Published in Am J Epidemiol on September 12, 2008
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Genotyping errors: causes, consequences and solutions. Nat Rev Genet (2005) 5.00
Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet (2002) 4.89
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Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms. Hum Hered (2002) 2.74
A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data. Am J Hum Genet (2001) 2.68
Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test. Am J Hum Genet (2003) 2.51
The impact of genotyping error on haplotype reconstruction and frequency estimation. Eur J Hum Genet (2002) 2.51
The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures. Am J Hum Genet (2001) 2.29
Air pollution and inflammation (interleukin-6, C-reactive protein, fibrinogen) in myocardial infarction survivors. Environ Health Perspect (2007) 2.24
Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels and parameters of the metabolic syndrome in 1,727 healthy Caucasians. Diabetes (2006) 2.23
Effects of differential genotyping error rate on the type I error probability of case-control studies. Hum Hered (2006) 2.21
What SNP genotyping errors are most costly for genetic association studies? Genet Epidemiol (2004) 2.00
Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium. Genet Epidemiol (2005) 1.93
Assessment and management of single nucleotide polymorphism genotype errors in genetic association analysis. Pac Symp Biocomput (2001) 1.62
Increasing power for tests of genetic association in the presence of phenotype and/or genotype error by use of double-sampling. Stat Appl Genet Mol Biol (2004) 1.61
A general method for dealing with misclassification in regression: the misclassification SIMEX. Biometrics (2006) 1.42
Estimation of magnitude in gene-environment interactions in the presence of measurement error. Stat Med (2004) 1.41
An overview of issues related to the correction of non-differential exposure measurement error in epidemiologic studies. Stat Med (1989) 1.37
Quantification of the power of Hardy-Weinberg equilibrium testing to detect genotyping error. Hum Hered (2006) 1.32
The ATGL gene is associated with free fatty acids, triglycerides, and type 2 diabetes. Diabetes (2006) 1.22
Allowing for genotyping error in analysis of unmatched case-control studies. Ann Hum Genet (2003) 1.21
Using duplicate genotyped data in genetic analyses: testing association and estimating error rates. Stat Appl Genet Mol Biol (2007) 1.16
Testing for association with a case-parents design in the presence of genotyping errors. Genet Epidemiol (2004) 1.16
Linear trend tests for case-control genetic association that incorporate random phenotype and genotype misclassification error. Genet Epidemiol (2007) 1.03
Genotyping error detection through tightly linked markers. Genetics (2003) 0.99
Incorporating individual error rate into association test of unmatched case-control design. Hum Hered (2004) 0.99
Repeated measurement sampling in genetic association analysis with genotyping errors. Genet Epidemiol (2007) 0.93
The impact of missing and erroneous genotypes on tagging SNP selection and power of subsequent association tests. Hum Hered (2006) 0.90
Estimating haplotype frequencies in pooled DNA samples when there is genotyping error. BMC Genet (2005) 0.87
Identification of probable genotyping errors by consideration of haplotypes. Eur J Hum Genet (2006) 0.87
Haplotype reconstruction error as a classical misclassification problem: introducing sensitivity and specificity as error measures. PLoS One (2008) 0.84
Effect of genotyping error on type-I error rate of affected sib pair studies with genotyped parents. Hum Hered (2005) 0.83
Quantifying bias due to allele misclassification in case-control studies of haplotypes. Genet Epidemiol (2006) 0.80
Incorporating genotyping uncertainty in haplotype frequency estimation in pedigree studies. Hum Hered (2007) 0.78
Susceptibility of biallelic haplotype and genotype frequencies to genotyping error. Biometrics (2006) 0.78
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet (2008) 35.06
Biological, clinical and population relevance of 95 loci for blood lipids. Nature (2010) 28.21
Genomewide association analysis of coronary artery disease. N Engl J Med (2007) 24.38
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet (2010) 23.08
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet (2008) 22.35
Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature (2010) 20.01
Particulate matter air pollution and cardiovascular disease: An update to the scientific statement from the American Heart Association. Circulation (2010) 19.30
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet (2010) 17.89
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet (2010) 16.96
Identification of ten loci associated with height highlights new biological pathways in human growth. Nat Genet (2008) 16.25
Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nat Genet (2008) 15.94
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nat Genet (2009) 15.15
A common genetic variant is associated with adult and childhood obesity. Science (2006) 14.95
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Nature (2007) 14.43
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet (2011) 13.25
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature (2011) 13.25
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature (2011) 13.23
Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet (2009) 12.44
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet (2008) 12.32
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet (2009) 12.19
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet (2012) 11.09
Variants in MTNR1B influence fasting glucose levels. Nat Genet (2008) 10.85
Long-term mortality after gastric bypass surgery. N Engl J Med (2007) 10.75
Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet (2009) 10.34
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat Genet (2011) 9.23
Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat Genet (2010) 8.55
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. Lancet (2012) 8.42
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nat Genet (2010) 7.94
Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet (2012) 7.59
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nat Genet (2010) 6.66
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat Genet (2010) 6.49
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat Genet (2006) 6.39
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat Genet (2009) 6.31
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. PLoS Genet (2009) 5.81
New loci associated with kidney function and chronic kidney disease. Nat Genet (2010) 5.58
Loss-of-function mutations in APOC3, triglycerides, and coronary disease. N Engl J Med (2014) 5.47
Lower estimated glomerular filtration rate and higher albuminuria are associated with mortality and end-stage renal disease. A collaborative meta-analysis of kidney disease population cohorts. Kidney Int (2011) 5.25
Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. PLoS Genet (2008) 5.23
Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease. Circulation (2008) 5.20
New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet (2009) 5.12
A genome-wide perspective of genetic variation in human metabolism. Nat Genet (2009) 5.00
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. PLoS Genet (2009) 4.97
Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants. PLoS One (2007) 4.92