Adjusting Family Relatedness in Data-driven Burden Test of Rare Variants

Health and function of participants in the Long Life Family Study: A comparison with other cohorts

(2016) Anne B. Newman et al.   Aging-US

Family-based association tests for sequence data, and comparisons with population-based association tests

(2013) Iuliana Ionita-Laza et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A Unified Mixed-Effects Model for Rare-Variant Association in Sequencing Studies

(2013) Jianping Sun et al.   GENETIC EPIDEMIOLOGY

Adjusted Sequence Kernel Association Test for Rare Variants Controlling for Cryptic and Family Relatedness

(2013) Karim Oualkacha et al.   GENETIC EPIDEMIOLOGY

Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c) levels in non-diabetic subjects: The Long Life Family Study (LLFS)

(2013) Ping An et al.   METABOLISM-CLINICAL AND EXPERIMENTAL

Rare Variant Analysis for Family-Based Design

(2013) Gourab De et al.   PLoS One

Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies

(2012) Seunggeun Lee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Two Adaptive Weighting Methods to Test for Rare Variant Associations in Family-Based Designs

(2012) Shurong Fang et al.   GENETIC EPIDEMIOLOGY

Sequence Kernel Association Test for Quantitative Traits in Family Samples

(2012) Han Chen et al.   GENETIC EPIDEMIOLOGY

Detecting Rare Variants for Quantitative Traits Using Nuclear Families

(2012) Wei Guo et al.   HUMAN HEREDITY

A General Framework for Detecting Disease Associations with Rare Variants in Sequencing Studies

(2011) Dan-Yu Lin et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

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

Assessing the Contribution Family Data Can Make to Case-Control Studies of Rare Variants

(2011) David Curtis   ANNALS OF HUMAN GENETICS

Population-based and family-based designs to analyze rare variants in complex diseases

(2011) Rémi Kazma et al.   GENETIC EPIDEMIOLOGY

Adaptive tests for association analysis of rare variants

(2011) Wei Pan et al.   GENETIC EPIDEMIOLOGY

A data-driven method for identifying rare variants with heterogeneous trait effects

(2011) Qunyuan Zhang et al.   GENETIC EPIDEMIOLOGY

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

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

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

A Data-Adaptive Sum Test for Disease Association with Multiple Common or Rare Variants

(2010) Fang Han et al.   HUMAN HEREDITY

Variance component model to account for sample structure in genome-wide association studies

(2010) Hyun Min Kang et al.   NATURE GENETICS

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

(2010) Dajiang J. Liu et al.   PLoS Genetics

A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression

(2009) Helen M. Knight et al.   AMERICAN JOURNAL OF HUMAN GENETICS

GWAF: an R package for genome-wide association analyses with family data

(2009) Ming-Huei Chen et al.   BIOINFORMATICS

Detecting rare variants for complex traits using family and unrelated data

(2009) Xiaofeng Zhu et al.   GENETIC EPIDEMIOLOGY

An evaluation of statistical approaches to rare variant analysis in genetic association studies

(2009) Andrew P. Morris et al.   GENETIC EPIDEMIOLOGY

Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis

(2009) M. Sabatelli et al.   HUMAN MOLECULAR GENETICS

Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility

(2009) Gabe Haller et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Multiple Rare Variants as a Cause of a Common Phenotype: Several Different Lactase Persistence Associated Alleles in a Single Ethnic Group

(2009) Catherine J. E. Ingram et al.   JOURNAL OF MOLECULAR EVOLUTION

Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes

(2009) S. Nejentsev et al.   SCIENCE

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

(2009) Bo Eskerod Madsen et al.   PLoS Genetics

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

(2008) Bingshan Li et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Efficient Control of Population Structure in Model Organism Association Mapping

(2008) H. M. Kang et al.   GENETICS

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

(2008) Weizhen Ji et al.   NATURE GENETICS