Georg Ehret focuses on Genome-wide association study, Genetics, Internal medicine, Genetic association and Blood pressure. His Genome-wide association study research incorporates elements of Polymorphism, Coronary artery disease, Medical genetics, Locus and Genetic architecture. Georg Ehret combines subjects such as Body mass index and Hematocrit with his study of Genetics.
His study in Internal medicine is interdisciplinary in nature, drawing from both Endocrinology and Cardiology. The concepts of his Genetic association study are interwoven with issues in Mean corpuscular hemoglobin, Hemoglobin, Mean corpuscular volume, Quantitative trait locus and Atrial fibrillation. He focuses mostly in the field of Blood pressure, narrowing it down to topics relating to Disease and, in certain cases, Stroke.
His primary areas of study are Genetics, Genome-wide association study, Internal medicine, Blood pressure and Genetic association. He interconnects Bioinformatics, Linkage disequilibrium, Medical genetics, Locus and Genetic architecture in the investigation of issues within Genome-wide association study. His research on Internal medicine also deals with topics like
His studies in Blood pressure integrate themes in fields like Disease, Risk factor and Genetic variation. His research in Single-nucleotide polymorphism intersects with topics in Polymorphism and Genomics. The various areas that Georg Ehret examines in his Renal function study include Kidney and Kidney disease.
Georg Ehret mainly investigates Internal medicine, Genome-wide association study, Genetics, Blood pressure and Atrial fibrillation. The Internal medicine study combines topics in areas such as Endocrinology and Cardiology. His studies deal with areas such as Imputation, Human genetics, Genetic association and Medical genetics as well as Genome-wide association study.
His Genetics study incorporates themes from Mean arterial pressure, Familial hypercholesterolemia and Pulse pressure. His Blood pressure study integrates concerns from other disciplines, such as Phenotype, Magnetic resonance imaging and Mendelian Randomization Analysis. His Atrial fibrillation study also includes fields such as
The scientist’s investigation covers issues in Genome-wide association study, Genetics, Medical genetics, Human genetics and Trait. His work carried out in the field of Genome-wide association study brings together such families of science as Diabetes mellitus genetics, Gene knockdown, Bioinformatics, Albuminuria and Regulation of gene expression. His Genetics research is multidisciplinary, relying on both Gout, Renal function and Insulin resistance.
His Medical genetics study combines topics in areas such as Mean arterial pressure, Pulse pressure, Blood pressure, Diastole and Heart failure. His Human genetics research includes themes of Evolutionary biology, Heritability, Genome, Genomics and Imputation.
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Discovery and refinement of loci associated with lipid levels
Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta;Gina M. Peloso;Gina M. Peloso;Gina M. Peloso.
Nature Genetics (2013)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg B. Ehret;Georg B. Ehret;Georg B. Ehret;Patricia B. Munroe;Kenneth M. Rice;Murielle Bochud.
Defining the role of common variation in the genomic and biological architecture of adult human height
Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam.
Nature Genetics (2014)
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.
Angelo Scuteri;Serena Sanna;Wei-Min Chen;Manuela Uda.
PLOS Genetics (2005)
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Faculty of Health; Institute of Health and Biomedical Innovation (2015)
Genome-wide association study of blood pressure and hypertension
Daniel Levy;Georg B. Ehret;Georg B. Ehret;Kenneth Rice;Germaine C. Verwoert.
Nature Genetics (2009)
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
Mary F. Feitosa;Aldi T. Kraja;Daniel I. Chasman;Yun J. Sung.
PLOS ONE (2018)
Common variants associated with plasma triglycerides and risk for coronary artery disease
Ron Do;Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta.
Nature Genetics (2013)
Multiple loci associated with indices of renal function and chronic kidney disease
Anna Köttgen;Nicole L. Glazer;Abbas Dehghan;Shih Jen Hwang.
Nature Genetics (2009)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Evangelos Evangelou;Evangelos Evangelou;Helen R. Warren;Helen R. Warren;David Mosen-Ansorena;Borbala Mifsud.
Nature Genetics (2018)
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