Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database.

World journal of pediatrics : WJP - 1 Aug 2021

Liu Jia-Lu, Shen Qian, Wu Ming-Yan, Zhu Guang-Hua, Li Yu-Feng, Wang Xiao-Wen, Tang Xiao-Shan, Bi Yun-Li, Gong Yi-Nv, Chen Jing, Fang Xiao-Yan, Zhai Yi-Hui, Wu Bing-Bing, Li Guo-Min, Sun Yu-Bo, Gao Xiao-Jie, Liu Cui-Hua, Jiang Xiao-Yun, Hao Sheng, Kang Yu-Lin, Gong Ying-Liang, Rong Li-Ping, Li Di, Wang Si, Ma Duan, Rao Jia, Xu Hong

Abstract excerpt

BACKGROUND: Primary vesicoureteral reflux (VUR) is a common congenital anomaly of the kidney and urinary tract (CAKUT) in childhood. The present study identified the possible genetic contributions to primary VUR in children. METHODS: Patients with primary VUR were enrolled and analysed based on a national multi-center registration network (Chinese Children Genetic Kidney Disease Database, CCGKDD) that covered 23...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Kidney

Share to Kidney Diseases

Share to Phenotype

Share to Urinary Tract

Share to Vesico-Ureteral Reflux

Source

Identifiers

PMID: 34059960
DOI: 10.1007/s12519-021-00428-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database.PMID 34059960Read ↗

Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort studySemantic proximity Read ↗

Deciphering the Mutation Spectrum in South Indian Children With Congenital Anomalies of the Kidney and Urinary TractSemantic proximity Read ↗

Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary TractSemantic proximity Read ↗

Deciphering the mutation spectrum in south Indian children with congenital anomalies of the kidney and urinary tract.Semantic proximity Read ↗

Congenital anomalies of the kidney and urinary tractSemantic proximity Read ↗

Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients.Semantic proximity Read ↗

Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.Semantic proximity Read ↗

Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary TractSemantic proximity Read ↗

Exome Reanalysis Identifies Novel Candidate Genes Associated with Congenital Anomalies of the Kidney and Urinary Tract in ChinaSemantic proximity Read ↗

Genetic Insights Into Nephrolithiasis and Renal Cancer Predisposition: Precision Medicine in Genes, Diagnosis, and Therapy.Semantic proximity Read ↗

Exome analysis links kidney malformations to developmental disorders and reveals causal genes.Semantic proximity Read ↗

Genetic Architecture of Childhood Kidney and Urological Diseases in ChinaSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.