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

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

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

From exomes to genomes: challenges and solutions in population-based genetic association studies

Por Auer, Paul L, Leal, Suzanne M
Publicado no Eur J Hum Genet (2017)

SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits

Por Li, Biao, Wang, Gao, Leal, Suzanne M.
Publicado em 2012

PhenoMan: phenotypic data exploration, selection, management and quality control for association studies of rare and common variants

Por Li, Biao, Wang, Gao, Leal, Suzanne M.
Publicado em 2014

Variant Association Tools for Quality Control and Analysis of Large-Scale Sequence and Genotyping Array Data

Por Wang, Gao T., Peng, Bo, Leal, Suzanne M.
Publicado em 2014

Genetic linkage analysis in the age of whole-genome sequencing

Por Ott, Jurg, Wang, Jing, Leal, Suzanne M.
Publicado no Nat Rev Genet (2015)

Generation of sequence-based data for pedigree-segregating Mendelian or Complex traits

Por Li, Biao, Wang, Gao T., Leal, Suzanne M.
Publicado no Bioinformatics (2015)