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Familial Cancer|August 14, 2014
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registryChristophe Rosty, Michael D Walsh, Noralane M Lindor, et al.
Annals of Surgical Oncology|January 30, 2013
Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriersAung Ko Win, Susan Parry, Bryan Parry, et al.
The Journal of Investigative Dermatology|June 12, 2018
Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based StudiesAnne E Cust, Martin Drummond, Peter A Kanetsky, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 5, 2009
The association of tumor microsatellite instability phenotype with family history of colorectal cancerBharati Bapat, Noralane M Lindor, John Baron, et al.
Familial Cancer|February 26, 2009
Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysisMichael D Walsh, Daniel D Buchanan, Rhiannon Walters, et al.
The Lancet. Digital Health|March 4, 2026
AI-based BRAIx risk score for the intermediate-term prediction of breast cancer: a population cohort studyHelen M L Frazer, John L Hopper, Tuong L Nguyen, et al.
The American Journal of Surgical Pathology|January 2, 2007
BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarraysAnita L Bane, Jeanne C Beck, Ira Bleiweiss, et al.
The American Journal of Surgical Pathology|December 6, 2012
Multiplicity and molecular heterogeneity of colorectal carcinomas in individuals with serrated polyposisChristophe Rosty, Michael D Walsh, Rhiannon J Walters, et al.
Carcinogenesis|July 16, 2014
A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association studyStephanie L Schmit, Fredrick R Schumacher, Christopher K Edlund, et al.
Pathology|December 27, 2011
Using tumour pathology to identify people at high genetic risk of breast and colorectal cancersJ L Hopper, M A Jenkins, J G Dowty, et al.
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