Prof Paul James
Honorary Professorial Fellow
Department of Medicine
454 Scholarly works
46 Projects
HIGHLIGHTS
2026
Journal article
Preparing healthcare providers to use polygenic risk scores: a qualitative study of learning needs and educational preferences.
DOI: 10.1136/bmjopen-2025-1118982026
Journal article
Breast cancer specialists' experiences and attitudes towards mainstream genetic testing for patients with breast cancer.
DOI: 10.1186/s13053-026-00340-32026
Journal article
Empirical evaluation of analytic validity of polygenic scores.
DOI: 10.1186/s13073-026-01654-62026
Journal article
Investigating the contribution of rare non-coding variants in BRCA1, BRCA2 and PALB2 to hereditary breast cancer.
DOI: 10.1038/s41523-026-00942-z2023
Research grants (ARC, NHMRC, MRFF)
Using Real World Data to Drive Cancer Care Research and Delivery
2023
Research grants (ARC, NHMRC, MRFF)
Trial Integration of Polygenic Scores for Common Cancers Into Standard Clinical Care
2021
Research grants (ARC, NHMRC, MRFF)
Diagnosis, Discovery and Novel Phenotype Characterisation Using Multimodal Genomics in Patients With Inherited Bone Marrow Failure and Related Disorders
RECENT SCHOLARLY WORKS
2026
Journal article
Abstract 4966: A single-cell spatial proteomic analysis of the TNBC microenvironment defines genotype-specific features
DOI: 10.1158/1538-7445.am2026-49662026
Journal article
Integrating breast tumour homologous recombination deficiency status to aid germline BRCA1 and BRCA2 variant classification
DOI: 10.1016/j.ebiom.2026.1061992026
Journal article
Consideration of inherited cancer risk on a continuum: An international and multidisciplinary perspective: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)
DOI: 10.1016/j.gim.2025.1016592026
Journal article
Large-scale meta-analysis and precision functional assays identify FANCM regions in which PTVs confer different risks for ER-negative and triple-negative breast cancer
DOI: 10.1016/j.breast.2025.1046192026
Journal article
Urgent need to recognize that Disease-Causing TP53 variants with atypical penetrance require distinct clinical recommendations.
DOI: 10.1093/jnci/djag0152026
Journal article
Feasibility and outcomes of the DNA Screen nationwide adult genomic screening pilot
DOI: 10.1038/s44360-025-00020-x
RECENT PROJECTS
2025
Research grants (ARC, NHMRC, MRFF)
Trial Implementation of Pharmacogenomics to Improve Complex Hospital Care
2024
Research grants (ARC, NHMRC, MRFF)
Salpingectomy With Delayed Oophorectomy to Prevent Ovarian Cancer (TUBA WISP II)