publication venue for
- Contribution of rare coding variants to complex trait heritability 2022
- Fluorescent Signal Probe Patterns Strongly Influence Performance of Methods to Estimate Covariate Effects on DNA Methylation Levels 2022
- Less is More: An Unbiased and Versatile Estimator of Genetic Variance Using Summary Statistics 2021
- A versatile, fast and unbiased method for estimation of gene-by-environment interaction effects on biobank-scale datasets 2021
- GWAS transethnic meta-analysis of BMI in similar to 700k individuals reveals novel gene-smoking interaction in African populations 2020
- Leveraging External Repositories to Generate Calibrated Rare Variant Gene Risk Scores 2019
- A Meta Genome-Wide Association Study Identifies a Novel Locus for Cardiovascular Disease in Type 1 Diabetes 2017
- Systematic Review and Meta-Analysis of the Association between FTO rs9939609 Obesity Polymorphism and Suicide in a Large-Scale Multiethnic Population 2017
- Genome-Wide Association Study of Duloxetine and Placebo Response in Major Depressive Disorder 2016
- Impact of Genetic Variants on Latent Class Modeling of Parenting Behavior in Neurodevelopmental Studies 2016
- Mendelian Randomization (MR) Predicts a Causal Role for Serum ACE, APOC-1, APOE, Clusterin, and GDF-15 in Alzheimer Disease (AD) 2016
- Quantifying risk of bias in systematic reviews of genetic association studies 2016
- Rewiring of Enhancer-Gene Interactions Drives PLAU Overexpression in the Pathogenesis of Quebec Platelet Disorder 2016
- BMI as an effect modifier of a novel triglyceride-associated epigenetic mark 2015
- Leveraging gene regulatory data in hypothesis-driven GWAS: The importance of shared tissue specificity 2015
- Methylome scan of PAI-1 plasma levels identifies a locus with putative epigenetic mediation of genetic effect 2015
- Novel method to estimate regional genetic associations improves genetic scores performance 2015
- A Maximum Likelihood Approach to Prioritize SNPs for Interactions Using Variance per Genotype 2012
- GWAS of Repeated Lipid Measures in Type 1 Diabetes Identifies a Novel Locus for Low-density Lipoprotein Cholesterol 2012
- Joint Modeling of Repeated Quantitative Trait Measures and Time to Event in Longitudinal Genetic Association Studies 2012
- Prioritizing SNPs for Gene-Environment and Gene-Gene Interactions: A method to Meta-analyze Levene's Test of Homogeneity of Variance 2012
- A Maximum Likelihood Approach to Prioritize SNPs for Interactions Using Variance per Genotype 2012
- Genome-Wide Association Studies Of Functional Traits: An Application To Lipid Density Profiles In Type 1 Diabetes 2012
- Genome-Wide Association Study (GWAS) Of Lactose Consumption Measured Longitudinally Identifies A Novel Variant 500kb Downstream Of The LCT Gene Region 2012
- A Repeated Measures Genome Wide Association Study of Blood Pressure in Type 1 Diabetes 2010
- Genetic Variation at Adenylate Cyclase 5 (ADCY5) is Associated with Glycemic Control in type 1 Diabetes 2010
- A Genome-Wide Association Study Identifies Variation near SORCS1 as a Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both HbA1c and Glucose 2009
- A High-resolution Scan in the MHC Region for Psoriatic Arthritis Reveals Associations that are not Confounded by Previously Known HLA Risk Alleles 2009
- A Multivariate Growth Curve Model for Ranking Genes in Replicated Time Course Microarray Experiments 2009
- Finding that Elusive Gene-Environment or Gene-Gene Interaction: Prioritizing SNPs for Quantitative Trait Interaction Testing 2009
- Weighted Kernel Fisher Discriminant Analysis (wKFDA) for Integrating Genomic and Clinical Data with Application to Breast Cancer Prediction 2009
- Evaluation of CNV calling algorithms in identifying T-ALL related cancer genes 2008
- Studying genomic impact of copy number variation on gene expression profiles using Sparse Canonical Correlation Analysis 2008
- Survival adjusted lung function severity score in Cystic Fibrosis modifier gene studies 2008
- Age specific effect of TGF beta 1 variants on pulmonary function in cystic fibrosis patients 2007
- The effect of MBL2 gene variants on the age of first infection in Cystic Fibrosis (CF) patients is modified by TGF beta 1 gene variants 2007
- Genome-wide sparse canonical correlation analysis of relationships of genes with complex phenotypes 2007
- Polymorphisms in polycyclic aromatic hydrocarbon (PAH) metabolism and conjugation genes and PAH-DNA adducts. in prostate cancer 2007
- A Bayesian hierarchical model for improving measurement of 5mC and 5hmC levels: Toward revealing associations between phenotypes and methylation states. 46:446-462. 2022
- Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure. 43:815-830. 2019
- A robust method to estimate regional polygenic correlation under misspecified linkage disequilibrium structure. 42:636-647. 2018
- Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels. 41:455-466. 2017
- Longitudinal Data Analysis in Genome‐Wide Association Studies. 38:S68-S73. 2014
- A Genome‐Wide Association Study for Venous Thromboembolism: The Extended Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. 37:512-521. 2013
- A fast algorithm to optimize SNP prioritization for gene-gene and gene-environment interactions. 35:729-738. 2011
- Gene‐ or region‐based analysis of genome‐wide association studies. 33:S105-S110. 2009
- Multivariate analysis of complex gene expression and clinical phenotypes with genetic marker data. 31:S103-S109. 2007
- Modeling Complex Disease with Demographic and Environmental Covariates and a Candidate Gene Marker. 21:S423-S428. 2001
- Effects of misclassification on estimates of relative risk in family history studies. 16:368-381. 1999
- Evidence of linkage in subtypes of alcoholism. 17:S253-S258. 1999
- Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings. 16:179-190. 1999
- Impact of prenatal diagnosis on revised livebirth prevalence estimates of Down syndrome in the Lothian region of Scotland, 1978–1992. 13:367-375. 1996
- Impact of prenatal diagnosis on revised livebirth prevalence estimates of Down syndrome in the Lothian region of Scotland, 1978–1992. 13:367-375. 1996