2023 - Research.com Genetics in Germany Leader Award
2022 - Research.com Best Female Scientist Award
Her primary areas of study are Genome-wide association study, Genetics, Single-nucleotide polymorphism, Internal medicine and Coronary artery disease. Her Genome-wide association study study integrates concerns from other disciplines, such as Quantitative trait locus, Disease, Allele and Locus. Genetics and Body mass index are commonly linked in her work.
Her studies in Single-nucleotide polymorphism integrate themes in fields like Genetic epidemiology, Cholesterol, Bioinformatics and Candidate gene. Her research integrates issues of Endocrinology and Cardiology in her study of Internal medicine. Her study in Coronary artery disease is interdisciplinary in nature, drawing from both Meta-analysis, Genotyping, Polymorphism and Haplotype.
Jeanette Erdmann mainly investigates Internal medicine, Genetics, Genome-wide association study, Coronary artery disease and Particle physics. Her Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology and Cardiology. Her work carried out in the field of Endocrinology brings together such families of science as Receptor and Genotype.
Her study in Gene, Locus, Allele, Allele frequency and Genetic variation are all subfields of Genetics. Her Genome-wide association study study introduces a deeper knowledge of Single-nucleotide polymorphism. Many of her studies on Coronary artery disease involve topics that are commonly interrelated, such as Genetic predisposition.
Jeanette Erdmann focuses on Genome-wide association study, Internal medicine, Genetics, Coronary artery disease and Gene. Her Genome-wide association study study is related to the wider topic of Single-nucleotide polymorphism. The Internal medicine study combines topics in areas such as Endocrinology, Mendelian randomization and Cardiology.
Many of her studies involve connections with topics such as Heart disease and Genetics. She interconnects Gastroenterology, Ldl triglycerides, Medical genetics, Myocardial infarction and Hazard ratio in the investigation of issues within Coronary artery disease. Her Genetic association research is multidisciplinary, relying on both Quantitative trait locus and Linkage disequilibrium.
Her primary areas of investigation include Genome-wide association study, Internal medicine, Genetics, Coronary artery disease and Disease. Her work deals with themes such as Periodontitis, Meta-analysis and Genetic association, which intersect with Genome-wide association study. Her Internal medicine research includes themes of Endocrinology, Mendelian randomization and Cardiology.
Her work on Allele, Gene, Expression quantitative trait loci and Candidate gene as part of general Genetics research is frequently linked to Research council, bridging the gap between disciplines. Her biological study spans a wide range of topics, including Gastroenterology, Susceptibility gene, Medical genetics, Myocardial infarction and Functional studies. The concepts of her Single-nucleotide polymorphism study are interwoven with issues in Precision medicine and Oncology.
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Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
Nature (2010)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda.
Nature Genetics (2010)
Genomewide association analysis of coronary artery disease.
Nilesh J. Samani;Jeanette Erdmann;Alistair S. Hall;Christian Hengstenberg.
The New England Journal of Medicine (2007)
Plasma HDL cholesterol and risk of myocardial infarction: A mendelian randomisation study
Benjamin F. Voight;Benjamin F. Voight;Benjamin F. Voight;Gina M. Peloso;Gina M. Peloso;Marju Orho-Melander;Ruth Frikke-Schmidt.
web science (2012)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Nature (2010)
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.
Nature (2011)
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Heribert Schunkert;Inke R. König;Sekar Kathiresan;Muredach P. Reilly.
Nature Genetics (2011)
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)
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
M Nikpay;A Goel;Won H-H.;L M Hall.
Nature Genetics (2015)
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)
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