about
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 studyCommon polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery diseaseGenetic studies of body mass index yield new insights for obesity biologyGenetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyNexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathyA genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathyGenetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association dataA genome-wide association study identifies LIPA as a susceptibility gene for coronary artery diseaseBiological, clinical and population relevance of 95 loci for blood lipidsGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskHundreds of variants clustered in genomic loci and biological pathways affect human heightGenome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.Genetic Loci associated with C-reactive protein levels and risk of coronary heart diseaseGenomewide association analysis of coronary artery diseaseShared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variantsPrediction of Causal Candidate Genes in Coronary Artery Disease LociMolecular variants of soluble guanylyl cyclase affecting cardiovascular riskHuman metabolic individuality in biomedical and pharmaceutical researchA comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery diseaseAssociation of the T8590C polymorphism of CYP4A11 with hypertension in the MONICA Augsburg echocardiographic substudyLack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservationRuns of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and MacrophagesDiscovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density ImputationMultiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular diseaseGenome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureRare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart diseaseGenome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studiesLarge-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyFunctional Characterization of the GUCY1A3 Coronary Artery Disease Risk Locus.Loss-of-function mutations in APOC3, triglycerides, and coronary diseaseAssociation of common polymorphisms in GLUT9 gene with gout but not with coronary artery disease in a large case-control study.A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease.Myeloid CD34+CD13+ precursor cells transdifferentiate into chondrocyte-like cells in atherosclerotic intimal calcificationIntegrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans.RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studiesNovel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.Genetic causes of myocardial infarction: new insights from genome-wide association studies.
P50
Q21090089-246792B0-C315-4194-8EC0-417F9DB53293Q21091170-825F1977-696C-482B-B39D-8D937CA83BF7Q22305005-7FC3FF99-7B37-4E7D-8BFE-42D7BAB0E66DQ24288778-A837EDC2-3347-4C4B-BA40-F526A55ADE49Q24313460-BEBDFE00-318E-47CA-9680-59C39F883C28Q24601469-71E8EFFD-090E-48DC-8748-26C60871B912Q24612121-8886C07D-328A-4E16-8868-0C6A56973468Q24615584-511779DF-8689-4FE6-970D-561E85D73D5EQ24622541-59C847B0-83C1-451D-9386-42C7B4F5D3E5Q24630394-B71C48DD-CC62-4D2A-B95F-FCF76D0ECD48Q24630979-73AD3AF2-6DD2-4CCA-873A-B22018457362Q24645076-E03697AB-490D-42D3-AEF7-44E178CEAB65Q24649709-6752A2FE-A138-415E-A97C-06EDB252E4B6Q24658344-A2B7AF78-9A44-4191-A419-347D94F926ABQ27008212-DED45D59-F18C-4A2E-AC0B-EF6924CA19B6Q27342192-6B4AEDD2-01B1-47B9-A721-6C5328D3F643Q28082172-D91228C2-38D1-4DA3-BA24-2168C545C6C4Q28247002-223E013D-DA86-4511-B32B-CA874C6916D1Q28267020-0C51393E-785C-4423-846C-C8CBB7145547Q28270884-4B639141-B15B-4049-A63E-42BA755034C9Q28293336-9136D5AC-D106-48D8-9102-4E12005B67A0Q28388875-247A1583-0130-4804-A404-A14F0F2940EAQ28546045-17B4D9B6-76C3-45FF-95C8-72B18A3A42FEQ28661433-A1198F32-8C35-4E2E-84CB-F8CED9ECD8ECQ28943288-E74A3C9E-F245-4D34-92A8-CCBC9FA4CD8BQ29147547-A720719E-390A-4E90-A422-6C7D99458E79Q29416988-9CD2E29C-FCC8-432C-89F7-B1006B621C85Q29417010-858B96AE-095D-42D1-A3EC-1497D4B43106Q29417023-22700312-90AA-4468-BCD4-FFD9D5877E03Q29615729-F1A61FED-4408-4F93-BDC1-B3AB8AE9FD82Q30252419-B49C3CBE-FDE9-4837-B070-3BD02F357A7CQ30408720-ED1D6FB0-C35A-4E18-9E5A-1DBBF2FB8022Q33327367-CB46886E-0EAB-4CD1-8C9C-08C74C000B19Q33518461-EFBD594A-9C66-4F7C-887A-A50D77FD6C94Q33916015-54A7B2F5-D2E6-4578-9BCE-5ADA1B50222DQ33947344-F7FF19A3-BCB0-4E64-A44A-EEE6891F400CQ34092395-AC6D8EC0-9712-4C7B-9CEA-DB1D1AEB8102Q34097785-8BA3B29A-BF07-4571-AE4D-0CCF69C5E47FQ34221038-B0FAA65C-C0EC-4375-B809-4F5195DE4278Q34247545-120A87E7-3D82-4F50-B0F0-AAE1D040683A
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jeanette Erdmann
@ast
Jeanette Erdmann
@br
Jeanette Erdmann
@ca
Jeanette Erdmann
@cs
Jeanette Erdmann
@cy
Jeanette Erdmann
@da
Jeanette Erdmann
@de
Jeanette Erdmann
@de-at
Jeanette Erdmann
@de-ch
Jeanette Erdmann
@en
type
label
Jeanette Erdmann
@ast
Jeanette Erdmann
@br
Jeanette Erdmann
@ca
Jeanette Erdmann
@cs
Jeanette Erdmann
@cy
Jeanette Erdmann
@da
Jeanette Erdmann
@de
Jeanette Erdmann
@de-at
Jeanette Erdmann
@de-ch
Jeanette Erdmann
@en
prefLabel
Jeanette Erdmann
@ast
Jeanette Erdmann
@br
Jeanette Erdmann
@ca
Jeanette Erdmann
@cs
Jeanette Erdmann
@cy
Jeanette Erdmann
@da
Jeanette Erdmann
@de
Jeanette Erdmann
@de-at
Jeanette Erdmann
@de-ch
Jeanette Erdmann
@en
P1053
P-7513-2014
P106
P1153
56254199300
57202594629
P21
P2798
P31
P3829
P496
0000-0002-4486-6231
P569
2000-01-01T00:00:00Z