Seq4SNPs: new software for retrieval of multiple, accurately annotated DNA sequences, ready formatted for SNP assay design. - Helen I. Field; Serena A. Scollen; Craig Luccarini; Caroline Baynes; Jonathan Morrison; Alison M. Dunning; Douglas F. Easton; Paul D. P. Pharoah (BMC Bioinform., 2009)

The admixture maximum likelihood test to test for association between rare variants and disease phenotypes. - Jonathan P. Tyrer; Qi Guo; Douglas F. Easton; Paul D. P. Pharoah (BMC Bioinform., 2013)

The effect of rare variants on inflation of the test statistics in case-control analyses. - Ailith Pirie; Angela M. Wood; Michael Lush; Jonathan P. Tyrer; Paul D. P. Pharoah (BMC Bioinform., 2015)

Dynamics of breast-cancer relapse reveal late-recurring ER-positive genomic subgroups. - Oscar M. Rueda; Stephen John Sammut; José A. Seoane; Suet-Feung Chin; Jennifer L. Caswell-Jin; Maurizio Callari; Rajbir Nath Batra; Bernard Pereira; Alejandra Bruna; H. Raza Ali; Elena Provenzano; Bin Liu; et al. (Nat., 2019)