| Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery EM Scott, A Halees, Y Itan, EG Spencer, Y He, MA Azab, SB Gabriel, ... Nature genetics 48 (9), 1071-1076, 2016 | 343 | 2016 |
| Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35) KJ Dick, M Eckhardt, C Paisán‐Ruiz, AA Alshehhi, C Proukakis, ... Human mutation 31 (4), E1251-E1260, 2010 | 219 | 2010 |
| Prevalence and pattern of epilepsy (Lath/Mirgi/Laran) in rural Kashmir, India R Koul, S Razdan, A Motta Epilepsia 29 (2), 116-122, 1988 | 191 | 1988 |
| Continuous midazolam infusion as treatment of status epilepticus RL Koul, GR Aithala, A Chacko, R Joshi, MS Elbualy Archives of Disease in Childhood 76 (5), 445-448, 1997 | 140 | 1997 |
| Cerebrovascular disease in rural Kashmir, India. S Razdan, RL Koul, A Motta, S Kaul Stroke 20 (12), 1691-1693, 1989 | 112 | 1989 |
| Evolutionarily assembled cis-regulatory module at a human ciliopathy locus JH Lee, JL Silhavy, JE Lee, L Al-Gazali, S Thomas, EE Davis, SL Bielas, ... Science 335 (6071), 966-969, 2012 | 96 | 2012 |
| Tolosa–Hunt syndrome: MRI appearances R Jain, S Sawhney, RL Koul, P Chand Journal of Medical Imaging and Radiation Oncology 52 (5), 447-451, 2008 | 88 | 2008 |
| PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights DL Johnstone, HH Al-Shekaili, M Tarailo-Graovac, NI Wolf, AS Ivy, ... Brain 142 (3), 542-559, 2019 | 74 | 2019 |
| A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23 KJ Dick, R Al-Mjeni, W Baskir, R Koul, MA Simpson, MA Patton, ... Neurology 71 (4), 248-252, 2008 | 73 | 2008 |
| Eight-year study of childhood status epilepticus: midazolam infusion in management and outcome R Koul, A Chako, H Javed, K Al Riyami Journal of child neurology 17 (12), 907-909, 2002 | 69 | 2002 |
| A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy S Al-Yahyaee, LI Al-Gazali, P De Jonghe, H Al-Barwany, M Al-Kindi, ... Neurology 66 (8), 1230-1234, 2006 | 64 | 2006 |
| Evaluation children with global developmental delay: A prospective study at Sultan Qaboos University Hospital, Oman R Koul, M Al-Yahmedy, A Al-Futaisi Oman medical journal 27 (4), 310, 2012 | 42 | 2012 |
| Ten-year prospective study (Clinical Spectrum) of childhood Guillain-Barré Syndrome in the Arabian Peninsula: comparison of outcome in patients in the pre—and post … R Koul, A Chacko, R Ahmed, T Varghese, H Javed, Z Al-Lamki Journal of child neurology 18 (11), 767-771, 2003 | 40 | 2003 |
| Eating epilepsy R Koul, S Koul, S Razdan Acta neurologica scandinavica 80 (1), 78-80, 1989 | 36 | 1989 |
| Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia N Akizu, NM Shembesh, T Ben-Omran, L Bastaki, A Al-Tawari, MS Zaki, ... The American Journal of Human Genetics 92 (3), 392-400, 2013 | 35 | 2013 |
| Prospective study of children with Guillain-Barre syndrome RL Koul, A Alfutaisi The Indian Journal of Pediatrics 75, 787-790, 2008 | 34 | 2008 |
| Clinical characteristics of childhood guillain-barré syndrome R Koul, A Al-Futaisi, A Chacko, M Fazalullah, S Al Nabhani, S Al-Awaidy, ... Oman Medical Journal 23 (3), 158, 2008 | 31 | 2008 |
| Novel mutation of GLRA1 in Omani families with hyperekplexia and mild mental retardation AM Al-Futaisi, MN Al-Kindi, AM Al-Mawali, RL Koul, S Al-Adawi, ... Pediatric neurology 46 (2), 89-93, 2012 | 26 | 2012 |
| Severe autosomal recessive rippling muscle disease RL Koul, RP Chand, A Chacko, M Ali, KM Brown, SR Bushnarmuth, ... Muscle & nerve 24 (11), 1542-1547, 2001 | 26 | 2001 |
| Rituximab in severe seronegative juvenile myasthenia gravis: review of the literature R Koul, A Al Futaisi, R Abdwani Pediatric neurology 47 (3), 209-212, 2012 | 25 | 2012 |
