Christopher Newton-Cheh spends much of his time researching Internal medicine, Genetics, Genome-wide association study, Cardiology and Genetic association. His study brings together the fields of Endocrinology and Internal medicine. As a part of the same scientific study, Christopher Newton-Cheh usually deals with the Genetics, concentrating on QT interval and frequently concerns with NOS1AP.
The various areas that Christopher Newton-Cheh examines in his Genome-wide association study study include Meta-analysis, Kidney, Disease and Blood pressure. The study incorporates disciplines such as Framingham Heart Study, PR interval and Hazard ratio in addition to Cardiology. His Genetic association study combines topics in areas such as Case-control study, Locus and Medical genetics.
Internal medicine, Genetics, Genome-wide association study, Cardiology and Single-nucleotide polymorphism are his primary areas of study. His research in Internal medicine tackles topics such as Endocrinology which are related to areas like Natriuretic peptide and C-reactive protein. His research investigates the link between Genetics and topics such as Cohort study that cross with problems in Cohort and Epidemiology.
His studies deal with areas such as Bioinformatics, Medical genetics, Disease, Genetic association and Locus as well as Genome-wide association study. His work in Cardiology tackles topics such as Odds ratio which are related to areas like Case-control study, Confidence interval and Prospective cohort study. His research integrates issues of Allele, Polymorphism, Genetic model and Genotyping in his study of Single-nucleotide polymorphism.
His primary areas of investigation include Internal medicine, Genome-wide association study, Cardiology, Atrial fibrillation and Cardiac conduction. Christopher Newton-Cheh has researched Internal medicine in several fields, including Virus and Endocrinology. His study with Genome-wide association study involves better knowledge in Genetics.
His Cardiology research integrates issues from Logistic regression, Bradycardia and Dosing. His Atrial fibrillation research focuses on subjects like Coronary artery disease, which are linked to Residual risk, Public health, Myocardial infarction, Acute coronary syndrome and Body mass index. His PR interval research incorporates elements of Cardiomyopathy, Single-nucleotide polymorphism and Disease.
His main research concerns Genome-wide association study, Internal medicine, Cardiac conduction, Medical genetics and Genetic association. His study on Genome-wide association study is covered under Genetics. The study of Internal medicine is intertwined with the study of Virus in a number of ways.
In his study, Missense mutation, Endocrinology, PR interval, Locus and Haplotype is strongly linked to QRS complex, which falls under the umbrella field of Cardiac conduction. His Medical genetics research focuses on Genetic architecture and how it connects with Mendelian randomization, Heritability, Long QT syndrome, QT interval and Genetic disorder. His research integrates issues of Pulse pressure, Blood pressure and Case-control study in his study of Genetic association.
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Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels
Richa Saxena;Benjamin F. Voight;Valeriya Lyssenko;Noël P. Burtt.
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)
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.
Multiple Biomarkers for the Prediction of First Major Cardiovascular Events and Death
Thomas J. Wang;Thomas J. Wang;Philimon Gona;Philimon Gona;Martin G. Larson;Martin G. Larson;Geoffrey H. Tofler.
The New England Journal of Medicine (2006)
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
Sekar Kathiresan;Sekar Kathiresan;Olle Melander;Candace Guiducci;Aarti Surti.
Nature Genetics (2008)
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)
Development of a risk score for atrial fibrillation (Framingham Heart Study): a community-based cohort study
Renate B Schnabel;Lisa M Sullivan;Daniel Levy;Michael J Pencina.
The Lancet (2009)
50 year trends in atrial fibrillation prevalence, incidence, risk factors, and mortality in the Framingham Heart Study: a cohort study
Renate B Schnabel;Xiaoyan Yin;Philimon Gona;Martin G Larson.
The Lancet (2015)
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
Weizhen Ji;Jia Nee Foo;Brian J O'Roak;Hongyu Zhao.
Nature Genetics (2008)
Polymorphisms Associated with Cholesterol and Risk of Cardiovascular Events
Sekar Kathiresan;Olle Melander;Dragi Anevski;Candace Guiducci.
The New England Journal of Medicine (2008)
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