| Timing of surgery following SARS‐CoV‐2 infection: an international prospective cohort study H Gacaferi, GS Collaborative, COVIDSurg Collaborative Anaesthesia 76 (6), 2021 | 538* | 2021 |
| SARS-CoV-2 infection and venous thromboembolism after surgery: an international prospective cohort study. C COVIDSurg, C GlobalSurg Anaesthesia 77 (1), 28-39, 2022 | 101 | 2022 |
| Mutation in noncoding RNA RNU12 causes early onset cerebellar ataxia MF Elsaid, N Chalhoub, T Ben‐Omran, P Kumar, H Kamel, K Ibrahim, ... Annals of neurology 81 (1), 68-78, 2017 | 79 | 2017 |
| Recurrence risk after a first febrile convulsion MS Bessisso, MF Elsaid, NA Almula, NK Kadomi, SH Zeidan, SB Azzam, ... Saudi medical journal 22 (3), 254-258, 2001 | 69 | 2001 |
| Autosomal recessive inheritance of GLUT1 deficiency syndrome J Klepper, H Scheffer, MF Elsaid, EJ Kamsteeg, M Leferink, T Ben-Omran Neuropediatrics 40 (05), 207-210, 2009 | 68 | 2009 |
| A common mutation in the CBS gene explains a high incidence of homocystinuria in the Qatari population MF El‐Said, R Badii, MS Bessisso, N Shahbek, MG El‐Ali, M El‐Marikhie, ... Human mutation 27 (7), 719-719, 2006 | 60 | 2006 |
| Effects of pre‐operative isolation on postoperative pulmonary complications after elective surgery: an international prospective cohort study COVIDSurg Collaborative, GlobalSurg Collaborative, D Nepogodiev, ... Anaesthesia 76 (11), 1454-1464, 2021 | 42 | 2021 |
| Gene therapy for spinal muscular atrophy: the Qatari experience HG Ali, K Ibrahim, MF Elsaid, RB Mohamed, MIA Abeidah, AO Al Rawwas, ... Gene Therapy 28 (10), 676-680, 2021 | 38 | 2021 |
| Altered PLP1 splicing causes hypomyelination of early myelinating structures SH Kevelam, JR Taube, RML van Spaendonk, E Bertini, K Sperle, ... Annals of clinical and translational neurology 2 (6), 648-661, 2015 | 35 | 2015 |
| Pattern of headache in school children in the State of Qatar. MS Bessisso, A Bener, MF Elsaid, FA Al-Khalaf, KA Huzaima Saudi medical journal 26 (4), 566-570, 2005 | 33 | 2005 |
| Neuro-imaging evaluation after the first afebrile seizure in children: A retrospective observational study R Al-Shami, AM Khair, M Elseid, K Ibrahim, A Al-Ahmad, A Elsetouhy, ... Seizure 43, 26-31, 2016 | 32 | 2016 |
| W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report L Elsaadany, M El-Said, R Ali, H Kamel, T Ben-Omran BMC Medical Genetics 17, 1-6, 2016 | 32 | 2016 |
| Acute bacterial meningitis in Qatar MF Elsaid, AA Flamerzi, MS Bessisso, SS Elshafie Saudi medical journal 27 (2), 198, 2006 | 28 | 2006 |
| Novel hypomyelinating leukoencephalopathy affecting early myelinating structures ME Steenweg, NI Wolf, JH Schieving, MF Elsaid, RL Friederich, ... Archives of neurology 69 (1), 125-128, 2012 | 26 | 2012 |
| Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy S Lakhani, R Doan, M Almureikhi, JN Partlow, M Al Saffar, MF Elsaid, ... European journal of medical genetics 60 (5), 245-249, 2017 | 25 | 2017 |
| Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance P Kumar, M Al-Shafai, WA Al Muftah, N Chalhoub, MF Elsaid, AA Aleem, ... BMC Research Notes 7, 1-13, 2014 | 20 | 2014 |
| Whole genome sequencing identifies a novel occludin mutation in microcephaly with band-like calcification and polymicrogyria that extends the phenotypic spectrum MF Elsaid, H Kamel, N Chalhoub, NA Aziz, K Ibrahim, T Ben-Omran, ... Am J Med Genet A 164 (6), 1614-1617, 2014 | 20 | 2014 |
| NT5C2 novel splicing variant expands the phenotypic spectrum of Spastic Paraplegia (SPG45): case report of a new member of thin corpus callosum SPG-Subgroup MF Elsaid, K Ibrahim, N Chalhoub, A Elsotouhy, N El Mudehki, ... BMC Medical Genetics 18, 1-7, 2017 | 18 | 2017 |
| Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant AA Aleem, MF Elsaid, N Chalhoub, A Chakroun, KAS Mohamed, ... Neuromuscular Disorders 30 (6), 457-471, 2020 | 17 | 2020 |
| Are heterocygotes for classical homocystinuria at risk of vitamin B12 and folic acid deficiency? MF Elsaid, A Bener, M Lindner, M Alzyoud, N Shahbek, MO Abdelrahman, ... Molecular genetics and metabolism 92 (1-2), 100-103, 2007 | 17 | 2007 |
Margaret Elizabeth RossWeill Cornell Medical CollegeVerified email at med.cornell.edu
