Published in Biostatistics on June 14, 2012
Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. Am J Hum Genet (2012) 5.48
The UK10K project identifies rare variants in health and disease. Nature (2015) 3.89
Rare-variant association analysis: study designs and statistical tests. Am J Hum Genet (2014) 3.42
The next-generation sequencing revolution and its impact on genomics. Cell (2013) 3.35
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Nat Genet (2012) 2.55
Sequence kernel association tests for the combined effect of rare and common variants. Am J Hum Genet (2013) 2.41
General framework for meta-analysis of rare variants in sequencing association studies. Am J Hum Genet (2013) 1.86
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk. Nat Genet (2014) 1.61
Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data. Genet Epidemiol (2013) 1.60
Family-based association tests for sequence data, and comparisons with population-based association tests. Eur J Hum Genet (2013) 1.55
The genetic architecture of type 2 diabetes. Nature (2016) 1.43
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. Eur J Hum Genet (2014) 1.41
The power of meta-analysis in genome-wide association studies. Annu Rev Genomics Hum Genet (2013) 1.40
Detecting rare variant effects using extreme phenotype sampling in sequencing association studies. Genet Epidemiol (2012) 1.35
A powerful and efficient set test for genetic markers that handles confounders. Bioinformatics (2013) 1.32
A unified mixed-effects model for rare-variant association in sequencing studies. Genet Epidemiol (2013) 1.29
Functional linear models for association analysis of quantitative traits. Genet Epidemiol (2013) 1.26
Properties and modeling of GWAS when complex disease risk is due to non-complementing, deleterious mutations in genes of large effect. PLoS Genet (2013) 1.24
Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population. JAMA (2014) 1.22
GEE-based SNP set association test for continuous and discrete traits in family-based association studies. Genet Epidemiol (2013) 1.14
Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism. Proc Natl Acad Sci U S A (2013) 1.13
Robust rare variant association testing for quantitative traits in samples with related individuals. Genet Epidemiol (2013) 1.06
Kernel machine SNP-set testing under multiple candidate kernels. Genet Epidemiol (2013) 1.04
Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants. Genet Epidemiol (2013) 1.04
Generalized functional linear models for gene-based case-control association studies. Genet Epidemiol (2014) 0.99
Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism. PLoS Genet (2014) 0.98
New loci and coding variants confer risk for age-related macular degeneration in East Asians. Nat Commun (2015) 0.97
Region-based association analysis of human quantitative traits in related individuals. PLoS One (2013) 0.97
HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome. J Am Soc Nephrol (2014) 0.96
The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. Front Genet (2013) 0.96
Identifying rare variants associated with complex traits via sequencing. Curr Protoc Hum Genet (2013) 0.95
A variational Bayes discrete mixture test for rare variant association. Genet Epidemiol (2014) 0.92
The admixture maximum likelihood test to test for association between rare variants and disease phenotypes. BMC Bioinformatics (2013) 0.91
A common variant near TGFBR3 is associated with primary open angle glaucoma. Hum Mol Genet (2015) 0.91
Methodology for the analysis of rare genetic variation in genome-wide association and re-sequencing studies of complex human traits. Brief Funct Genomics (2014) 0.91
Rare variant association testing by adaptive combination of P-values. PLoS One (2014) 0.90
Evaluation of gene-based association tests for analyzing rare variants using Genetic Analysis Workshop 18 data. BMC Proc (2014) 0.90
FFBSKAT: fast family-based sequence kernel association test. PLoS One (2014) 0.90
Filtering genetic variants and placing informative priors based on putative biological function. BMC Genet (2016) 0.89
TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits. PLoS One (2015) 0.88
Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data. BMC Proc (2014) 0.88
Progress in methods for rare variant association. BMC Genet (2016) 0.88
A flexible approach for the analysis of rare variants allowing for a mixture of effects on binary or quantitative traits. PLoS Genet (2013) 0.88
A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing. Front Genet (2015) 0.88
Gene-based GWAS and biological pathway analysis of the resilience of executive functioning. Brain Imaging Behav (2014) 0.87
Exome array analysis identifies CAV1/CAV2 as a susceptibility locus for intraocular pressure. Invest Ophthalmol Vis Sci (2014) 0.87
Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic. Bioinformatics (2014) 0.87
Region-Based Association Test for Familial Data under Functional Linear Models. PLoS One (2015) 0.87
Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort. PLoS One (2015) 0.86
Association testing of clustered rare causal variants in case-control studies. PLoS One (2014) 0.85
Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes. PLoS One (2015) 0.85
The value of statistical or bioinformatics annotation for rare variant association with quantitative trait. Genet Epidemiol (2013) 0.84
Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African Americans. PLoS Genet (2014) 0.84
A weighted U-statistic for genetic association analyses of sequencing data. Genet Epidemiol (2014) 0.84
What will diabetes genomes tell us? Curr Diab Rep (2012) 0.84
Test for rare variants by environment interactions in sequencing association studies. Biometrics (2015) 0.84
No large-effect low-frequency coding variation found for myocardial infarction. Hum Mol Genet (2014) 0.84
Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland. Am J Hum Genet (2014) 0.84
Sequence Kernel Association Analysis of Rare Variant Set Based on the Marginal Regression Model for Binary Traits. Genet Epidemiol (2015) 0.84
Blocking approach for identification of rare variants in family-based association studies. PLoS One (2014) 0.83
Impact of genetic variants in human scavenger receptor class B type I (SCARB1) on plasma lipid traits. Circ Cardiovasc Genet (2014) 0.82
Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants. Mol Autism (2015) 0.82
Association of rare haplotypes on ULK4 and MAP4 genes with hypertension. BMC Proc (2016) 0.81
Selection and explosive growth alter genetic architecture and hamper the detection of causal rare variants. Genome Res (2016) 0.81
High-throughput sequencing of the synaptome in major depressive disorder. Mol Psychiatry (2015) 0.81
Greater power and computational efficiency for kernel-based association testing of sets of genetic variants. Bioinformatics (2014) 0.81
Detecting genomic clustering of risk variants from sequence data: cases versus controls. Hum Genet (2013) 0.81
A method for analyzing multiple continuous phenotypes in rare variant association studies allowing for flexible correlations in variant effects. Eur J Hum Genet (2016) 0.81
A unified sparse representation for sequence variant identification for complex traits. Genet Epidemiol (2014) 0.81
Longitudinal SNP-set association analysis of quantitative phenotypes. Genet Epidemiol (2016) 0.80
Identification of rare variants in Alzheimer's disease. Front Genet (2014) 0.80
Phenotypic extremes in rare variant study designs. Eur J Hum Genet (2015) 0.80
Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia. PLoS One (2014) 0.80
Methods for association analysis and meta-analysis of rare variants in families. Genet Epidemiol (2015) 0.80
On the simultaneous association analysis of large genomic regions: a massive multi-locus association test. Bioinformatics (2013) 0.80
Beyond Rare-Variant Association Testing: Pinpointing Rare Causal Variants in Case-Control Sequencing Study. Sci Rep (2016) 0.80
Weighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies. PLoS One (2015) 0.80
USAT: A Unified Score-Based Association Test for Multiple Phenotype-Genotype Analysis. Genet Epidemiol (2015) 0.79
Detecting the Genomic Signature of Divergent Selection in Presence of Gene Flow. Curr Genomics (2015) 0.79
On Efficient and Accurate Calculation of Significance P-Values for Sequence Kernel Association Testing of Variant Set. Ann Hum Genet (2016) 0.79
Adaptive combination of P-values for family-based association testing with sequence data. PLoS One (2014) 0.78
An efficient resampling method for calibrating single and gene-based rare variant association analysis in case-control studies. Biostatistics (2015) 0.78
Testing genetic association with rare and common variants in family data. Genet Epidemiol (2014) 0.78
Incorporating gene-environment interaction in testing for association with rare genetic variants. Hum Hered (2014) 0.78
A New Method for Detecting Associations with Rare Copy-Number Variants. PLoS Genet (2015) 0.78
GWAS to Sequencing: Divergence in Study Design and Analysis. Genes (Basel) (2014) 0.78
Assessing association between protein truncating variants and quantitative traits. Bioinformatics (2013) 0.78
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease. Acta Neuropathol (2016) 0.78
Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples. Hum Hered (2016) 0.78
A novel random effect model for GWAS meta-analysis and its application to trans-ethnic meta-analysis. Biometrics (2016) 0.78
Joint analysis of multiple phenotypes: summary of results and discussions from the Genetic Analysis Workshop 19. BMC Genet (2016) 0.78
Comparison of haplotype-based statistical tests for disease association with rare and common variants. Brief Bioinform (2015) 0.78
Rare Variants in the Complement Factor H-Related Protein 5 Gene Contribute to Genetic Susceptibility to IgA Nephropathy. J Am Soc Nephrol (2016) 0.78
A fast and powerful tree-based association test for detecting complex joint effects in case-control studies. Bioinformatics (2014) 0.78
Lipoprotein lipase gene sequencing and plasma lipid profile. J Lipid Res (2013) 0.78
Boosting the Power of the Sequence Kernel Association Test by Properly Estimating Its Null Distribution. Am J Hum Genet (2016) 0.78
A general approach for combining diverse rare variant association tests provides improved robustness across a wider range of genetic architectures. Eur J Hum Genet (2015) 0.77
Rare variants detection with kernel machine learning based on likelihood ratio test. PLoS One (2014) 0.77
The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis. Genes Immun (2015) 0.77
Low-frequency coding variants at 6p21.33 and 20q11.21 are associated with lung cancer risk in Chinese populations. Am J Hum Genet (2015) 0.77
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. Am J Hum Genet (2008) 26.79
Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science (2004) 21.65
A groupwise association test for rare mutations using a weighted sum statistic. PLoS Genet (2009) 19.64
Rare-variant association testing for sequencing data with the sequence kernel association test. Am J Hum Genet (2011) 18.88
Calibrating a coalescent simulation of human genome sequence variation. Genome Res (2005) 15.04
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL. Nat Genet (2007) 13.78
Pooled association tests for rare variants in exon-resequencing studies. Am J Hum Genet (2010) 13.18
Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. Am J Hum Genet (2007) 10.92
An evaluation of statistical approaches to rare variant analysis in genetic association studies. Genet Epidemiol (2010) 10.54
The Dallas Heart Study: a population-based probability sample for the multidisciplinary study of ethnic differences in cardiovascular health. Am J Cardiol (2004) 9.43
Testing for an unusual distribution of rare variants. PLoS Genet (2011) 9.28
Comparison of maximum statistics for hypothesis testing when a nuisance parameter is present only under the alternative. Biometrics (2005) 5.59
Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed models. Biometrics (2007) 4.66
Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models. BMC Bioinformatics (2008) 3.70
Hypothesis testing in semiparametric additive mixed models. Biostatistics (2003) 3.63
Comparison of statistical tests for disease association with rare variants. Genet Epidemiol (2011) 3.42
Haplotype-based association analysis via variance-components score test. Am J Hum Genet (2007) 2.93
Rare-variant association testing for sequencing data with the sequence kernel association test. Am J Hum Genet (2011) 18.88
Quality of life and satisfaction with outcome among prostate-cancer survivors. N Engl J Med (2008) 18.60
LKB1 modulates lung cancer differentiation and metastasis. Nature (2007) 7.80
Powerful SNP-set analysis for case-control genome-wide association studies. Am J Hum Genet (2010) 6.60
Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. Am J Hum Genet (2012) 5.48
A powerful and flexible multilocus association test for quantitative traits. Am J Hum Genet (2008) 4.96
450K epigenome-wide scan identifies differential DNA methylation in newborns related to maternal smoking during pregnancy. Environ Health Perspect (2012) 4.89
Aberrant lipid metabolism disrupts calcium homeostasis causing liver endoplasmic reticulum stress in obesity. Nature (2011) 4.78
Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed models. Biometrics (2007) 4.66
Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models. BMC Bioinformatics (2008) 3.70
Hypothesis testing in semiparametric additive mixed models. Biostatistics (2003) 3.63
Sequence kernel association tests for the combined effect of rare and common variants. Am J Hum Genet (2013) 2.41
Genetic variants on 15q25.1, smoking, and lung cancer: an assessment of mediation and interaction. Am J Epidemiol (2012) 2.16
SNP set association analysis for familial data. Genet Epidemiol (2012) 2.08
Semiparametric modeling of longitudinal measurements and time-to-event data--a two-stage regression calibration approach. Biometrics (2008) 2.05
VEGF polymorphisms and survival in early-stage non-small-cell lung cancer. J Clin Oncol (2008) 1.94
General framework for meta-analysis of rare variants in sequencing association studies. Am J Hum Genet (2013) 1.86
Mixtures of varying coefficient models for longitudinal data with discrete or continuous nonignorable dropout. Biometrics (2004) 1.85
Impact of physician asthma care education on patient outcomes. Pediatrics (2006) 1.70
A comparison of methods for estimating the causal effect of a treatment in randomized clinical trials subject to noncompliance. Biometrics (2008) 1.70
A varying-coefficient Cox model for the effect of age at a marker event on age at menopause. Biometrics (2005) 1.68
Clinical presentation, recurrence, and survival in patients with neuroendocrine tumors: results from a prospective institutional database. Endocr Relat Cancer (2013) 1.62
Family-based association tests for sequence data, and comparisons with population-based association tests. Eur J Hum Genet (2013) 1.55
Genome-wide analysis of survival in early-stage non-small-cell lung cancer. J Clin Oncol (2009) 1.52
Development and validation of a prioritization rule for obtaining an immediate 12-lead electrocardiogram in the emergency department to identify ST-elevation myocardial infarction. Am Heart J (2012) 1.52
A tobit variance-component method for linkage analysis of censored trait data. Am J Hum Genet (2003) 1.49
Pharmacologic prophylaxis and risk factors for intraoperative floppy-iris syndrome in phacoemulsification performed by resident physicians. J Cataract Refract Surg (2010) 1.47
The effect of correlation in false discovery rate estimation. Biometrika (2011) 1.46
Scaled marginal models for multiple continuous outcomes. Biostatistics (2003) 1.46
Air pollution-associated changes in lung function among asthmatic children in Detroit. Environ Health Perspect (2005) 1.45
Identification of driver genes in hepatocellular carcinoma by exome sequencing. Hepatology (2013) 1.41
Finding disease variants in Mendelian disorders by using sequence data: methods and applications. Am J Hum Genet (2011) 1.40
Detecting rare variant effects using extreme phenotype sampling in sequencing association studies. Genet Epidemiol (2012) 1.35
Ascertainment-adjusted parameter estimates revisited. Am J Hum Genet (2002) 1.34
Genotypes and haplotypes of matrix metalloproteinase 1, 3 and 12 genes and the risk of lung cancer. Carcinogenesis (2005) 1.33
Sparse linear discriminant analysis for simultaneous testing for the significance of a gene set/pathway and gene selection. Bioinformatics (2009) 1.32
Semiparametric Maximum Likelihood Estimation in Normal Transformation Models for Bivariate Survival Data. Biometrika (2008) 1.31
The role of choice in health education intervention trials: a review and case study. Soc Sci Med (2003) 1.30
Kernel machine approach to testing the significance of multiple genetic markers for risk prediction. Biometrics (2011) 1.30
Genome-wide association analysis for multiple continuous secondary phenotypes. Am J Hum Genet (2013) 1.29
Kernel machine SNP-set analysis for censored survival outcomes in genome-wide association studies. Genet Epidemiol (2011) 1.29
Staging reproductive aging: a comparison of proposed bleeding criteria for the menopausal transition. Menopause (2004) 1.27
Progression of subclinical coronary atherosclerosis: does obesity make a difference? Circulation (2005) 1.27
Vascular endothelial growth factor genotypes, haplotypes, gender, and the risk of non-small cell lung cancer. Clin Cancer Res (2008) 1.24
Quantitative quality-assessment techniques to compare fractionation and depletion methods in SELDI-TOF mass spectrometry experiments. Bioinformatics (2007) 1.22
Test for interactions between a genetic marker set and environment in generalized linear models. Biostatistics (2013) 1.20
Arsenic and the epigenome: interindividual differences in arsenic metabolism related to distinct patterns of DNA methylation. J Biochem Mol Toxicol (2013) 1.19
Exposure to airborne particulate matter is associated with methylation pattern in the asthma pathway. Epigenomics (2013) 1.17
Neuropsychological effects of low-level manganese exposure in welders. Neurotoxicology (2010) 1.16
Apoptosis gene polymorphisms, age, smoking and the risk of non-small cell lung cancer. Carcinogenesis (2008) 1.15
GEE-based SNP set association test for continuous and discrete traits in family-based association studies. Genet Epidemiol (2013) 1.14
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Genet Epidemiol (2010) 1.14
Risk factors for low bone mineral density and the 6-year rate of bone loss among premenopausal and perimenopausal women. Osteoporos Int (2004) 1.13
Toenail, blood, and urine as biomarkers of manganese exposure. J Occup Environ Med (2011) 1.12
A Large-scale genetic association study of esophageal adenocarcinoma risk. Carcinogenesis (2010) 1.12
Neonatal genome-wide methylation patterns in relation to birth weight in the Norwegian Mother and Child Cohort. Am J Epidemiol (2014) 1.11
Evaluation of Viable Dynamic Treatment Regimes in a Sequentially Randomized Trial of Advanced Prostate Cancer. J Am Stat Assoc (2012) 1.11
Sparse principal component analysis for identifying ancestry-informative markers in genome-wide association studies. Genet Epidemiol (2012) 1.10
Two-stage functional mixed models for evaluating the effect of longitudinal covariate profiles on a scalar outcome. Biometrics (2007) 1.09
Missing covariates in longitudinal data with informative dropouts: bias analysis and inference. Biometrics (2005) 1.09
Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma. Front Genet (2013) 1.08
Increased power for the analysis of label-free LC-MS/MS proteomics data by combining spectral counts and peptide peak attributes. Mol Cell Proteomics (2010) 1.08
Evaluation of cytochrome P450-derived eicosanoids in humans with stable atherosclerotic cardiovascular disease. Atherosclerosis (2012) 1.07
Cervical multilevel intraspinal stem cell therapy: assessment of surgical risks in Gottingen minipigs. Spine (Phila Pa 1976) (2011) 1.07
Variable selection and estimation in generalized linear models with the seamless L0 penalty. Can J Stat (2012) 1.06
Fetal window of vulnerability to airborne polycyclic aromatic hydrocarbons on proportional intrauterine growth restriction. PLoS One (2012) 1.06
Cigarette smoking increases copy number alterations in nonsmall-cell lung cancer. Proc Natl Acad Sci U S A (2011) 1.05
Identifying genetic marker sets associated with phenotypes via an efficient adaptive score test. Biostatistics (2012) 1.04
Interictal epileptiform discharges do not change before seizures during sleep. Epilepsia (2002) 1.03
Arsenic reduction in drinking water and improvement in skin lesions: a follow-up study in Bangladesh. Environ Health Perspect (2012) 1.03
Prognostic significance of MTOR pathway component expression in neuroendocrine tumors. J Clin Oncol (2013) 1.02
Genetic polymorphisms of VEGF, interactions with cigarette smoking exposure and esophageal adenocarcinoma risk. Carcinogenesis (2008) 1.01
Assessment of occupational exposure to manganese and other metals in welding fumes by portable X-ray fluorescence spectrometer. J Occup Environ Hyg (2010) 1.00
Coronary artery calcification progression is heritable. Circulation (2007) 0.99
Powerful tests for detecting a gene effect in the presence of possible gene-gene interactions using garrote kernel machines. Biometrics (2011) 0.99
Insulin-like growth factor pathway genetic polymorphisms, circulating IGF1 and IGFBP3, and prostate cancer survival. J Natl Cancer Inst (2014) 0.98
Plasma neutrophil elastase and elafin imbalance is associated with acute respiratory distress syndrome (ARDS) development. PLoS One (2009) 0.98
Asking the correct questions to assess asthma symptoms. Clin Pediatr (Phila) (2005) 0.95
Estimation in semiparametric transition measurement error models for longitudinal data. Biometrics (2009) 0.94
Prior biological knowledge-based approaches for the analysis of genome-wide expression profiles using gene sets and pathways. Stat Methods Med Res (2009) 0.94
Cytochrome P450-derived eicosanoids and vascular dysfunction in coronary artery disease patients. Atherosclerosis (2013) 0.94
SEMIPARAMETRIC REGRESSION WITH TIME-DEPENDENT COEFFICIENTS FOR FAILURE TIME DATA ANALYSIS. Stat Sin (2010) 0.93
The effect of patient choice of intervention on health outcomes. Contemp Clin Trials (2008) 0.93
Parental management of asthma triggers within a child's environment. J Allergy Clin Immunol (2004) 0.92
Interactions among genetic variants in apoptosis pathway genes, reflux symptoms, body mass index, and smoking indicate two distinct etiologic patterns of esophageal adenocarcinoma. J Clin Oncol (2010) 0.92
Time-dependent cross ratio estimation for bivariate failure times. Biometrika (2011) 0.92
Parity and risk of lung cancer in women. Am J Epidemiol (2010) 0.91
Spatial Linear Mixed Models with Covariate Measurement Errors. Stat Sin (2009) 0.91
Estimating Causal Effects in Trials Involving Multi-Treatment Arms Subject to Non-compliance: A Bayesian framework. J R Stat Soc Ser C Appl Stat (2010) 0.90
Epigenome-wide DNA methylation changes with development of arsenic-induced skin lesions in Bangladesh: a case-control follow-up study. Environ Mol Mutagen (2014) 0.89
SEMIPARAMETRIC TRANSFORMATION MODELS WITH RANDOM EFFECTS FOR CLUSTERED FAILURE TIME DATA. Stat Sin (2008) 0.89
Mediation analysis when a continuous mediator is measured with error and the outcome follows a generalized linear model. Stat Med (2014) 0.89