Braxton D Mitchell

发表

Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies

Seunggeun Lee, Tamar Sofer, Xihong Lin, 2018, bioRxiv.

Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.

Braxton D Mitchell, J. O'connell, A. Shuldiner, 2008, Arthritis and rheumatism.

Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction

Udo Hoffmann, David M Herrington, Eric Boerwinkle, 2011, Circulation.

Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: The Trans-Omics for Precision Medicine Program

James A Perry, Eric Boerwinkle, Josée Dupuis, 2019, bioRxiv.

Obesity Increases Risk of Ischemic Stroke in Young Adults

Braxton D Mitchell, Andrew B Mitchell, Yu-Ching Cheng, 2015, Stroke.

Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.

Lawrence F Bielak, Patricia A Peyser, Braxton D Mitchell, 2010, Archives of internal medicine.

Approaches for unraveling the joint genetic determinants of schizophrenia and bipolar disorder.

Braxton D Mitchell, B. Mitchell, Ping-I Lin, 2007, Schizophrenia bulletin.

Association between bilirubin and cardiovascular disease risk factors: using Mendelian randomization to assess causal inference

Braxton D Mitchell, Brian W Whitcomb, B. Whitcomb, 2012, BMC Cardiovascular Disorders.

CUBN is a gene locus for albuminuria.

Sylvia Stracke, Ming-Huei Chen, Luigi Ferrucci, 2011, Journal of the American Society of Nephrology : JASN.

Sensory gating endophenotype based on its neural oscillatory pattern and heritability estimate.

L Elliot Hong, Braxton D Mitchell, Ann Summerfelt, 2008, Archives of general psychiatry.

Cardiac size and sex-matching in heart transplantation : size matters in matters of sex and the heart.

Keshava Rajagopal, Michael Eberlein, Braxton D Mitchell, 2014, JACC. Heart failure.

Downregulated kynurenine 3-monooxygenase gene expression and enzyme activity in schizophrenia and genetic association with schizophrenia endophenotypes.

L Elliot Hong, Braxton D Mitchell, R. Schwarcz, 2011, Archives of general psychiatry.

Genetic epidemiology of insulin resistance and visceral adiposity. The IRAS Family Study design and methods.

Carl D Langefeld, Marian Rewers, Braxton D Mitchell, 2003, Annals of epidemiology.

Genetic variation in adiponectin receptor 1 and adiponectin receptor 2 is associated with type 2 diabetes in the Old Order Amish.

Jian Wang, Braxton D Mitchell, J. O’Connell, 2005, Diabetes.

Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease: A Genome-Wide Analysis of Common Variants

Pankaj Sharma, Sudha Seshadri, Cathie Sudlow, 2014, Stroke.

Quantitative Trait Loci on Chromosomes 2p, 4p, and 13q Influence Bone Mineral Density of the Forearm and Hip in Mexican Americans

John Blangero, Laura Almasy, Thomas D Dyer, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Does having children extend life span? A genealogical study of parity and longevity in the Amish.

Richa Agarwala, Alejandro A Schäffer, Braxton D Mitchell, 2006, The journals of gerontology. Series A, Biological sciences and medical sciences.

Type 2 diabetes is associated with increased bone mineral density in Mexican-American women.

Braxton D Mitchell, B. Mitchell, R. Bauer, 2003, Archives of medical research.

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Christian Gieger, Alex Doney, Inês Barroso, 2010, Nature Genetics.

Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile

Christian Gieger, Inês Barroso, Meena Kumari, 2011, Nature Genetics.

The association between cardiovascular autonomic neuropathy and mortality in individuals with diabetes: a meta-analysis.

Braxton D Mitchell, R. Freeman, B. Mitchell, 2003, Diabetes care.

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

Tom R. Gaunt, Fotios Drenos, Meena Kumari, 2012, American journal of human genetics.

New loci associated with kidney function and chronic kidney disease

Uwe Völker, Luigi Ferrucci, Reinhold Schmidt, 2010, Nature Genetics.

Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology

Andrew Carroll, Eric Boerwinkle, Andrew D. Johnson, 2017, Nature Genetics.

Design and rationale for examining neuroimaging genetics in ischemic stroke

Polina Golland, Reinhold Schmidt, Adrian V. Dalca, 2017, Neurology: Genetics.

Eating behavior in the Old Order Amish: heritability analysis and a genome-wide linkage analysis.

Braxton D Mitchell, C. Bell, A. Shuldiner, 2002, The American journal of clinical nutrition.

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

Alex Doney, Beverley Balkau, Meena Kumari, 2010, Nature Genetics.

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.

Sylvia Stracke, Christian Gieger, Alex Doney, 2012, Human molecular genetics.

Familial aggregation of eye-tracking endophenotypes in families of schizophrenic patients.

L Elliot Hong, Braxton D Mitchell, L. Hong, 2006, Archives of general psychiatry.

Variation Within the Gene Encoding the Upstream Stimulatory Factor 1 Does Not Influence Susceptibility to Type 2 Diabetes in Samples From Populations With Replicated Evidence of Linkage to Chromosome 1q

Philippe Froguel, Mark Walker, Mark I McCarthy, 2006, Diabetes.

Do Candidate Genes Affect the Brain’s White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans

Peter Kochunov, Thomas E. Nichols, Neda Jahanshad, 2017, bioRxiv.

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.

Christian Gieger, Ingo Ruczinski, Tom R. Gaunt, 2012, American journal of human genetics.

Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium.

Dana C Crawford, Florian Kronenberg, Eric Boerwinkle, 2012, Atherosclerosis.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Claude Bouchard, William Wheeler, Peter Kraft, 2014 .

Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function.

Ramaiah Nagaraja, David Schlessinger, Andrea Maschio, 2008, American journal of human genetics.