Published in Am Heart J on June 01, 2005
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Gene polymorphisms in association with self-reported stroke in US adults. Appl Clin Genet (2010) 0.75
De novo mutations in epileptic encephalopathies. Nature (2013) 7.42
Genic intolerance to functional variation and the interpretation of personal genomes. PLoS Genet (2013) 5.58
A simple and improved correction for population stratification in case-control studies. Am J Hum Genet (2007) 4.29
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An evaluation of copy number variation detection tools from whole-exome sequencing data. Hum Mutat (2014) 1.56
Physician-diagnosed depression as a correlate of hospitalizations in patients receiving long-term hemodialysis. Am J Kidney Dis (2005) 1.27
A permutation procedure to correct for confounders in case-control studies, including tests of rare variation. Am J Hum Genet (2012) 1.25
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Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study. BMC Genet (2005) 0.94
Discovery of proteins related to coronary artery disease using industrial-scale proteomics analysis of pooled plasma. Am Heart J (2006) 0.87
Inference for case-control studies when exposure status is both informatively missing and misclassified. Stat Med (2006) 0.86
A weighted accumulation test for associating rare genetic variation with quantitative phenotypes. BMC Proc (2011) 0.86
Estimating crude or common odds ratios in case-control studies with informatively missing exposure data. Am J Epidemiol (2002) 0.86
Testing the effect of rare compound-heterozygous and recessive mutations in case--parent sequencing studies. Genet Epidemiol (2015) 0.85
Determinants of exhaled nitric oxide levels in healthy, nonsmoking African American adults. J Allergy Clin Immunol (2007) 0.85
Genetic variation in HTR2A influences serotonin transporter binding potential as measured using PET and [11C]DASB. Int J Neuropsychopharmacol (2010) 0.85
A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting. BMC Infect Dis (2014) 0.85
Stratification-score matching improves correction for confounding by population stratification in case-control association studies. Genet Epidemiol (2012) 0.85
Leveraging prior information to detect causal variants via multi-variant regression. PLoS Comput Biol (2013) 0.85
Missing data in the 2 x 2 table: patterns and likelihood-based analysis for cross-sectional studies with supplemental sampling. Stat Med (2003) 0.82
The genetics of neuropsychiatric diseases: looking in and beyond the exome. Annu Rev Neurosci (2015) 0.81
A regression-based association test for case-control studies that uses inferred ancestral haplotype similarity. Ann Hum Genet (2009) 0.79
Long-term survival estimates for imatinib versus interferon-alpha plus low-dose cytarabine for patients with newly diagnosed chronic-phase chronic myeloid leukemia. Cancer (2004) 0.78
Where the rubber meets the road in pharmacogenetics: assessment of gene-environment interactions. Am Heart J (2003) 0.75
Power calculations for large multi-arm placebo-controlled studies of dichotomous outcomes. Stat Med (2003) 0.75
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