Tamim H. Shaikh

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics

Xiaowu Gai, Peter S. White, Hongbo M. Xie, 2010, BMC Bioinformatics.

A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay

Deborah L. Levy, Gregory M. Cooper, Brian L. Browning, 2010, Nature Genetics.

Copy number variation at 1q21.1 associated with neuroblastoma

Sharon J. Diskin, John M. Maris, Struan F. A. Grant, 2009, Nature.

Segmental duplications: an 'expanding' role in genomic instability and disease

Tamim H. Shaikh, T. Shaikh, B. Emanuel, 2001, Nature Reviews Genetics.