Rongchun Wang

Changsha, China

Last Updated: 09/26/2026

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Found 14 publications

PCDSOS: a novel clinical predictive tool for screening primary ciliary dyskinesia in adult bronchiectasis patients-a multicenter derivation and external validation study.

PCDSOS: a novel clinical predictive tool for screening primary ciliary dyskinesia in adult bronchiectasis patients-a multicenter derivation and external validation study.

Journal: BMC medicine

Published: October 29, 2025

A novel COL3A1 variant associated with vascular Ehlers-Danlos syndrome in a patient presents as recurrent pneumothorax with cavities.

A novel COL3A1 variant associated with vascular Ehlers-Danlos syndrome in a patient presents as recurrent pneumothorax with cavities.

Journal: QJM : monthly journal of the Association of Physicians

Published: March 30, 2023

Polybacterial infection in patients with stable bronchiectasis revealed by metagenomic next-generation sequencing.

Polybacterial infection in patients with stable bronchiectasis revealed by metagenomic next-generation sequencing.

Journal: The Journal of infection

Published: February 26, 2023

Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice.

Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice.

Journal: Frontiers of medicine

Published: November 15, 2022

Clinical phenotypes of primary ciliary dyskinesia.

Clinical phenotypes of primary ciliary dyskinesia.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Published: May 11, 2022

Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia.

Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia.

Journal: Frontiers in genetics

Published: May 10, 2022

Case Report: DNAAF4 Variants Cause Primary Ciliary Dyskinesia and Infertility in Two Han Chinese Families.

Case Report: DNAAF4 Variants Cause Primary Ciliary Dyskinesia and Infertility in Two Han Chinese Families.

Journal: Frontiers in genetics

Published: May 03, 2022

Novel RSPH4A Variants Associated With Primary Ciliary Dyskinesia-Related Infertility in Three Chinese Families.

Novel RSPH4A Variants Associated With Primary Ciliary Dyskinesia-Related Infertility in Three Chinese Families.

Journal: Frontiers in genetics

Published: April 17, 2022

Identification of a Novel OFD1 Variant in a Patient with Primary Ciliary Dyskinesia.

Identification of a Novel OFD1 Variant in a Patient with Primary Ciliary Dyskinesia.

Journal: Pharmacogenomics and personalized medicine

Published: March 16, 2022

Novel Compound Heterozygous Variants in CCDC40 Associated with Primary Ciliary Dyskinesia and Multiple Morphological Abnormalities of the Sperm Flagella.

Novel Compound Heterozygous Variants in CCDC40 Associated with Primary Ciliary Dyskinesia and Multiple Morphological Abnormalities of the Sperm Flagella.

Journal: Pharmacogenomics and personalized medicine

Published: February 04, 2022

Identification of Two Novel DNAAF2 Variants in Two Consanguineous Families with Primary Ciliary Dyskinesia.

Identification of Two Novel DNAAF2 Variants in Two Consanguineous Families with Primary Ciliary Dyskinesia.

Journal: Pharmacogenomics and personalized medicine

Published: September 16, 2021

DRC1 deficiency caused primary ciliary dyskinesia and MMAF in a Chinese patient.

DRC1 deficiency caused primary ciliary dyskinesia and MMAF in a Chinese patient.

Journal: Journal of human genetics

Published: September 06, 2021

Showing 1-12 of 14

Last Updated: 09/26/2026