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Role of DNA copy number variation in dyslipidemias.
Iacocca MA, Hegele RA. Iacocca MA, et al. Among authors: hegele ra. Curr Opin Lipidol. 2018 Apr;29(2):125-132. doi: 10.1097/MOL.0000000000000483. Curr Opin Lipidol. 2018. PMID: 29303791 Review.
Polygenic influences on dyslipidemias.
Dron JS, Hegele RA. Dron JS, et al. Among authors: hegele ra. Curr Opin Lipidol. 2018 Apr;29(2):133-143. doi: 10.1097/MOL.0000000000000482. Curr Opin Lipidol. 2018. PMID: 29300201 Review.
Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia.
Dron JS, Wang J, Berberich AJ, Iacocca MA, Cao H, Yang P, Knoll J, Tremblay K, Brisson D, Netzer C, Gouni-Berthold I, Gaudet D, Hegele RA. Dron JS, et al. Among authors: hegele ra. J Lipid Res. 2018 Aug;59(8):1529-1535. doi: 10.1194/jlr.P086280. Epub 2018 Jun 4. J Lipid Res. 2018. PMID: 29866657 Free PMC article.
ClinVar database of global familial hypercholesterolemia-associated DNA variants.
Iacocca MA, Chora JR, Carrié A, Freiberger T, Leigh SE, Defesche JC, Kurtz CL, DiStefano MT, Santos RD, Humphries SE, Mata P, Jannes CE, Hooper AJ, Wilemon KA, Benlian P, O'Connor R, Garcia J, Wand H, Tichy L, Sijbrands EJ, Hegele RA, Bourbon M, Knowles JW; ClinGen FH Variant Curation Expert Panel. Iacocca MA, et al. Among authors: hegele ra. Hum Mutat. 2018 Nov;39(11):1631-1640. doi: 10.1002/humu.23634. Hum Mutat. 2018. PMID: 30311388 Free PMC article.
Severe hypertriglyceridemia is primarily polygenic.
Dron JS, Wang J, Cao H, McIntyre AD, Iacocca MA, Menard JR, Movsesyan I, Malloy MJ, Pullinger CR, Kane JP, Hegele RA. Dron JS, et al. Among authors: hegele ra. J Clin Lipidol. 2019 Jan-Feb;13(1):80-88. doi: 10.1016/j.jacl.2018.10.006. Epub 2018 Oct 24. J Clin Lipidol. 2019. PMID: 30466821 Free article.
964 results