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[1]Wang W, Su L, Tan YQ, Meng L, He J, Tan C, Yi D, Cheng D, Zhang H, Lu G, Du J, Lin G, Zhang Q, Tu C.Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia[期刊]. 英国.Human Reproduction, 2023, 38 (7) : 1399-1411.
[2]Tu C, Wen J, Wang W, Zhu Q, Gou LT, Tan YQ, Chen Y, Cheng J, Li Z, Meng L, Li Y, He W, Tan C, Xie C, Fu SM, Du J, Lu G, Lin G, Gou LT.Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression[期刊]. 英国.Cell Discovery, 2023, 9 (1) : 87.
[3]Wang W, Tian S, Zhang F, Tan YQ, Nie H, Tu C, Liu C, Li Y, Li D, Yang X, Meng L, Hu T, Zhang Q, Du J, Fan L, Lu G, Lin G.CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis[期刊]. 英国.Human Molecular Genetics, 2021, 30 (23) : 2240-2254.
[4]Wang W, Tan YQ, Tu C, Nie H, Meng L, Li Y, Yuan S, Zhang Q, Du J, Wang J, Gong F, Fan L, Lu GX, Lin G.Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations[期刊]. 英国.Journal of Medical Genetics, 2019, 56 (11) : 750-757.
[5]Wang W, Meng L, Tu CF, Tan YQ, He J, Su L, Li Y, Tan C, Xu X, Nie H, Zhang H, Du J, Lu G, Luo M, Lin G.Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice[期刊]. 英国.Molecular Human Reproduction, 2022
[6]Yi S, Wang W, Tan YQ, Tu C, Zhang Q, Su L, Meng L, Li Y, Tan C, Liu Q, Zhang H, Fan L, Lu G, Hu L, Du J, Lin G.Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia[期刊]. 英国.Molecular Human Reproduction, 2024, 30 (2) : gaae002.
[7]Wang W, Dai J, Du J, Hu X, He W, Gu Y, Wan Z, Zhang Y, Luo K, Li W, Zhang Q, Gong F, Lu G, Hu L, Tan YQ, Lin G.Decade-long application of preimplantation genetic testing for DMD/BMD: analysis of five clinical strategies and embryo recombination patterns[期刊]. 德国.Human Genetics, 2025, 144 (4) : 405-416.
[8]Hu X, Wang W, Lin G, Du J, Cheng D, Gu Y, Wan Z, Dai J, Zhang Y, Luo K, Li W, Zhang Q, Gong F, Lu G, Tan YQ.Preimplantation genetic testing for facioscapulohumeral dystrophy caused by contractions of 4q35 D4Z4 repeats[期刊]. 英国.Reproductive BioMedicine Online, 2025, 51 (2) : 104879.
[9]Hu X, Wang W, Lin G, Du J, Luo K, Dai J, Zhang Y, Wan Z, He W, Zhang S, Yang L, Tan Q, Li W, Zhang Q, Gong F, Lu G, Tan YQ.Extended application of PGT-M strategies for small pathogenic CNVs[期刊]. 美国.Journal of Assisted Reproduction and Genetics, 2024, 41 (3) : 739-750.
[10]Tu C, Wang W, Tan YQ, Hu T, Lu G, Lin G.Genetic underpinnings of asthenozoospermia[期刊]. 荷兰.Best Practice & Research Clinical Endocrinology & Metabolism, 2020, 34 (6) : 101472.
[11]Wang W, He Y, Liao P.A gene polymorphism in PD-L1 promoter region is not associated with PD-L1 expression and patients' survival in gastric cancer[期刊]. 德国.Cancer Immunology, Immunotherapy, 2017, 66 (10) : 1379-1381.
[12]Li W, Wang W, Chen L, Liao P, Song K, Zhu Z, Wang K, Liu Z, Zhang W, Xie S, He Y, Mcleod HL.High levels of tumor-infiltrating lymphocytes showed better clinical outcomes in FOLFOX-treated gastric cancer patients[期刊]. 英国.Pharmacogenomics, 2020, 21 (11) : 751-759.
[13]Wang W, McLeod HL, Liu J, He Y.Prospect for immune checkpoint blockade: dynamic and comprehensive monitorings pave the way[期刊]. 英国.Pharmacogenomics, 2017, 18 (13) : 1299-1304.
[14]李永, wangweili, tanyueqiu, 谭琛, 谢春波, tuchaofeng.精子领在精子形成中的作用及功能研究进展[期刊]. 中国.中国科学:生命科学, 2024, 54 (01) : 34-45.
[15]胡也娜, wangweili, tanyueqiu, tuchaofeng, linge, 胡亮.精子表观遗传变化介导的父系代际遗传[期刊]. 中国.中华医学遗传学杂志, 2025, 42 (1) : 114-121.

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