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40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004
Rare and low-frequency coding variants alter human adult height
Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation
Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability
Analysis of protein-coding genetic variation in 60,706 humans
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
35th Annual Meeting of the European Association for the Study of Diabetes
