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O. Alsmadi · SciRah

Researcher profile · Semantic Scholar

O. Alsmadi

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O. Alsmadi — researcher profile on SciRah

h-index: 28
Works: 102
Citations: 2,353

Most-cited papers

Imaging Native β-Actin mRNA in Motile Fibroblasts
Sanjay Tyagi, O. Alsmadi
2004138 citations Open access
Semantic Scholar
High-throughput genotyping of single nucleotide polymorphisms with rolling circle amplification
A. Faruqi, S. Hosono, M. Driscoll, F. Dean +10 more
2001BMC Genomics133 citations Open access
Semantic Scholar
Metabolic Disease Risk in Children by Salivary Biomarker Analysis
J. Goodson, A. Kantarcı, M. Hartman, G. Denis +14 more
2014PLoS ONE116 citations Open access
Semantic Scholar
The salivary microbiome is altered in the presence of a high salivary glucose concentration
J. Goodson, M. Hartman, Ping Shi, H. Hasturk +11 more
2017PLoS ONE108 citations Open access
Semantic Scholar
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, Safaa Al-Hissi +11 more
2012Journal of Clinical Immunology85 citations
Semantic Scholar
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 +5 more
2009BMC Medical Genetics85 citations Open access
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
Whole genome amplification from a single cell: a new era for preimplantation genetic diagnosis
S. Coskun, O. Alsmadi
2007Prenatal Diagnosis65 citations
Semantic Scholar
Genetic Study of Saudi Diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes
O. Alsmadi, K. Al-Rubeaan, S. Wakil, F. Imtiaz +6 more
2008Diabetes/Metabolism Research Reviews62 citations
Semantic Scholar
Imaging native beta-actin mRNA in motile fibroblasts.
Sanjay Tyagi, O. Alsmadi
2004Biophysical Journal59 citations
Semantic Scholar
Obesity and Dental Decay: Inference on the Role of Dietary Sugar
J. Goodson, M. Tavares, Xiaoshan Wang, R. Niederman +9 more
2013PLoS ONE57 citations Open access
Semantic Scholar
Clinical, Immunological, and Molecular Characterization of Hyper-IgM Syndrome Due to CD40 Deficiency in Eleven Patients
B. Al-Saud, Zobaida Al-Sum, Hanadi Alassiri, A. Al-ghonaium +9 more
2013Journal of Clinical Immunology56 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
Pleiotropic Effects of YC-1 Selectively Inhibit Pathological Retinal Neovascularization and Promote Physiological Revascularization in a Mouse Model of Oxygen-Induced Retinopathy
Michael Deniro, A. Al-Halafi, F. Al-Mohanna, O. Alsmadi +1 more
2010Molecular Pharmacology51 citations
Semantic Scholar
A Review of Adult Obesity Prevalence, Trends, Risk Factors, and Epidemiologic Methods in Kuwait
S. Karageorgi, O. Alsmadi, K. Behbehani
2013Journal of Obesity45 citations Open access
Semantic Scholar
Antibody-Dependent Cellular Cytotoxicity Directed against Cells Expressing Human Immunodeficiency Virus Type 1 Envelope of Primary or Laboratory-Adapted Strains by Human and Chimpanzee Monoclonal Antibodies of Different Epitope Specificities
O. Alsmadi, S. A. Tilley
1998Journal of Virology42 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
Sequence and analysis of a whole genome from Kuwaiti population subgroup of Persian ancestry
Gaurav Thareja, S. John, Prashantha Hebbar, K. Behbehani +2 more
2015BMC Genomics36 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
Genome at Juncture of Early Human Migration: A Systematic Analysis of Two Whole Genomes and Thirteen Exomes from Kuwaiti Population Subgroup of Inferred Saudi Arabian Tribe Ancestry
O. Alsmadi, S. John, Gaurav Thareja, Prashantha Hebbar +3 more
2014PLoS ONE35 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
Modulating the hypoxia-inducible factor signaling pathway as a therapeutic modality to regulate retinal angiogenesis.
Michael Deniro, O. Alsmadi, F. Al-Mohanna
2009Experimental Eye Research34 citations
Semantic Scholar
Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics
S. John, Dinu Antony, M. Eaaswarkhanth, Prashantha Hebbar +7 more
2018Scientific Reports31 citations Open access
Semantic Scholar
Insight into the impact of diabetes mellitus on the increased risk of hepatocellular carcinoma: mini-review
Maisa Mahmoud Ali Kamkar, R. Ahmad, O. Alsmadi, K. Behbehani
2014Journal of Diabetes and Metabolic Disorders31 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
Major Histocompatibility Complex Class II Deficiency in Kuwait: Clinical Manifestations, Immunological Findings and Molecular Profile
W. Al-Herz, O. Alsmadi, Motasem Melhem, M. Recher +2 more
2013Journal of Clinical Immunology29 citations
Semantic Scholar
Salivary glucose concentration exhibits threshold kinetics in normal-weight, overweight, and obese children
M. Hartman, J. Goodson, R. Barake, O. Alsmadi +6 more
2014Diabetes, Metabolic Syndrome and Obesity : Targets and Therapy28 citations Open access
Semantic Scholar
Kuwaiti population subgroup of nomadic Bedouin ancestry—Whole genome sequence and analysis
S. John, Gaurav Thareja, Prashantha Hebbar, K. Behbehani +2 more
2014Genomics Data25 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
Association of FTO rs9939609 with Obesity in the Kuwaiti Population: A Public Health Concern?
Ahmad E. Al-Serri, S. Al-Bustan, M. Kamkar, Daisy Thomas +4 more
2018Medical Principles and Practice23 citations Open access
Semantic Scholar
Continuous Metabolic Syndrome Scores for Children Using Salivary Biomarkers
Ping Shi, J. Goodson, M. Hartman, H. Hasturk +11 more
2015PLoS ONE23 citations Open access
Semantic Scholar
Ocular manifestations in chronic granulomatous disease in Saudi Arabia.
S. Al-Muhsen, A. Al-Hemidan, Amer Al-Shehri, A. Al-Harbi +7 more
2009Journal of AAPOS23 citations
Semantic Scholar
Genetic and clinical characteristics of pediatric patients with familial hemophagocytic lymphohistiocytosis
A. Al-Ahmari, O. Alsmadi, A. Sheereen, T. Elamin +9 more
2021Blood Research22 citations Open access
Semantic Scholar
Mutations underlying 3-Hydroxy-3-Methylglutaryl CoA Lyase deficiency in the Saudi population
M. Al-Sayed, F. Imtiaz, O. Alsmadi, Mohammed S. Rashed +1 more
2006BMC Medical Genetics22 citations Open access
Semantic Scholar
ANGPTL8/Betatrophin R59W variant is associated with higher glucose level in non-diabetic Arabs living in Kuwaits
Mohamed Abu-Farha, Motasem Melhem, J. Abubaker, K. Behbehani +2 more
2016Lipids in Health and Disease21 citations Open access
Semantic Scholar
A novel mutation in purine nucleoside phosphorylase in a child with normal uric acid levels.
B. Al-Saud, O. Alsmadi, S. Al-Muhsen, A. Al-ghonaium +4 more
2009Clinical Biochemistry20 citations
Semantic Scholar
Haplotypes Encompassing the KIAA0391 and PSMA6 Gene Cluster Confer a Genetic Link for Myocardial Infarction and Coronary Artery Disease
O. Alsmadi, P. Muiya, H. Khalak, H. Al-Saud +4 more
2009Annals of Human Genetics20 citations
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
Mitochondrial DNA D-loop sequencing reveals obesity variants in an Arab population
M. Eaaswarkhanth, Motasem Melhem, Prem Sharma, R. Nizam +5 more
2019The Application of Clinical Genetics19 citations Open access
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
Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria
M. Al-Sayed, S. AlAhmed, O. Alsmadi, H. Khalil +3 more
2005Journal of Inherited Metabolic Disease19 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
Caveolin-1 Variant Is Associated With the Metabolic Syndrome in Kuwaiti Children
R. Nizam, E. Al-Ozairi, J. Goodson, Motesam Melhem +20 more
2018Frontiers 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
Epidemiology of Chronic Granulomatous Disease of Childhood in Eastern Province, Saudi Arabia
F. Suliaman, Nasir K. Amra, S. Sheikh, S. Al-Muhsen +1 more
200917 citations
Semantic Scholar
ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait
R. Behbehani, Motasem Melhem, Ghazi Alghanim, K. Behbehani +1 more
2014British Journal of Ophthalmology16 citations Open access
Semantic Scholar
Salivary Biomarkers in Pediatric Metabolic Disease Research.
M. Hartman, J. Goodson, R. Barake, O. Alsmadi +5 more
2016Pediatric Endocrinology Reviews: diabetes, nutrition, metabolism15 citations
Semantic Scholar
The Nexus between VEGF and NFκB Orchestrates a Hypoxia-Independent Neovasculogenesis
Michael Deniro, F. Al-Mohanna, O. Alsmadi, F. Al-Mohanna
2013PLoS ONE15 citations Open access
Semantic Scholar

Frequent co-authors

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K. Behbehani×16
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K. Behbehani — researcher profile on SciRah
Fadi Alkayal×13
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Fadi Alkayal — researcher profile on SciRah
S. John×12
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S. John — researcher profile on SciRah
Prashantha Hebbar×12
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T. Thanaraj — researcher profile on SciRah

Motasem Melhem×11

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Motasem Melhem — researcher profile on SciRah

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B. Meyer — researcher profile on SciRah

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N. Elkum — researcher profile on SciRah

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M. Hartman — researcher profile on SciRah

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S. Al-Mutawa×6

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S. Al-Mutawa — researcher profile on SciRah