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Wanyu Fu

Observed name: Fu, Wanyu
ORCID: 0009-0001-8542-5491
Observed ORCID: 0009-0001-8542-5491
OpenAlex ID: A5110668778
Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population
2022 · Jianlong Zhuang, Chunnuan Chen, et al. · Archives of Pathology & Laboratory Medicine · 26
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Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, China
2021 · Jianlong Zhuang, Chunnuan Chen, et al. · BMC Pregnancy and Childbirth · 16
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Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism array
2021 · Jianlong Zhuang, Na Zhang, et al. · Molecular Cytogenetics · 14
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A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures
2023 · Jianlong Zhuang, Meihua Xie, et al. · BMC Medical Genomics · 6
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Sub-Exome Target Sequencing in a Family With Syndactyly Type IV Due to a Novel Partial Duplication of the LMBR1 Gene: First Case Report in Fujian Province of China
2020 · Lijing Shi, Hui Huang, et al. · Frontiers in Genetics · 5
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Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview
2022 · Jianlong Zhuang, Chunnuan Chen, et al. · Molecular Cytogenetics · 4
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Etiological diagnosis of miscarriage by combining use of chromosomal microarray analysis and whole-exome sequencing
2025 · Jianlong Zhuang, Wanyu Fu, et al. · European journal of medical research · 2
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Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study
2024 · Jianlong Zhuang, Na Zhang, et al. · Molecular Cytogenetics · 2
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Prenatal Etiology Diagnosis of Rare Compound Heterozygous PROC Gene Variants in a Fetus With Ocular Ultrasonic Anomaly Using Whole Exome Sequencing
2026 · Jianlong Zhuang, Nan Huang, et al. · Molecular Genetics & Genomic Medicine · 1
Prenatal diagnosis and molecular cytogenetic analysis of Xp22.31 microdeletions and microduplications in Chinese populations
2026 · Jianlong Zhuang, Wanyu Fu, et al. · BMC Pregnancy and Childbirth
First clinical and molecular characterization of two rare complex β-globin variants in Chinese population using third generation sequencing
2026 · Lixian Zhang, Jianlong Zhuang, et al. · Annals of Hematology
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Identification of Two Novel Variants in CRYGD and OCRL Genes in the Chinese Population With Hereditary Congenital Cataracts Using Whole Exome Sequencing
2026 · Jianlong Zhuang, Nan Huang, et al. · Human Mutation
[A case of neonatal Cornelia de Lange syndrome caused by a novel variant of SMC1A gene].
2021 · Yanqing Li, Yuanbai Wang, et al. · PubMed
Additional file 1 of Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, China
2021 · Jianlong Zhuang, Chunnuan Chen, et al. · Figshare
A familial case of Syndactyly type IV due to a novel duplication of ~222.23 kb covering exons 2-17 of the LMBR1 gene: a case report
2018 · Lijing Shi, Hui Huang, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Works count: 18
Citation count: 76
H-index: 5
I10-index: 3
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