Niall J. Cardin

Does Accounting for Gene-Environment Interactions Help Uncover Association between Rare Variants and Complex Diseases?

John S. Witte, Rémi Kazma, J. Witte, 2013, Human Heredity.

A second generation human haplotype map of over 3.1 million SNPs

Zhaohui S. Qin, Gudmundur A. Thorisson, L. M. Sung, 2007, Nature.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Simon C. Potter, P. Donnelly, C. Spencer, 2007, Nature.

Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls

Jake K. Byrnes, Tomas W. Fitzgerald, P. Donnelly, 2010, Nature.

Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls

Jake K. Byrnes, Tomas W. Fitzgerald, Renwick, 2010 .

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

Simon C. Potter, C. Spencer, A. Silman, 2007, Nature.

Mutational Landscape of Aggressive Prostate Tumors in African American Men.

J. Mefford, J. Witte, W. Catalona, 2016, Cancer research.

Approximating the coalescent with recombination

G. McVean, Niall J Cardin, Niall J. Cardin, 2005, Philosophical Transactions of the Royal Society B: Biological Sciences.

A Bayesian Method for Detecting and Characterizing Allelic Heterogeneity and Boosting Signals in Genome-Wide Association Studies

Peter Donnelly, Niall Cardin, Jonathan Marchini, 2009, 1010.4670.

Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV array

Peter Donnelly, Chris Holmes, Niall Cardin, 2011, Genetic epidemiology.