| Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield S Anazi, S Maddirevula, E Faqeih, H Alsedairy, F Alzahrani, ... Molecular psychiatry 22 (4), 615-624, 2017 | 226 | 2017 |
| Genomic and phenotypic delineation of congenital microcephaly R Shaheen, S Maddirevula, N Ewida, S Alsahli, GMH Abdel-Salam, ... Genetics in Medicine 21 (3), 545-552, 2019 | 102 | 2019 |
| FARS2 deficiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance M Almannai, J Wang, H Dai, AW El-Hattab, EA Faqeih, MA Saleh, ... Molecular genetics and metabolism 125 (3), 281-291, 2018 | 32 | 2018 |
| Idiopathic intracranial hypertension in children: diagnostic and management approach A Albakr, MH Hamad, AH Alwadei, FA Bashiri, HH Hassan, H Idris, ... Sudanese Journal of Paediatrics 16 (2), 67, 2016 | 31 | 2016 |
| Acute necrotizing encephalopathy of childhood: a multicenter experience in Saudi Arabia FA Bashiri, S Al Johani, MH Hamad, AY Kentab, AH Alwadei, K Hundallah, ... Frontiers in pediatrics 8, 526, 2020 | 24 | 2020 |
| Management of convulsive status epilepticus in children: an adapted clinical practice guideline for pediatricians in Saudi Arabia FA Bashiri, MH Hamad, YS Amer, MM Abouelkheir, S Mohamed, ... Neurosciences Journal 22 (2), 146-155, 2017 | 20 | 2017 |
| Loss‐of‐function mutation in RUSC2 causes intellectual disability and secondary microcephaly AH Alwadei, R Benini, A Mahmoud, A Alasmari, EJ Kamsteeg, M Alfadhel Developmental Medicine & Child Neurology 58 (12), 1317-1322, 2016 | 15 | 2016 |
| Phenotypic characterization of KCTD3‐related developmental epileptic encephalopathy EA Faqeih, M Almannai, MM Saleh, AH AlWadei, MM Samman, ... Clinical genetics 93 (5), 1081-1086, 2018 | 14 | 2018 |
| Clinico‐radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate … M Scala, SB Wortmann, N Kaya, MD Stellingwerff, A Pistorio, E Glamuzina, ... Human mutation 43 (3), 403-419, 2022 | 9 | 2022 |
| Clinical, molecular, and biochemical delineation of asparagine synthetase deficiency in Saudi cohort E Alharby, EA Faqeih, M Saleh, S Alameer, M Almuntashri, A Pastore, ... Genetics in Medicine 22 (12), 2071-2080, 2020 | 8 | 2020 |
| Childhood absence epilepsy: Electro-clinical manifestations, treatment options, and outcome in a tertiary educational center FA Bashiri, MH Hamad, AY Kentab, AH Alwadei International Journal of Pediatrics and Adolescent Medicine 9 (2), 131-135, 2022 | 5 | 2022 |
| SHQ1-associated neurodevelopmental disorder: Report of the first homozygous variant in unrelated patients and review of the literature A AlHargan, MA AlMuhaizea, R Almass, AH Alwadei, M Daghestani, ... Human Genome Variation 10 (1), 7, 2023 | 3 | 2023 |
| Pediatric neurology workforce in Saudi Arabia BM Al-Nahdi, MW Ashgar, MY Domyati, AH AlWadei, RS Albaradie, ... Journal of Pediatric Neurology 15 (04), 166-170, 2017 | 3 | 2017 |
| Efficacy and safety of corpus callosotomy versus vagus nerve stimulation as long-term adjunctive therapies in children with Lennox–Gastaut syndrome: Experience of a tertiary … GM Alanazi, TF ALOsaimi, AH Alwadei, AD Al-Otaibi, LA Jad, AA Al-Attas Neurosciences Journal 27 (2), 59-64, 2022 | 2 | 2022 |
| Pediatric intracranial hypertension: Experience from 2 Tertiary Centers FA Bashiri, HK Al Abdulsalam, SM Hassan, WA Al Twaijri, FI Almalki, ... Neurosciences Journal 24 (4), 257-263, 2019 | 1 | 2019 |
| Clinical and molecular characteristics of neuronal ceroid lipofuscinosis in Saudi Arabia MM Saleh, AM Hamhom, A Al-Otaibi, M AlGhamdi, Y Housawi, YI Aljadhai, ... Pediatric Neurology 155, 149-155, 2024 | | 2024 |
| Case Report: A rare treatable metabolic syndrome (Brown-Vialetto-Van Laere syndrome) masquerading as chronic inflammatory demyelinating polyneuropathy from Saudi Arabia AY Kentab, Y Alsalloum, M Labani, A Hudairi, MH Hamad, DZ Jamjoom, ... Frontiers in Pediatrics 12, 1377515, 2024 | | 2024 |
| Paroxysmal nonepileptic events in children and adolescents admitted to the epilepsy monitoring unit: A retrospective study A Kaki, M Almutairi, R Alharbi, A Alotaibi, A Alwadei, F Bamogaddam, ... Brain Disorders 11, 100082, 2023 | | 2023 |
| Hereditary Hyperekplexia in Saudi Arabia A Aldhilan, A Alhakeem, S Al Hajjaj, M Abukhalid, H Aldhalaan, E Salah, ... Pediatric Neurology 134, 78-82, 2022 | | 2022 |
| Predicting future handedness and hemispheric dominance during infancy by analyzing sleep spindles AH Alwadei, TF AlOsaimi, MA Bayounis, GA AlHajaj, FA Bashiri Neurosciences Journal 25 (3), 188-192, 2020 | | 2020 |
