Wenmiao L. Liu

Qingdao, China

Last Updated: 09/26/2026

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Found 29 publications

Genetic characterization of DDX11 variants identified in a Chinese family with Warsaw breakage syndrome.

Genetic characterization of DDX11 variants identified in a Chinese family with Warsaw breakage syndrome.

Journal: Seizure

Published: February 23, 2026

Autism Spectrum Disorder Caused by a Novel De Novo SCN2A Mutation: A Case Report.

Autism Spectrum Disorder Caused by a Novel De Novo SCN2A Mutation: A Case Report.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: February 01, 2026

Association between smoking status and the risk of depressive symptoms among the elderly in Shandong Province

Association between smoking status and the risk of depressive symptoms among the elderly in Shandong Province

Journal: Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi

Published: December 24, 2025

rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation.

rs9789446 genotype as susceptibility biomarkers for congenital hypothyroidism based on population and family validation.

Journal: Frontiers in genetics

Published: October 09, 2025

A case report of transcatheter aortic valve replacement for severe aortic regurgitation caused by Takayasu's arteritis

A case report of transcatheter aortic valve replacement for severe aortic regurgitation caused by Takayasu's arteritis

Journal: Zhonghua xin xue guan bing za zhi

Published: November 18, 2024

Two novel heterozygous HPDL variants in a Chinese family with a neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities.

Two novel heterozygous HPDL variants in a Chinese family with a neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities.

Journal: Gene

Published: August 09, 2024

A study on the dual use of e-cigarettes and cigarettes among adolescents in Shandong Province

A study on the dual use of e-cigarettes and cigarettes among adolescents in Shandong Province

Journal: Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi

Published: April 28, 2024

A novel hemizygous CD40L mutation of X-linked hyper IgM syndromes and compound heterozygous DOCK8 mutations of hyper IgE syndromes in two Chinese families.

A novel hemizygous CD40L mutation of X-linked hyper IgM syndromes and compound heterozygous DOCK8 mutations of hyper IgE syndromes in two Chinese families.

Journal: Immunogenetics

Published: January 20, 2024

Abnormal H3K4 enzyme catalytic activity and neuronal morphology caused by ASH1L mutations in individuals with Tourette syndrome.

Abnormal H3K4 enzyme catalytic activity and neuronal morphology caused by ASH1L mutations in individuals with Tourette syndrome.

Journal: European child & adolescent psychiatry

Published: April 08, 2023

ASH1L may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control study.

ASH1L may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control study.

Journal: Brain and behavior

Published: July 29, 2021

Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases.

Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases.

Journal: Endocrine

Published: June 10, 2020

Compound heterozygous DYSF variants causing limb-girdle muscular dystrophy type 2B in a Chinese family.

Compound heterozygous DYSF variants causing limb-girdle muscular dystrophy type 2B in a Chinese family.

Journal: The journal of gene medicine

Published: January 16, 2020

Showing 1-12 of 29

Last Updated: 09/26/2026