His primary scientific interests are in Genetics, Genome-wide association study, Internal medicine, Single-nucleotide polymorphism and Molecular biology. His Genetics research incorporates themes from Body mass index and Case-control study. His biological study spans a wide range of topics, including Polymorphism, Coronary artery disease, Cholesterol, Genetic association and Locus.
His work on Blood lipids is typically connected to Mendelian randomization as part of general Cholesterol study, connecting several disciplines of science. His Internal medicine study combines topics from a wide range of disciplines, such as Pathology, Endocrinology and Cardiology. Thomas Quertermous has included themes like GATA2, Complementary DNA, Integrin, Cell biology and Lipase in his Molecular biology study.
Thomas Quertermous spends much of his time researching Internal medicine, Endocrinology, Genetics, Gene and Cell biology. His study ties his expertise on Cardiology together with the subject of Internal medicine. His works in Genome-wide association study, Single-nucleotide polymorphism, Allele, Candidate gene and Genetic architecture are all subjects of inquiry into Genetics.
His research in Genome-wide association study focuses on subjects like Coronary artery disease, which are connected to Bioinformatics and Case-control study. His research investigates the connection between Gene and topics such as Molecular biology that intersect with problems in Recombinant DNA, Biochemistry, Plasminogen activator, Complementary DNA and Antibody. Thomas Quertermous has researched Cell biology in several fields, including Endothelial stem cell, Embryonic stem cell, Angiogenesis, Cellular differentiation and Integrin.
Thomas Quertermous mostly deals with Gene, Genome-wide association study, Genetics, Internal medicine and Genetic association. His Gene research is multidisciplinary, incorporating perspectives in Computational biology and Cell type. His work carried out in the field of Genome-wide association study brings together such families of science as Bioinformatics, Quantitative trait locus, Expression quantitative trait loci, Allele and Locus.
All of his Genetics and Single-nucleotide polymorphism, Enhancer, Allele frequency and Kidney investigations are sub-components of the entire Genetics study. His Single-nucleotide polymorphism research is multidisciplinary, incorporating elements of Diabetes mellitus, Type 2 diabetes, Medical genetics and Genetic architecture. His Internal medicine research is multidisciplinary, relying on both Endocrinology and Cardiology.
Thomas Quertermous mainly investigates Genome-wide association study, Gene, Bioinformatics, Cell biology and Genetics. His Genome-wide association study study deals with Genetic association intersecting with Quantitative trait locus. As a part of the same scientific study, he usually deals with the Gene, concentrating on Cancer research and frequently concerns with Actin cytoskeleton, Contraction, Immunohistochemistry and Hyperplasia.
His Bioinformatics research includes elements of Exome sequencing, Mutation and Single-nucleotide polymorphism. His studies in Cell biology integrate themes in fields like Phenotype, Cell, Cell type and Transcriptome. His studies examine the connections between Kidney and genetics, as well as such issues in Transmembrane transporter activity, with regards to Internal medicine.
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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)
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)
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)
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)
Large-scale association analysis identifies new risk loci for coronary artery disease
Panos Deloukas;Stavroula Kanoni;Christina Willenborg;Martin Farrall.
Nature Genetics (2013)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
E. K. Speliotes;C. J. Willer;S. I. Berndt;K. L. Monda.
Faculty of Health; Institute of Health and Biomedical Innovation (2010)
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