Gaoli Jiang

Linking childhood interstitial lung disease to IARS-related disorder: clinical and preliminary functional studies in four new cases.

Journal: Human genomics

Published: October 15, 2025

Clinical and Genetic Study of a Pseudo-Dominant Primary Ciliary Dyskinesia Pedigree: The First DNAAF1-Associated Family Reported in Chinese Population.

Journal: Molecular genetics & genomic medicine

Published: September 18, 2025

Functional characterization of two novel NKX2-1 frameshift variants that cause pulmonary surfactant dysfunction.

Journal: Pediatric research

Published: June 09, 2023

Clinical features and outcomes of children's interstitial lung disease accompanied with connective tissue disease: A prospective cohort study.

Journal: Respiratory medicine

Published: January 14, 2023

Respiratory symptoms as initial manifestations of interstitial lung disease in clinically amyopathic juvenile dermatomyositis: a case report with literature review.

Journal: BMC pediatrics

Published: May 11, 2021

Clinical features and molecular genetic analysis of thanatophoric dysplasia type I in a neonate with a de novo c.2419 T > C (p. Ter807Arg) (X807R) mutation in FGFR3.

Journal: Experimental and molecular pathology

Published: May 08, 2019

Clinical and genetic spectrum of interstitial lung disease in Chinese children associated with surfactant protein C mutations.

Journal: Italian journal of pediatrics

Published: March 19, 2019

Reference data for BabyBody-plethysmographic measurements in Chinese neonates and infants.

Journal: Respirology (Carlton, Vic.)

Published: October 26, 2016

Lung function measurements using body plethysmography in young children with acute lower respiratory tract infection

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

Published: September 17, 2014

Risk factors for acute respiratory syncytial virus infection of lower respiratory tract in hospitalized infants

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

Published: June 28, 2014

Linking childhood interstitial lung disease to IARS-related disorder: clinical and preliminary functional studies in four new cases.

Linking childhood interstitial lung disease to IARS-related disorder: clinical and preliminary functional studies in four new cases.

Clinical and Genetic Study of a Pseudo-Dominant Primary Ciliary Dyskinesia Pedigree: The First DNAAF1-Associated Family Reported in Chinese Population.

Clinical and Genetic Study of a Pseudo-Dominant Primary Ciliary Dyskinesia Pedigree: The First DNAAF1-Associated Family Reported in Chinese Population.

Functional characterization of two novel NKX2-1 frameshift variants that cause pulmonary surfactant dysfunction.

Functional characterization of two novel NKX2-1 frameshift variants that cause pulmonary surfactant dysfunction.

Clinical features and outcomes of children's interstitial lung disease accompanied with connective tissue disease: A prospective cohort study.

Clinical features and outcomes of children's interstitial lung disease accompanied with connective tissue disease: A prospective cohort study.

Respiratory symptoms as initial manifestations of interstitial lung disease in clinically amyopathic juvenile dermatomyositis: a case report with literature review.

Respiratory symptoms as initial manifestations of interstitial lung disease in clinically amyopathic juvenile dermatomyositis: a case report with literature review.

Clinical features and molecular genetic analysis of thanatophoric dysplasia type I in a neonate with a de novo c.2419 T > C (p. Ter807Arg) (X807R) mutation in FGFR3.

Clinical features and molecular genetic analysis of thanatophoric dysplasia type I in a neonate with a de novo c.2419 T > C (p. Ter807Arg) (X807R) mutation in FGFR3.

Clinical and genetic spectrum of interstitial lung disease in Chinese children associated with surfactant protein C mutations.

Clinical and genetic spectrum of interstitial lung disease in Chinese children associated with surfactant protein C mutations.

Reference data for BabyBody-plethysmographic measurements in Chinese neonates and infants.

Reference data for BabyBody-plethysmographic measurements in Chinese neonates and infants.

Lung function measurements using body plethysmography in young children with acute lower respiratory tract infection

Lung function measurements using body plethysmography in young children with acute lower respiratory tract infection

Risk factors for acute respiratory syncytial virus infection of lower respiratory tract in hospitalized infants

Risk factors for acute respiratory syncytial virus infection of lower respiratory tract in hospitalized infants

Clinical features and molecular genetic analysis of thanatophoric dysplasia type I in a neonate with a de novo c.2419 T > C (p. Ter807Arg) (X807R) mutation in FGFR3.

Clinical features and molecular genetic analysis of thanatophoric dysplasia type I in a neonate with a de novo c.2419 T > C (p. Ter807Arg) (X807R) mutation in FGFR3.