[PDF][PDF] Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data
…, D Drogan, S Padmanabhan, S Li, A Yesupriya… - Bmj, 2014 - bmj.com
Objective To use the rs1229984 variant in the alcohol dehydrogenase 1B gene (ADH1B) as
an instrument to investigate the causal role of alcohol in cardiovascular disease. Design …
an instrument to investigate the causal role of alcohol in cardiovascular disease. Design …
A navigator for human genome epidemiology
Recent successes in large-scale genetic association studies call for renewed attention to
integrating research results, not only among studies, but across disciplines1. At the molecular …
integrating research results, not only among studies, but across disciplines1. At the molecular …
[HTML][HTML] Genetic variants associated with fasting blood lipids in the US population: Third National Health and Nutrition Examination Survey
M Chang, A Yesupriya, RM Ned, PW Mueller… - BMC medical …, 2010 - Springer
Background The identification of genetic variants related to blood lipid levels within a large,
population-based and nationally representative study might lead to a better understanding of …
population-based and nationally representative study might lead to a better understanding of …
[HTML][HTML] A systematic review of cancer GWAS and candidate gene meta-analyses reveals limited overlap but similar effect sizes
CQ Chang, A Yesupriya, JL Rowell… - European Journal of …, 2014 - nature.com
Candidate gene and genome-wide association studies (GWAS) represent two complementary
approaches to uncovering genetic contributions to common diseases. We systematically …
approaches to uncovering genetic contributions to common diseases. We systematically …
Racial/ethnic variation in the association of lipid-related genetic variants with blood lipids in the US adult population
M Chang, RM Ned, Y Hong, A Yesupriya… - Circulation …, 2011 - Am Heart Assoc
Background— Genome-wide association studies (GWAS) have identified a number of single-nucleotide
polymorphisms (SNPs) associated with serum lipid level in populations of …
polymorphisms (SNPs) associated with serum lipid level in populations of …
[HTML][HTML] Prospective study of methylenetetrahydrofolate reductase (MTHFR) variant C677T and risk of all-cause and cardiovascular disease mortality among 6000 US …
…, R Clarke, WD Flanders, T Liu, A Yesupriya… - The American journal of …, 2012 - Elsevier
Background: The association between blood homocysteine concentration and the risk of
cardiovascular disease (CVD) remains controversial, but few studies have examined the …
cardiovascular disease (CVD) remains controversial, but few studies have examined the …
Trends in laboratory test volumes for Medicare Part B reimbursements, 2000–2010
…, TD Alspach, JR Astles, A Yesupriya… - … of Pathology and …, 2014 - meridian.allenpress.com
Context.—Changes in reimbursements for clinical laboratory testing may help us assess the
effect of various variables, such as testing recommendations, market forces, changes in …
effect of various variables, such as testing recommendations, market forces, changes in …
Prevalence in the United States of selected candidate gene variants: third national health and nutrition examination survey, 1991–1994
…, CL Sanders, R Welch, A Yesupriya… - American journal of …, 2009 - academic.oup.com
Population-based allele frequencies and genotype prevalence are important for measuring
the contribution of genetic variation to human disease susceptibility, progression, and …
the contribution of genetic variation to human disease susceptibility, progression, and …
[HTML][HTML] GAPscreener: an automatic tool for screening human genetic association literature in PubMed using the support vector machine technique
W Yu, M Clyne, SM Dolan, A Yesupriya, A Wulf, T Liu… - BMC …, 2008 - Springer
Background Synthesis of data from published human genetic association studies is a critical
step in the translation of human genome discoveries into health applications. Although …
step in the translation of human genome discoveries into health applications. Although …
The ACE I/D Polymorphism in US Adults: Limited Evidence of Association With Hypertension-Related Traits and Sex-Specific Effects by Race/Ethnicity
RM Ned, A Yesupriya, G Imperatore… - American journal of …, 2012 - academic.oup.com
Background: The insertion/deletion (I/D) variant (rs4646994) of the angiotensin I-converting
enzyme (ACE) gene is one of the most studied polymorphisms in relation to blood pressure …
enzyme (ACE) gene is one of the most studied polymorphisms in relation to blood pressure …
