| Characterizing the grape transcriptome. Analysis of expressed sequence tags from multiple Vitis species and development of a compendium of gene expression during berry development F Goes da Silva, A Iandolino, F Al-Kayal, MC Bohlmann, MA Cushman, ... Plant physiology 139 (2), 574-597, 2005 | 234 | 2005 |
| Comparison of methods for isolating high-quality RNA from leaves of grapevine EAR Tattersall, A Ergul, F AlKayal, L DeLuc, JC Cushman, GR Cramer American Journal of Enology and Viticulture 56 (4), 400-406, 2005 | 98 | 2005 |
| Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population O Alsmadi, K Al-Rubeaan, G Mohamed, F Alkayal, H Al-Saud, NA Al-Saud, ... BMC medical genetics 9, 1-7, 2008 | 97 | 2008 |
| Vitamin D insufficiency in Arabs and South Asians positively associates with polymorphisms in GC and CYP2R1 genes N Elkum, F Alkayal, F Noronha, MM Ali, M Melhem, M Al-Arouj, ... PloS one 9 (11), e113102, 2014 | 89 | 2014 |
| Expressed sequence tag (EST) profiling in hyper saline shocked Dunaliella salina reveals high expression of protein synthetic apparatus components F Alkayal, RL Albion, RL Tillett, LT Hathwaik, MS Lemos, JC Cushman Plant Science 179 (5), 437-449, 2010 | 70 | 2010 |
| Genetic substructure of Kuwaiti population reveals migration history O Alsmadi, G Thareja, F Alkayal, R Rajagopalan, SE John, P Hebbar, ... PloS one 8 (9), e74913, 2013 | 57 | 2013 |
| Specific and complete human genome amplification with improved yield achieved by phi29 DNA polymerase and a novel primer at elevated temperature O Alsmadi, F Alkayal, D Monies, BF Meyer BMC Research Notes 2, 1-7, 2009 | 56 | 2009 |
| Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3) O Alsmadi, BF Meyer, F Alkuraya, S Wakil, F Alkayal, H Al-Saud, ... European Journal of Human Genetics 17 (1), 14-21, 2009 | 36 | 2009 |
| Genetic risk variants for metabolic traits in Arab populations P Hebbar, N Elkum, F Alkayal, SE John, TA Thanaraj, O Alsmadi Scientific reports 7 (1), 40988, 2017 | 32 | 2017 |
| Molecular analysis of T-B-NK+severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia O Alsmadi, A Al-Ghonaium, S Al-Muhsen, R Arnaout, H Al-Dhekri, ... BMC medical genetics 10, 1-7, 2009 | 32 | 2009 |
| Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia M Melhem, M Abu‐Farha, D Antony, AA Madhoun, C Bacchelli, F Alkayal, ... European Journal of Haematology 98 (3), 218-227, 2017 | 30 | 2017 |
| Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population P Hebbar, R Nizam, M Melhem, F Alkayal, N Elkum, SE John, ... Journal of lipid research 59 (10), 1951-1966, 2018 | 25 | 2018 |
| Leptin in association with common variants of MC3R mediates hypertension O Alsmadi, M Melhem, P Hebbar, G Thareja, SE John, F Alkayal, ... American journal of hypertension 27 (7), 973-981, 2014 | 22 | 2014 |
| Higher levels of ANGPTL5 in the circulation of subjects with obesity and type 2 diabetes are associated with insulin resistance G Alghanim, MG Qaddoumi, N Alhasawi, P Cherian, I Al-Khairi, R Nizam, ... Frontiers in Endocrinology 10, 495, 2019 | 20 | 2019 |
| MC4R variant rs17782313 associates with increased levels of DNAJC27, ghrelin, and visfatin and correlates with obesity and hypertension in a Kuwaiti cohort MM Hammad, M Abu-Farha, P Hebbar, P Cherian, I Al Khairi, M Melhem, ... Frontiers in Endocrinology 11, 535480, 2020 | 19 | 2020 |
| Frequency of common HFEvariants in the Saudi population: a high throughput molecular beacon-based study OA Alsmadi, F Al-Kayal, M Al-Hamed, BF Meyer BMC Medical Genetics 7, 1-7, 2006 | 19 | 2006 |
| FTO Variant rs1421085 Associates With Increased Body Weight, Soft Lean Mass, and Total Body Water Through Interaction With Ghrelin and Apolipoproteins in … P Hebbar, M Abu-Farha, A Mohammad, F Alkayal, M Melhem, J Abubaker, ... Frontiers in genetics 10, 1411, 2020 | 16 | 2020 |
| Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population P Hebbar, M Abu-Farha, F Alkayal, R Nizam, N Elkum, M Melhem, ... Scientific reports 10 (1), 152, 2020 | 16 | 2020 |
| Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population P Hebbar, JA Abubaker, M Abu-Farha, O Alsmadi, N Elkum, F Alkayal, ... Human genetics 140, 505-528, 2021 | 15 | 2021 |
| The TCN2 variant of rs9606756 [Ile23Val] acts as risk loci for obesity‐related traits and mediates by interacting with Apo‐A1 P Hebbar, F Alkayal, R Nizam, M Melhem, N Elkum, SE John, M Abufarha, ... Obesity 25 (6), 1098-1108, 2017 | 15 | 2017 |
