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- Publications
- Influence
Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids
- Tanya M. Teslovich, K. Musunuru, +206 authors S. Kathiresan
- Biology, Medicine
- Nature
- 5 August 2010
Plasma concentrations of total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol and triglycerides are among the most important risk factors for coronary artery… Expand
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
- S. Kathiresan, O. Melander, +23 authors M. Orho-Melander
- Biology, Medicine
- Nature Genetics
- 13 January 2008
Blood concentrations of lipoproteins and lipids are heritable risk factors for cardiovascular disease. Using genome-wide association data from three studies (n = 8,816 that included 2,758 individuals… Expand
Common variants at 30 loci contribute to polygenic dyslipidemia
- S. Kathiresan, C. Willer, +58 authors L. Cupples
- Biology, Medicine
- Nature Genetics
- 2009
Blood low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol and triglyceride levels are risk factors for cardiovascular disease. To dissect the polygenic basis of… Expand
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
- B. F. Voight, G. Peloso, +123 authors S. Kathiresan
- Medicine
- The Lancet
- 11 August 2012
Summary Background High plasma HDL cholesterol is associated with reduced risk of myocardial infarction, but whether this association is causal is unclear. Exploiting the fact that genotypes are… Expand
Genome-wide association study identifies eight loci associated with blood pressure
- C. Newton‐Cheh, T. Johnson, +155 authors P. Munroe
- Biology, Medicine
- Nature Genetics
- 1 June 2009
Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, identification of common genetic variants influencing blood pressure has proven challenging. We… Expand
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
- V. Lyssenko, R. Lupi, +13 authors L. Groop
- Biology, Medicine
- The Journal of clinical investigation
- 1 August 2007
Genetic variants in the gene encoding for transcription factor-7-like 2 (TCF7L2) have been associated with type 2 diabetes (T2D) and impaired beta cell function, but the mechanisms have remained… Expand
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
- K. Musunuru, Alanna Strong, +27 authors D. Rader
- Biology, Medicine
- Nature
- 5 August 2010
Recent genome-wide association studies (GWASs) have identified a locus on chromosome 1p13 strongly associated with both plasma low-density lipoprotein cholesterol (LDL-C) and myocardial infarction… Expand
Prediction of non-alcoholic fatty liver disease and liver fat using metabolic and genetic factors.
- A. Kotronen, M. Peltonen, +9 authors H. Yki–Järvinen
- Medicine, Biology
- Gastroenterology
- 1 September 2009
BACKGROUND & AIMS
Our aims were to develop a method to accurately predict non-alcoholic fatty liver disease (NAFLD) and liver fat content based on routinely available clinical and laboratory data and… Expand
A common variant in PNPLA3, which encodes adiponutrin, is associated with liver fat content in humans
- A. Kotronen, L. Johansson, +13 authors H. Yki–Järvinen
- Biology, Medicine
- Diabetologia
- 18 February 2009
Aims/hypothesisIt has recently been suggested that the rs738409 G allele in PNPLA3, which encodes adiponutrin, is strongly associated with increased liver fat content in three different ethnic… Expand
The genetic architecture of type 2 diabetes
- C. Fuchsberger, J. Flannick, +298 authors M. McCarthy
- Biology, Medicine
- Nature
- 1 August 2016
The genetic architecture of common traits, including the number, frequency, and effect sizes of inherited variants that contribute to individual risk, has been long debated. Genome-wide association… Expand