Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses
and triglyceride measures in Finnish men from the METSIM study

James P. Davis1¶, Jeroen R. Huyghe2¶, Adam E. Locke2, Anne U. Jackson2, Xueling Sim2,
Heather M. Stringham2, Tanya M. Teslovich2, Ryan P. Welch2, Christian Fuchsberger2,
Narisu Narisu3, Peter S. Chines3, Antti J. Kangas4, Pasi Soininen4,5, Mika Ala-Korpela4,5,6,
Johanna Kuusisto7, Francis S. Collins3, Markku Laakso7¶, Michael Boehnke2¶, Karen L. Mohlke1¶*

1) Department of Genetics, University of North Carolina, Chapel Hill, NC, 27599 USA
2) Department of Biostatistics and Center for Statistical Genetics, University of Michigan, Ann Arbor, MI, 48109 USA
3) National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 20892 USA
4) Computational Medicine, Faculty of Medicine, University of Oulu and Biocenter Oulu, Oulu, Finland
5) NMR Metabolomics Laboratory, School of Pharmacy, University of Eastern Finland, Kuopio, Finland
6) School of Social and Community Medicine, University of Bristol and
   Medical Research Council Integrative Epidemiology Unit at the University of Bristol, Bristol, United Kingdom
7) Institute of Clinical Medicine, Internal Medicine, University of Eastern Finland and Kuopio University Hospital, 70210 Kuopio, Finland

¶ These authors contributed equally to this work.

* Corresponding author