Studies
Treatment of Genetic Screening of Hypertriglyceridemia type I, III, and V - HTG Amsterdam
Treatment of Genetic Screening of Hypertriglyceridemia type I, III, and V - HTG Amsterdam
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Overview
Selected Publications (3)
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
C. T. Johansen, Jian Wang, M. Lanktree, et al.. (2010). Nature Genetics. Cited 470 times.
https://doi.org/10.1038/ng.628
Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia
R. P. Surendran, M. Visser, S. Heemelaar, et al.. (2012). Journal of Internal Medicine. Cited 235 times.
https://doi.org/10.1111/j.1365-2796.2012.02516.x
An Increased Burden of Common and Rare Lipid-Associated Risk Alleles Contributes to the Phenotypic Spectrum of Hypertriglyceridemia
C. T. Johansen, Jian Wang, M. Lanktree, et al.. (2011). Arteriosclerosis, Thrombosis, and Vascular Biology. Cited 92 times.
https://doi.org/10.1161/ATVBAHA.111.226365
