Combined genotype and haplotype tests for region-based association studies

Robust and Powerful Tests for Rare Variants Using Fisher's Method to Combine Evidence of Association From Two or More Complementary Tests

(2012) Andriy Derkach et al.   GENETIC EPIDEMIOLOGY

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

(2012) J-C Lambert et al.   MOLECULAR PSYCHIATRY

Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

(2011) Michael C. Wu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Rare variants in the CYP27B1 gene are associated with multiple sclerosis

(2011) Sreeram V. Ramagopalan et al.   ANNALS OF NEUROLOGY

Rare Nonsynonymous Variants in Alpha-4 Nicotinic Acetylcholine Receptor Gene Protect Against Nicotine Dependence

(2011) Pingxing Xie et al.   BIOLOGICAL PSYCHIATRY

Pathway-based analysis using reduced gene subsets in genome-wide association studies

(2011) Jingyuan Zhao et al.   BMC BIOINFORMATICS

Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations

(2011) Belinda K. Cornes et al.   HUMAN MOLECULAR GENETICS

Genome-wide and gene-based association implicates FRMD6 in alzheimer disease

(2011) Mun-Gwan Hong et al.   HUMAN MUTATION

A New Testing Strategy to Identify Rare Variants with Either Risk or Protective Effect on Disease

(2011) Iuliana Ionita-Laza et al.   PLoS Genetics

Testing for an Unusual Distribution of Rare Variants

(2011) Benjamin M. Neale et al.   PLoS Genetics

To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests

(2010) Yun Li et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

(2010) Alkes L. Price et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Powerful SNP-Set Analysis for Case-Control Genome-wide Association Studies

(2010) Michael C. Wu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome-wide association studies using haplotype clustering with a new haplotype similarity

(2010) Lina Jin et al.   GENETIC EPIDEMIOLOGY

Assembly of large genomes using second-generation sequencing

(2010) M. C. Schatz et al.   GENOME RESEARCH

Collagen-related genes influence the glaucoma risk factor, central corneal thickness

(2010) Eranga N. Vithana et al.   HUMAN MOLECULAR GENETICS

Phenotype-Haplotype Correlation of IRF5 in Systemic Sclerosis: Role of 2 Haplotypes in Disease Severity

(2010) P. DIEUDE et al.   JOURNAL OF RHEUMATOLOGY

An Evolutionary Framework for Association Testing in Resequencing Studies

(2010) C. Ryan King et al.   PLoS Genetics

Central Corneal Thickness and its Associations With Ocular and Systemic Factors: The Singapore Malay Eye Study

(2009) Daniel H.W. Su et al.   AMERICAN JOURNAL OF OPHTHALMOLOGY

Detecting rare variants for complex traits using family and unrelated data

(2009) Xiaofeng Zhu et al.   GENETIC EPIDEMIOLOGY

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

(2009) David-Alexandre Trégouët et al.   NATURE GENETICS

Methodology of the Singapore Indian Chinese Cohort (SICC) Eye Study: Quantifying ethnic variations in the epidemiology of eye diseases in Asians

(2009) Raghavan Lavanya et al.   OPHTHALMIC EPIDEMIOLOGY

Genome-Wide and Candidate Gene Association Study of Cigarette Smoking Behaviors

(2009) Neil Caporaso et al.   PLoS One

A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic

(2009) Bo Eskerod Madsen et al.   PLoS Genetics

Inferring the Joint Demographic History of Multiple Populations from Multidimensional SNP Frequency Data

(2009) Ryan N. Gutenkunst et al.   PLoS Genetics

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

(2009) Bryan N. Howie et al.   PLoS Genetics

Prevalence and Causes of Low Vision and Blindness in an Urban Malay Population

(2008) Tien Yin Wong   ARCHIVES OF OPHTHALMOLOGY

HapCUT: an efficient and accurate algorithm for the haplotype assembly problem

(2008) V. Bansal et al.   BIOINFORMATICS

Generalized linear modeling with regularization for detecting common disease rare haplotype association

(2008) Wei Guo et al.   GENETIC EPIDEMIOLOGY

An MCMC algorithm for haplotype assembly from whole-genome sequence data

(2008) V. Bansal et al.   GENOME RESEARCH

Central corneal thickness in adult Chinese. Association with ocular and general parameters. The Beijing Eye Study

(2008) Haitao Zhang et al.   GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

Assessing the Evolutionary Impact of Amino Acid Mutations in the Human Genome

(2008) Adam R. Boyko et al.   PLoS Genetics

Permutation-based adjustments for the significance of partial regression coefficients in microarray data analysis

(2007) Brandie D. Wagner et al.   GENETIC EPIDEMIOLOGY

An Entropy-Based Measure for QTL Mapping Using Extreme Samples of Population

(2007) Yu-Mei Li et al.   HUMAN HEREDITY