BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Gorman KM, Meyer E, Kurian MA. Review of the phenotype of early-onset generalised progressive dystonia due to mutations in KMT2B. Eur J Paediatr Neurol 2018;22:245-56. [PMID: 29289525 DOI: 10.1016/j.ejpn.2017.11.009] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 3.4] [Reference Citation Analysis]
Number Citing Articles
1 Owczarzak LR, Hogan KE, Dineen RT, Gill CE, Li MH. A New Pathologic KMT2B Variant Associated with Childhood Onset Dystonia Presenting as Variable Phenotypes among Family Members. Tremor and Other Hyperkinetic Movements 2022;12:7. [DOI: 10.5334/tohm.679] [Reference Citation Analysis]
2 Mun JK, Kim AR, Ahn JH, Kim M, Cho JW, Lee JI, Cho KR, Youn J. Successful Pallidal Stimulation in a Patient with KMT2B-Related Dystonia. J Mov Disord 2020;13:154-8. [PMID: 32241076 DOI: 10.14802/jmd.19087] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
3 Horisawa S, Azuma K, Akagawa H, Nonaka T, Kawamata T, Taira T. Radiofrequency ablation for DYT-28 dystonia: short term follow-up of three adult cases. Ann Clin Transl Neurol 2020;7:2047-51. [PMID: 32886413 DOI: 10.1002/acn3.51170] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
4 Bally JF, Camargos S, Oliveira Dos Santos C, Kern DS, Lee T, Pereira da Silva-Junior F, Puga RD, Cardoso F, Barbosa ER, Yadav R, Ozelius LJ, de Carvalho Aguiar P, Lang AE. DYT-TUBB4A (DYT4 Dystonia): New Clinical and Genetic Observations. Neurology 2021;96:e1887-97. [PMID: 32943487 DOI: 10.1212/WNL.0000000000010882] [Reference Citation Analysis]
5 Zech M, Lam DD, Winkelmann J. Update on KMT2B-Related Dystonia. Curr Neurol Neurosci Rep 2019;19:92. [PMID: 31768667 DOI: 10.1007/s11910-019-1007-y] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 5.3] [Reference Citation Analysis]
6 Kanduc D. The comparative biochemistry of viruses and humans: an evolutionary path towards autoimmunity. Biol Chem 2019;400:629-38. [PMID: 30504522 DOI: 10.1515/hsz-2018-0271] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 3.7] [Reference Citation Analysis]
7 Marogianni C, Georgouli D, Dadouli K, Ntellas P, Rikos D, Hadjigeorgiou GM, Spanaki C, Xiromerisiou G. Identification of a novel de novo KMT2B variant in a Greek dystonia patient via exome sequencing genotype-phenotype correlations of all published cases. Mol Biol Rep 2021;48:371-9. [PMID: 33300088 DOI: 10.1007/s11033-020-06057-3] [Reference Citation Analysis]
8 Carecchio M, Invernizzi F, Gonzàlez-Latapi P, Panteghini C, Zorzi G, Romito L, Leuzzi V, Galosi S, Reale C, Zibordi F, Joseph AP, Topf M, Piano C, Bentivoglio AR, Girotti F, Morana P, Morana B, Kurian MA, Garavaglia B, Mencacci NE, Lubbe SJ, Nardocci N. Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study. Mov Disord 2019;34:1516-27. [PMID: 31216378 DOI: 10.1002/mds.27771] [Cited by in Crossref: 24] [Cited by in F6Publishing: 23] [Article Influence: 8.0] [Reference Citation Analysis]
9 Pearson TS, Pons R. Movement Disorders in Children. Continuum (Minneap Minn) 2019;25:1099-120. [PMID: 31356295 DOI: 10.1212/CON.0000000000000756] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
10 Dai L, Ding C, Fang F. An inherited KMT2B duplication variant in a Chinese family with dystonia and/or development delay. Parkinsonism Relat Disord 2019;63:227-8. [PMID: 30196991 DOI: 10.1016/j.parkreldis.2018.08.021] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
11 Fagan RJ, Dingwall AK. COMPASS Ascending: Emerging clues regarding the roles of MLL3/KMT2C and MLL2/KMT2D proteins in cancer. Cancer Lett 2019;458:56-65. [PMID: 31128216 DOI: 10.1016/j.canlet.2019.05.024] [Cited by in Crossref: 27] [Cited by in F6Publishing: 23] [Article Influence: 9.0] [Reference Citation Analysis]
12 Lange LM, Junker J, Loens S, Baumann H, Olschewski L, Schaake S, Madoev H, Petkovic S, Kuhnke N, Kasten M, Westenberger A, Domingo A, Marras C, König IR, Camargos S, Ozelius LJ, Klein C, Lohmann K. Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review. Mov Disord 2021;36:1086-103. [PMID: 33502045 DOI: 10.1002/mds.28485] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 6.0] [Reference Citation Analysis]
13 Brás A, Ribeiro JA, Sobral F, Moreira F, Morgadinho A, Januário C. Early-onset oromandibular-laryngeal dystonia and Charlot gait: New phenotype of DYT-KMT2B. Neurology 2019;92:919-919. [DOI: 10.1212/wnl.0000000000007469] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
14 Zhou X, Wu J, Sun Y. An atypical case of early-onset dystonia with a novel missense variant in KMT2B. Parkinsonism & Related Disorders 2019;63:224-6. [DOI: 10.1016/j.parkreldis.2018.09.020] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]
15 Lee S, Ochoa E, Barwick K, Cif L, Rodger F, Docquier F, Pérez-Dueñas B, Clark G, Martin E, Banka S, Kurian MA, Maher ER. Comparison of methylation episignatures in KMT2B- and KMT2D-related human disorders. Epigenomics 2022. [PMID: 35506254 DOI: 10.2217/epi-2021-0521] [Reference Citation Analysis]
16 Damásio J, Santos M, Samões R, Araújo M, Macedo M, Sardoeira A, Cavaco S, Freitas J, Barros J, Oliveira J, Sequeiros J. Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype. Clin Genet 2021;100:743-7. [PMID: 34477219 DOI: 10.1111/cge.14055] [Reference Citation Analysis]
17 Cao Z, Yao H, Bao X, Wen Y, Liu B, Wang S, Yang H. DYT28 Responsive to Pallidal Deep Brain Stimulation. Mov Disord Clin Pract 2020;7:97-9. [PMID: 31970221 DOI: 10.1002/mdc3.12862] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]