Genetic Association Studies of Copy-Number Variation: Should Assignment of Copy Number States Precede Testing?

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

(2011) Daniel Moreno-De-Luca et al.   AMERICAN JOURNAL OF HUMAN GENETICS

False discovery rates and copy number variation

(2011) Bradley Efron et al.   BIOMETRIKA

A fused lasso latent feature model for analyzing multi-sample aCGH data

(2011) G. Nowak et al.   BIOSTATISTICS

Bayesian Random Segmentation Models to Identify Shared Copy Number Aberrations for Array CGH Data

(2011) Veerabhadran Baladandayuthapani et al.   JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

(2011) Dalila Pinto et al.   NATURE BIOTECHNOLOGY

Copy number variation and cytidine analogue cytotoxicity: A genome-wide association approach

(2010) Krishna R Kalari et al.   BMC GENOMICS

Radiation pharmacogenomics: A genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines

(2010) N. Niu et al.   GENOME RESEARCH

Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study

(2010) Gaëlle Marenne et al.   HUMAN MUTATION

Reference-unbiased copy number variant analysis using CGH microarrays

(2010) Young Seok Ju et al.   NUCLEIC ACIDS RESEARCH

Towards a comprehensive structural variation map of an individual human genome

(2010) Andy W Pang et al.   GENOME BIOLOGY

High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

(2009) T. H. Shaikh et al.   GENOME RESEARCH

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

(2009) K. J. McKernan et al.   GENOME RESEARCH

Origins and functional impact of copy number variation in the human genome

(2009) Donald F. Conrad et al.   NATURE

Gemcitabine and Arabinosylcytosin Pharmacogenomics: Genome-Wide Association and Drug Response Biomarkers

(2009) Liang Li et al.   PLoS One

High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians

(2009) Hajime Matsuzaki et al.   GENOME BIOLOGY

The Fine-Scale and Complex Architecture of Human Copy-Number Variation

(2008) George H. Perry et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Gemcitabine and Cytosine Arabinoside Cytotoxicity: Association with Lymphoblastoid Cell Expression

(2008) L. Li et al.   CANCER RESEARCH

Kernel-Based Association Test

(2008) Hsin-Chou Yang et al.   GENETICS

Mapping and sequencing of structural variation from eight human genomes

(2008) Jeffrey M. Kidd et al.   NATURE

Accurate whole human genome sequencing using reversible terminator chemistry

(2008) David R. Bentley et al.   NATURE

A robust statistical method for case-control association testing with copy number variation

(2008) Chris Barnes et al.   NATURE GENETICS

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

(2008) Sharon J. Diskin et al.   NUCLEIC ACIDS RESEARCH

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

(2008) T. Walsh et al.   SCIENCE