| Mutations in prickle orthologs cause seizures in flies, mice, and humans H Tao, JR Manak, L Sowers, X Mei, H Kiyonari, T Abe, NS Dahdaleh, ... The American Journal of Human Genetics 88 (2), 138-149, 2011 | 158 | 2011 |
| Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase L Paemka, VB Mahajan, SN Ehaideb, JM Skeie, MC Tan, S Wu, AJ Cox, ... PLoS genetics 11 (3), e1005022, 2015 | 81 | 2015 |
| KCNT1‐related epilepsy: An international multicenter cohort of 27 pediatric cases F Borlot, A Abushama, N Morrison‐Levy, P Jain, K Puthenveettil Vinayan, ... Epilepsia 61 (4), 679-692, 2020 | 55 | 2020 |
| Evidence of a wide gap between COVID-19 in humans and animal models: a systematic review SN Ehaideb, ML Abdullah, B Abuyassin, A Bouchama Critical Care 24, 1-23, 2020 | 52 | 2020 |
| Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality J Alghamdi, M Alaamery, T Barhoumi, M Rashid, H Alajmi, N Aljasser, ... Genomics 113 (4), 1733-1741, 2021 | 50 | 2021 |
| prickle modulates microtubule polarity and axonal transport to ameliorate seizures in flies SN Ehaideb, A Iyengar, A Ueda, GJ Iacobucci, C Cranston, AG Bassuk, ... Proceedings of the National Academy of Sciences 111 (30), 11187-11192, 2014 | 49 | 2014 |
| PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders L Paemka, VB Mahajan, JM Skeie, LP Sowers, SN Ehaideb, ... PloS one 8 (12), e80737, 2013 | 49 | 2013 |
| Novel homozygous mutation in the WWOX gene causes seizures and global developmental delay: Report and review SN Ehaideb, MJ Al-Bu Ali, JJ Al-Obaid, KM Aljassim, M Alfadhel Translational neuroscience 9 (1), 203-208, 2018 | 32 | 2018 |
| Mutation of orthologous prickle genes causes a similar epilepsy syndrome in flies and humans SN Ehaideb, EA Wignall, J Kasuya, WH Evans, A Iyengar, HL Koerselman, ... Annals of clinical and translational neurology 3 (9), 695-707, 2016 | 16 | 2016 |
| A systematic review uncovers a wide-gap between COVID-19 in humans and animal models SN Ehaideb, ML Abdullah, B Abuyassin, A Bouchama MedRxiv, 2020.07. 15.20147041, 2020 | 4 | 2020 |
| Novel compensatory mechanisms enable the mutant KCNT1 channels to induce seizures SN Ehaideb, GT Decker, P Smith, D Davis, B Zhang bioRxiv, 191171, 2017 | 2 | 2017 |
| Escalating climate-related health risks for Hajj pilgrims to Mecca S Yezli, S Ehaideb, Y Yassin, B Alotaibi, A Bouchama Journal of Travel Medicine, taae042, 2024 | | 2024 |
| Insights into pathophysiology and therapeutic strategies for heat stroke: Lessons from a baboon model M Abdullah, S Ehaideb, G Roberts, A Bouchama Experimental Physiology, 2023 | | 2023 |
| Abnormal larval neuromuscular junction morphology and physiology in Drosophila prickle isoform mutants with known axonal transport defects and adult seizure … A Ueda, TCDG O’Harrow, X Xing, S Ehaideb, JR Manak, CF Wu Journal of neurogenetics 36 (2-3), 65-73, 2022 | | 2022 |
| Abnormal larval neuromuscular junction morphology and physiology in Drosophila Prickle isoform mutants with defective axonal transport and adult seizure behavior T O’Harrow, A Ueda, X Xing, S Ehaideb, JR Manak, CF Wu bioRxiv, 2021.12. 31.474668, 2022 | | 2022 |
| A systematic review uncovers a wide-gap between COVID-19 in humans and animal models (preprint) SN Ehaideb, ML Abdullah, B Abuyassin, A Bouchama | | 2020 |
| Evidence of a wide gap between COVID-19 in humans and animal models: a systematic SN Ehaideb, ML Abdullah, B Abuyassin, A Bouchama | | 2020 |
| Allostatic Compensatory Mechanisms Enable the Mutant KCNT1 Channels to Induce Seizures and Hyperexcitability SN Ehaideb, GT Decker, P Smith, N Messimore, D Davis, B Zhang Available at SSRN 3188397, 2018 | | 2018 |
| Elucidating the mechanism of prickle associated epilepsy in flies SN Ehaideb The University of Iowa, 2015 | | 2015 |
| The pksple seizure‐associated isoform of prickle is co‐expressed in the same cells as the pkpk isoform in Drosophila larval brains N Anderson, G Yuan, D Wadkins, S Ehaideb, C Cranston, JR Manak | | |
