Chunyan Wang
No.399 WanYuan Road
Minhang, 201102, China
Minhang, 201102, China
Last Updated: 09/26/2026
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Found 21 publications
Urinary ANGPTL3: a novel noninvasive biomarker for podocyte injury in pediatric glomerular diseases.
Urinary ANGPTL3: a novel noninvasive biomarker for podocyte injury in pediatric glomerular diseases.
Journal: Journal of translational medicine
Published: December 30, 2025
Maternal Exposure to 2,4-Di-tert-butylphenol During Pregnancy in a Mouse Model Leads to Abnormal Development of the Urinary System in Offspring.
Journal: Toxics
Published: October 21, 2025
From mutation to symptoms: a multi-center study on HNF1B-related nephropathy in Chinese children.
Journal: BMC nephrology
Published: July 16, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 08, 2024
GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract.
Journal: Human genomics
Published: October 15, 2023
Coupling Global Context and Local Contents for Weakly-Supervised Semantic Segmentation.
Journal: IEEE transactions on neural networks and learning systems
Published: May 23, 2023
Recessive CHRM5 variant as a potential cause of neurogenic bladder.
Journal: American journal of medical genetics. Part A
Published: February 01, 2023
Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal Kidney.
Journal: Nephron
Published: January 04, 2023
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract.
Journal: American journal of medical genetics. Part A
Published: September 09, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
Journal: European urology open science
Published: August 10, 2022
Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.
Journal: Journal of the American Society of Nephrology : JASN
Published: January 27, 2022
Last Updated: 09/26/2026