Genetic Epidemiology

Journal

Publication Venue For

  • Assessing pleiotropy and mediation in genetic loci associated with chronic obstructive pulmonary disease.  43:318-329. 2019
  • A Genome-Wide Association Study of Early Spontaneous Preterm Delivery.  39:217-226. 2015
  • Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.  38:447-456. 2014
  • Pathway analysis approaches for rare and common variants: Insights from genetic analysis workshop 18.  38. 2014
  • Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.  37:560-570. 2013
  • Pathway-Based Approaches for Sequencing-Based Genome-Wide Association Studies.  37:478-494. 2013
  • Haplotype-Based Methods for Detecting Uncommon Causal Variants With Common SNPs.  36:572-582. 2012
  • Genotype Imputation for African Americans Using Data From HapMap Phase II Versus 1000 Genomes Projects.  36:508-516. 2012
  • A data-driven method for identifying rare variants with heterogeneous trait effects.  35:679-685. 2011
  • Bayesian analysis of rare variants in genetic association studies.  35:57-69. 2011
  • Association test of multiallelic gene copy numbers in family trios.  34:2-6. 2010
  • Visualizing disease associations: Graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease.  34:92-99. 2010
  • Genome-wide admixture mapping for coronary artery calcification in African Americans: The NHLBI family heart study.  32:264-272. 2008
  • Powerful designs for genetic association studies that consider twins and sibling pairs with discordant genotypes.  31:789-796. 2007
  • Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program.  31:195-210. 2007
  • Data mining of RNA expression and DNA genotype data: Presentation Group 5 contributions to Genetic Analysis Workshop 15.  31:S43-S50. 2007
  • New joint covariance- and marginal-based tests for association and linkage for quantitative traits for random and non-random sampling.  28:48-57. 2005
  • Evidence for major genes influencing pulmonary function in the NHLBI Family Heart Study.  19:81-94. 2000
  • A multivariate model for the analysis of sibship covariance structure using marker information and multiple quantitative traits.  14:921-926. 1997
  • Lack of evidence for maternal effect in familial Alzheimer's disease.  10:461-464. 1993
  • Segregation analysis for high density lipoprotein in the berkeley data.  10:629-634. 1993
  • Autoimmune thyroid disease in type I diabetic families.  6:137-141. 1989
  • HLA may be involved in resistance and susceptibility to affective disorders.  6:293-298. 1989
  • Using survival methods to estimate age-at-onset distributions for genetic diseases with an application to Huntington disease.  6:361-371. 1989
  • A synergistic three allele model for the HLA‐linked components of coeliac disease predisposition.  3:277-282. 1986
  • Family and population analysis of multiple sclerosis.  3:381-386. 1986
  • Multilocus Linkage Analysis of the German Asthma Data.  21:S210-S215.

    • International Standard Serial Number (issn)

  • 0741-0395

    • Electronic International Standard Serial Number (eissn)

  • 1098-2272