Publications by authors named "Wanli Meng"

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Synthesis and biological activity of the marine-derived leonurine analogue N-(4-guanidinobutyl)-2-(4-hydroxyphenyl)-2-oxoacetamide.
Ning Li, Xing-Long Dai, Gui-Xin Xiong, Wan-Li Meng, Jie Hao

J Asian Nat Prod Res· November 2025

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Haplotype-Resolved Genotyping and Association Analysis of 1,020 β-Thalassemia Patients by Targeted Long-Read Sequencing.
Yuhua Ye, Chao Niu, Aiping Mao, Lang Qin, Jiahan Zhan, Wanli Meng, Yumeng Liu

Adv Sci (Weinh)· March 2025

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Targeted long-read sequencing facilitates effective carrier screening for complex monogenic diseases including spinal muscular atrophy, α-/β-thalassemia, 21-hydroxylase deficiency, and fragile-X syndrome.
Shuyuan Li, Renyi Hua, Xu Han, Yan Xu, Ming Li, Wanli Meng

J Transl Med· March 2025

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Long-read sequencing enables comprehensive molecular genetic diagnosis of Fabry disease.
Fengxia Yao, Na Hao, Danhua Li, Weimin Zhang, Jingwen Zhou, Wanli Meng

Hum Genomics· November 2024

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Evaluating the clinical efficacy of a long-read sequencing-based approach for carrier screening of spinal muscular atrophy.
Ju Long, Di Cui, Chunhui Yu, Wanli Meng

Hum Genomics· September 2024

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Design, synthesis and antibacterial activity evaluation of ebselen derivatives in NDM-1 producing bacteria.
Wanli Meng, Chenyu Liu, Guangxin Wu, Zhongyue Bai, Zhihao Wang

RSC Med Chem· June 2024

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A high-fidelity long-read sequencing-based approach enables accurate and effective genetic diagnosis of spinal muscular atrophy.
Jinli Bai, Yujin Qu, Wenchen Huang, Wanli Meng, Jiahan Zhan

Clin Chim Acta· January 2024

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Molecular characterization of a novel 83.9-kb deletion of the α-globin upstream regulatory elements by long-read sequencing.
Jianjiang Feng, Aiping Mao, Ye Lu, Haihong Shi, Wanli Meng

Blood Cells Mol Dis· November 2023

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Evaluating the clinical utility of a long-read sequencing-based approach in genetic testing of fragile-X syndrome.
Fei Hou, Aiping Mao, Shan Shan, Yan Li, Wanli Meng

Clin Chim Acta· November 2023

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The comprehensive analysis of thalassemia alleles (CATSA) based on single-molecule real-time technology (SMRT) is a more powerful strategy in the diagnosis of thalassemia caused by rare variants.
Jianjiang Feng, Di Cui, Caipeng Li, Yingsong Yang, Qiuli Li, Wanli Meng

Clin Chim Acta· November 2023

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Identification of a novel 10.3 kb deletion causing α-thalassemia by third-generation sequencing: Pedigree analysis and genetic diagnosis.
Runhong Xu, Hui Li, Song Yi, Jun Du, Jianguo Jin, Wanli Meng

Clin Biochem· March 2023

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Case report: Long-read sequencing identified a novel 14.9-kb deletion of the α-globin gene locus in a family with α-thalassemia in China.
Yan Yuan, Xia Zhou, Jing Deng, Qun Zhu, Zanping Peng, Wanli Meng

Front Genet· March 2023

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Comprehensive Analysis of Fragile X Syndrome: Full Characterization of the FMR1 Locus by Long-Read Sequencing.
Qiaowei Liang, Yingdi Liu, Yaning Liu, Ranhui Duan, Wanli Meng

Clin Chem· December 2022

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Knocking out Analysis of the CpxP gene using Crispr/Cas9 in Escherichia coli MG1655.
Xiaoliang He, Yuwen Ren, Wanli Meng, Xinran Yu, Xiaohui Zhou

AMB Express· September 2020

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