Chenyang Xu
Department Of Otolaryngology Head And Neck Surgery, Ldey.cn
Lanzhou, China
Lanzhou, China
Last Updated: 09/26/2026
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Found 23 publications
A Novel LMX1A Frameshift Variant Underlies Familial Phenotypic Heterogeneity in DFNA7.
Journal: Human mutation
Published: August 30, 2025
Chronic Maxillary Sinusitis Secondary to a Retained Wooden Foreign Body: A Case Report.
Journal: Ear, nose, & throat journal
Published: May 16, 2025
A Novel Intronic Variant Causes Aberrant Splicing of PCDH15 in a Family With Usher Syndrome Type 1F.
A Novel Intronic Variant Causes Aberrant Splicing of PCDH15 in a Family With Usher Syndrome Type 1F.
Journal: Molecular genetics & genomic medicine
Published: May 14, 2025
Accelerated Identification and Preliminary Validation of a Pathogenic Missense Variant in the L1CAM Gene in a Pregnant Woman With Sonographic Anomalies Using AlphaMissense.
Journal: Molecular genetics & genomic medicine
Published: May 01, 2025
Life-threatening pediatric retropharyngeal abscess: A case report on delayed complication of endoscopic fishbone removal in an infant.
Journal: Medicine
Published: March 27, 2025
Genetic analysis of two novel variants in a Chinese pedigree affected with intellectual disorder
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 09, 2024
Saliva Sample-Based Non-Invasive Carrier Screening for Spinal Muscular Atrophy, Hereditary Hearing Loss, and Thalassemia in 13,926 Women of Reproductive Age From South Zhejiang.
Journal: Molecular genetics & genomic medicine
Published: February 17, 2024
PLPPR4 haploinsufficiency causes neurodevelopmental disorders by disrupting synaptic plasticity via mTOR signalling.
Journal: Journal of cellular and molecular medicine
Published: April 06, 2023
Characteristics and mechanisms of mosaicism in prenatal diagnosis cases by application of SNP array.
Characteristics and mechanisms of mosaicism in prenatal diagnosis cases by application of SNP array.
Journal: Molecular cytogenetics
Published: February 27, 2023
Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next-generation sequencing in a Chinese family with nonsyndromic hearing loss.
Journal: Journal of clinical laboratory analysis
Published: July 12, 2022
Analysis of ARID1B gene variants in two Chinese pedigrees with Coffin-Siris syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 22, 2022
Implicit theories of body weight and engagement in healthy lifestyles among young adults: The mediating effect of self-control.
Journal: Journal of health psychology
Published: December 29, 2021
Last Updated: 09/26/2026