Yongan Zhou

机构：Shanxi Medical University, Second Hospital of Shanxi Medical University · ORCID：0000-0001-5015-7688

发表论文 36 篇 · 总被引 139 次 · h-index 6

代表论文

• Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province (2019 · Molecular Genetics & Genomic Medicine · 被引 29)
• A Novel α-Galactosidase A Splicing Mutation Predisposes to Fabry Disease (2019 · Frontiers in Genetics · 被引 21)
• GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder (2019 · Genetics and Molecular Biology · 被引 10)
• The multi-tyrosine kinase inhibitor TKI258, alone or in combination with RAD001, is effective for treatment of human leukemia with BCR-ABL translocation in vitro. (2014 · PubMed · 被引 7)
• A novel splicing pathogenic variant in COL1A1 causing osteogenesis imperfecta (OI) type I in a Chinese family (2020 · Molecular Genetics & Genomic Medicine · 被引 6)
• Functional evaluation of a novel GLA causative mutation in Fabry disease (2019 · Molecular Genetics & Genomic Medicine · 被引 6)