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For: 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]
Number Citing Articles
1 Kim YC, Jeong BH. Transcriptomic analysis identifies novel potential biomarkers and highlights cilium-related biological processes in the early stages of prion disease in mice. Prion 2022;16:84-90. [PMID: 35786398 DOI: 10.1080/19336896.2022.2095186] [Reference Citation Analysis]
2 Zanusso G, Colaizzo E, Poleggi A, Masullo C, Romeo R, Ferrari S, Bongianni M, Fiorini M, Tiple D, Vaianella L, Sbriccoli M, Porreca F, Equestre M, Pocchiari M, Cardone F, Ladogana A. Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene. IJMS 2022;23:10210. [DOI: 10.3390/ijms231810210] [Reference Citation Analysis]
3 Kim YC, Jeong BH. Creutzfeldt-Jakob Disease Incidence, South Korea, 2001-2019. Emerg Infect Dis 2022;28:1863-6. [PMID: 35997603 DOI: 10.3201/eid2809.212050] [Reference Citation Analysis]
4 Menendez L, Milo R, Cohen OS, Chapman J, Rosenmann H, Nitsan Z, Kahana E, Appel S. Genetic Creutzfeldt-Jakob disease in Turkish Jews-demographic and clinical features. Acta Neurol Scand 2022. [PMID: 35974683 DOI: 10.1111/ane.13684] [Reference Citation Analysis]
5 Chen EH, Kao HW, Lee CH, Huang JYC, Wu KP, Chen RP. 2.2 Å Cryo-EM Tetra-Protofilament Structure of the Hamster Prion 108-144 Fibril Reveals an Ordered Water Channel in the Center. J Am Chem Soc 2022. [PMID: 35857020 DOI: 10.1021/jacs.2c05479] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Won S, Kim Y, Lee Y, Park C, Kim W, Jeong B. The First Evaluation of Proteinase K-Resistant Prion Protein (PrPSc) in Korean Appendix Specimens. Medicina 2022;58:947. [DOI: 10.3390/medicina58070947] [Reference Citation Analysis]
7 Kim KH, Kim Y, Jeong B. Novel Polymorphisms and Genetic Characteristics of the Prion Protein Gene in Pheasants. Front Vet Sci 2022;9:935476. [DOI: 10.3389/fvets.2022.935476] [Reference Citation Analysis]
8 Xiao K, Pang MF, Zhao YQ, Gao LP, Wu YZ, Wang Y, Shi Q, Dong XP. Difference of geographic distributions of the Chinese patients with prion diseases in the permanent resident places and referring places. Prion 2022;16:58-65. [PMID: 35638100 DOI: 10.1080/19336896.2022.2080921] [Reference Citation Analysis]
9 Kim Y, Kim Y, Jeong B. Novel Single Nucleotide Polymorphisms (SNPs) and Genetic Features of the Prion Protein Gene (PRNP) in Quail (Coturnix japonica). Front Vet Sci 2022;9:870735. [DOI: 10.3389/fvets.2022.870735] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Guo Y, Xu Y, Lin X, Zhen Z, Yi F, Guan H, Shi Q, Sun W, Yang A, Dong X, Wang J. Creutzfeldt-Jakob Disease: Alterations of Gut Microbiota. Front Neurol 2022;13:832599. [DOI: 10.3389/fneur.2022.832599] [Reference Citation Analysis]
11 Yerukala Sathipati S, Tsai MJ, Shukla SK, Ho SY, Liu Y, Beheshti A. MicroRNA signature for estimating the survival time in patients with bladder urothelial carcinoma. Sci Rep 2022;12:4141. [PMID: 35264666 DOI: 10.1038/s41598-022-08082-7] [Reference Citation Analysis]
12 Roh I, Kim Y, Won S, Park K, Park H, Hwang J, Kang H, Sohn H, Jeong B. Association Study of the M132L Single Nucleotide Polymorphism With Susceptibility to Chronic Wasting Disease in Korean Elk: A Meta-Analysis. Front Vet Sci 2022;8:804325. [DOI: 10.3389/fvets.2021.804325] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
13 Shi Q, Xiao K, Chen C, Zhou W, Gao LP, Wu YZ, Wang Y, Hu C, Gao C, Dong XP. Characteristics of Chinese patients with genetic CJD who have E196A or E196K mutation in PRNP: comparative analysis of patients identified in the Chinese National CJD Surveillance System. BMJ Open 2021;11:e054551. [PMID: 34782343 DOI: 10.1136/bmjopen-2021-054551] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Kim YC, Jeong BH. The First Meta-Analysis of the M129V Single-Nucleotide Polymorphism (SNP) of the Prion Protein Gene (PRNP) with Sporadic Creutzfeldt-Jakob Disease. Cells 2021;10:3132. [PMID: 34831353 DOI: 10.3390/cells10113132] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
15 Roh IS, Kim YC, Kim HJ, Won SY, Jeong MJ, Hwang JY, Kang HE, Sohn HJ, Jeong BH. Polymorphisms of the prion-related protein gene are strongly associated with cervids' susceptibility to chronic wasting disease. Vet Rec 2021;:e940. [PMID: 34562285 DOI: 10.1002/vetr.940] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
16 Lu H, Jing D, Chen Y, Cui C, Gao R, Wang L, Liang Z, Chen K, Wu L. Metabolic Changes Detected by 18F-FDG PET in the Preclinical Stage of Familial Creutzfeldt-Jakob Disease. J Alzheimers Dis 2020;77:1513-21. [PMID: 32925055 DOI: 10.3233/JAD-200576] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Shi Q, Chen C, Xiao K, Zhou W, Gao LP, Chen DD, Wu YZ, Wang Y, Hu C, Gao C, Dong XP. Genetic Prion Disease: Insight from the Features and Experience of China National Surveillance for Creutzfeldt-Jakob Disease. Neurosci Bull 2021;37:1570-82. [PMID: 34487324 DOI: 10.1007/s12264-021-00764-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Kim YC, Park KJ, Hwang JY, Park HC, Kang HE, Sohn HJ, Jeong BH. In-depth examination of PrPSc in Holstein cattle carrying the E211K somatic mutation of the bovine prion protein gene (PRNP). Transbound Emerg Dis 2021. [PMID: 34470082 DOI: 10.1111/tbed.14309] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
19 Halder P, Mitra P. Human prion protein: exploring the thermodynamic stability and structural dynamics of its pathogenic mutants. J Biomol Struct Dyn 2021;:1-17. [PMID: 34338141 DOI: 10.1080/07391102.2021.1957715] [Reference Citation Analysis]
20 Kim YC, Lee J, Lee DW, Jeong BH. Large-scale lipidomic profiling identifies novel potential biomarkers for prion diseases and highlights lipid raft-related pathways. Vet Res 2021;52:105. [PMID: 34289911 DOI: 10.1186/s13567-021-00975-1] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
21 Chen EH, Lin KM, Sang JC, Ho MR, Lee CH, Shih O, Su CJ, Yeh YQ, Jeng US, Chen RP. Condition-dependent structural collapse in the intrinsically disordered N-terminal domain of prion protein. IUBMB Life 2021. [PMID: 34288372 DOI: 10.1002/iub.2528] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Shi Q, Shen XJ, Gao LP, Xiao K, Zhou W, Wang Y, Chen C, Dong XP. A Chinese patient with the clinical features of Parkinson's disease contains a single copy of octarepeat deletion in PRNP case report. Prion 2021;15:121-5. [PMID: 34224312 DOI: 10.1080/19336896.2021.1946376] [Reference Citation Analysis]
23 Jing D, Chen Y, Xie K, Cui Y, Cui C, Liu L, Lu H, Ye J, Gao R, Wang L, Liang Z, Zhang Z, Wu L. White Matter Integrity Involvement in the Preclinical Stage of Familial Creutzfeldt-Jakob Disease: A Diffusion Tensor Imaging Study. Front Aging Neurosci 2021;13:655667. [PMID: 34093166 DOI: 10.3389/fnagi.2021.655667] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Watson N, Brandel JP, Green A, Hermann P, Ladogana A, Lindsay T, Mackenzie J, Pocchiari M, Smith C, Zerr I, Pal S. The importance of ongoing international surveillance for Creutzfeldt-Jakob disease. Nat Rev Neurol 2021;17:362-79. [PMID: 33972773 DOI: 10.1038/s41582-021-00488-7] [Cited by in Crossref: 27] [Cited by in F6Publishing: 31] [Article Influence: 27.0] [Reference Citation Analysis]
25 Won SY, Kim YC, Jeong BH. Evaluation of proteinase K-resistant prion protein (PrPres) in Korean native black goats carrying a potential scrapie-susceptible haplotype of the prion protein gene (PRNP). Acta Vet Hung 2021;69:88-93. [PMID: 33844641 DOI: 10.1556/004.2021.00009] [Reference Citation Analysis]
26 Kim YC, Won SY, Jeong MJ, Jeong BH. Absence of proteinase K-resistant PrP in Korean Holstein cattle carrying potential bovine spongiform encephalopathy-related E211K somatic mutation. Transbound Emerg Dis 2021. [PMID: 33660931 DOI: 10.1111/tbed.14053] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 7.0] [Reference Citation Analysis]
27 Jeong MJ, Kim YC, Jeong BH. The First Report of the Prion Protein Gene (PRNP) Sequence in Pekin Ducks (Anas platyrhynchos domestica): The Potential Prion Disease Susceptibility in Ducks. Genes (Basel) 2021;12:193. [PMID: 33525657 DOI: 10.3390/genes12020193] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
28 Kim HH, Kim YC, Kim K, Kim AD, Jeong BH. Novel Polymorphisms and Genetic Features of the Prion Protein Gene (PRNP) in Cats, Hosts of Feline Spongiform Encephalopathy. Genes (Basel) 2020;12:E13. [PMID: 33374431 DOI: 10.3390/genes12010013] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
29 Xiao K, Zhou W, Gao LP, Wu YZ, Wang Y, Chen C, Gao C, Shi Q, Dong XP. Clinical and Laboratory Features of Three Rare Chinese V210I gCJD Patients. Pathogens 2020;9:E800. [PMID: 32998248 DOI: 10.3390/pathogens9100800] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
30 Roh IS, Kim YC, Kim HJ, Won SY, Jeong MJ, Kang HE, Sohn HJ, Jeong BH. Identification of the prion-related protein gene (PRNT) sequences in various species of the Cervidae family. Mol Biol Rep 2020;47:6155-64. [PMID: 32737828 DOI: 10.1007/s11033-020-05697-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
31 Kim YC, Won SY, Jeong BH. Identification of Prion Disease-Related Somatic Mutations in the Prion Protein Gene (PRNP) in Cancer Patients. Cells 2020;9:E1480. [PMID: 32560489 DOI: 10.3390/cells9061480] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
32 Won SY, Kim YC, Jeong BH. First Report of the Potential Bovine Spongiform Encephalopathy (BSE)-Related Somatic Mutation E211K of the Prion Protein Gene (PRNP) in Cattle. Int J Mol Sci 2020;21:E4246. [PMID: 32549191 DOI: 10.3390/ijms21124246] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
33 Kim DJ, Kim YC, Kim AD, Jeong BH. Novel Polymorphisms and Genetic Characteristics of the Prion Protein Gene (PRNP) in Dogs-A Resistant Animal of Prion Disease. Int J Mol Sci 2020;21:E4160. [PMID: 32532135 DOI: 10.3390/ijms21114160] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
34 Wu X, Cui Z, Guomin X, Wang H, Zhang X, Li Z, Sun Q, Qi F. Rare genetic E196A mutation in a patient with Creutzfeldt-Jakob disease: a case report and literature. Prion 2020;14:143-8. [PMID: 32501129 DOI: 10.1080/19336896.2020.1769528] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
35 Kim YC, Won SY, Do K, Jeong BH. Identification of the novel polymorphisms and potential genetic features of the prion protein gene (PRNP) in horses, a prion disease-resistant animal. Sci Rep 2020;10:8926. [PMID: 32488112 DOI: 10.1038/s41598-020-65731-5] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
36 Won SY, Kim YC, Do K, Jeong BH. Absence of Strong Genetic Linkage Disequilibrium between Single Nucleotide Polymorphisms (SNPs) in the Prion Protein Gene (PRNP) and the Prion-Like Protein Gene (PRND) in the Horse, a Prion-Resistant Species. Genes (Basel) 2020;11:E518. [PMID: 32392732 DOI: 10.3390/genes11050518] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
37 Zhang M, Zhang H, Yao H, Guo C, Lin D. Biophysical characterization of oligomerization and fibrillization of the G131V pathogenic mutant of human prion protein. Acta Biochim Biophys Sin (Shanghai) 2019;51:1223-32. [PMID: 31735962 DOI: 10.1093/abbs/gmz124] [Reference Citation Analysis]
38 Kim YC, Won SY, Jeong BH. Absence of single nucleotide polymorphisms (SNPs) in the open reading frame (ORF) of the prion protein gene (PRNP) in a large sampling of various chicken breeds. BMC Genomics 2019;20:922. [PMID: 31795947 DOI: 10.1186/s12864-019-6315-8] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
39 Kim YC, Kim SK, Jeong BH. Scrapie susceptibility-associated indel polymorphism of shadow of prion protein gene (SPRN) in Korean native black goats. Sci Rep 2019;9:15261. [PMID: 31649311 DOI: 10.1038/s41598-019-51625-8] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 6.3] [Reference Citation Analysis]
40 Chen C, Hu C, Shi Q, Zhou W, Xiao K, Wang Y, Liu L, Chen J, Xia Y, Dong XP. Profiles of 14-3-3 and Total Tau in CSF Samples of Chinese Patients of Different Genetic Prion Diseases. Front Neurosci 2019;13:934. [PMID: 31551692 DOI: 10.3389/fnins.2019.00934] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
41 Chandrasekaran P, Santosh Kumar C, Rangachari K, Sekar K. Disassociation of β1-α1-β2 from the α2-α3 domain of prion protein (PrP) is a prerequisite for the conformational conversion of PrPC into PrPSc: Driven by the free energy landscape. International Journal of Biological Macromolecules 2019;136:368-76. [DOI: 10.1016/j.ijbiomac.2019.06.099] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
42 Dai Y, Lang Y, Ding M, Zhang B, Han X, Duan G, Cui L. Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report. Prion 2019;13:132-6. [PMID: 31238786 DOI: 10.1080/19336896.2019.1631679] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
43 Jeong MJ, Jeong BH. No polymorphisms in the coding region of the prion-like protein gene in Thoroughbred racehorses. Acta Vet Hung 2019;67:174-82. [PMID: 31238729 DOI: 10.1556/004.2019.019] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
44 Won SY, Kim YC, Kim K, Kim AD, Jeong BH. The First Report of Polymorphisms and Genetic Features of the prion-like Protein Gene (PRND) in a Prion Disease-Resistant Animal, Dog. Int J Mol Sci 2019;20:E1404. [PMID: 30897750 DOI: 10.3390/ijms20061404] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 6.3] [Reference Citation Analysis]
45 Xiao K, Shi Q, Zhou W, Zhang BY, Wang Y, Chen C, Ma Y, Gao C, Dong XP. T188K-Familial Creutzfeldt-Jacob Disease, Predominant Among Chinese, has a Reactive Pattern in CSF RT-QuIC Different from D178N-Fatal Familial Insomnia and E200K-Familial CJD. Neurosci Bull 2019;35:519-21. [PMID: 30838505 DOI: 10.1007/s12264-019-00354-z] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 3.0] [Reference Citation Analysis]
46 Jeong MJ, Kim YC, Jeong BH. Prion-like protein gene (PRND) polymorphisms associated with scrapie susceptibility in Korean native black goats. PLoS One 2018;13:e0206209. [PMID: 30359416 DOI: 10.1371/journal.pone.0206209] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis]
47 Ladogana A, Kovacs GG. Genetic Creutzfeldt-Jakob disease. Handb Clin Neurol 2018;153:219-42. [PMID: 29887139 DOI: 10.1016/B978-0-444-63945-5.00013-1] [Cited by in Crossref: 25] [Cited by in F6Publishing: 10] [Article Influence: 6.3] [Reference Citation Analysis]
48 Kim YC, Jeong BH. The first report of polymorphisms and genetic characteristics of the prion protein gene (PRNP) in horses. Prion 2018;12:245-52. [PMID: 30165784 DOI: 10.1080/19336896.2018.1513316] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
49 Zheng Z, Zhang M, Wang Y, Ma R, Guo C, Feng L, Wu J, Yao H, Lin D. Structural basis for the complete resistance of the human prion protein mutant G127V to prion disease. Sci Rep 2018;8:13211. [PMID: 30181558 DOI: 10.1038/s41598-018-31394-6] [Cited by in Crossref: 23] [Cited by in F6Publishing: 24] [Article Influence: 5.8] [Reference Citation Analysis]
50 Kim YC, Jeong MJ, Jeong BH. The first report of genetic variations in the chicken prion protein gene. Prion 2018;12:197-203. [PMID: 29966485 DOI: 10.1080/19336896.2018.1471922] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 4.0] [Reference Citation Analysis]
51 Kim Y, Jeong B. Bovine spongiform encephalopathy (BSE) associated polymorphisms of the prion-like protein gene (PRND) in Korean dairy cattle and Hanwoo. Journal of Dairy Research 2018;85:7-11. [DOI: 10.1017/s0022029917000814] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
52 Ito Y, Sanjo N, Hizume M, Kobayashi A, Ohgami T, Satoh K, Hamaguchi T, Yamada M, Kitamoto T, Mizusawa H, Yokota T. Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene. Biochem Biophys Res Commun 2018;496:1055-61. [PMID: 29382530 DOI: 10.1016/j.bbrc.2018.01.119] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
53 Gao C, Shi Q, Wei J, Zhou W, Xiao K, Wang J, Shi Q, Dong XP. The associations of two SNPs in miRNA-146a and one SNP in ZBTB38-RASA2 with the disease susceptibility and the clinical features of the Chinese patients of sCJD and FFI. Prion 2018;12:34-41. [PMID: 29216791 DOI: 10.1080/19336896.2017.1405885] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
54 De Souza RKM, Josviak ND, Batistela MS, Santos PSF, Landemberger MC, Ramina R. First case of V180I rare mutation in a Brazilian patient with Creutzfeldt-Jakob disease. Prion 2017;11:465-8. [PMID: 29095671 DOI: 10.1080/19336896.2017.1397869] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
55 Shi Q, Zhou W, Chen C, Zhang BY, Xiao K, Wang Y, Dong XP. Rare E196A mutation in PRNP gene of 3 Chinese patients with Creutzfeldt-Jacob disease. Prion 2016;10:331-7. [PMID: 27310471 DOI: 10.1080/19336896.2016.1190897] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 1.8] [Reference Citation Analysis]
56 Elezgarai SR, Fernández-Borges N, Eraña H, Sevillano AM, Charco JM, Harrathi C, Saá P, Gil D, Kong Q, Requena JR, Andréoletti O, Castilla J. Generation of a new infectious recombinant prion: a model to understand Gerstmann-Sträussler-Scheinker syndrome. Sci Rep 2017;7:9584. [PMID: 28851967 DOI: 10.1038/s41598-017-09489-3] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 1.8] [Reference Citation Analysis]
57 Puligheddu M, Congiu P, Laccu I, Figorilli M, Gioi G, Polizzi L, Pisanu P, Marrosu F, Provini F. Overlap Parasomnia Disorder in a case of Creutzfeldt-Jakob Disease. Sleep Medicine 2017;36:75-7. [DOI: 10.1016/j.sleep.2017.05.014] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 1.8] [Reference Citation Analysis]
58 Cistaro A, Cassalia L, Ferrara C, Atzori C, Vai D, Quartuccio N, Fania P, Vaudano GP, Imperiale D. Brain 18F-FDG PET/CT findings in a case of genetic Creutzfeldt–Jakob disease due to V203I heterozygous mutation in the PRNP gene. J Neurol 2017;264:170-3. [DOI: 10.1007/s00415-016-8327-5] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
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60 Schmitz M, Dittmar K, Llorens F, Gelpi E, Ferrer I, Schulz-Schaeffer WJ, Zerr I. Hereditary Human Prion Diseases: an Update. Mol Neurobiol 2017;54:4138-49. [PMID: 27324792 DOI: 10.1007/s12035-016-9918-y] [Cited by in Crossref: 55] [Cited by in F6Publishing: 50] [Article Influence: 9.2] [Reference Citation Analysis]
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63 Shi Q, Zhou W, Chen C, Zhang BY, Xiao K, Zhang XC, Shen XJ, Li Q, Deng LQ, Dong JH, Lin WQ, Huang P, Jiang WJ, Lv J, Han J, Dong XP. The Features of Genetic Prion Diseases Based on Chinese Surveillance Program. PLoS One 2015;10:e0139552. [PMID: 26488179 DOI: 10.1371/journal.pone.0139552] [Cited by in Crossref: 38] [Cited by in F6Publishing: 41] [Article Influence: 5.4] [Reference Citation Analysis]
64 Edward DP, Alkatan H, Rafiq Q, Eberhart C, Al Mesfer S, Ghazi N, Al Safieh L, Kondkar AA, Abu Amero KK. MicroRNA profiling in intraocular medulloepitheliomas. PLoS One 2015;10:e0121706. [PMID: 25807141 DOI: 10.1371/journal.pone.0121706] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 1.6] [Reference Citation Analysis]