Genetic Epidemiology
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Publication Venue For
- Multiethnic polygenic risk scores improve risk prediction in diverse populations.. 41:811-823. 2017
- A genetic stochastic process model for genome-wide joint analysis of biomarker dynamics and disease susceptibility with longitudinal data.. 41:620-635. 2017
- Gene-environment interactions in cancer epidemiology: a National Cancer Institute Think Tank report.. 37:643-657. 2013
- An "almost exhaustive" search-based sequential permutation method for detecting epistasis in disease association studies.. 34:434-443. 2010
- Haplotype associations with quantitative traits in the presence of complex multilocus and heterogeneous effects.. 33:63-78. 2009
- X-LRT: a likelihood approach to estimate genetic risks and test association with X-linked markers using a case-parents design.. 32:370-380. 2008
- Robust estimation and testing of haplotype effects in case-control studies.. 32:29-40. 2008
- Methods for interaction analyses using family-based case-control data: conditional logistic regression versus generalized estimating equations.. 31:883-893. 2007
- Interpreting analyses of continuous covariates in affected sibling pair linkage studies.. 31:541-552. 2007
- Inference on haplotype/disease association using parent-affected-child data: the projection conditional on parental haplotypes method.. 31:211-223. 2007
- Interpretation of simultaneous linkage and family-based association tests in genome screens.. 31:134-142. 2007
- Multistage designs in the genomic era: providing balance in complex disease studies.. 31 Suppl 1:S118-S123. 2007
- Simple methods for assessing haplotype-environment interactions in case-only and case-control studies.. 31:75-90. 2007
- Summary of contributions to GAW15 Group 13: candidate gene association studies.. 31 Suppl 1:S110-S117. 2007
- Linkage analysis with gene-environment interaction: model illustration and performance of ordered subset analysis.. 30:409-422. 2006
- Genetic association tests based on ranks (GATOR) for quantitative traits with and without censoring.. 30:248-258. 2006
- Ordered subset analysis in genetic linkage mapping of complex traits.. 27:53-63. 2004
- Genotype-based association test for general pedigrees: the genotype-PDT.. 25:203-213. 2003
- Effects of covariates: a summary of Group 5 contributions.. 25 Suppl 1:S43-S49. 2003
- Life after the screen: making sense of many P-values.. 21 Suppl 1:S546-S551. 2001
- Complete genomic screen for disease susceptibility loci in nuclear families.. 17 Suppl 1:S473-S478. 1999
- Increased risk for familial ovarian cancer among Jewish women: a population-based case-control study.. 15:51-59. 1998
- Testing for contributions of mitochondrial DNA mutations to complex diseases.. 15:451-469. 1998
- False positive rates in a genomic screen for complex quantitative traits.. 14:891-896. 1997
- No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease.. 14:307-315. 1997
- Sequential sib-pair and association studies to detect genes in quantitative traits.. 14:885-890. 1997
- Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations.. 13:117-137. 1996
- Genetic analysis of durations: correlated frailty model applied to survival of Danish twins.. 12:529-538. 1995
- Identification of susceptibility loci contributing to a complex disease using conventional segregation, linkage, and association methods.. 12:601-606. 1995
- Clustering of high density lipoprotein cholesterol levels in premenopausal and postmenopausal female twins.. 10:563-567. 1993
- Linkage analysis in familial Alzheimer disease: description of the Duke and Boston data sets.. 10:361-364. 1993
- Relationship of epithelial ovarian cancer to other malignancies within families.. 5:355-367. 1988
- Smoking Dependent and Independent Causal Effects of Educational Ascertainment and Alcohol Use on Lung Cancer 2021
- The Association of Accelerated Epigenetic Age with Time-to-death Mediated by Subclinical and Clinical Vascular Outcomes 2021
- Racial differences in methylation pathway-structured predictive models and breast cancer survival 2020
- The role of brain-derived neurotropic factor (BDNF) genetic variants in exercise training 2020
- FamRVC Program for Family-based Rare Variant Association Tests for Censored Traits and its Applications to Age-at-onset of Alzheimer's Disease 2019
- Genome-wide Analysis of Non-completion of Controlled Exercise Trials in Sedentary Adults 2019
- Genetics of the measure of physiological dysregulation: findings from the health and retirement study 2018
- Harmonizing psychosocial stress and CVD-risk variables for developing robust estimates of GxE analyses 2018
- Incorporating prior information into set-based analyses using higher criticism statistics with an application to amyotrophic lateral sclerosis 2018
- Understanding of DNA methylation in the biological basis of stress related cardiovascular disease 2018
- Gender Differences in Brain-Derived Neurotrophic Factor (BDNF) Val66Met Variants and Stressful Life Events on Psychological and Metabolic Phenotypes 2017
- Genetics of the Measure of Physiological Dysregulation: Insights from Longitudinal Data 2017
- Genome-wide Meta-analysis of 24 Age-related Phenotypes Leveraging Longitudinal Follow-up and Genetic Heterogeneity Identified Abundant Associations in a Modest Sample of 26,371 Individuals 2017
- The effect of Brain- Derived Neurotrophic Factor (BDNF) Val66Met Variants on the Path from Psychosocial Stress to Depression, Body Mass Index and Pre-Clinical Atherosclerosis 2017
- Brain-Derived Neurotrophic Factor Val66Met Variants (RS6265) are Associated with Coronary Heart Disease (CHD) Outcomes in a Patient Sample 2016
- Follow-up of GxE Interactions: EBF1 GxE Association, Synthetic Chronic Psychosocial Stress, and Dropout from a Structured Exercise Program 2016
- High-Resolution Analyses of Effects of Polygenic Risk Scores on Time-to-Event Outcomes in Longitudinal Studies 2016
- On Approaches to Improve Power in Analyses of Genetic Effects on Time-To-Event Outcomes in Longitudinal Studies 2015
- Unfolding heterogeneity of complex traits has strong potential for advancing GWAS 2015
- Developmental Processes can Drive Inter-chromosomal Linkage Disequilibrium 2012
- Heavy Metals, Organic Solvents and Multiple Sclerosis: An Exploratory Analysis of Gene-environment Interactions 2012
- Relationship Between the APOE Polymorphism and Risks of Cancer and Alzheimer's Disease: Application of the Genetic Stochastic Process Model 2012
- The Role of Genes and Life Course in Late Life Diseases 2012
- Complex Modalities Of Gene Action On Phenotypes With Post Reproductive Manifestation: The Case Of Genetic Trade-Off 2012
- Trade-Off In The Effects Of The APOE Polymorphism On The Ages At Onset Of CVD And Cancer: Insights From The Genetic Stochastic Process Model 2012
- Evaluation of Effects of Genetic polymorphisms and Age Trajectories of Physiological Indices on survival 2010
- Evaluation of Genotype-specific Age Patterns of Hazard Rates Using Joint Analysis of Genetic and Non-genetic Subsamples of Longitudinal Data 2009
- Polymorphisms in the Angiotensin-Converting Enzyme (ACE) Gene as Determinants of Cardiovascular Diseases Risks and Short Life in Framingham Heart Study 2009
- The Role of Polymorphisms in the ACE and ADRB2 Genes in Incidence of Myocardial Infarction in Framingham Heart Study Participants 2009
- Effects of ACE D/I Polymorphism and 11 SNPs Heterozygosity in the Same Gene on Health Risks in Framingham Study 2008
- Heritability of Endophenotypes of Pulmonary & Physical Function in Long Life Family Study 2008
- Interacting Effect of ACE D/I Polymorphism and Smoking on Health Risks in Framingham Study 2008
- Stochastic Model for Joint Analysis of Genetic and Non-Genetic Data from Longitudinal Studies of Aging, Health and Longevity 2008
- Using in silico priors for pathway modeling 2008
- Integration of SIMIA and SIMLAPLOT: A graphical user interface for complex disease simulation and analysis 2007
- A visualization tool for genetic parameters in complex human traits 2007
- Relationship between genotype variants in coronary artery disease (CAD) and HDL level 2007