84 patients with 21-Hydroxylase deficiency in southern China.

Journal: Steroids

Published: February 13, 2019

Zulin Liu

Estrogen deficiency and risk of hearing loss in pediatric Turner syndrome.

Estrogen deficiency and risk of hearing loss in pediatric Turner syndrome.

TCL1A in naïve B cells as a therapeutic target for type 1 diabetes.

TCL1A in naïve B cells as a therapeutic target for type 1 diabetes.

Novel ANKRD17 variants implicate synaptic and mitochondrial disruptions in intellectual disability and autism spectrum disorder.

Novel ANKRD17 variants implicate synaptic and mitochondrial disruptions in intellectual disability and autism spectrum disorder.

Long-term efficacy and safety of PEGylated recombinant human growth hormone in treating Chinese children with growth hormone deficiency: a 5-year retrospective study.

Long-term efficacy and safety of PEGylated recombinant human growth hormone in treating Chinese children with growth hormone deficiency: a 5-year retrospective study.

Efficacy and safety of leuprorelin 3-month depot (11.25 mg) for idiopathic central precocious puberty treatment of Chinese girls: a single-center retrospective study.

Efficacy and safety of leuprorelin 3-month depot (11.25 mg) for idiopathic central precocious puberty treatment of Chinese girls: a single-center retrospective study.

ARID2, a rare cause of Coffin-Siris syndrome: A novel microdeletion at 12q12q13.11 causing severe short stature and literature review.

ARID2, a rare cause of Coffin-Siris syndrome: A novel microdeletion at 12q12q13.11 causing severe short stature and literature review.

Clinical application of artificial intelligence in longitudinal image analysis of bone age among GHD patients.

Clinical application of artificial intelligence in longitudinal image analysis of bone age among GHD patients.

Indicators of glucose dysregulation and the relationship with iron overload in Chinese children with beta thalassemia major.

Indicators of glucose dysregulation and the relationship with iron overload in Chinese children with beta thalassemia major.

Gender roles and behavioral problems in children with 21-hydroxylase deficiency in Southern China.

Gender roles and behavioral problems in children with 21-hydroxylase deficiency in Southern China.

Analysis of phenotypes and genotypes in 84 patients with 21-Hydroxylase deficiency in southern China.

Analysis of phenotypes and genotypes in 84 patients with 21-Hydroxylase deficiency in southern China.

Efficacy and safety of leuprorelin 3-month depot (11.25 mg) for idiopathic central precocious puberty treatment of Chinese girls: a single-center retrospective study.

Efficacy and safety of leuprorelin 3-month depot (11.25 mg) for idiopathic central precocious puberty treatment of Chinese girls: a single-center retrospective study.