A Functional SNP in the NKX2.5-binding Site of ITPR3 Promoter Is Associated With Susceptibility to Systemic Lupus Erythematosus in Japanese Population | Oishi, T | Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University of Tokyo, 4-6-1 Shirokanedai, Minato, Department of Medicine, Kidney Center, Tokyo Women's Medical University, Tokyo | 18219441 |
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Polymorphisms of the IL12B and IL23R Genes Are Associated With Psoriasis | Nair, RP | Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan | 18219280 |
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Two-stage Candidate Gene Study of Chromosome 3p Demonstrates an Association Between Nonsynonymous Variants in the MST1R Gene and Crohn's Disease | Beckly, JB | Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK | 18200509 |
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Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans | Kathiresan, S | Massachusetts General Hospital | 18193044 |
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Newly identified loci that influence lipid concentrations and risk of coronary artery disease | Willer, C, J | University of Michigan | 18193043 |
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Association of variants in the sterol regulatory element-binding factor 1 (SREBF1) gene with type 2 diabetes, glycemia, and insulin resistance | Grarup, N | Steno Diabetes Center, Copenhagen | 18192539 |
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Vitamin D Deficiency and Risk for Cardiovascular Disease | Judd, S | Emory University School of Medicine | 18180395 |
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Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 With Susceptibility to Type 2 Diabetes in a Japanese Population | Omori, S | Laboratory for Diabetic Nephropathy, SNP Research Center | 18162508 |
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SNPs in PPARG associate with type 2 diabetes and interact with physical activity. | Kilpelainen, T | Institute of Biomedicine, Physiology, University of Kuopio | 18091023 |
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Interleukin (IL)-23 Receptor Is a Major Susceptibility Gene for Graves' Ophthalmopathy, The IL-23/T-helper 17 Axis Extends to Thyroid Autoimmunity | Huber, AK | Division of Endocrinology, The Vontz Center, ML 0547, University of Cincinnati College of Medicine, Cincinnati, Ohio | 18073300 |
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Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population | Shen, G, Q | Cleveland Clinic | 18066490 |
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Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome. | Winkelmann, J | GSF - Research Center for Environment and Health | 18058820 |
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A genome-wide association study of sporadic ALS in a homogenous Irish population. | Cronin, S | Department of Clinical Neurological Sciences, Royal College of Surgeons in Ireland, Dublin 2, Ireland | 18057069 |
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Four SNPs on Chromosome 9p21 in a South Korean Population Implicate a Genetic Locus That Confers High Cross-Race Risk for Development of Coronary Artery Disease | Shen, G, Q | Lerner Research Institute, Cleveland Clinic | 18048766 |
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ATG16L1 and IL23R Are Associated With Inflammatory Bowel Diseases but Not With Celiac Disease in the Netherlands | Weersma, RK | Department of Gastroenterology and Hepatology, University Medical Center Groningen, The Netherlands | 18047540 |
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A985G polymorphism of the endothelin-2 gene and atrial fibrillation in patients with hypertrophic cardiomyopathy. | Nagai, T | Ehime University Graduate School of Medicine | 18037749 |
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High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project | Kato, N | International Medical Center of Japan | 18003638 |
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Identification of Two Independent Risk Factors for Lupus Within the MHC in United Kingdom Families | Fernando, MMA | Section of Molecular Genetics and Rheumatology, Imperial College London, London, United Kingdom | 17997607 |
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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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