Associated Papers
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk.
Oliver KL et al.
Epilepsia, 2023
Novel Mutation With Literature Review WW Domain-Containing Oxidoreductase (WWOX) Gene.
Sukkar G et al.
Cureus, 2022
Modeling genetic epileptic encephalopathies using brain organoids.
Steinberg DJ et al.
Embo Molecular Medicine, 2021
Neurological Disorders Associated with WWOX Germline Mutations-A Comprehensive Overview.
Banne E et al.
Cells, 2021
WWOX Loss of Function in Neurodevelopmental and Neurodegenerative Disorders.
Aldaz CM et al.
International Journal of Molecular Sciences, 2020
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery.
Hengel H et al.
European Journal of Human Genetics : Ejhg, 2020
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development.
Iacomino M et al.
Frontiers in Neuroscience, 2020
Germline mutation and aberrant transcripts of WWOX in a syndrome with multiple primary tumors.
Xu A et al.
The Journal of Pathology, 2019
The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature.
Piard J et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
Early infantile-onset epileptic encephalopathy 28 due to a homozygous microdeletion involving the WWOX gene in a region of uniparental disomy.
Davids M et al.
Human Mutation, 2019
The WWOX Gene Influences Cellular Pathways in the Neuronal Differentiation of Human Neural Progenitor Cells.
Kośla K et al.
Frontiers in Cellular Neuroscience, 2019
West syndrome, developmental and epileptic encephalopathy, and severe CNS disorder associated with WWOX mutations.
Shaukat Q et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2018
Modeling WWOX Loss of Function in vivo: What Have We Learned?
Tanna M et al.
Frontiers in Oncology, 2018
Novel Homozygous Mutation in the WWOX Gene Causes Seizures and Global Developmental Delay: Report and Review.
Ehaideb SN et al.
Translational Neuroscience, 2018
Novel mutations in WWOX, RARS2, and C10orf2 genes in consanguineous Arab families with intellectual disability.
Alkhateeb AM et al.
Metabolic Brain Disease, 2016
A novel whole exon deletion in WWOX gene causes early epilepsy, intellectual disability and optic atrophy.
Ben-Salem S et al.
Journal of Molecular Neuroscience : Mn, 2015
The fragile site WWOX gene and the developing brain.
Tabarki B et al.
Experimental Biology and Medicine (maywood, N.j.), 2015
Introduction to a thematic issue for WWOX.
Chang NS
Experimental Biology and Medicine (maywood, N.j.), 2015
WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation.
Mignot C et al.
Journal of Medical Genetics, 2015
WW domain-containing oxidoreductase in neuronal injury and neurological diseases.
Chang HT et al.
Oncotarget, 2014
WWOX at the crossroads of cancer, metabolic syndrome related traits and CNS pathologies.
Aldaz CM et al.
Biochimica Et Biophysica Acta, 2014
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.
Mallaret M et al.
Brain : a Journal of Neurology, 2014