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2020 – today
- 2026
[j5]John Baierl, Yi-Wen Hsiao, Michelle R. Jones, Pei-Chen Peng
, Paul D. P. Pharoah:
Measuring the accuracy of electronic health record-based phenotyping in the All of Us Research Program to optimize statistical power for genetic association testing. J. Am. Medical Informatics Assoc. 33(3): 611-620 (2026)
2010 – 2019
- 2019
- [j4]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:
Dynamics of breast-cancer relapse reveal late-recurring ER-positive genomic subgroups. Nat. 567(7748): 399-404 (2019) - 2015
- [j3]Ailith Pirie, Angela M. Wood, Michael Lush, Jonathan P. Tyrer, Paul D. P. Pharoah:
The effect of rare variants on inflation of the test statistics in case-control analyses. BMC Bioinform. 16: 53:1-53:5 (2015) - 2013
- [j2]Jonathan P. Tyrer, Qi Guo, Douglas F. Easton, Paul D. P. Pharoah:
The admixture maximum likelihood test to test for association between rare variants and disease phenotypes. BMC Bioinform. 14: 177 (2013)
2000 – 2009
- 2009
- [j1]Helen I. Field, Serena A. Scollen, Craig Luccarini, Caroline Baynes, Jonathan Morrison, Alison M. Dunning, Douglas F. Easton, Paul D. P. Pharoah:
Seq4SNPs: new software for retrieval of multiple, accurately annotated DNA sequences, ready formatted for SNP assay design. BMC Bioinform. 10 (2009)
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