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Cited by in F6Publishing
For: Sferra A, Fattori F, Rizza T, Flex E, Bellacchio E, Bruselles A, Petrini S, Cecchetti S, Teson M, Restaldi F, Ciolfi A, Santorelli FM, Zanni G, Barresi S, Castiglioni C, Tartaglia M, Bertini E. Defective kinesin binding of TUBB2A causes progressive spastic ataxia syndrome resembling sacsinopathy. Human Molecular Genetics 2018;27:1892-904. [DOI: 10.1093/hmg/ddy096] [Cited by in Crossref: 11] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]
Number Citing Articles
1 Xiao H, He H, Wu T, Ni X, Liu F, Yin F, Peng J. Functional Investigation of TUBB4A Variants Associated with Different Clinical Phenotypes. Mol Neurobiol 2022. [PMID: 35668344 DOI: 10.1007/s12035-022-02900-9] [Reference Citation Analysis]
2 Lange LM, Gonzalez-Latapi P, Rajalingam R, Tijssen MAJ, Ebrahimi-Fakhari D, Gabbert C, Ganos C, Ghosh R, Kumar KR, Lang AE, Rossi M, van der Veen S, van de Warrenburg B, Warner T, Lohmann K, Klein C, Marras C; on behalf of the Task Force on Genetic Nomenclature in Movement Disorders. Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update. Mov Disord 2022. [PMID: 35481685 DOI: 10.1002/mds.28982] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 Krajka V, Vulinovic F, Genova M, Tanzer K, Jijumon AS, Bodakuntla S, Tennstedt S, Mueller-Fielitz H, Meier B, Janke C, Klein C, Rakovic A. H-ABC- and dystonia-causing TUBB4A mutations show distinct pathogenic effects. Sci Adv 2022;8:eabj9229. [PMID: 35275727 DOI: 10.1126/sciadv.abj9229] [Reference Citation Analysis]
4 Narváez-Bandera I, Suárez-Gómez D, Isaza CE, Cabrera-Ríos M. Multiple Criteria Optimization (MCO): A gene selection deterministic tool in RStudio. PLoS One 2022;17:e0262890. [PMID: 35085348 DOI: 10.1371/journal.pone.0262890] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
5 Uniyal A, Akhilesh, Singh Rathore A, Kumari Keshri P, Pratap Singh S, Singh S, Tiwari V. Inhibition of pan-Aurora kinase attenuates evoked and ongoing pain in nerve injured rats via regulating KIF17-NR2B mediated signaling. Int Immunopharmacol 2022;106:108622. [PMID: 35183034 DOI: 10.1016/j.intimp.2022.108622] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
6 Lou Y, Lu J, Zhang Y, Gu P, Wang H, Qian F, Zhou W, Zhang W, Zhong H, Han B. The centromere-associated protein CENPU promotes cell proliferation, migration, and invasiveness in lung adenocarcinoma. Cancer Lett 2022;532:215599. [PMID: 35176420 DOI: 10.1016/j.canlet.2022.215599] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Schmidt L, Wain KE, Hajek C, Estrada-Veras JI, Guillen Sacoto MJ, Wentzensen IM, Malhotra A, Clause A, Perry D, Moreno-De-Luca A, Bell M. Expanding the Phenotype of TUBB2A-Related Tubulinopathy: Three Cases of a Novel, Heterozygous TUBB2A Pathogenic Variant p.Gly98Arg. Mol Syndromol 2021;12:33-40. [PMID: 33776625 DOI: 10.1159/000512160] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Sferra A, Nicita F, Bertini E. Microtubule Dysfunction: A Common Feature of Neurodegenerative Diseases. Int J Mol Sci 2020;21:E7354. [PMID: 33027950 DOI: 10.3390/ijms21197354] [Cited by in Crossref: 9] [Cited by in F6Publishing: 22] [Article Influence: 4.5] [Reference Citation Analysis]
9 Brock S, Vanderhasselt T, Vermaning S, Keymolen K, Régal L, Romaniello R, Wieczorek D, Storm TM, Schaeferhoff K, Hehr U, Kuechler A, Krägeloh-Mann I, Haack TB, Kasteleijn E, Schot R, Mancini GMS, Webster R, Mohammad S, Leventer RJ, Mirzaa G, Dobyns WB, Bahi-Buisson N, Meuwissen M, Jansen AC, Stouffs K. Defining the phenotypical spectrum associated with variants in TUBB2A. J Med Genet 2021;58:33-40. [PMID: 32571897 DOI: 10.1136/jmedgenet-2019-106740] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
10 Martinelli C, Battaglini M, Pucci C, Gioi S, Caracci C, Macaluso G, Doccini S, Santorelli FM, Ciofani G. Development of Nanostructured Lipid Carriers for the Delivery of Idebenone in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. ACS Omega 2020;5:12451-66. [PMID: 32548430 DOI: 10.1021/acsomega.0c01282] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
11 Cai S, Li J, Wu Y, Jiang Y. De novo mutations of TUBB2A cause infantile-onset epilepsy and developmental delay. J Hum Genet 2020;65:601-8. [PMID: 32203252 DOI: 10.1038/s10038-020-0739-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
12 Sferra A, Petrini S, Bellacchio E, Nicita F, Scibelli F, Dentici ML, Alfieri P, Cestra G, Bertini ES, Zanni G. TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics. Int J Mol Sci 2020;21:E1385. [PMID: 32085672 DOI: 10.3390/ijms21041385] [Cited by in Crossref: 5] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
13 Muñoz-Lasso DC, Romá-Mateo C, Pallardó FV, Gonzalez-Cabo P. Much More Than a Scaffold: Cytoskeletal Proteins in Neurological Disorders. Cells 2020;9:E358. [PMID: 32033020 DOI: 10.3390/cells9020358] [Cited by in Crossref: 25] [Cited by in F6Publishing: 31] [Article Influence: 12.5] [Reference Citation Analysis]
14 Stregapede F, Travaglini L, Rebelo AP, Cintra VP, Bellacchio E, Bosco L, Alfieri P, Pro S, Zuchner S, Bertini E, Nicita F. Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation. Clin Genet 2019;97:521-6. [DOI: 10.1111/cge.13668] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
15 Ricca I, Morani F, Bacci GM, Nesti C, Caputo R, Tessa A, Santorelli FM. Clinical and molecular studies in two new cases of ARSACS. Neurogenetics 2019;20:45-9. [PMID: 30680480 DOI: 10.1007/s10048-019-00564-7] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
16 Parodi L, Coarelli G, Stevanin G, Brice A, Durr A. Hereditary ataxias and paraparesias: clinical and genetic update. Current Opinion in Neurology 2018;31:462-71. [DOI: 10.1097/wco.0000000000000585] [Cited by in Crossref: 44] [Cited by in F6Publishing: 51] [Article Influence: 11.0] [Reference Citation Analysis]
17 Romaniello R, Arrigoni F, Fry AE, Bassi MT, Rees MI, Borgatti R, Pilz DT, Cushion TD. Tubulin genes and malformations of cortical development. Eur J Med Genet 2018;61:744-54. [PMID: 30016746 DOI: 10.1016/j.ejmg.2018.07.012] [Cited by in Crossref: 43] [Cited by in F6Publishing: 50] [Article Influence: 10.8] [Reference Citation Analysis]