Publications

If you are a collaborator and your publications are not listed please let us know.

Click on publication citation to see the abstract and PubMed link.

Using tumour pathology to identify people at high genetic risk of breast and colorectal cancers

Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome

Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22

Performance of PREMM(1,2,6), MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

Phenotype and polyp landscape in serrated polyposis syndrome: a series of 100 patients from genetics clinics

Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry

Quality assessment and correlation of microsatellite instability and immunohistochemical markers among population- and clinic-based colorectal tumors results from the Colon Cancer Family Registry

Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes

Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery

Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers

Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis

Estimates of familial risks from family data are biased when ascertainment of families is not independent of family history

The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history

Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes

Genotype-environment interactions in microsatellite stable/microsatellite instability-low colorectal cancer: results from a genome-wide association study

Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases

Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer

Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer

Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes

Determining the frequency of de novo germline mutations in DNA mismatch repair genes

Mutation deep within an intron of MSH2 causes Lynch syndrome

Investigating the potential role of genetic and epigenetic variation of DNA methyltransferase genes in hyperplastic polyposis syndrome

Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study

Cigarette smoking, genetic variants in carcinogen-metabolizing enzymes, and colorectal cancer risk

Total 144 articles in this section.
Pages Previous 1 . [2] . 3 . 4 . 5 . 6 Next