Genetics and Analysis of Quantitative Traits,

Por Leal, Suzanne M.
Publicado em 2001

A Tribute to Marcy Carlson Speer, 1959–2007

Por Leal, Suzanne M
Publicado em 2007

Genetic Maps of Microsatellite and Single-Nucleotide Polymorphism Markers: Are the Distances Accurate?

Por Leal, Suzanne M.
Publicado no Genet Epidemiol (2003)

Detection of Genotyping Errors and Pseudo-SNPs Via Deviations From Hardy-Weinberg Equilibrium

Por Leal, Suzanne M.
Publicado no Genet Epidemiol (2005)

Effects of Stratification in the Analysis of Affected-Sib-Pair Data: Benefits and Costs

Por Leal, Suzanne M., Ott, Jurg
Publicado em 2000

Discovery of Rare Variants via Sequencing: Implications for the Design of Complex Trait Association Studies

Por Li, Bingshan, Leal, Suzanne M.
Publicado em 2009

Deviations from Hardy-Weinberg Equilibrium in Parental and Unaffected Sibling Genotype Data

Por Li, Bingshan, Leal, Suzanne M.
Publicado em 2009

Ignoring Intermarker Linkage Disequilibrium Induces False-Positive Evidence of Linkage for Consanguineous Pedigrees when Genotype Data Is Missing for Any Pedigree Member

Por Li, Bingshan, Leal, Suzanne M.
Publicado em 2008

Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data

Por Li, Bingshan, Leal, Suzanne M.
Publicado em 2008

Variability of Genotype-specific Penetrance Probabilities in the Calculation of Risk Support Intervals

Por Leal, Suzanne M., Ott, Jurg
Publicado no Genet Epidemiol (1995)

A Bootstrap Approach to Estimating Power for Linkage Heterogeneity

Por Leal, Suzanne M., Ott, Jurg
Publicado no Genet Epidemiol (1993)

Analysis of Two-locus Traits Under Heterogeneity for Recessive Versus Dominant Inheritance

Por Leal, Suzanne M., Ott, Jurg
Publicado no Genet Epidemiol (1997)

Novel Selection Criteria for Genome Scans of Complex Traits

Por Wille, Anja, Leal, Suzanne M.
Publicado no Genet Epidemiol (2001)

A Novel Adaptive Method for the Analysis of Next-Generation Sequencing Data to Detect Complex Trait Associations with Rare Variants Due to Gene Main Effects and Interactions

Por Liu, Dajiang J., Leal, Suzanne M.
Publicado em 2010

Replication Strategies for Rare Variant Complex Trait Association Studies via Next-Generation Sequencing

Por Liu, Dajiang J., Leal, Suzanne M.
Publicado em 2010

A flexible likelihood framework for detecting associations with secondary phenotypes in genetic studies using selected samples: application to sequence data

Por Liu, Dajiang J, Leal, Suzanne M
Publicado em 2012

A Unified Framework for Detecting Rare Variant Quantitative Trait Associations in Pedigree and Unrelated Individuals via Sequence Data

Por Liu, Dajiang J., Leal, Suzanne M.
Publicado em 2012

Estimating Genetic Effects and Quantifying Missing Heritability Explained by Identified Rare-Variant Associations

Por Liu, Dajiang J., Leal, Suzanne M.
Publicado em 2012

SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations

Por Liu, Dajiang J., Leal, Suzanne M.
Publicado em 2012

A Unified Method for Detecting Secondary Trait Associations with Rare Variants: Application to Sequence Data

Por Liu, Dajiang J., Leal, Suzanne M.
Publicado em 2012