Wanqi Wang

Changchun, China

Last Updated: 09/26/2026

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Found 11 publications

A network meta-analysis of strategies for endoscopic submucosal dissection procedures from the perspectives of efficacy, duration and safety.

A network meta-analysis of strategies for endoscopic submucosal dissection procedures from the perspectives of efficacy, duration and safety.

Journal: BMC gastroenterology

Published: October 14, 2025

Cartilage-hair hypoplasia in a patient with compound heterozygous variants in the RMRP gene: A case report.

Cartilage-hair hypoplasia in a patient with compound heterozygous variants in the RMRP gene: A case report.

Journal: Medicine

Published: August 24, 2025

Concurrent 12p trisomy and 4q34.2-q35.2 deletion detected by WES-CNV: Case report.

Concurrent 12p trisomy and 4q34.2-q35.2 deletion detected by WES-CNV: Case report.

Journal: Medicine

Published: August 19, 2025

De novo missense mutation in MYT1l leading to autosomal dominant intellectual disability 39 and autism spectrum disorder: a case report.

De novo missense mutation in MYT1l leading to autosomal dominant intellectual disability 39 and autism spectrum disorder: a case report.

Journal: Frontiers in pediatrics

Published: July 25, 2025

De novo frameshift mutation in SYNGAP1 resulting in autosomal dominant mental retardation type 5 and autism spectrum disorder: a case report.

De novo frameshift mutation in SYNGAP1 resulting in autosomal dominant mental retardation type 5 and autism spectrum disorder: a case report.

Journal: Frontiers in pediatrics

Published: July 23, 2025

Therapeutic effects of Icariside II on radiation cystitis: revealing the mechanistic role of the FN1/Itgαvβ6-PI3K/AKT signaling pathway using single-cell RNA sequencing.

Therapeutic effects of Icariside II on radiation cystitis: revealing the mechanistic role of the FN1/Itgαvβ6-PI3K/AKT signaling pathway using single-cell RNA sequencing.

Journal: International journal of surgery (London, England)

Published: April 16, 2025

Case Report: Novel ADA2 variants cause atypical adenosine deaminase 2 deficiency.

Case Report: Novel ADA2 variants cause atypical adenosine deaminase 2 deficiency.

Journal: Frontiers in genetics

Published: August 10, 2024

A case of Sandhoff disease caused by a novel β-hexosaminidase B (HEXB) mutation c.118delG (p.A40fs*24): A case report from China.

A case of Sandhoff disease caused by a novel β-hexosaminidase B (HEXB) mutation c.118delG (p.A40fs*24): A case report from China.

Journal: Medicine

Published: June 16, 2023

Thyroid hormone resistance resulting from a novel mutation in the THRB gene in a Chinese child: A case report.

Thyroid hormone resistance resulting from a novel mutation in the THRB gene in a Chinese child: A case report.

Journal: Medicine

Published: April 28, 2023

A nonsense mutation in the CUL3 gene in a Chinese patient with autism spectrum disorder and epilepsy: A case report.

A nonsense mutation in the CUL3 gene in a Chinese patient with autism spectrum disorder and epilepsy: A case report.

Journal: Medicine

Published: April 07, 2023

Case report: Heterogeneous mutations of SOX10 gene in a Chinese infant with Waardenburg syndrome type 4C.

Case report: Heterogeneous mutations of SOX10 gene in a Chinese infant with Waardenburg syndrome type 4C.

Journal: Frontiers in pediatrics

Published: March 17, 2022

Showing 1-11 of 11

Last Updated: 09/26/2026