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Author
- Alkayal, Fadi1
- Alsmadi, Osama1
- Cai, Tianxi1
- Elkum, Naser1
- Furtado, Jeremy D1
- Gray, Brianna E1
- Hebbar, Prashantha1
- Jensen, Majken K1
- Jiang, Gordon Z1
- John, Sumi Elsa1
- Kang, Moonil1
- Koch, Manja1
- Melhem, Motasem1
- Nizam, Rasheeba1
- Overvad, Kim1
- Sacks, Frank1
- Sung, Joohon1
- Thanaraj, Thangavel Alphonse1
- Tjønneland, Anne1
- Tuomilehto, Jaakko1
JLR Patient-Oriented and Epidemiological Research
3 Results
- Patient-Oriented and Epidemiological ResearchOpen Access
A genome-wide search for gene-by-obesity interaction loci of dyslipidemia in Koreans shows diverse genetic risk alleles
Journal of Lipid ResearchVol. 60Issue 12p2090–2101Published online: October 29, 2019- Moonil Kang
- Joohon Sung
Cited in Scopus: 2Dyslipidemia is a well-established risk factor for CVD. Studies suggest that similar fat accumulation in a given population might result in different levels of dyslipidemia risk among individuals; for example, despite similar or leaner body composition compared with Caucasians, Asians of Korean descent experience a higher prevalence of dyslipidemia. These variations imply a possible role of gene-obesity interactions on lipid profiles. Genome-wide association studies have identified more than 500 loci regulating plasma lipids, but the interaction structure between genes and obesity traits remains unclear. - Patient-Oriented and Epidemiological ResearchOpen Access
Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population
Journal of Lipid ResearchVol. 59Issue 10p1951–1966Published online: August 14, 2018- Prashantha Hebbar
- Rasheeba Nizam
- Motasem Melhem
- Fadi Alkayal
- Naser Elkum
- Sumi Elsa John
- and others
Cited in Scopus: 14Abnormal blood lipid levels are influenced by genetic and lifestyle/dietary factors. Although many genetic variants associated with blood lipid traits have been identified in Europeans, similar data in Middle Eastern populations are limited. We performed a genome-wide association study with Arab individuals (discovery cohort: 1,353; replication cohort: 1,176) from Kuwait to identify possible associations of genetic variants with high lipid levels. We used Illumina HumanOmniExpress BeadChip and candidate SNP genotyping in the discovery and replication phases, respectively. - Patient-Oriented and Epidemiological ResearchOpen Access
Associations of anthropometry and lifestyle factors with HDL subspecies according to apolipoprotein C-III
Journal of Lipid ResearchVol. 58Issue 6p1196–1203Published online: April 1, 2017- Manja Koch
- Jeremy D. Furtado
- Gordon Z. Jiang
- Brianna E. Gray
- Tianxi Cai
- Frank Sacks
- and others
Cited in Scopus: 16The presence of apoC-III on HDL impairs HDL's inverse association with coronary heart disease (CHD). Little is known about modifiable factors explaining variation in HDL subspecies defined according to apoC-III. The aim was to investigate cross-sectional associations of anthropometry and lifestyle with HDL subspecies in 3,631 participants from the Diet, Cancer, and Health study originally selected for a case-cohort study (36% women; age 50–65 years) who were all free of CHD. Greater adiposity and less activity were associated with higher HDL containing apoC-III and lower HDL lacking apoC-III.