His primary areas of study are Internal medicine, Genome-wide association study, Genetics, Endocrinology and Single-nucleotide polymorphism. His research integrates issues of Diabetes mellitus and Cardiology in his study of Internal medicine. His Genome-wide association study research incorporates elements of Kidney disease, Renal function, Bioinformatics, Genetic association and Heritability.
His research investigates the connection between Genetics and topics such as Old Order Amish that intersect with issues in Genetic determinism. His Endocrinology study integrates concerns from other disciplines, such as Genetic variation and Allele. His studies in Single-nucleotide polymorphism integrate themes in fields like Genotyping and Allele frequency.
His primary scientific interests are in Internal medicine, Genetics, Endocrinology, Genome-wide association study and Single-nucleotide polymorphism. His Internal medicine research includes elements of Diabetes mellitus and Cardiology. His Diabetes mellitus research is multidisciplinary, relying on both Epidemiology, Gerontology and Risk factor.
His Endocrinology research is multidisciplinary, incorporating elements of Old Order Amish and Allele frequency. Within one scientific family, Braxton D. Mitchell focuses on topics pertaining to Heritability under Genome-wide association study, and may sometimes address concerns connected to Bone mineral. He works mostly in the field of Obesity, limiting it down to topics relating to Body mass index and, in certain cases, Blood pressure, as a part of the same area of interest.
Braxton D. Mitchell focuses on Genetics, Internal medicine, Genome-wide association study, Genetic association and Whole genome sequencing. His work deals with themes such as Endocrinology and Cardiology, which intersect with Internal medicine. Braxton D. Mitchell focuses mostly in the field of Genome-wide association study, narrowing it down to matters related to Heritability and, in some cases, Old Order Amish.
His research on Stroke also deals with topics like
Braxton D. Mitchell spends much of his time researching Genome-wide association study, Genetics, Internal medicine, Genetic association and Genetic variation. His research on Genome-wide association study concerns the broader Single-nucleotide polymorphism. Particularly relevant to Odds ratio is his body of work in Internal medicine.
His studies deal with areas such as Data mining, Generalized linear mixed model, Kernel, Type I and type II errors and Covariate as well as Genetic association. His Genetic variation study also includes fields such as
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Diabetic Autonomic Neuropathy
Aaron I. Vinik;Raelene E. Maser;Braxton D. Mitchell;Roy Freeman.
Diabetes Care (2003)
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)
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)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)
J Dupuis;C Langenberg;I Prokopenko;R Saxena.
Nature Genetics (2010)
Prospective Analysis of The Insulin-Resistance Syndrome (Syndrome X)
Steven M Haffner;Rodolfo A Valdez;Helen P Hazuda;Braxton D Mitchell.
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)
Association of Cytochrome P450 2C19 Genotype With the Antiplatelet Effect and Clinical Efficacy of Clopidogrel Therapy
Alan R. Shuldiner;Jeffrey R. O’Connell;Kevin P. Bliden;Amish Gandhi.
Cardiovascular risk factors in confirmed prediabetic individuals. Does the clock for coronary heart disease start ticking before the onset of clinical diabetes
Steven M. Haffner;Michael P. Stern;Helen P. Hazuda;Braxton D. Mitchell.
Hyperinsulinaemia: the key feature of a cardiovascular and metabolic syndrome
E. Ferrannini;E. Ferrannini;S. M. Haffner;B. D. Mitchell;M. P. Stern.
Analysis of shared heritability in common disorders of the brain
Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
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