Search
Skip to Search Results- 3Hegele, Robert A.
- 3Young, T. Kue
- 2Ban, Matthew R.
- 2Bjerregaard, Peter
- 2Wang, Jian
- 1Burnett, John R.
- 2Complex disease
- 2Genetics
- 2Greenland
- 2Single nucleotide polymorphisms
- 1Aboriginal
- 1Adipose triglyceride lipase
-
Rare ATGL haplotypes are associated with increased plasma triglyceride concentrations in the Greenland Inuit
Download2012-03-18
Johansen, Christopher T., Gallinger, Zane R., Wang, Jian, Ban, Matthew R., Young, T. Kue, Bjerregaard, Peter, Hegele, Robert A.
"Objectives: To genotype common genetic variants found in the adipose triglyceride lipase (ATGL) gene and test them for association with cardiovascular disease risk factors in the Greenland Inuit. Study design: Candidate gene association study of discrete and quantitative traits related to...
-
Common variants APOC3, APOA5, APOE and PON1 are associated with variation in plasma lipoprotein traits in Greenlanders
Download2007-12-01
Lahiry, Piya, Ban, Matthew R., Pollex, Rebecca L., Sawyez, Cynthia G., Huff, Murray W., Young, T. Kue, Bjerregaard, Peter, Hegele, Robert A.
"Objectives: We undertook studies of the association between common genomic variations in APOC3, APOA5, APOE and PON1 genes and variation in biochemical phenotypes in a sample of Greenlanders. Study Design: Genetic association study of quantitative lipoprotein traits. Methods: In a sample of...
-
2000-08-01
Wang, Jian, Burnett, John R., Near, Susan, Young, T. Kue, Zinman, Bernard, Hanley, Anthony J. G., Connelly, Philip W., Harris, Stewart B., Hegele, Robert A.
"Mutations in ABCA1, a member of the ATP-binding cassette family, have been shown to underlie Tangier disease (TD) and familial hypoalphalipoproteinemia (FHA), which are genetic disorders that are characterized by depressed concentrations of plasma high density lipoprotein (HDL) cholesterol. An...