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Fadi Alkayal · SciRah

Researcher profile · Semantic Scholar

Fadi Alkayal

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Fadi Alkayal — researcher profile on SciRah

h-index: 16
Works: 28
Citations: 689

Most-cited papers

Comparison of Methods for Isolating High-Quality RNA from Leaves of Grapevine
E. Tattersall, A. Ergül, Fadi Alkayal, L. Deluc +2 more
2005American Journal of Enology and Viticulture86 citations
Semantic Scholar
Weak or no association of TCF7L2 variants with Type 2 diabetes risk in an Arab population
O. Alsmadi, K. Al-Rubeaan, G. Mohamed, Fadi Alkayal +5 more
2008BMC Medical Genetics83 citations Open access
Semantic Scholar
Vitamin D Insufficiency in Arabs and South Asians Positively Associates with Polymorphisms in GC and CYP2R1 Genes
N. Elkum, Fadi Alkayal, Fiona Noronha, Maisa M. Ali +6 more
2014PLoS ONE75 citations Open access
Semantic Scholar
Expressed sequence tag (EST) profiling in hyper saline shocked Dunaliella salina reveals high expression of protein synthetic apparatus components.
Fadi Alkayal, Rebecca L. Albion, R. Tillett, Leyla T. Hathwaik +2 more
2010Plant Science61 citations
Semantic Scholar
Genetic Substructure of Kuwaiti Population Reveals Migration History
O. Alsmadi, Gaurav Thareja, Fadi Alkayal, R. Rajagopalan +4 more
2013PLoS ONE56 citations Open access
Semantic Scholar
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)
O. Alsmadi, B. Meyer, F. Alkuraya, S. Wakil +4 more
2009European Journal of Human Genetics40 citations Open access
Semantic Scholar
Specific and complete human genome amplification with improved yield achieved by phi29 DNA polymerase and a novel primer at elevated temperature
O. Alsmadi, Fadi Alkayal, D. Monies, B. Meyer
2009BMC Research Notes36 citations Open access
Semantic Scholar
Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia
Motasem Melhem, Mohamed Abu-Farha, Dinu Antony, A. Al Madhoun +7 more
2017European Journal of Haematology34 citations Open access
Semantic Scholar
Genetic risk variants for metabolic traits in Arab populations
Prashantha Hebbar, N. Elkum, Fadi Alkayal, S. John +2 more
2017Scientific Reports29 citations Open access
Semantic Scholar
MC4R Variant rs17782313 Associates With Increased Levels of DNAJC27, Ghrelin, and Visfatin and Correlates With Obesity and Hypertension in a Kuwaiti Cohort
Maha M. Hammad, Mohamed Abu-Farha, Prashantha Hebbar, Preethi Cherian +7 more
2020Frontiers in Endocrinology24 citations Open access
Semantic Scholar
Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population
Prashantha Hebbar, R. Nizam, Motasem Melhem, Fadi Alkayal +5 more
202019 citations
Semantic Scholar
Leptin in association with common variants of MC3R mediates hypertension.
O. Alsmadi, Motasem Melhem, Prashantha Hebbar, Gaurav Thareja +4 more
2014American Journal of Hypertension19 citations
Semantic Scholar
Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population
Prashantha Hebbar, J. Abubaker, Mohamed Abu-Farha, O. Alsmadi +10 more
2020Human Genetics18 citations Open access
Semantic Scholar
Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population
Prashantha Hebbar, Mohamed Abu-farha, Fadi Alkayal, R. Nizam +12 more
2020Scientific Reports18 citations Open access
Semantic Scholar
FTO Variant rs1421085 Associates With Increased Body Weight, Soft Lean Mass, and Total Body Water Through Interaction With Ghrelin and Apolipoproteins in Arab Population
Prashantha Hebbar, Mohamed Abu-Farha, Anwar Mohammad, Fadi Alkayal +4 more
2020Frontiers in Genetics17 citations Open access
Semantic Scholar
The TCN2 variant of rs9606756 [Ile23Val] acts as risk loci for obesity‐related traits and mediates by interacting with Apo‐A1
Prashantha Hebbar, Fadi Alkayal, R. Nizam, Motasem Melhem +5 more
2017Obesity17 citations
Semantic Scholar
Higher Levels of ANGPTL5 in the Circulation of Subjects With Obesity and Type 2 Diabetes Are Associated With Insulin Resistance
Ghazi Alghanim, M. Qaddoumi, N. Alhasawi, Preethi Cherian +8 more
2019Frontiers in Endocrinology16 citations Open access
Semantic Scholar
Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population[S]
Prashantha Hebbar, R. Nizam, Motasem Melhem, Fadi Alkayal +5 more
2018Journal of Lipid Research14 citations Open access
Semantic Scholar
Investigation of genetic variation and lifestyle determinants in vitamin D levels in Arab individuals
Massimo Mezzavilla, S. Tomei, Fadi Alkayal, Motasem Melhem +5 more
2018Journal of Translational Medicine9 citations Open access
Semantic Scholar
Genetic variants associated with warfarin dosage in Kuwaiti population.
S. John, Dinu Antony, M. Eaaswarkhanth, Prashantha Hebbar +4 more
2017Pharmacogenomics (London)5 citations
Semantic Scholar
ANGPTL3 Variants Associate with Lower Levels of Irisin and C-Peptide in a Cohort of Arab Individuals
M. Alanbaei, Mohamed Abu-farha, Prashantha Hebbar, Motasem Melhem +8 more
2021Genes4 citations Open access
Semantic Scholar
Survivin and MKI67 mRNA Expression in Bladder Washings of Patients with Superficial Urothelial Cell Carcinoma Correlate with Tumor Stage and Grade but Do Not Predict Tumor Recurrence
O. Alsmadi, Fadi Alkayal, M. Al-Sayed, M. Rashed +2 more
20064 citations
Semantic Scholar
Response to leptin and nitric oxide in blood pressure regulation in humans.
O. Alsmadi, Motasem Melhem, Prashantha Hebbar, A. Channanath +5 more
2014American Journal of Hypertension2 citations Open access
Semantic Scholar
LCGreen I-based real-time PCR assays for detecting common ASL and HMGCL variants.
O. Alsmadi, Fadi Alkayal, M. Al-Sayed, M. Rashed +2 more
2006Clinical Chemistry2 citations
Semantic Scholar
Underlying Molecular Genetic Defects in T- B- NK+ Severe Combined Immunodeficiency Disease in Saudi Arabia
H. Al-Mousa, A. Alghonaim, H. Al-Dhekri, S. Al-Muhsen +8 more
20081 citations
Semantic Scholar
Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population
Prashantha Hebbar, J. Abubaker, Mohamed Abu-Farha, O. Alsmadi +10 more
2020Human Genetics0 citations Open access
Semantic Scholar
. Amylin (an insulin co-secretor) is significantly reduced at one year after Laparoscopy Sleeve Gastrectomy in both morbidly obese diabetic and non-diabetic patients
F. Al-asfar, E. Al-Ozairi, E. Alshawaf, S. Al-Beloushi +4 more
20170 citations
Semantic Scholar
Title : Novel G 6 B gene variant cause familial autosomal recessive thrombocytopenia and anemia Running title : Melhem et al . G 6 B NOVEL VARIANT CAUSE THROMBOCYTOPENIA AND ANEMIA
Motasem Melhem, Mohamed Abu-Farha, Dinu Antony, A. Al Madhoun +8 more
20160 citations
Semantic Scholar

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