Johansen, Christopher T <br/><br/>
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia.  [electronic resource] 

 -  Arteriosclerosis, thrombosis, and vascular biology  Aug 2011 
 - 1916-26 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1524-4636 
<br/><br/><label>Standard No.: </label>10.1161/ATVBAHA.111.226365  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Alleles<br/>Apolipoprotein E2--genetics<br/>Case-Control Studies<br/>Cholesterol, HDL--blood<br/>Cholesterol, LDL--blood<br/>Female<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Humans<br/>Hyperlipoproteinemia Type IV--blood<br/>Hypertriglyceridemia--blood<br/>Lipids--blood<br/>Male<br/>Middle Aged<br/>Multifactorial Inheritance<br/>Phenotype<br/>Risk Factors<br/>Triglycerides--blood