Association between bilirubin and cardiovascular disease risk factors: using Mendelian randomization to assess causal inference.
BMC Cardiovasc Disord., 12:16 (2012)
Serum alanine aminotransferase is correlated with hematocrit in healthy human subjects.
Scand. J. Clin. Lab. Invest., May;72(3):258-64 (2012)
A functional haplotype in EIF2AK3, an ER stress sensor, is associated with lower bone mineral density.
J. Bone Miner. Res., Feb;27(2):331-41 (2012)
The genetic interface between gestational diabetes and type 2 diabetes.
J. Matern. Fetal. Neonatal. Med., Jan;25(1):36-40 (2012)
Genotype-based changes in serum uric acid affect blood pressure.
Kidney Int., Mar;81(5):502-7 (2012)
Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.
Arch. Intern. Med., Nov;170(20):1850-5 (2010)
The relation between CYP2C19 genotype and phenotype in stented patients on maintenance dual antiplatelet therapy.
Am. Heart J., Mar;161(3):598-604 (2011)
A common variant in fibroblast growth factor binding protein 1 (FGFBP1) is associated with bone mineral density and influences gene expression in vitro.
Bone., Aug;47(2):272-80 (2010)
Genotyping: one piece of the puzzle to personalize antiplatelet therapy.
J. Am. Coll. Cardiol., Jul;56(2):112-6 (2010)
Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification.
Arterioscler. Thromb. Vasc. Biol., Dec;30(12):2648-54 (2010)
Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.
Arthritis Rheum., Sep;58(9):2874-81 (2008)
The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults.
Am. J. Epidemiol., Nov;168(9):1016-23 (2008)
A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection.
Science., Dec;322(5908):1702-5 (2008)
From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.
Proc. Natl. Acad. Sci. U.S.A., Jan;106(1):226-31 (2009)
Serum 25-hydroxyvitamin d levels are not associated with subclinical vascular disease or C-reactive protein in the old order amish.
Calcif. Tissue Int., Mar;84(3):195-202 (2009)
Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study.
Hum. Genet., Oct;126(4):567-74 (2009)
Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy.
JAMA., Aug;302(8):849-57 (2009)
The effect of elinogrel on high platelet reactivity during dual antiplatelet therapy and the relation to CYP2C19*2 genotype: first experience in patients.
J. Thromb. Haemost., Jan;8(1):43-53 (2010)
Single nucleotide polymorphism upstream of interleukin 28B associated with phase 1 and phase 2 of early viral kinetics in patients infected with HCV genotype 1.
J. Hepatol., Mar;56(3):557-63 (2012)
Determinants of blood pressure response to low-salt intake in a healthy adult population.
J Clin Hypertens (Greenwich)., Nov;13(11):795-800 (2011)