His primary areas of study are Internal medicine, Genome-wide association study, Genetics, Blood pressure and Endocrinology. In his study, Pulse wave velocity and Stroke is strongly linked to Cardiology, which falls under the umbrella field of Internal medicine. The study incorporates disciplines such as Bioinformatics, Medical genetics, Disease, Allele and Genetic association in addition to Genome-wide association study.
His Blood pressure study incorporates themes from Anesthesia, Diuretic and Risk factor. In his research on the topic of Endocrinology, Hyperuricemia and Urate transport is strongly related with SLC2A9. His research integrates issues of Population stratification, Human genetics and CDKN2BAS in his study of Allele frequency.
Morris J. Brown focuses on Internal medicine, Endocrinology, Blood pressure, Genetics and Aldosterone. Within one scientific family, he focuses on topics pertaining to Cardiology under Internal medicine, and may sometimes address concerns connected to Atenolol and Stroke. His work carried out in the field of Endocrinology brings together such families of science as Receptor and Antagonist.
His Blood pressure research incorporates elements of Hemodynamics, Surgery, Disease and Bioinformatics. His study in Genome-wide association study, Single-nucleotide polymorphism, Locus, Gene and Candidate gene falls within the category of Genetics. His Genome-wide association study study integrates concerns from other disciplines, such as Allele and Genetic association.
Morris J. Brown mainly focuses on Internal medicine, Blood pressure, Endocrinology, Aldosterone and Genetics. His Internal medicine research is multidisciplinary, incorporating perspectives in Transcriptome and Cardiology. His Blood pressure research incorporates themes from Genetic analysis, Placebo, Disease and Genetic association.
His research in Endocrinology intersects with topics in Mutation, Microarray analysis techniques and Wnt signaling pathway. His study in Genome-wide association study, Single-nucleotide polymorphism, Genetic variation, Candidate gene and Gene is done as part of Genetics. Morris J. Brown combines subjects such as Bioinformatics, Medical genetics, Allele, Locus and Genetic architecture with his study of Genome-wide association study.
The scientist’s investigation covers issues in Genome-wide association study, Blood pressure, Internal medicine, Genetics and Endocrinology. His studies in Genome-wide association study integrate themes in fields like Bioinformatics, Medical genetics, Allele, Genetic association and Genetic architecture. His Blood pressure study combines topics in areas such as Spironolactone, Placebo, Randomized controlled trial and Disease.
As part of one scientific family, Morris J. Brown deals mainly with the area of Disease, narrowing it down to issues related to the Pulse pressure, and often Genetic testing, Biobank and Risk factor. His work on Aldosterone, Vascular resistance, Hemodynamics and Primary aldosteronism as part of general Internal medicine study is frequently connected to GNRHR, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. His Endocrinology study frequently draws connections between related disciplines such as Somatic cell.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton;David G. Clayton;Lon R. Cardon;Nick Craddock.
Nature (2007)
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)
Randomised controlled trial of vitamin E in patients with coronary disease: Cambridge Heart Antioxidant Study (CHAOS)
N.G Stephens;N.G Stephens;A Parsons;A Parsons;M.J Brown;P.M Schofield.
The Lancet (1996)
A Randomised Controlled Trial of Vitamin E in Patients with Coronary Disease: The Cambridge Heart Antioxidant Study (CHAOS)
NG Stephens;A Parsons;PM Schofield;MJ Mitchinson.
Clinical Science (1996)
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)
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Cristen J. Willer;Elizabeth K. Speliotes;Elizabeth K. Speliotes;Ruth J. F. Loos;Shengxu Li.
Nature Genetics (2009)
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)
Morbidity and mortality in patients randomised to double-blind treatment with a long-acting calcium-channel blocker or diuretic in the International Nifedipine GITS study: Intervention as a Goal in Hypertension Treatment (INSIGHT)
Morris J Brown;Christopher R Palmer;Alain Castaigne;Peter W de Leeuw.
The Lancet (2000)
Guidelines for management of hypertension: report of the fourth working party of the British Hypertension Society, 2004—BHS IV
Williams B;Poulter Nr;Brown Mj;Davis M.
Journal of Human Hypertension (2004)
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