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Author
- Choi, Jungmin1
- Chu, Catherine1
- Dong, Weilai1
- Hung, Wei-Chien1
- Jin, Sheng Chih1
- Kane, John P1
- Kwok, Pui-Yan1
- Lao, Richard1
- Levy-Sakin, Michal1
- Li, Boyang1
- Li, Mo1
- Lifton, Richard P1
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- Lopez-Giraldez, Francesc1
- Malloy, Mary J1
- Movsesyan, Irina1
- Poon, Annie1
- Pullinger, Clive R1
- Vaka, Dedeepya1
- Wong, Karen HY1
- Zhao, Hongyu1
Keyword
- CHD1
- CNV1
- copy number variant1
- coronary heart disease1
- dyslipidemia1
- gene ontology1
- genetics1
- Genomic Resource in Arteriosclerosis1
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- scavenger receptor class B, type 11
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Regular Research Articles
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- Research ArticleOpen Access
Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia
Journal of Lipid ResearchVol. 63Issue 6100209Published online: April 20, 2022- Weilai Dong
- Karen H.Y. Wong
- Youbin Liu
- Michal Levy-Sakin
- Wei-Chien Hung
- Mo Li
- and others
Cited in Scopus: 0Low levels of high density lipoprotein-cholesterol (HDL-C) are associated with an elevated risk of arteriosclerotic coronary heart disease. Heritability of HDL-C levels is high. In this research discovery study, we used whole-exome sequencing to identify damaging gene variants that may play significant roles in determining HDL-C levels. We studied 204 individuals with a mean HDL-C level of 27.8 ± 6.4 mg/dl (range: 4–36 mg/dl). Data were analyzed by statistical gene burden testing and by filtering against candidate gene lists.