Xueqin Cheng

72 Guangzhou Road
Nanjing, 210029, China

Last Updated: 09/26/2026

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Found 8 publications

Clinical phenotypes and genetic analysis of 30 children with Gitelman syndrome.

Clinical phenotypes and genetic analysis of 30 children with Gitelman syndrome.

Journal: Frontiers in pediatrics

Published: April 12, 2026

Association between healthy lifestyle score and thyroid function biomarkers in adults: a cross-sectional analysis.

Association between healthy lifestyle score and thyroid function biomarkers in adults: a cross-sectional analysis.

Journal: The British journal of nutrition

Published: February 04, 2026

Rare Biallelic CTU2 Variants in an Individual With CAKUT: Clinical Characterization and Minigene Splicing Analysis.

Rare Biallelic CTU2 Variants in an Individual With CAKUT: Clinical Characterization and Minigene Splicing Analysis.

Journal: Molecular genetics & genomic medicine

Published: December 31, 2025

Repeat kidney biopsy in pediatric lupus nephritis: an analysis of associated clinical-pathological features and outcomes.

Repeat kidney biopsy in pediatric lupus nephritis: an analysis of associated clinical-pathological features and outcomes.

Journal: Frontiers in pediatrics

Published: December 14, 2025

Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine.

Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine.

Journal: BMC nephrology

Published: September 05, 2025

Are children with IgA nephropathy different from adult patients?

Are children with IgA nephropathy different from adult patients?

Journal: Pediatric nephrology (Berlin, Germany)

Published: February 01, 2024

Compound heterozygous variants of ANKFY1 in a child with infantile-onset proteinuria and movement disorder.

Compound heterozygous variants of ANKFY1 in a child with infantile-onset proteinuria and movement disorder.

Journal: Clinical kidney journal

Published: October 25, 2023

The identification of a novel CCNQ gene tail extension variant contributing to syndactyly, telecanthus and anogenital and renal malformations syndrome.

The identification of a novel CCNQ gene tail extension variant contributing to syndactyly, telecanthus and anogenital and renal malformations syndrome.

Journal: Clinical genetics

Published: April 25, 2022

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Last Updated: 09/26/2026