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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.
Identity
International Standard Serial Number (issn)
0741-0395
Electronic International Standard Serial Number (eissn)
1098-2272