| Beneficial effects of lamivudine in hepatitis B virus-related decompensated cirrhosis D Kapoor, RC Guptan, SM Wakil, SN Kazim, R Kaul, SR Agarwal, ... Journal of hepatology 33 (2), 308-312, 2000 | 251 | 2000 |
| 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 | 221 | 2017 |
| A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer NA Al-Tassan, N Whiffin, FJ Hosking, C Palles, SM Farrington, ... Scientific reports 5 (1), 10442, 2015 | 141 | 2015 |
| Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases Saudi Mendeliome Group falkuaya@ kfshrc. edu. sa Genome biology 16, 1-14, 2015 | 138 | 2015 |
| Vertical transmission of hepatitis B virus despite maternal lamivudine therapy SN Kazim, SM Wakil, LA Khan, SE Hasnain, SK Sarin The Lancet 359 (9316), 1488-1489, 2002 | 132 | 2002 |
| Association of a Mutation in LACC1 With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis SM Wakil, DM Monies, M Abouelhoda, N Al‐Tassan, H Al‐Dusery, ... Arthritis & rheumatology 67 (1), 288-295, 2015 | 130 | 2015 |
| Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases H Al-Mousa, M Abouelhoda, DM Monies, N Al-Tassan, A Al-Ghonaium, ... Journal of Allergy and Clinical Immunology 137 (6), 1780-1787, 2016 | 129 | 2016 |
| A European spectrum of pharmacogenomic biomarkers: implications for clinical pharmacogenomics C Mizzi, E Dalabira, J Kumuthini, N Dzimiri, I Balogh, N Başak, R Böhm, ... PloS one 11 (9), e0162866, 2016 | 115 | 2016 |
| Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis S May-Wilson, A Sud, PJ Law, K Palin, S Tuupanen, A Gylfe, ... European Journal of Cancer 84, 228-238, 2017 | 100 | 2017 |
| Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty five patients Z Alsum, A Hawwari, O Alsmadi, S Al-Hissi, E Borrero, A Abu-staiteh, ... Journal of clinical immunology 33, 55-67, 2013 | 95 | 2013 |
| Associations of autozygosity with a broad range of human phenotypes DW Clark, Y Okada, KHS Moore, D Mason, N Pirastu, I Gandin, ... Nature communications 10 (1), 4957, 2019 | 92 | 2019 |
| Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy S Bohlega, SN Abu-Amero, SM Wakil, P Carroll, R Al-Amr, B Lach, ... Neurology 62 (9), 1518-1521, 2004 | 86 | 2004 |
| Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer H Rodriguez‐Broadbent, PJ Law, A Sud, K Palin, S Tuupanen, A Gylfe, ... International journal of cancer 140 (12), 2701-2708, 2017 | 84 | 2017 |
| Genetic Study of Saudi Diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes O Alsmadi, K Al‐Rubeaan, SM Wakil, F Imtiaz, G Mohamed, H Al‐Saud, ... Diabetes/metabolism research and reviews 24 (2), 137-140, 2008 | 74 | 2008 |
| Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer D Jarvis, JS Mitchell, PJ Law, K Palin, S Tuupanen, A Gylfe, UA Hänninen, ... British journal of cancer 115 (2), 266-272, 2016 | 71 | 2016 |
| Prevalence and profile of mutations associated with lamivudine therapy in Indian patients with chronic hepatitis B in the surface and polymerase genes of hepatitis B virus SM Wakil, SN Kazim, LA Khan, S Raisuddin, MK Parvez, RC Guptan, ... Journal of medical virology 68 (3), 311-318, 2002 | 70 | 2002 |
| A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs SM Wakil, R Ram, NP Muiya, M Mehta, E Andres, N Mazhar, B Baz, ... Atherosclerosis 245, 62-70, 2016 | 67 | 2016 |
| Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohort R Shaheen, N Patel, H Shamseldin, F Alzahrani, R Al-Yamany, ... Genetics in Medicine 18 (7), 686-695, 2016 | 64 | 2016 |
| Mutations in SMG9, encoding an essential component of nonsense-mediated decay machinery, cause a multiple congenital anomaly syndrome in humans and mice R Shaheen, S Anazi, T Ben-Omran, MZ Seidahmed, LB Caddle, K Palmer, ... The American Journal of Human Genetics 98 (4), 643-652, 2016 | 60 | 2016 |
| A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies D Monies, HN Alhindi, MA Almuhaizea, M Abouelhoda, AM Alazami, ... Human Genomics 10, 1-7, 2016 | 51 | 2016 |
Fowzan S Alkuraya, MDProfessor of Human Genetics, Alfaisal University and KFSHRC, Riyadh, Saudi ArabiaVerified email at kfshrc.edu.sa
