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Cited by in F6Publishing
For: Moe Lee S, Ran Ju Y, Choi BY, Wook Hyeon J, Sun Park J, Kyeong Kim C, Yeon Kim S. Genotype patterns and characteristics of PRNP in the Korean population. Prion 2012;6:375-82. [PMID: 22561193 DOI: 10.4161/pri.20195] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 0.8] [Reference Citation Analysis]
Number Citing Articles
1 Bagyinszky E, Kang MJ, Pyun J, Giau VV, An SSA, Kim S. Early-onset Alzheimer's disease patient with prion (PRNP) p.Val180Ile mutation. Neuropsychiatr Dis Treat 2019;15:2003-13. [PMID: 31410005 DOI: 10.2147/NDT.S215277] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
2 Wang J, Xiao K, Zhou W, Shi Q, Dong XP. Analysis of 12 Chinese Patients with Proline-to-Leucine Mutation at Codon 102-Associated Gerstmann-Sträussler-Scheinker Disease. J Clin Neurol 2019;15:184-90. [PMID: 30877692 DOI: 10.3988/jcn.2019.15.2.184] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
3 Takada LT, Kim M, Metcalf S, Gala II, Geschwind MD. Prion disease. Neurogenetics, Part II. Elsevier; 2018. pp. 441-64. [DOI: 10.1016/b978-0-444-64076-5.00029-6] [Cited by in Crossref: 18] [Cited by in F6Publishing: 6] [Article Influence: 4.5] [Reference Citation Analysis]
4 Lee SM, Chung M, Hyeon JW, Jeong SW, Ju YR, Kim H, Lee J, Kim S, An SS, Cho SB, Lee YS, Kim SY. Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders. PLoS One 2016;11:e0157540. [PMID: 27341347 DOI: 10.1371/journal.pone.0157540] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
5 Chen C, Dong XP. Epidemiological characteristics of human prion diseases. Infect Dis Poverty 2016;5:47. [PMID: 27251305 DOI: 10.1186/s40249-016-0143-8] [Cited by in Crossref: 82] [Cited by in F6Publishing: 89] [Article Influence: 13.7] [Reference Citation Analysis]
6 Shi Q, Shen XJ, Zhou W, Xiao K, Zhang XM, Zhang BY, Dong XP. Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease. Prion 2014;8:411-4. [PMID: 25482600 DOI: 10.4161/19336896.2014.967040] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
7 Shi Q, Shen X, Zhou W, Xiao K, Zhang X, Zhang B, Dong X. Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jacob disease. prion 2014;8. [DOI: 10.4161/pri.32080] [Reference Citation Analysis]
8 Jeong BH, Kim YS. Genetic studies in human prion diseases. J Korean Med Sci 2014;29:623-32. [PMID: 24851016 DOI: 10.3346/jkms.2014.29.5.623] [Cited by in Crossref: 64] [Cited by in F6Publishing: 66] [Article Influence: 8.0] [Reference Citation Analysis]
9 Lloyd SE, Mead S, Collinge J. Genetics of prion diseases. Curr Opin Genet Dev 2013;23:345-51. [PMID: 23518043 DOI: 10.1016/j.gde.2013.02.012] [Cited by in Crossref: 55] [Cited by in F6Publishing: 58] [Article Influence: 6.1] [Reference Citation Analysis]