Mutluay Arslan
Sağlık Bilimleri Üniversitesi(TR)University of Health Sciences Antigua(AG)
Publications by Year
Research Areas
Epilepsy research and treatment, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Asthma and respiratory diseases, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy(2015)268 cited
- → De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome(2013)220 cited
- → Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies(2017)159 cited
- → KIAA0586is Mutated in Joubert Syndrome(2015)80 cited
- → A multicenter cross-sectional study to evaluate the clinical characteristics and nutritional status of children with cerebral palsy(2018)49 cited
- → Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes(2024)43 cited