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Xingkun Yang

A Cell‐free DNA Barcode‐Enabled Single‐Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β‐Thalassemia
2019 · Xingkun Yang, Qinghua Zhou, et al. · Advanced Science · 47
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Integrated miRNA‐mRNA Expression Profiles Revealing Key Molecules in Ovarian Cancer Based on Bioinformatics Analysis
2021 · Chao Li, Zhantong Hong, et al. · BioMed Research International · 12
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High-throughput primer design by scoring in piecewise logistic model for multiple polymerase chain reaction variants
2022 · Huaping Zeng, Kexin Chen, et al. · Scientific Reports · 3
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Mosaic tetrasomy 9p detected by CNV-seq but missed by traditional karyotyping in a prenatal case without dysmorphic features
2025 · Xingkun Yang, Yasi Zhou, et al. · Molecular Cytogenetics · 2
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Case Report: Genetic Analysis of a Small Supernumerary Marker Chromosome in a Unique Case of Mosaic Turner Syndrome
2022 · Chao Li, Weiyao Luo, et al. · Frontiers in Pediatrics · 2
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Case Report: A Novel Compound Heterozygous Mutation of the FRMD4A Gene Identified in a Chinese Family With Global Developmental Delay, Intellectual Disability, and Ataxia
2021 · Yuhua Pan, Xiaoling Guo, et al. · Frontiers in Pediatrics · 2
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Detection of Rare Thalassemia Variants Using Accurate Circular Consensus Long‐Read Sequencing
2026 · Xiaoqiang Zhou, Yue Chen, et al. · Human Mutation · 1
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A Rare Case of Bardet-Biedl Syndrome Caused by a Heterozygous Point Variant in BBS7 and a CNV Involved BBS7
2025 · Xingkun Yang, Xiaoqiang Zhou, et al. · Molecular Syndromology · 1
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[Noninvasive prenatal genetic testing in 6804 pregnant women aged less than 35 years with positive results in serum screening].
2019 · Xingkun Yang, Xiaoling Guo, et al. · PubMed · 1
Study on the value of thromboelastography in the assessment of thrombosis risk in perinatal women
2025 · Wei Liu, Jieqing Zhang, et al.
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A missense variant in the SOX5 gene (c.221C > T) is associated with intellectual disability
2025 · Xiujuan Yang, Xiujuan Yang, et al. · Orphanet Journal of Rare Diseases
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Case Report: Novel CNGA3 compound heterozygous variants cause achromatopsia in three patients from a family
2024 · Xiaoqiang Zhou, Yasi Zhou, et al. · Frontiers in Genetics
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A Missense Mutation in the SOX5 Gene (c.221C>T) Causes Mental Retardation in a Chinese Family
2023 · Yang Xiujuan, Gan Zhongzhi, et al. · SSRN Electronic Journal
Application of high-throughput sequencing in noninvasive detection of fetal chromosome aneuploidies
2015 · Jin Zhong, Xingkun Yang, et al. · Int J Genet
Works count: 14
Citation count: 71
H-index: 3
I10-index: 2
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