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Sherifa A. Hamed

King Khalid University · SA
Area of research
Psychiatry and Mental health · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Epilepsy research and treatment, Pharmacological Effects and Toxicity Studies, Neuroscience and Neuropharmacology Research, and Hereditary Neurological Disorders.
h-index
40
citations
5,338
works
180
NIH funding
primary concept
email

Recent publications

Pediatric functional seizures: Demographics, clinical and psychological characteristics and risk factors.
2026cited by 0position: contributordoi
Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.
2026cited by 0position: contributordoi
Epilepsy secondary to intracranial calcification cause by hypothyroidism and chronic hypocalcaemia: a case report
Iberoamerican Journal of Medicine 2026cited by 0position: contributordoi
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD
Brain 2025cited by 7position: middledoi
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.
2025cited by 4position: contributordoi
SLK is mutated in individuals with a neurodevelopmental disorder
eBioMedicine 2025cited by 2position: contributordoi
From Expert Judgment to Structured Guidelines: A Brief History and Bright Future of DNA Variant Interpretation.
2025cited by 1position: contributordoi
Case-based genomics education and training of neurologists: an Egyptian initiative.
2025cited by 0position: contributordoi
The HUGO Clinical Genomics & Genomic Medicine Education Survey: clinicians globally need and want genomic medicine training.
2025cited by 0position: contributordoi
Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy
Journal of Clinical Investigation 2025cited by 0position: contributordoi
The effect of anticholinergic drugs on cognition of patients with Parkinson's disease: a cohort study from the Egyptian population.
2024cited by 4position: contributordoi
The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson's disease.
2024cited by 4position: contributordoi
The effect of epilepsy and antiseizure medications on cardiac autonomic functions in children with epilepsy.
2024cited by 3position: contributordoi
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study.
2023cited by 142position: contributordoi
Restless leg syndrome in patients with chronic kidney disease: a hospital-based study from Upper Egypt.
2023cited by 8position: contributordoi
The effectiveness of cerebrolysin, a multi-modal neurotrophic factor, for treatment of post-covid-19 persistent olfactory, gustatory and trigeminal chemosensory dysfunctions: a randomized clinical trial.
2023cited by 6position: contributordoi
Evaluation of chronic idiopathic tinnitus and its psychosocial triggers.
2023cited by 3position: contributordoi
Idiopathic steno-occlusive disease with bilateral internal carotid artery occlusion: A Case Report.
2023cited by 2position: contributordoi
Peripartum depression and its predictors: A longitudinal observational hospital-based study.
2022cited by 2position: contributordoi
Vestibular function in children with generalized epilepsy and treated with valproate.
2022cited by 1position: contributordoi
Biallelic variants in <i>HPDL</i> cause pure and complicated hereditary spastic paraplegia
Brain 2021cited by 50position: middledoi
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
2021cited by 41position: contributordoi
Behavioral assessment of children and adolescents with Graves' disease: A prospective study.
2021cited by 13position: contributordoi
Behavioral problems in children with primary monosymptomatic nocturnal enuresis.
2021cited by 10position: contributordoi
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome.
2021cited by 9position: contributordoi
Behavioral assessment of females with congenital adrenal hyperplasia.
2021cited by 5position: contributordoi
Vestibular Function in Children with Type 1 Diabetes: Videonystagmography Testing.
2021cited by 3position: contributordoi
Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
2021cited by 0position: contributordoi
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
Nature Genetics 2020cited by 174position: middledoi
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
2020cited by 119position: contributordoi

Grants

No grants ingested yet.

Frequent collaborators

· 15 papers (2019–2026)Stephanie Efthymiou · Cyprus Institute of Neurology and Genetics11 papers (2019–2026)Reza Maroofian · University of Cincinnati7 papers (2019–2021)Fowzan S. Alkuraya · University of Medicine and Health Sciences6 papers (2019–2025)Henry Houlden · Cyprus Institute of Neurology and Genetics5 papers (2020–2026)Gian Luigi Marseglia · University of Pavia4 papers (2019–2020)Jana Vandrovcova · National Hospital for Neurology and Neurosurgery4 papers (2019–2020)Nicholas W. Wood · University College London4 papers (2019–2023)Rita Horvath · Országos Korányi Tbc és Pulmonológiai Intézet4 papers (2020–2025)Mary M. Reilly · Genomics (United Kingdom)4 papers (2019–2026)Sylvia Boesch · Technical University of Munich4 papers (2019–2021)Mohd. Farooq Shaikh · Monash University Malaysia3 papers (2019–2025)Stephan Züchner · University of Miami3 papers (2020–2026)Yalda Jamshidi · Radboud University Medical Center3 papers (2020–2025)Efthimios Dardiotis · Universidad Metropolitana de Honduras3 papers (2019–2020)Davide Pareyson · Sydney Children’s Hospitals Network2 papers (2020–2020)Adriana Rebelo · University of Miami2 papers (2020–2020)Dimitri M. Kullmann · National Health Service2 papers (2019–2019)Jonathan Baets · University of Antwerp2 papers (2021–2025)Filippo Maria Santorelli · Fondazione Stella Maris2 papers (2021–2021)