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Cited by in F6Publishing
For: Iacomino M, Baldassari S, Tochigi Y, Kośla K, Buffelli F, Torella A, Severino M, Paladini D, Mandarà L, Riva A, Scala M, Balagura G, Accogli A, Nigro V, Minetti C, Fulcheri E, Zara F, Bednarek AK, Striano P, Suzuki H, Salpietro V. Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development. Front Neurosci 2020;14:644. [PMID: 32581702 DOI: 10.3389/fnins.2020.00644] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Riva A, Nobile G, Giacomini T, Ognibene M, Scala M, Balagura G, Madia F, Accogli A, Romano F, Tortora D, Severino M, Scudieri P, Baldassari S, Musante I, Uva P, Salpietro V, Torella A, Nigro V, Capra V, Nobili L, Striano P, Mancardi MM, Zara F, Iacomino M. A Phenotypic-Driven Approach for the Diagnosis of WOREE Syndrome. Front Pediatr 2022;10:847549. [DOI: 10.3389/fped.2022.847549] [Reference Citation Analysis]
2 Steinberg DJ, Aqeilan RI. WWOX-Related Neurodevelopmental Disorders: Models and Future Perspectives. Cells 2021;10:3082. [PMID: 34831305 DOI: 10.3390/cells10113082] [Reference Citation Analysis]
3 Breton VL, Aquilino MS, Repudi S, Saleem A, Mylvaganam S, Abu-Swai S, Bardakjian BL, Aqeilan RI, Carlen PL. Altered neocortical oscillations and cellular excitability in an in vitro Wwox knockout mouse model of epileptic encephalopathy. Neurobiol Dis 2021;160:105529. [PMID: 34634460 DOI: 10.1016/j.nbd.2021.105529] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Steinberg DJ, Repudi S, Saleem A, Kustanovich I, Viukov S, Abudiab B, Banne E, Mahajnah M, Hanna JH, Stern S, Carlen PL, Aqeilan RI. Modeling genetic epileptic encephalopathies using brain organoids. EMBO Mol Med 2021;13:e13610. [PMID: 34268881 DOI: 10.15252/emmm.202013610] [Reference Citation Analysis]
5 Hsu CY, Lee KT, Sun TY, Sze CI, Huang SS, Hsu LJ, Chang NS. WWOX and Its Binding Proteins in Neurodegeneration. Cells 2021;10:1781. [PMID: 34359949 DOI: 10.3390/cells10071781] [Reference Citation Analysis]
6 Banne E, Abudiab B, Abu-Swai S, Repudi SR, Steinberg DJ, Shatleh D, Alshammery S, Lisowski L, Gold W, Carlen PL, Aqeilan RI. Neurological Disorders Associated with WWOX Germline Mutations-A Comprehensive Overview. Cells 2021;10:824. [PMID: 33916893 DOI: 10.3390/cells10040824] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
7 Aldaz CM, Hussain T. WWOX Loss of Function in Neurodevelopmental and Neurodegenerative Disorders. Int J Mol Sci 2020;21:E8922. [PMID: 33255508 DOI: 10.3390/ijms21238922] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 5.5] [Reference Citation Analysis]