| Variants within the MMP3 gene are associated with Achilles tendinopathy, possible interaction with the COL5A1 gene | Raleigh, S | Division of Health and Life Sciences, University of Northampton | 19042922 |
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| Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss | Francis, P | Macular Degeneration Center, Casey Eye Institute, Oregon Health & Science University | 19015224 |
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| Genetic Variation in the KIF1B Locus Influences Susceptibility to Multiple Sclerosis | Aulchenko, YS | Genetic Epidemiology Unit, Department of Epidemiology and Biostatistics and Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands | 18997785 |
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| The Expanding Genetic Overlap Between Multiple Sclerosis and Type I Diabetes | Staff | International Multiple Sclerosis Genetics Consortium | 18987646 |
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| Screening for replication of genome-wide SNP associations in sporadic ALS. | Cronin, S | Department of Clinical Neurological Sciences, Royal College of Surgeons in Ireland, Dublin 2, Ireland | 18987618 |
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| Genomewide association study for susceptibility genes contributing to familial Parkinson disease. | Pankratz, N | Indiana University School of Medicine, Health Information and Translational Sciences Building, Indianapolis, IN | 18985386 |
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| TheTRIB3Q84R Polymorphism and Risk of Early-Onset Type 2 Diabetes | Prudente, S | CSS-Mendel Institute | 18984671 |
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| Meta-analysis of Genome-Wide Association Study Data Identifies Additional Type 1 Diabetes Risk Loci | Cooper, JD | Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK | 18978792 |
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| SNP analyses of postprandial responses in(an)orexigenic hormones and feelings of hunger reveal long-term physiological adaptations to facilitate homeostasis | Hoed, M | Department of Human Biology, Maastricht University | 18957934 |
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| Variation Within the CLEC16A Gene Shows Consistent Disease Association With Both Multiple Sclerosis and Type 1 Diabetes in Sardinia | Zoledziewska, M | Dipartimento di Scienze Biomediche, University of Sassari, Sassari, Italy | 18946483 |
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| Identification of a Novel Risk Locus for Multiple Sclerosis at 13q31.3 by a Pooled Genome-Wide Scan of 500,000 Single Nucleotide Polymorphisms | Comabella, M | Unitat de Neuroimmunologia Clínica, CEM-Cat, Hospital Universitari Vall d'Hebron, Barcelona, Spain | 18941528 |
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| Associations between single nucleotide polymorphisms in folate uptake and metabolizing genes with blood folate, homocysteine, and DNA uracil concentrations | DeVos, L | Eberly College of Science, Pennsylvania State University | 18842806 |
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| Further Assessment of the Complement Component 2 and Factor B Region Associated with Age-Related Macular Degeneration | McKay, G | Centre for Vision Sciences, Queen's University of Belfast | 18806297 |
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| Functional SNPs in CD244 Increase the Risk of Rheumatoid Arthritis in a Japanese Population | Suzuki, A | Laboratory for Autoimmune Diseases, Center for Genomic Medicine, RIKEN, Yokohama, Kanagawa 230-0045, Japan | 18794858 |
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| Common Variants at CD40 and Other Loci Confer Risk of Rheumatoid Arthritis | Raychaudhuri, S | Program in Medical and Population Genetics, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, Massachusetts | 18794853 |
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| Common Variants in the Adiponectin Gene (ADIPOQ) Associated With Plasma Adiponectin Levels, Type 2 Diabetes, and Diabetes-Related Quantitative Traits | Hivert, M | General Medicine Division, Massachusetts General Hospital | 18776141 |
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| Toll-Like Receptor-3 and Geographic Atrophy in Age-Related Macular Degeneration | Yang, Z | Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu | 18753640 |
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| High Ratio of Triglycerides to HDL-Cholesterol Predicts Extensive Coronary Disease | Lemos da Luz, P | Universidade de Sao Paulo | 18719750 |
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| Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study | Linsel-Nitschke, P | Universitat zu Lubeck | 18714375 |
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| Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation Study | Linsel-Nitschke, P | Universitat zu Lubeck | 18714375 |
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| STAT4, A Risk Factor for Type 1 Diabetes? | Zervou, MI | Medical School, University of Crete, Heraklion, Greece | 18703106 |
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| Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis | Orton, SM | Wellcome Trust Centre for Human Genetics and Department of Clinical Neurology, University of Oxford | 18689381 |
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| Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate Genes | Gaulton, K | Department of Genetics, University of North Carolina at Chapel Hill | 18678618 |
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| Human fasting plasma concentrations of vitamin E and carotenoids, and their association with genetic variants in apo C-III, cholesteryl ester transfer protein, hepatic lipase, intestinal fatty acid binding protein and microsomal triacylglycerol transfer protein | Borel, P | Nutriments Lipidiques et Prevention des Maladies Metaboliques | 18662427 |
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| The -589C>T polymorphism in the interleukin-4 gene (IL-4) is associated with a reduced risk of myocardial infarction in young individuals. | Paffen, E | Leiden University Medical Center | 18662263 |
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