BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Kawarai T, Miyamoto R, Nakagawa E, Koichihara R, Sakamoto T, Mure H, Morigaki R, Koizumi H, Oki R, Montecchiani C, Caltagirone C, Orlacchio A, Hattori A, Mashimo H, Izumi Y, Mezaki T, Kumada S, Taniguchi M, Yokochi F, Saitoh S, Goto S, Kaji R. Phenotype variability and allelic heterogeneity in KMT2B-Associated disease. Parkinsonism Relat Disord 2018;52:55-61. [PMID: 29653907 DOI: 10.1016/j.parkreldis.2018.03.022] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 4.8] [Reference Citation Analysis]
Number Citing Articles
1 Ma J, Wang L, Yang Y, Li S, Wan X. Identification of Novel KMT2B Variants in Chinese Dystonia Patients via Whole-Exome Sequencing. Front Neurol 2019;10:729. [PMID: 31338059 DOI: 10.3389/fneur.2019.00729] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
2 Ng A, Galosi S, Salz L, Wong T, Schwager C, Amudhavalli S, Gelineau-Morel R, Chowdhury S, Friedman J; Rady Children’s Institute for Genomic Medicine Investigators. Failure to thrive - an overlooked manifestation of KMT2B-related dystonia: a case presentation. BMC Neurol 2020;20:246. [PMID: 32546208 DOI: 10.1186/s12883-020-01798-x] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [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 Wilson KD, Porter EG, Garcia BA. Reprogramming of the epigenome in neurodevelopmental disorders. Crit Rev Biochem Mol Biol 2021;:1-40. [PMID: 34601997 DOI: 10.1080/10409238.2021.1979457] [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 Cif L, Demailly D, Lin JP, Barwick KE, Sa M, Abela L, Malhotra S, Chong WK, Steel D, Sanchis-Juan A, Ngoh A, Trump N, Meyer E, Vasques X, Rankin J, Allain MW, Applegate CD, Attaripour Isfahani S, Baleine J, Balint B, Bassetti JA, Baple EL, Bhatia KP, Blanchet C, Burglen L, Cambonie G, Seng EC, Bastaraud SC, Cyprien F, Coubes C, d'Hardemare V, Doja A, Dorison N, Doummar D, Dy-Hollins ME, Farrelly E, Fitzpatrick DR, Fearon C, Fieg EL, Fogel BL, Forman EB, Fox RG, Gahl WA, Galosi S, Gonzalez V, Graves TD, Gregory A, Hallett M, Hasegawa H, Hayflick SJ, Hamosh A, Hully M, Jansen S, Jeong SY, Krier JB, Krystal S, Kumar KR, Laurencin C, Lee H, Lesca G, François LL, Lynch T, Mahant N, Martinez-Agosto JA, Milesi C, Mills KA, Mondain M, Morales-Briceno H, Ostergaard JR, Pal S, Pallais JC, Pavillard F, Perrigault PF, Petersen AK, Polo G, Poulen G, Rinne T, Roujeau T, Rogers C, Roubertie A, Sahagian M, Schaefer E, Selim L, Selway R, Sharma N, Signer R, Soldatos AG, Stevenson DA, Stewart F, Tchan M, Verma IC, de Vries BBA, Wilson JL, Wong DA, Zaitoun R, Zhen D, Znaczko A, Dale RC, de Gusmão CM, Friedman J, Fung VSC, King MD, Mohammad SS, Rohena L, Waugh JL, Toro C, Raymond FL, Topf M, Coubes P, Gorman KM, Kurian MA; Deciphering Developmental Disorders Study., Genomics England Research Consortium., NIHR BioResource., Undiagnosed Diseases Network. KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation. Brain 2020;143:3242-61. [PMID: 33150406 DOI: 10.1093/brain/awaa304] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 9.0] [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 Tisch S, Kumar KR. Pallidal Deep Brain Stimulation for Monogenic Dystonia: The Effect of Gene on Outcome. Front Neurol 2020;11:630391. [PMID: 33488508 DOI: 10.3389/fneur.2020.630391] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Rajan R, Garg K, Saini A, Radhakrishnan DM, Carecchio M, Bk B, Singh M, Srivastava AK. GPi-DBS for KMT2B-Associated Dystonia: Systematic Review and Meta-Analysis. Mov Disord Clin Pract 2022;9:31-7. [PMID: 35005062 DOI: 10.1002/mdc3.13374] [Reference Citation Analysis]
10 Abel M, Pfister R, Hussein I, Alsalloum F, Onyinzo C, Kappl S, Zech M, Demmel W, Staudt M, Kudernatsch M, Berweck S. Deep Brain Stimulation in KMT2B-Related Dystonia: Case Report and Review of the Literature With Special Emphasis on Dysarthria and Speech. Front Neurol 2021;12:662910. [PMID: 34054706 DOI: 10.3389/fneur.2021.662910] [Reference Citation Analysis]
11 Macerollo A, Sajin V, Bonello M, Barghava D, Alusi SH, Eldridge PR, Osman-farah J. Deep brain stimulation in dystonia: State of art and future directions. Journal of Neuroscience Methods 2020;340:108750. [DOI: 10.1016/j.jneumeth.2020.108750] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
12 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]
13 Li XY, Dai LF, Wan XH, Guo Y, Dai Y, Li SL, Fang F, Wang XH, Zhang WH, Liu TH, Xie ZH, Fang T, Wang L, Ding CH. Clinical phenotypes, genotypes and treatment in Chinese dystonia patients with KMT2B variants. Parkinsonism Relat Disord 2020;77:76-82. [PMID: 32634684 DOI: 10.1016/j.parkreldis.2020.06.002] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
14 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]
15 Larsh T, Wu SW, Vadivelu S, Grant GA, O'Malley JA. Deep Brain Stimulation for Pediatric Dystonia. Semin Pediatr Neurol 2021;38:100896. [PMID: 34183138 DOI: 10.1016/j.spen.2021.100896] [Reference Citation Analysis]
16 Rajan R, Garg K, Saini A, Kumar M, Binukumar BK, Scaria V, Aggarwal R, Gupta A, Vishnu VY, Garg A, Singh MB, Bhatia R, Srivastava AK, Padma Srivastava MV, Singh M. Pallidal Deep Brain Stimulation for KMT2B Related Dystonia in An Indian Patient. Ann Indian Acad Neurol 2021;24:586-8. [PMID: 34728955 DOI: 10.4103/aian.AIAN_1316_20] [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]
18 Keller Sarmiento IJ, Mencacci NE. Genetic Dystonias: Update on Classification and New Genetic Discoveries. Curr Neurol Neurosci Rep 2021;21:8. [PMID: 33564903 DOI: 10.1007/s11910-021-01095-1] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
19 Kim HJ, Jeon B. Arching deep brain stimulation in dystonia types. J Neural Transm (Vienna) 2021;128:539-47. [PMID: 33740122 DOI: 10.1007/s00702-021-02304-4] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Alterman RL, Filippidis AS. Genetic Subtypes and Deep Brain Stimulation in Dystonia. Mov Disord Clin Pract 2018;5:357-60. [PMID: 30838292 DOI: 10.1002/mdc3.12660] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]