Author

Xueqin Xu

Institution: Wenzhou Central Hospital

Observed institution: Wenzhou Central Hospital

ORCID: 0000-0002-5861-1301

Observed ORCID: 0000-0002-5861-1301

OpenAlex ID: A5034004957

Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next‐generation sequencing in a Chinese family with nonsyndromic hearing loss

2022 · Yanbao Xiang, Chenyang Xu, et al. · Journal of Clinical Laboratory Analysis · 6

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

2025 · Chenyang Xu, Yanbao Xiang, et al. · Molecular Genetics & Genomic Medicine · 3

Prenatal Diagnosis and Postnatal Follow‐Up of 19 Fetuses With 16p13.11 Microduplication in a Cohort of 12,038 Pregnancies From South Zhejiang

2026 · Xiaoxiao Lv, Shufei Li, et al. · Molecular Genetics & Genomic Medicine

A Novel Intronic Variant Causes Aberrant Splicing of PCDH15 in a Family With Usher Syndrome Type 1F

2026 · Qifan Ma, Chenyang Xu, et al. · Molecular Genetics & Genomic Medicine

Works count: 4

Citation count: 9

H-index: 2

I10-index: