| Impact of common type 2 diabetes risk polymorphisms in the DESIR prospective study. | Vaxillaire, M | UMR8090 and Institute of Biology, Lille 2 University, CNRS and Pasteur Institute | 17977958 |
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| Polymorphisms in the IDE-KIF11-HHEX gene locus are reproducibly associated with type 2 diabetes in a Japanese population. | Furukawa, Y | The First Department of Medicine, Wakayama Medical University | 17971426 |
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| Association of apolipoprotein E genotypes with lipid levels and coronary risk | Bennet, AM | Department of Public Health and Primary Care, University of Cambridge, Cambridge, England | 17878422 |
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| STAT4 and the Risk of Rheumatoid Arthritis and Systemic Lupus Erythematosus | Remmers, EF | National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD | 17804842 |
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| TRAF1-C5 as a Risk Locus for Rheumatoid Arthritis--A Genomewide Study | Plenge, RM | Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA | 17804836 |
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| Variation in complement factor 3 is associated with risk of age-related macular degeneration | Maller, J | Center for Human Genetic Research, Massachusetts General Hospital | 17767156 |
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| The association of common polymorphisms in the QPCT gene with bone mineral density in the Chinese population. | Huang, Q, Y | Department of Medicine, The University of Hong Kong, Hong Kong, Hong Kong. | 17687619 |
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| Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease Gene | Franke, A | Institute for Clinical Molecular Biology, Christian-Albrechts University Kiel, Kiel, Germany | 17684544 |
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| Neutrophil function and metabolism in individuals with diabetes mellitus | Alba-Loureiro, T, C | Instituto de Ciencias Biomedicas, Universidade de Sao Paulo | 17665039 |
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| Genetic Variations in NALP1 Are Associated With Generalized Vitiligo in a Romanian Population | Jin, Y | Human Medical Genetics Program, School of Medicine, University of Colorado, Aurora, CO | 17637824 |
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| Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. | Winkelmann, J | GSF - Research Center for Environment and Health | 17637780 |
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| Genomewide Association Analysis of Coronary Artery Disease | Samani, N, J | University of Leicester | 17634449 |
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| A genetic risk factor for periodic limb movements in sleep. | Stefansson, H | deCODE Genetics, Reykjavik, Iceland | 17634447 |
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| Evidence for sugar addiction: Behavioral and neurochemical effects of intermittent, excessive sugar intake | Avena, N, M | Princeton University | 17617461 |
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| The ITGAV rs3738919-C Allele Is Associated With Rheumatoid Arthritis in the European Caucasian Population, A Family-Based Study | Jacq, L | Evry-Paris VII Universities, 91057 Evry-Genopole cedex, France | 17615072 |
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| A Genome-Wide Association Study for Celiac Disease Identifies Risk Variants in the Region Harboring IL2 and IL21 | van Heel, DA | Centre for Gastroenterology, Institute of Cell and Molecular Science, Queen Mary University of London, London E1 2AT, UK | 17558408 |
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| Genome-wide Association Study of 14,000 Cases of Seven Common Diseases and 3,000 Shared Controls | Staff | Wellcome Trust Case Control Consortium | 17554300 |
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| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Burton, P, R | Wellcome Trust Case Control Consortium | 17554300 |
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| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. | Burton, P | Genetic Epidemiology Group, Department of Health Sciences, University of Leicester, Adrian Building, University Road | 17554300 |
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| Robust Associations of Four New Chromosome Regions From Genome-Wide Analyses of Type 1 Diabetes | Todd, JA | Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Department of Medical Genetics, University of Cambridge, Addenbrooke's Hospital, Cambridge CB2 0XY, UK | 17554260 |
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| Association between sleep and morning testosterone levels in older men | Penev, P, D | The University of Chicago | 17520786 |
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| A common variant on chromosome 9p21 affects the risk of myocardial infarction | Helgadottir, A | deCODE Genetics | 17478679 |
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| Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes | Zeggini, E | Oxford Centre for Diabetes, Endocrinology and Medicine, University of Oxford, Churchill Hospital | 17463249 |
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| A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. | Scott, L | Department of Biostatistics and Center for Statistical Genetics, University of Michigan | 17463248 |
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| Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels | Saxena, R | Broad Institute of Harvard and Massachusetts Institute of Technology (MIT) | 17463246 |
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