Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs

Whole-genome sequence variation, population structure and demographic history of the Dutch population

(2014) Laurent C Francioli et al.   NATURE GENETICS

Rare Nonsynonymous Exonic Variants in Addiction and Behavioral Disinhibition

(2013) Scott I. Vrieze et al.   BIOLOGICAL PSYCHIATRY

Genetic Variants Regulating Immune Cell Levels in Health and Disease

(2013) Valeria Orrù et al.   CELL

The Impact of Improved Microarray Coverage and Larger Sample Sizes on Future Genome-Wide Association Studies

(2013) Karla J. Lindquist et al.   GENETIC EPIDEMIOLOGY

Imputation-Based Genomic Coverage Assessments of Current Human Genotyping Arrays

(2013) Sarah C. Nelson et al.   G3-Genes Genomes Genetics

zCall: a rare variant caller for array-based genotyping

(2012) Jacqueline I. Goldstein et al.   BIOINFORMATICS

Improved whole-chromosome phasing for disease and population genetic studies

(2012) Olivier Delaneau et al.   NATURE METHODS

The Minnesota Center for Twin and Family Research Genome-Wide Association Study

(2012) Michael B. Miller et al.   Twin Research and Human Genetics

A Genome-Wide Association Scan on the Levels of Markers of Inflammation in Sardinians Reveals Associations That Underpin Its Complex Regulation

(2012) Silvia Naitza et al.   PLoS Genetics

The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits

(2012) Benjamin F. Voight et al.   PLoS Genetics

HAPGEN2: simulation of multiple disease SNPs

(2011) Zhan Su et al.   BIOINFORMATICS

The variant call format and VCFtools

(2011) P. Danecek et al.   BIOINFORMATICS

Low-coverage sequencing: Implications for design of complex trait association studies

(2011) Y. Li et al.   GENOME RESEARCH

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

(2011) Hilma Holm et al.   NATURE GENETICS

Promise and pitfalls of the Immunochip

(2011) Adrian Cortes et al.   ARTHRITIS RESEARCH & THERAPY

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

(2010) Yun Li et al.   GENETIC EPIDEMIOLOGY

Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis

(2010) Serena Sanna et al.   NATURE GENETICS

Genotype imputation for genome-wide association studies

(2010) Jonathan Marchini et al.   NATURE REVIEWS GENETICS

Genetic loci linked to Type 1 Diabetes and Multiple Sclerosis families in Sardinia

(2008) Maristella Pitzalis et al.   BMC Medical Genetics