Supplementary materials

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2010

	Draisma HHM et al. Equating, or Correction for Between-Block Effects with Application to Body Fluid LC-MS and NMR Metabolomics Data Sets. Analytical Chemistry, Volume 82, No. 3, 1039-1046, 2010 Supporting information
	Freathy RM et al for the Early Growth Genetics (EGG) Consortium. Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Nature Genetics, Volume 42, Number 5, 430-435, 2010 Supplementary table 1 (Excel file) Supplementary table 2 (Excel file) Supporting information
	MAGIC. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nature Genetics, Volume 42, Number 2, 105-116, 2010 Supplementary Text and Figures: Supplementary Note, Supplementary Tables 2–4 and Supplementary Figures 1–4 Supplementary Table 1 (Excel file): Study characteristics for discovery (a) and replication (b) cohorts
	Talens RP, Boomsma DI, Tobi EW, Kremer D, Jukema JW, Willemsen G, Putter H, Slagboom PE, Heijmans BT. Variation, patterns, and temporal stability of DNA methylation: considerations for epigenetic epidemiology. The FASEB Journal, Volume 24, Issue 9, 3135-3144, 2010 Supplementary material
	Terracciano A et al. Genome-wide association scan for five major dimensions of personality. Molecular Psychiatry, Volume 15, Issue 6, 647-656, 2010 Supplementary table A (Excel file) Supplementary table B (Excel file)
	Teslovich TM et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature, Volume 466, 707-713, 2010 Supplementary information
	Thorgeirsson TE et al. Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior. Nature Genetics, Volume 42, Number 5, 448-453, 2010 Supplementary information
	The Tobacco and Genetics Consortium. Genome-wide meta-analyses identify multiple loci associated with smoking behavior. Nature Genetics, Volume 42, Number 5, 441-447, 2010 Supplementary information Supplementary table (Excel file)

2009

	Aulchenko YS et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics, Volume 41, Number 1, 47-55, 2009 Supplementary material
	Estrada K et al. A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. Human Molecular Genetics, Volume 18, No. 18, 3516-3524, 2009 Supplementary material
	Sullivan PF et al. Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Molecular Psychiatry, Volume 14, 359-375, 2009 Supplementary information Supplementary table (Excel file)
	Vink JM, Smit AB, Geus de EJC, Sullivan PF, Willemsen G, Hottenga JJ, Smit JH, Hoogendijk WJ, Zitman FG, Peltonen L, Kaprio J, Pedersen NL, Magnusson PK, Spector TD, Ohm Kyvik K, Morley KI, Heath AC, Martin NG, Westendorp RGJ, Slagboom PE, Tiemeier H, Hofman A, Uitterlinden AG, Aulchenko YS, Amin N, Duijn van C, Penninx BW, Boomsma DI. Genome-wide Association Study of Smoking Initiation and Current Smoking. The American Journal of Human Genetics, Volume 84, Issue 3, 367-379, 2009 Supplemental data (Excel file)