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Yilun Tao

Observed names: Y.-L. Tao, Yi-Lun Tao, 陶逸伦
Institution: Changzhi University
ORCID: 0000-0002-8787-9622
Observed ORCID: 0000-0002-8787-9622
OpenAlex ID: A5066260530
Cloning, expression, and characterization of the β-glucosidase hydrolyzing secoisolariciresinol diglucoside to secoisolariciresinol from Bacteroides uniformis ZL1
2013 · Y.-L. Tao, D.-H. Yang, et al. · Applied Microbiology and Biotechnology · 29
Biotransformation of the SDG in defatted flaxseed into END co-cultured by three single bacterial colonies
2013 · Hong-Yun Zhu, Miao-Xin Li, et al. · Process Biochemistry · 12
Combining Z-Score and Maternal Copy Number Variation Analysis Increases the Positive Rate and Accuracy in Non-Invasive Prenatal Testing
2022 · Liheng Chen, Lihong Wang, et al. · Frontiers in Genetics · 11
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Spectrum of PAH gene mutations and genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Shanxi province
2020 · Yilun Tao, Dong Han, et al. · Brain and Development · 10
A GATA3 gene mutation that causes incorrect splicing and HDR syndrome: a case study and literature review
2023 · Yilun Tao, Lin Yang, et al. · Frontiers in Genetics · 9
Novel JAG1 variants leading to Alagille syndrome in two Chinese cases
2024 · Xiufang Feng, Jiangyuan Ping, et al. · Scientific Reports · 7
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Case Report: Complete Maternal Uniparental Disomy of Chromosome 2 With a Novel UNC80 Splicing Variant c.5609-4G> A in a Chinese Patient With Infantile Hypotonia With Psychomotor Retardation and Characteristic Facies 2
2021 · Yilun Tao, Dong Han, et al. · Frontiers in Genetics · 7
Identification of a novel homozygous nonsense variant in a Chinese patient with ethylmalonic encephalopathy and a genotype-phenotype spectrum review
2020 · Yilun Tao, Dong Han, et al. · Clinica Chimica Acta · 5
Newborn screening for inherited metabolic disorders in central China: a retrospective study of 153,956 infants using non-derivatized tandem mass spectrometry
2025 · Dong Han, Yilun Tao, et al. · Scientific Reports · 3
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Novel HPD mutation p. A244V compound with p. T219M causing tyrosinemia type III in a Chinese girl and review of the genotype–phenotype spectrum
2023 · Dong Han, Lihong Wang, et al. · Molecular Genetics & Genomic Medicine · 3
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Typical pantothenate kinase-associated neurodegeneration caused by compound heterozygous mutations in PANK2 gene in a Chinese patient: a case report and literature review
2023 · Yilun Tao, Chen Zhao, et al. · Frontiers in Neurology · 3
A retrospective analysis of 6942 amniocentesis cases
2025 · Qingsha An, Yuxiao Huang, et al. · BMC Pregnancy and Childbirth · 2
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Uncovering genetic contributors to developmental delay and intellectual disability: a focus on CNVs in pediatric patients
2025 · Yilun Tao, Hongzhi Guo, et al. · Frontiers in Genetics · 2
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Novel GJB2 mutation c.188delT compound with c.235delC causing non-syndromic hearing loss in a Chinese family: A case report
2024 · Yilun Tao, Zhipeng Hu, et al. · Medicine · 1
Clinical utility of chromosomal microarray analysis for genetic diagnosis in 708 cases of spontaneous abortion tissues
2026 · Yuxiao Huang, Qingsha An, et al. · BMC Pregnancy and Childbirth
Prenatal SNP-array chromosomal microarray analysis in 3,549 pregnancies: indication-specific yields and clinical implications
2026 · Yilun Tao, Yuefeng Wei, et al. · BMC Pregnancy and Childbirth
ALPL Mutations With Dominant‐Negative Effect in Infantile Hypophosphatasia Monozygotic Twins
2026 · Luna Hao, Na Huang, et al. · Human Mutation
A P2RX2 exon-2 complex indel disrupts splicing and reduces P2X2 output: implications for DFNA41 and variable expressivity
2026 · 陶逸伦 · China National GeneBank DataBase
Novel ACAD8 variants identified in Isobutyryl-CoA dehydrogenase deficiency: challenges in phenotypic variability and management
2025 · Yilun Tao, Dong Han, et al. · Frontiers in Genetics
Identification of a novel splice site variant in the GATA3 gene in a Chinese patient with hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome, and a review of genotype-phenotype spectrum
2023 · Yilun Tao · Zenodo (CERN European Organization for Nuclear Research)
Works count: 20
Citation count: 104
H-index: 7
I10-index: 4
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