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Terho Lehtimäki

Researcher at University of Tampere

Publications -  1375
Citations -  129159

Terho Lehtimäki is an academic researcher from University of Tampere. The author has contributed to research in topics: Population & Genome-wide association study. The author has an hindex of 142, co-authored 1304 publications receiving 106981 citations. Previous affiliations of Terho Lehtimäki include Boston University & National Institutes of Health.

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The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

Thomas W. Winkler, +438 more
- 01 Oct 2015 - 
TL;DR: In this paper, the authors performed meta-analyses of 114 studies with genome-wide chip and/or Metabochip data by the Genetic Investigation of Anthropometric Traits (GIANT) Consortium.
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Sonja I. Berndt, +385 more
- 01 May 2013 - 
TL;DR: A genome-wide search for loci associated with the upper versus the lower 5th percentiles of body mass index, height and waist-to-hip ratio as well as clinical classes of obesity, including up to 263,407 individuals of European ancestry finds a large overlap in genetic structure and the distribution of variants between traits based on extremes and the general population and little etiological heterogeneity between obesity subgroups.
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Risk of acute coronary events and serum concentration of asymmetrical dimethylarginine

TL;DR: The findings suggest that ADMA is a predictors of acute coronary events in middle-aged men from eastern Finland.
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Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA

TL;DR: The LPA locus link with cardiovascular risk exemplifies how detailed metabolic profiling may inform underlying aetiology via extensive associations with very-low-density lipoprotein and triglyceride metabolism and strengthens the argument for safe LPA-targeted intervention to reduce cardiovascular risk.
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Association analyses based on false discovery rate implicate new loci for coronary artery disease.

Christopher P. Nelson, +90 more
- 17 Jul 2017 - 
TL;DR: This approach identified 13 new loci at genome-wide significance, 12 of which were on the previous list of loci meeting the 5% FDR threshold, thus providing strong support that the remaining loci identified by FDR represent genuine signals.