BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Lin Y, Lan Y, Wan L, Huang C, Lin C, Hsueh K, Chen D, Lin T, Tsai F. The NBS1 Genetic Polymorphisms and the Risk of the Systemic Lupus Erythematosus in Taiwanese Patients. J Clin Immunol 2010;30:643-8. [DOI: 10.1007/s10875-010-9427-0] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
Number Citing Articles
1 Babushkina NP, Postrigan AE, Kucher AN. Involvement of Variants in the Genes Encoding BRCA1-Associated Genome Surveillance Complex (BASC) in the Development of Human Common Diseases. Mol Biol 2021;55:278-96. [DOI: 10.1134/s0026893321020047] [Reference Citation Analysis]
2 Li X, Li Z, Yang M, Luo Y, Hu L, Xiao Z, Huang A, Huang J. Two tSNPs in BRIP1 are associated with breast cancer during TDT analysis. Mol Genet Genomic Med 2021;9:e1578. [PMID: 33403820 DOI: 10.1002/mgg3.1578] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Mireles-Canales MP, González-Chávez SA, Quiñonez-Flores CM, León-López EA, Pacheco-Tena C. DNA Damage and Deficiencies in the Mechanisms of Its Repair: Implications in the Pathogenesis of Systemic Lupus Erythematosus. J Immunol Res 2018;2018:8214379. [PMID: 30116756 DOI: 10.1155/2018/8214379] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 2.8] [Reference Citation Analysis]
4 Li Y, Wu Z, Zhang S, Chen S, Li P, Li J, Cao C, Liu B, Zhang F, Li Y. Genetic Variants of IκB Kinase β (IKBKB) and Polymerase β (POLB) Were Not Associated with Systemic Lupus Erythematosus Risk in a Chinese Han Population. PLoS One 2015;10:e0132556. [PMID: 26167925 DOI: 10.1371/journal.pone.0132556] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
5 Smetsers S, Muter J, Bristow C, Patel L, Chandler K, Bonney D, Wynn RF, Whetton AD, Will AM, Rockx D, Joenje H, Strathdee G, Shanks J, Klopocki E, Gille JJP, Dorsman J, Meyer S. Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminoma. Familial Cancer 2012;11:661-5. [DOI: 10.1007/s10689-012-9553-3] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 1.5] [Reference Citation Analysis]