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Wenxin Lin

Clinical and genetic analysis of a case with centronuclear myopathy caused by SPEG gene mutation: a case report and literature review
2021 · Gang Zhang, Min Xu, et al. · BMC Pediatrics · 12
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Clinical and genetic analysis of a case of late onset carbamoyl phosphate synthase I deficiency caused by CPS1 mutation and literature review
2023 · Shangyu Wang, Jinglin Chen, et al. · BMC Medical Genomics · 8
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Case Report: Identification of a de novo Microdeletion 1q44 in a Patient With Seizures and Developmental Delay
2021 · Yiehen Tung, Haiying Lu, et al. · Frontiers in Genetics · 8
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Identification of 1q21.1 microduplication in a family: A case report
2023 · Ting-Ting Huang, Hai-Feng Xu, et al. · World Journal of Clinical Cases · 4
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Novel compound heterozygous GPR56 gene mutation in a twin with lissencephaly: A case report
2022 · Wen-Xin Lin, Ying-Ying Chai, et al. · World Journal of Clinical Cases · 3
Clinical indicators associated with tuberculous meningitis using multiple correspondence analysis
2025 · Xujie Zhu, Rui Li, et al. · Diagnostic Microbiology and Infectious Disease · 1
The reach-rigor paradox in health communication: a comparative analysis of congenital heart disease content quality and engagement on TikTok and Bilibili
2026 · Ming-Tang Ye, Yang Wang, et al. · BMC Cardiovascular Disorders
A Twins Case of Lissencephaly With GPR56 Compound Heterozygous Mutations and Literatures Review
2021 · Wenxin Lin, Yingying Chai, et al. · Research Square
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Introduction of defense genes that confer broad-spectrum disease-resistance into tomato plants
2001 · Wenxin Lin, Jianli Wu, et al.
Works count: 9
Citation count: 36
H-index: 4
I10-index: 1
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