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Cited by in F6Publishing
For: Su T, Yan Y, Xu S, Zhang K, Xu S. Early onset epileptic encephalopathy caused by novel compound heterozygous mutation of WWOX gene. Int J Dev Neurosci 2020;80:157-61. [PMID: 32037574 DOI: 10.1002/jdn.10013] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Baryła I, Kośla K, Bednarek AK. WWOX and metabolic regulation in normal and pathological conditions. J Mol Med (Berl) 2022. [PMID: 36271927 DOI: 10.1007/s00109-022-02265-5] [Reference Citation Analysis]
2 Su T, Yan Y, Hu Q, Liu Y, Xu S. De novo DYNC1H1 mutation causes infantile developmental and epileptic encephalopathy with brain malformations. Molec Gen & Gen Med. [DOI: 10.1002/mgg3.1874] [Reference Citation Analysis]
3 Steinberg DJ, Aqeilan RI. WWOX-Related Neurodevelopmental Disorders: Models and Future Perspectives. Cells 2021;10:3082. [PMID: 34831305 DOI: 10.3390/cells10113082] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
4 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: 7] [Cited by in F6Publishing: 6] [Article Influence: 7.0] [Reference Citation Analysis]