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Nature (London), ISSN 0028-0836, 2010, Volume 466, Issue 7307, pp. 707 - 713
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Cardiology. Vascular system | Heart | Biological and medical sciences | Medical sciences | Coronary heart disease | Humans | Asian Continental Ancestry Group - genetics | Genetic Loci - genetics | Male | Coronary Artery Disease - blood | Europe - ethnology | Lipids - blood | N-Acetylgalactosaminyltransferases - genetics | Protein Phosphatase 1 - genetics | Cholesterol, LDL - blood | Female | Lipid Metabolism - genetics | N-Acetylgalactosaminyltransferases - metabolism | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Reproducibility of Results | Liver - metabolism | African Americans - genetics | Genotype | Phenotype | Protein Phosphatase 1 - metabolism | Animals | Coronary Artery Disease - therapy | Coronary Artery Disease - genetics | Triglycerides - blood | Cholesterol, HDL - blood | Polymorphism, Single Nucleotide - genetics | Mice | Genetic research | Genetic aspects | Genomes | Blood lipids | Properties | Identification and classification | Women | Plasma | Lipids | Lipoproteins | Genetic engineering | Cholesterol | Index Medicus | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Endokrinologi och diabetes | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Endocrinology and Diabetes
Journal Article
Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 4, pp. 333 - U153
Fundamental and applied biological sciences. Psychology | Cardiology. Vascular system | Heart | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Coronary heart disease | Genetic Predisposition to Disease | Genome-Wide Association Study | Coronary Artery Disease - etiology | Gene Frequency | Humans | Middle Aged | Risk Factors | Male | Case-Control Studies | Alleles | Coronary Artery Disease - genetics | Adult | Female | Aged | Polymorphism, Single Nucleotide | Genetic aspects | Disease susceptibility | Research | Single nucleotide polymorphisms | Health aspects | Risk factors | Studies | Genomes | Gene expression | Chromosomes | Meta-analysis | Index Medicus | Medicin och hälsovetenskap
Journal Article
Nature (London), ISSN 0028-0836, 2015, Volume 518, Issue 7537, pp. 102 - +
no | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetics, Population | Myocardial Infarction - blood | Myocardial Infarction - genetics | Receptors, LDL - genetics | Apolipoprotein A-V | Genetic Predisposition to Disease - genetics | Apolipoproteins A - genetics | National Heart, Lung, and Blood Institute (U.S.) | Age Factors | United States | Humans | Middle Aged | Male | Mutation - genetics | Case-Control Studies | Exome - genetics | Age of Onset | Alleles | Coronary Artery Disease - genetics | Triglycerides - blood | Cholesterol, LDL - blood | Female | Heterozygote | Usage | Low density lipoproteins | Exome sequencing | Physiological aspects | Genetic aspects | Research | Diagnosis | Heart attack | Risk factors | Proteins | Studies | Algorithms | Heart attacks | Genes | Cardiovascular disease | Triglycerides | Mutation | Cholesterol | Index Medicus | Medicin och hälsovetenskap
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Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
The Lancet (British edition), ISSN 0140-6736, 08/2012, Volume 380, Issue 9841, pp. 572 - 580
Internal Medicine | ENDOTHELIAL LIPASE | METAANALYSIS | BLOOD CHOLESTEROL | ATHEROSCLEROSIS | GENETIC-VARIANTS | LOCI | CORONARY-HEART-DISEASE | UMCG Approved | HIGH-DENSITY-LIPOPROTEIN | ISCHEMIC CARDIOVASCULAR-DISEASE | ARTERY-DISEASE | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Cardiology. Vascular system | Heart | General aspects | Biological and medical sciences | Metabolic diseases | Medical sciences | Coronary heart disease | Disorders of blood lipids. Hyperlipoproteinemia | Mendelian Randomization Analysis - methods | Myocardial Infarction - blood | Myocardial Infarction - genetics | Genetic Predisposition to Disease | Myocardial Infarction - epidemiology | Prospective Studies | Gene Frequency | Humans | Risk Factors | Biomarkers - blood | Case-Control Studies | Cholesterol, HDL - blood | Cholesterol, LDL - blood | Polymorphism, Single Nucleotide | Myocardial Infarction - etiology | Lipase - genetics | Genetic aspects | High density lipoproteins | Health aspects | Heart attack | Risk factors | Studies | Plasma | Heart attacks | Diet | Cardiovascular disease | Lipids | Cholesterol | Index Medicus | Abridged Index Medicus | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Endokrinologi och diabetes | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Endocrinology and Diabetes
Journal Article
Nature (London), ISSN 0028-0836, 2016, Volume 536, Issue 7614, pp. 41 - +
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Exome | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Sample Size | DNA Mutational Analysis | Diabetes Mellitus, Type 2 - genetics | Humans | Alleles | Genetic Variation - genetics | Genotyping Techniques | Europe - ethnology | Type 2 diabetes | Genomic structural variations | Nucleotide sequencing | Research | Analysis | DNA sequencing | Studies | Genetics | Genomes | Diabetes | Health risk assessment | Genes | Index Medicus | health risk | ancestry | pathology | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | Article | genetic structure | Klinisk medicin | genetic code | genetics | Endokrinologi och diabetes | genetic predisposition | Diabetes Mellitus, Type 2 | priority journal | ethnology | human | sample size | Endocrinology and Diabetes | Genetic Predisposition to Disease | gene sequence | Europe | genotyping technique | physiology | genetic variation | European | genotype | non insulin dependent diabetes mellitus | genome | Clinical Medicine | genetic analysis | exome | controlled study | allele | genome-wide association study | dna mutational analysis | diabetes
Journal Article
Nature genetics, ISSN 1061-4036, 06/2009, Volume 41, Issue 6, pp. 703 - 707
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Diabetes. Impaired glucose tolerance | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Diabetes Mellitus, Type 1 - epidemiology | Meta-Analysis as Topic | Humans | Male | HLA Antigens - genetics | Antigens, CD - genetics | Chromosomes, Human, Pair 17 - genetics | Interferon-Induced Helicase, IFIH1 | Chromosomes, Human, Pair 2 - genetics | Chromosome Mapping - methods | Female | Diabetes Mellitus, Type 1 - immunology | Chromosomes, Human, Pair 1 - genetics | Siblings | Genome-Wide Association Study | Risk Assessment | Protein Tyrosine Phosphatase, Non-Receptor Type 22 - genetics | Diabetes Mellitus, Type 1 - genetics | Genotype | CTLA-4 Antigen | DNA - genetics | DEAD-box RNA Helicases - genetics | Algorithms | Polymorphism, Single Nucleotide - genetics | Family | Usage | Type 1 diabetes | Genetic aspects | Single nucleotide polymorphisms | Research | Risk factors | Meta-analysis | Studies | Genomics | Quality control | Mental health | Colleges & universities | Principal components analysis | Genetic testing | Diabetes | Index Medicus | Medicin och hälsovetenskap
Journal Article