Exome-wide rare loss-of-function variant enrichment study in 21,347 Han Chinese individuals identifies four new susceptibility genes for psoriasis [healthy controls]

Exome-wide rare loss-of-function variant enrichment study in 21,347 Han Chinese individuals identifies four new susceptibility genes for psoriasis [psoriasis patients]

An Exome-Wide Association Study Identifies New Susceptibility Loci for the Risk of Nicotine Dependence in African-American Populations

use of aCGH in a large series of prenatal samples

Hox-C9 activates the intrinsic pathway of apoptosis and is associated with spontaneous regression in neuroblastoma

Genomic Subtypes of Breast Cancer Identified by Array Comparative Genomic Hybridization

Discovery of a Trans-Omics Biomarker Signature that Predisposes High Risk Diabetic Patients to Diabetic Kidney Disease

MMRC expression and aCGH reference collection

Genetic Study of anti-EGFR Antibody Therapy Response in Colorectal Carcinoma

Analysis of copy number variants on chromosome 21 in Down syndrome-associated congenital heart defects

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss

Comparative genomic hybridization of a Burkholderia cenocepacia collection

High-resolution comparative genomic hybridization of inflammatory breast cancer and identification of candidate genes

High resolution X chromosome copy number analysis in fertile and POI females

CGH array used to identify de novo copy number variations in offspring of BaP exposed parents.

Cancer Process Study

Substantial interindividual and limited intraindividual genomic diversity among tumors from men with metastatic prostate cancer

Array comparative genomic hybridization data from 313 CLL specimens to study outcome associations

Fine mapping of regulatory loci for mammalian gene expression using radiation hybrids

Detection of de novo and homozygous copy number variants in 99 autism simplex trios