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For: Feng H, Khalil S, Neubig RR, Sidiropoulos C. A mechanistic review on GNAO1-associated movement disorder. Neurobiol Dis 2018;116:131-41. [PMID: 29758257 DOI: 10.1016/j.nbd.2018.05.005] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
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4 Liu Y, Zhang Q, Wang J, Liu J, Yang W, Yan X, Ouyang Y, Yang H. Both subthalamic and pallidal deep brain stimulation are effective for GNAO1 -associated dystonia: three case reports and a literature review. Ther Adv Neurol Disord 2022;15:175628642210935. [DOI: 10.1177/17562864221093507] [Reference Citation Analysis]
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7 Feng H, Larrivee CL, Demireva EY, Xie H, Leipprandt JR, Neubig RR. Mouse models of GNAO1-associated movement disorder: Allele- and sex-specific differences in phenotypes. PLoS One 2019;14:e0211066. [PMID: 30682176 DOI: 10.1371/journal.pone.0211066] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 2.3] [Reference Citation Analysis]
8 Al Masseri Z, Alsayed M. Gonadal mosaicism in GNAO1 causing neurodevelopmental disorder with involuntary movements; two additional variants. Molecular Genetics and Metabolism Reports 2022;31:100864. [DOI: 10.1016/j.ymgmr.2022.100864] [Reference Citation Analysis]
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11 E GX, Basang WD, Zhu YB. Whole-genome analysis identifying candidate genes of altitude adaptive ecological thresholds in yak populations. J Anim Breed Genet 2019;136:371-7. [PMID: 31062447 DOI: 10.1111/jbg.12403] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
12 Yamashita Y, Ogawa T, Ogaki K, Kamo H, Sukigara T, Kitahara E, Izawa N, Iwamuro H, Oyama G, Kamagata K, Hatano T, Umemura A, Kosaki R, Kubota M, Shimo Y, Hattori N. Neuroimaging evaluation and successful treatment by using directional deep brain stimulation and levodopa in a patient with GNAO1-associated movement disorder: A case report. J Neurol Sci 2020;411:116710. [PMID: 32044685 DOI: 10.1016/j.jns.2020.116710] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
13 Méneret A, Mohammad SS, Cif L, Doummar D, DeGusmao C, Anheim M, Barth M, Damier P, Demonceau N, Friedman J, Gallea C, Gras D, Gurgel-Giannetti J, Innes EA, Necpál J, Riant F, Sagnes S, Sarret C, Seliverstov Y, Paramanandam V, Shetty K, Tranchant C, Doulazmi M, Vidailhet M, Pringsheim T, Roze E. Efficacy of Caffeine in ADCY5-Related Dyskinesia: A Retrospective Study. Mov Disord 2022. [PMID: 35384065 DOI: 10.1002/mds.29006] [Reference Citation Analysis]
14 Yang X, Niu X, Yang Y, Cheng M, Zhang J, Chen J, Yang Z, Zhang Y. Phenotypes of GNAO1 Variants in a Chinese Cohort. Front Neurol 2021;12:662162. [PMID: 34122306 DOI: 10.3389/fneur.2021.662162] [Reference Citation Analysis]
15 Akamine S, Okuzono S, Yamamoto H, Setoyama D, Sagata N, Ohgidani M, Kato TA, Ishitani T, Kato H, Masuda K, Matsushita Y, Ono H, Ishizaki Y, Sanefuji M, Saitsu H, Matsumoto N, Kang D, Kanba S, Nakabeppu Y, Sakai Y, Ohga S. GNAO1 organizes the cytoskeletal remodeling and firing of developing neurons. FASEB J 2020;34:16601-21. [PMID: 33107105 DOI: 10.1096/fj.202001113R] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
16 Delorme C, Giron C, Bendetowicz D, Méneret A, Mariani LL, Roze E. Current challenges in the pathophysiology, diagnosis, and treatment of paroxysmal movement disorders. Expert Rev Neurother 2021;21:81-97. [PMID: 33089715 DOI: 10.1080/14737175.2021.1840978] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
17 Larsh T, Friedman N, Fernandez H. Child Neurology: Genetically determined dystonias with childhood onset. Neurology 2020;94:892-5. [DOI: 10.1212/wnl.0000000000009040] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Baizabal-carvallo JF, Cardoso F. Chorea in children: etiology, diagnostic approach and management. J Neural Transm 2020;127:1323-42. [DOI: 10.1007/s00702-020-02238-3] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
19 Wang D, Dao M, Muntean BS, Giles AC, Martemyanov KA, Grill B. Genetic modeling of GNAO1 disorder delineates mechanisms of Gαo dysfunction. Hum Mol Genet 2021:ddab235. [PMID: 34508586 DOI: 10.1093/hmg/ddab235] [Reference Citation Analysis]