John F. Peden mostly deals with Genetics, Genome-wide association study, Single-nucleotide polymorphism, Internal medicine and Genetic association. His Genetics research is multidisciplinary, relying on both Body mass index and Obesity. His Genome-wide association study study combines topics in areas such as SNP, Genetic variability and Blood pressure.
His Single-nucleotide polymorphism research incorporates themes from Odds ratio and Case-control study. His Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology and Cardiology. His study in Genetic association is interdisciplinary in nature, drawing from both Quantitative trait locus and Bioinformatics.
His main research concerns Genetics, Genome-wide association study, Internal medicine, Single-nucleotide polymorphism and Genetic association. His Genome-wide association study study combines topics from a wide range of disciplines, such as Allelic heterogeneity, Coronary artery disease, Linkage disequilibrium, Case-control study and Allele frequency. His Internal medicine research is multidisciplinary, incorporating elements of Gastroenterology, Endocrinology, Mendelian randomization and Cardiology.
John F. Peden combines subjects such as Methylenetetrahydrofolate reductase and Haplotype with his study of Single-nucleotide polymorphism. His research integrates issues of Body mass index, Bioinformatics, Blood pressure, Meta-analysis and Waist–hip ratio in his study of Genetic association. His research in Candidate gene intersects with topics in Genetic variation and Allele.
Genetics, Internal medicine, Germline mutation, Body mass index and Obesity are his primary areas of study. Genome-wide association study, Missense mutation, Aniridia, Mutation and Congenital cataracts are the core of his Genetics study. His multidisciplinary approach integrates Genome-wide association study and Kidney development in his work.
His Internal medicine study combines topics in areas such as SNP, Mendelian randomization, Transmembrane transporter activity and Surgery. The Germline mutation study which covers Transcriptome that intersects with Breast cancer, Cancer, Mutation, Genome and Disease. His Obesity research is multidisciplinary, incorporating elements of Gout and Locus.
His primary areas of investigation include Genetics, Body mass index, Obesity, Genome-wide association study and Energy metabolism. His Genetics study frequently draws connections to other fields, such as Uric acid. In his study, SNP is inextricably linked to Locus, which falls within the broad field of Uric acid.
His Energy metabolism research incorporates elements of Adipogenesis and Insulin secretion. His biological study spans a wide range of topics, including Exome sequencing, Genetic variability, Genomics, Genetic association and Genetic variation. His studies in Exome sequencing integrate themes in fields like Computational biology and 1000 Genomes Project.
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A global reference for human genetic variation.
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Josée Dupuis;Josée Dupuis;Claudia Langenberg;Inga Prokopenko;Richa Saxena;Richa Saxena.
Nature Genetics (2010)
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.
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.
A genome-wide association search for type 2 diabetes genes in African Americans.
N D Palmer;C W McDonough;P J Hicks;B H Roh.
PLOS ONE (2012)
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)
Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease
R Clarke;J F Peden;J C Hopewell;T Kyriakou.
The New England Journal of Medicine (2009)
Large-scale association analysis identifies new risk loci for coronary artery disease
Panos Deloukas;Stavroula Kanoni;Christina Willenborg;Martin Farrall.
Nature Genetics (2013)
Genome-wide association study identifies eight loci associated with blood pressure
Christopher Newton-Cheh;Christopher Newton-Cheh;Toby Johnson;Toby Johnson;Vesela Gateva;Martin D. Tobin.
Nature Genetics (2009)
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