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| 31118516 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. | Nature | 2019 |
| 29360107 | Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2018 |
| 30061737 | Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. | Nat Genet | 2018 |
| 29899519 | Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. | Nat Commun | 2018 |
| 30275531 | Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. | Nat Genet | 2018 |
| 29481666 | Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. | Hum Mol Genet | 2018 |
| 29562163 | A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease. | N Engl J Med | 2018 |
| 29290336 | Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development. | Am J Hum Genet | 2018 |
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| 29632382 | Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. | Nat Genet | 2018 |
| 29727688 | Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes. | Am J Hum Genet | 2018 |
| 29257133 | Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. | Sci Data | 2017 |
| 28506971 | Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease. | Circ Res | 2017 |
| 28341696 | A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. | Diabetes | 2017 |
| 28538136 | Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease. | N Engl J Med | 2017 |
| 28566273 | An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. | Diabetes | 2017 |
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| 27980614 | Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19. | BMC Proc | 2016 |
| 27356620 | Prosaposin is a regulator of progranulin levels and oligomerization. | Nat Commun | 2016 |
| 27355579 | Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. | PLoS Genet | 2016 |
| 27398621 | The genetic architecture of type 2 diabetes. | Nature | 2016 |
| 27980644 | Independent test assessment using the extreme value distribution theory. | BMC Proc | 2016 |
| 26426971 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. | PLoS Genet | 2015 |
| 25625282 | Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. | PLoS Genet | 2015 |
| 26551672 | Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. | Nat Genet | 2015 |
| 24509480 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. | Nat Genet | 2014 |
| 24497850 | Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci. | PLoS Genet | 2014 |
| 24584071 | Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. | Nat Genet | 2014 |
| 23263489 | Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. | Nat Genet | 2013 |
| 23768515 | General framework for meta-analysis of rare variants in sequencing association studies. | Am J Hum Genet | 2013 |
| 24097068 | Discovery and refinement of loci associated with lipid levels. | Nat Genet | 2013 |
| 24097064 | Common variants associated with plasma triglycerides and risk for coronary artery disease. | Nat Genet | 2013 |
| 23835345 | Mendelian randomization studies do not support a causal role for reduced circulating adiponectin levels in insulin resistance and type 2 diabetes. | Diabetes | 2013 |
| 22415877 | No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels. | Diabetes | 2012 |
| 22479202 | Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. | PLoS Genet | 2012 |
| 22885924 | Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. | Nat Genet | 2012 |
| 22885922 | Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. | Nat Genet | 2012 |
| 22876189 | The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. | PLoS Genet | 2012 |
| 22001757 | Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. | Nat Genet | 2011 |
| 20634204 | LocusZoom: regional visualization of genome-wide association scan results. | Bioinformatics | 2010 |
| 20935630 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. | Nat Genet | 2010 |
| 20686565 | Biological, clinical and population relevance of 95 loci for blood lipids. | Nature | 2010 |
| 20935629 | Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. | Nat Genet | 2010 |
| 18179894 | A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. | Am J Hum Genet | 2008 |
| 18077723 | Chronic CD4+ T-cell activation and depletion in human immunodeficiency virus type 1 infection: type I interferon-mediated disruption of T-cell dynamics. | J Virol | 2008 |
| 17658953 | Population bottlenecks as a potential major shaping force of human genome architecture. | PLoS Genet | 2007 |
| 16773128 | A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment. | Eur J Hum Genet | 2006 |
| 15780141 | Therapeutic targets for HIV-1 infection in the host proteome. | Retrovirology | 2005 |
| 15922682 | Dissection of the sets of genes that control the behavior of biglycan-deficient pre-osteoblasts using oligonucleotide microarrays. | Bone | 2005 |