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Cited by in F6Publishing
For: Guo W, Zhu X, Yan L, Qiao J. The present and future of whole-exome sequencing in studying and treating human reproductive disorders. Journal of Genetics and Genomics 2018;45:517-25. [DOI: 10.1016/j.jgg.2018.08.004] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
1 Deng Y, Ou Z, Li R, Chen Z, Liang P, Sun L. Affected-embryo-based SNP haplotyping with NGS for the preimplantation genetic testing of Marfan syndrome. Syst Biol Reprod Med 2021;67:298-306. [PMID: 34053377 DOI: 10.1080/19396368.2021.1926574] [Reference Citation Analysis]
2 Liu F, Zhao Y, Beier S, Jiang Y, Thorwarth P, H Longin CF, Ganal M, Himmelbach A, Reif JC, Schulthess AW. Exome association analysis sheds light onto leaf rust (Puccinia triticina) resistance genes currently used in wheat breeding (Triticum aestivum L.). Plant Biotechnol J 2020;18:1396-408. [PMID: 31782598 DOI: 10.1111/pbi.13303] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
3 Luo H, Chen C, Yang Y, Zhang Y, Yuan Y, Wang W, Wu R, Peng Z, Han Y, Jiang L, Yao R, An X, Zhang W, Le Y, Xiang J, Yi N, Huang H, Li W, Zhang Y, Sun J. Preimplantation genetic testing for a family with usher syndrome through targeted sequencing and haplotype analysis. BMC Med Genomics 2019;12:157. [PMID: 31699113 DOI: 10.1186/s12920-019-0600-x] [Reference Citation Analysis]
4 Qin M, Zhu X, Zhang Z, Li X, Yan Z, Wang Y, Guan S, He Y, Zhang W, Yan L, Qiao J, Zhi X. Genetic analysis and preimplantation genetic diagnosis of Chinese Marfan syndrome patients. J Genet Genomics 2019;46:319-23. [PMID: 31279624 DOI: 10.1016/j.jgg.2019.04.003] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
5 Guo W, Lai Y, Yan Z, Wang Y, Nie Y, Guan S, Kuo Y, Zhang W, Zhu X, Peng M, Zhi X, Wei Y, Yan L, Qiao J. Trio-whole-exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations. Hum Mutat 2020;41:432-48. [PMID: 31680349 DOI: 10.1002/humu.23935] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
6 Guo W, Nie Y, Yan Z, Zhu X, Wang Y, Guan S, Kuo Y, Zhang W, Zhi X, Wei Y, Yan L, Qiao J. Genetic testing and PGD for unexplained recurrent fetal malformations with MAGEL2 gene mutation. Sci China Life Sci 2019;62:886-94. [PMID: 31152388 DOI: 10.1007/s11427-019-9541-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]