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For: Roszak A, Lianeri M, Jagodzinski PP. Involvement of the XRCC1 Arg399Gln gene polymorphism in the development of cervical carcinoma. Int J Biol Markers 2011;26:216-20. [PMID: 21928248 DOI: 10.5301/JBM.2011.8581] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 1.5] [Reference Citation Analysis]
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1 Das AP, Saini S, Tyagi S, Chaudhary N, Agarwal SM. Elucidation of Increased Cervical Cancer Risk Due to Polymorphisms in XRCC1 (R399Q and R194W), ERCC5 (D1104H), and NQO1 (P187S). Reprod Sci 2022. [PMID: 36195778 DOI: 10.1007/s43032-022-01096-6] [Reference Citation Analysis]
2 Shao X, Yang X, Liu Y, Song Q, Pan X, Chen W, Jiang W, Xu D, Song Y, Chen R. Genetic polymorphisms in DNA repair genes and their association with risk of cervical cancer: A systematic review and meta-analysis. J Obstet Gynaecol Res 2022. [PMID: 35732591 DOI: 10.1111/jog.15325] [Reference Citation Analysis]
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4 Zhao S, Tadesse S, Kidane D. Significance of base excision repair to human health. Int Rev Cell Mol Biol 2021;364:163-93. [PMID: 34507783 DOI: 10.1016/bs.ircmb.2021.05.002] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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8 Lin WY, Lee CC, Liu HP, Chou IC, Sheu JJ, Wan L, Lin YJ, Tsai Y, Tsai FJ. Association of genetic variations in X-ray repair cross-complementing group 1 and Tourette syndrome. J Clin Lab Anal 2012;26:321-4. [PMID: 23001975 DOI: 10.1002/jcla.21525] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
9 Li Y, Liu F, Tan SQ, Wang Y, Li SW. X-ray repair cross-complementing group 1 (XRCC1) genetic polymorphisms and cervical cancer risk: a huge systematic review and meta-analysis. PLoS One 2012;7:e44441. [PMID: 22984511 DOI: 10.1371/journal.pone.0044441] [Cited by in Crossref: 25] [Cited by in F6Publishing: 30] [Article Influence: 2.3] [Reference Citation Analysis]
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