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Nature Genetics, ISSN 1061-4036, 03/2009, Volume 41, Issue 3, pp. 283 - 285
Journal Article
PLoS Genetics, ISSN 1553-7390, 09/2017, Volume 13, Issue 9, pp. e1007040 - e1007040
Cardiovascular diseases (CVD) and type 2 diabetes (T2D) are closely interrelated complex diseases likely sharing overlapping pathogenesis driven by aberrant... 
METABOLIC SYNDROME | MULTIDIMENSIONAL DATA INTEGRATION | INSULIN-RESISTANCE | GENETICS & HEREDITY | ATHEROSCLEROSIS | MITOCHONDRIAL DYSFUNCTION | CHAIN AMINO-ACIDS | EXTRACELLULAR-MATRIX | ASSOCIATION | CORONARY-ARTERY-DISEASE | KEY REGULATORS | United States | Amino Acids, Branched-Chain - metabolism | Diabetes Mellitus, Type 2 - genetics | Humans | Glycoproteins - metabolism | Male | Insulin-Like Growth Factor I - genetics | Gene Regulatory Networks | Cardiovascular Diseases - genetics | Ethnic Groups - genetics | Hydroxymethylglutaryl CoA Reductases - metabolism | Extracellular Matrix Proteins - metabolism | Disease Models, Animal | Glycoproteins - genetics | Genome-Wide Association Study | Reproducibility of Results | Extracellular Matrix Proteins - genetics | Gene Expression Regulation | Caveolin 1 - genetics | Lipid Metabolism | Caveolin 1 - metabolism | Animals | Adipocytes - metabolism | Glucose - metabolism | Mice | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Hydroxymethylglutaryl CoA Reductases - genetics | Insulin-Like Growth Factor I - metabolism | Type 2 diabetes | Genetic aspects | Cardiovascular diseases | Gene expression | Statistics | Health aspects | Prevalence studies (Epidemiology) | Heart | Networks | Animal models | Insulin-like growth factor I | Pathogenesis | Genomics | Chain branching | Amino acids | Cardiovascular disease | Lipids | Genomes | Biology | Epidemiology | Consortia | Glucose metabolism | Metabolites | Genetics | Extracellular matrix | Physiology | Oxidation | Lipid metabolism | Departments | Immune response | Diabetes mellitus | Calcium channels (voltage-gated) | siRNA | Metabolism | Quantitative trait loci | Immune systems | Medicine | Ethnicity | Collaboration | Insulin resistance | Diabetes | Aberration | Endocrinology | Index Medicus | Life Sciences | Human health and pathology | Endocrinology and metabolism | Biochemistry, Molecular Biology | Cardiology and cardiovascular system
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2007, Volume 357, Issue 5, pp. 443 - 453
Journal Article
by Perret, Claire and Blankenberg, Stefan and Stark, Klaus and Braund, Peter S and Rubin, Diana and Deloukas, Panos and Ball, Stephen G and Schäfer, Arne and Thompson, John R and Voight, Benjamin F and Zeller, Tanja and Schunkert, Heribert and Ouwehand, Willem H and Merlini, Piera Angelica and Schrezenmeir, Jürgen and Linsel-Nitschke, Patrick and Bernardinelli, Luisa and Elosua, Roberto and Wright, Ben and Peyvandi, Flora and Schillert, Arne and Meisinger, Christa and Hengstenberg, Christian and Samani, Nilesh J and Salomaa, Veikko and Peltonen, Leena and Melander, Olle and Schreiber, Stefan and Trégouët, David-Alexandre and Mokhtari, Nour Eddine El and Schwarz, Daniel F and Balmforth, Anthony J and Kathiresan, Sekar and Wagner, Arnika K and Siscovick, David S and Schwartz, Stephen M and Bugert, Peter and Ardissino, Diego and König, Inke R and Aherrahrou, Zouhair and Wild, Philipp and Erdmann, Jeanette and Baumert, Jens and Renner, Wilfried and Bruse, Petra and Klüter, Harald and Altshuler, David and März, Winfried and Wichmann, H-Erich and Ziegler, Andreas and Fischer, Marcus and Hall, Alistair S and Cambien, Francois and Meitinger, Thomas and Großhennig, Anika and Tiret, Laurence and O'Donnell, Christopher J and Peters, Annette and Italian Atherosclerosis Thrombosis and Cardiogenics Consortium and Myocardial Infarction Genetics Con and Wellcome Trust Case Control Consor and Italian Atherosclerosis, Thrombosis, and Vascular Biology Working Group and Wellcome Trust Case Control Consortium and Myocardial Infarction Genetics Consortium and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Lund University and Lunds universitet
Nature Genetics, ISSN 1061-4036, 03/2009, Volume 41, Issue 3, pp. 280 - 282
Journal Article
European Heart Journal, ISSN 0195-668X, 05/2011, Volume 32, Issue 9, pp. 1065 - 1076
Journal Article
Circulation, ISSN 0009-7322, 04/2008, Volume 117, Issue 13, pp. 1675 - 1684
Journal Article
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 07/2013, Volume 33, Issue 7, pp. 1722 - 1727
Journal Article
PLoS Genetics, ISSN 1553-7390, 12/2011, Volume 7, Issue 12, pp. e1002367 - e1002367
Journal Article
PLOS ONE, ISSN 1932-6203, 08/2008, Volume 3, Issue 8, pp. e2986 - e2986
Background: Rare mutations of the low-density lipoprotein receptor gene (LDLR) cause familial hypercholesterolemia, which increases the risk for coronary... 
POPULATION | HEART-DISEASE | METAANALYSIS | MYOCARDIAL-INFARCTION | CARDIOVASCULAR EVENTS | BIOLOGY | POLYMORPHISM | HYPERCHOLESTEROLEMIA | PREVALENCE | EPIDEMIOLOGY | GENOME-WIDE ASSOCIATION | Receptors, LDL - genetics | Oligonucleotide Array Sequence Analysis | Risk Assessment | Humans | Risk Factors | Cholesterol, LDL - drug effects | Chromosome Mapping | Random Allocation | Case-Control Studies | Genetic Variation | Cholesterol, LDL - genetics | Coronary Disease - prevention & control | Anticholesteremic Agents - therapeutic use | Coronary Disease - genetics | Cholesterol, LDL - blood | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 10 | Medical research | Hypercholesterolemia | Blood cholesterol | Low density lipoproteins | Genes | Medicine, Experimental | Genetic research | Genetics | Genetic aspects | Single nucleotide polymorphisms | Coronary heart disease | Risk factors | Lipoproteins (low density) | Risk | Lipids | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Gene polymorphism | Epidemiology | Consortia | Confidence intervals | Randomization | Population | Lipoprotein (low density) receptors | Children | Heart diseases | Statistical analysis | Mortality | Coronary artery | Health risks | Environmental health | Genetic diversity | Regression analysis | Metabolism | LDLR gene | Apolipoproteins | Coronary artery disease | Low density lipoprotein | Cholesterol | Studies | Genetic variance | Hospitals | Coronary vessels | Alleles | Biomarkers | Receptor density | Adults | Mutation | Polymorphism | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2014, Volume 9, Issue 7, pp. e102612 - e102612
Journal Article