BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Spaull RVV, Soo AKS, Hogarth P, Hayflick SJ, Kurian MA. Towards Precision Therapies for Inherited Disorders of Neurodegeneration with Brain Iron Accumulation. Tremor Other Hyperkinet Mov (N Y) 2021;11:51. [PMID: 34909266 DOI: 10.5334/tohm.661] [Reference Citation Analysis]
2 Zech M, Steel D, Kurian MA, Winkelmann J. Reply to "Truncating VPS16 Mutations are Rare in Early-Onset Dystonia". Ann Neurol 2021;89:626. [PMID: 33305837 DOI: 10.1002/ana.25988] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 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]
4 Siegert S, Mindler GT, Brücke C, Kranzl A, Patsch J, Ritter M, Janecke AR, Vodopiutz J. Expanding the Phenotype of the FAM149B1-Related Ciliopathy and Identification of Three Neurogenetic Disorders in a Single Family. Genes (Basel) 2021;12:1648. [PMID: 34828254 DOI: 10.3390/genes12111648] [Reference Citation Analysis]
5 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]
6 Doummar D, Treven M, Qebibo L, Devos D, Ghoumid J, Ravelli C, Kranz G, Krenn M, Demailly D, Cif L, Davion JB, Zimprich F, Burglen L, Zech M. Childhood-onset progressive dystonia associated with pathogenic truncating variants in CHD8. Ann Clin Transl Neurol 2021;8:1986-90. [PMID: 34415117 DOI: 10.1002/acn3.51444] [Reference Citation Analysis]
7 Trenado C, Cif L, Pedroarena-Leal N, Ruge D. Electrophysiological Signature and the Prediction of Deep Brain Stimulation Withdrawal and Insertion Effects. Front Neurol 2021;12:754701. [PMID: 34917015 DOI: 10.3389/fneur.2021.754701] [Reference Citation Analysis]
8 Buzo EL, De la Casa-fages B, Sánchez MG, Sánchez JP, Carballal CF, Vidorreta JG, Sierra OM, Chicote AC, Grandas F. Pallidal deep brain stimulation response in two siblings with atypical adult-onset dystonia related to a KMT2B variant. Journal of the Neurological Sciences 2022;438:120295. [DOI: 10.1016/j.jns.2022.120295] [Reference Citation Analysis]
9 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]
10 Pozojevic J, Beetz C, Westenberger A. The importance of genetic testing for dystonia patients and translational research. J Neural Transm (Vienna) 2021;128:473-81. [PMID: 33876307 DOI: 10.1007/s00702-021-02329-9] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 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]
12 Ciolfi A, Foroutan A, Capuano A, Pedace L, Travaglini L, Pizzi S, Andreani M, Miele E, Invernizzi F, Reale C, Panteghini C, Iascone M, Niceta M, Gavrilova RH, Schultz-Rogers L, Agolini E, Bedeschi MF, Prontera P, Garibaldi M, Galosi S, Leuzzi V, Soliveri P, Olson RJ, Zorzi GS, Garavaglia BM, Tartaglia M, Sadikovic B. Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile. Clin Epigenetics 2021;13:157. [PMID: 34380541 DOI: 10.1186/s13148-021-01145-y] [Reference Citation Analysis]
13 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]
14 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]
15 Mulroy E, Vijiaratnam N, De Roquemaurel A, Bhatia KP, Zrinzo L, Foltynie T, Limousin P. A practical guide to troubleshooting pallidal deep brain stimulation issues in patients with dystonia. Parkinsonism Relat Disord 2021;87:142-54. [PMID: 34074583 DOI: 10.1016/j.parkreldis.2021.05.017] [Reference Citation Analysis]
16 Yellajoshyula D, Pappas SS, Dauer WT. Oligodendrocyte and Extracellular Matrix Contributions to Central Nervous System Motor Function: Implications for Dystonia. Mov Disord 2022. [PMID: 34989453 DOI: 10.1002/mds.28892] [Reference Citation Analysis]
17 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]