Paul D. P. Pharoah

According to our database, Paul D. P. Pharoah authored at least 5 papers between 2009 and 2026.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2026

Measuring the accuracy of electronic health record-based phenotyping in the <i>All of Us</i> Research Program to optimize statistical power for genetic association testing.

John Baierl, Yi-Wen Hsiao, Michelle R. Jones, Pei-Chen Peng, Paul D. P. Pharoah

J. Am. Medical Informatics Assoc., 2026

2019

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, Michelle Parisien, Cheryl Gillett, Steven McKinney, Andrew R. Green, Leigh Murphy, Arnie Purushotham, Ian O. Ellis, Paul D. P. Pharoah, Cristina Rueda, Samuel Aparicio, Carlos Caldas, Christina Curtis

Nat., 2019

2015

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

2013

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

2009

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