| The subjective meaning of sleep quality, a comparison of individuals with and without insomnia. | Harvey, A, G | Department of Psychology, University of California, Berkeley, C | 18363315 |
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| Polymorphisms associated with cholesterol and risk of cardiovascular events | Kathiresan, S | Massachusetts General Hospital | 18354102 |
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| Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis. | Meurs, J | Department of Internal Medicine, Erasmus MC, Rotterdam | 18349089 |
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| Polymorphisms of the Tumor Suppressor Gene LSAMP are Associated with Left Main Coronary Artery Disease | Wang, L | John P. Hussma Institute for Human Genomics University of Miami | 18318786 |
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| HTRA1Variants in Exudative Age-Related Macular Degeneration and Interactions with Smoking and CFH | Tam, P | Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong | 18316707 |
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| Hyperglycemia enhances coagulation and reduces neutrophil degranulation, whereas hyperinsulinemia inhibits fibrinolysis during human endotoxemia | Stegenga, M, E | Center for Infection and Immunity University of Amsterdam | 18316629 |
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| Newly Identified Genetic Risk Variants for Celiac Disease Related to the Immune Response | Hunt, KA | Institute of Cell and Molecular Science, Barts and The London School of Medicine and Dentistry, London, UK | 18311140 |
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| 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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