Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits.Speliotes EK, Yerges-Armstrong LM, Wu J, Hernaez R, Kim LJ, Palmer CD, Gudnason V, Eiriksdottir G, Garcia ME, Launer LJ, Nalls MA, Clark JM, Mitchell BD, Shuldiner AR, Butler JL, Tomas M, Hoffmann U, Hwang SJ, Massaro JM, O'Donnell CJ, Sahani DV, Salomaa V, Schadt EE, Schwartz SM, Siscovick DS, NASH CRN, GIANT Consortium, MAGIC Investigators, Voight BF, Carr JJ, Feitosa MF, Harris TB, Fox CS, Smith AV, Kao WH, Hirschhorn JN, Borecki IB, GOLD Consortium
(2011)
PLoS Genet 7: e1001324
MeSH Terms: Adaptor Proteins, Signal Transducing, Adult, Aged, Aged, 80 and over, Blood Glucose, Case-Control Studies, Chondroitin Sulfate Proteoglycans, Cohort Studies, Fatty Liver, Genome-Wide Association Study, Humans, Insulin, Lectins, C-Type, Lipase, Male, Membrane Proteins, Middle Aged, Mutation, Missense, Nerve Tissue Proteins, Neurocan, Non-alcoholic Fatty Liver Disease, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Tomography, X-Ray ComputedAdded February 15, 2014