Dongjuan J. Wang

Ministry Of Education Key Laboratory Of Child Development And Disorders, Chongqing Key Laboratory Of Child Rare Diseases In Infection And Immunity, Chongqing Municipal Health Commission Key Laboratory Of Children's Vital Organ Development And Diseases
Chongqing, China

Last Updated: 09/26/2026

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Found 11 publications

Elevated IL1RL1 expression is correlated with the persistence of childhood allergies.

Elevated IL1RL1 expression is correlated with the persistence of childhood allergies.

Journal: The Journal of asthma : official journal of the Association for the Care of Asthma

Published: July 10, 2026

Genetic characterization and screening of congenital adrenal hyperplasia by long-read sequencing in a cohort of 21,239 newborns.

Genetic characterization and screening of congenital adrenal hyperplasia by long-read sequencing in a cohort of 21,239 newborns.

Journal: Genome medicine

Published: July 31, 2025

Hypocitrullinemia as an Early Diagnostic Biomarker for MT-ATP6 Mitochondrial Diseases.

Hypocitrullinemia as an Early Diagnostic Biomarker for MT-ATP6 Mitochondrial Diseases.

Journal: Journal of molecular neuroscience : MN

Published: May 24, 2025

Clinical analysis of systemic juvenile idiopathic arthritis with Kawasaki disease-like symptoms

Clinical analysis of systemic juvenile idiopathic arthritis with Kawasaki disease-like symptoms

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: November 20, 2024

Corrigendum: Disease spectrum, prevalence, genetic characteristics of inborn errors of metabolism in 21,840 hospitalized infants in Chongqing, China, 2017-2022.

Corrigendum: Disease spectrum, prevalence, genetic characteristics of inborn errors of metabolism in 21,840 hospitalized infants in Chongqing, China, 2017-2022.

Journal: Frontiers in genetics

Published: June 15, 2024

Disease spectrum, prevalence, genetic characteristics of inborn errors of metabolism in 21,840 hospitalized infants in Chongqing, China, 2017-2022.

Disease spectrum, prevalence, genetic characteristics of inborn errors of metabolism in 21,840 hospitalized infants in Chongqing, China, 2017-2022.

Journal: Frontiers in genetics

Published: March 05, 2024

Clinical phenotypic and genotypic analysis of 5 pediatric patients with β-ketothiolase deficiency

Clinical phenotypic and genotypic analysis of 5 pediatric patients with β-ketothiolase deficiency

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: December 28, 2023

Integrative identification of the pathogenic role of a novel G6PD missense mutation c.697G>C.

Integrative identification of the pathogenic role of a novel G6PD missense mutation c.697G>C.

Journal: Annals of translational medicine

Published: March 12, 2021

C4OH is a potential newborn screening marker-a multicenter retrospective study of patients with beta-ketothiolase deficiency in China.

C4OH is a potential newborn screening marker-a multicenter retrospective study of patients with beta-ketothiolase deficiency in China.

Journal: Orphanet journal of rare diseases

Published: December 11, 2020

Chinese expert brief consensus on newborn screening of inherited metabolic disorders during the novel coronavirus infection epidemic.

Chinese expert brief consensus on newborn screening of inherited metabolic disorders during the novel coronavirus infection epidemic.

Journal: Annals of translational medicine

Published: May 13, 2020

Maternal high-fat diet feeding during pregnancy and lactation augments lung inflammation and remodeling in the offspring.

Maternal high-fat diet feeding during pregnancy and lactation augments lung inflammation and remodeling in the offspring.

Journal: Respiratory physiology & neurobiology

Published: September 18, 2014

Showing 1-11 of 11

Last Updated: 09/26/2026