M. Clendenning

发表

Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing

D. Schaid, D. Serie, Y. Asmann, 2013, Cancer Epidemiology, Biomarkers & Prevention.

Mutation deep within an intron of MSH2 causes Lynch syndrome

J. Hopper, A. Spurdle, M. Jenkins, 2011, Familial Cancer.

Identification of nine new susceptibility loci for endometrial cancer

Peter Kraft, Mark McEvoy, Julian Peto, 2018, Nature Communications.

A Genomic Test for Colorectal Cancer Risk: Is This Acceptable and Feasible in Primary Care?

J. Emery, J. Dowty, M. Jenkins, 2020, Public Health Genomics.

Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.

Alexander M. Metcalf, A. Spurdle, F. Lose, 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome

Aung Ko Win, J. Potter, G. Giles, 2019, British Journal of Cancer.

Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas

Aung Ko Win, D. English, G. Giles, 2017, Familial Cancer.

Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome)

Aung Ko Win, A. Spurdle, C. Rosty, 2014, The application of clinical genetics.

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

Aung Ko Win, J. Hopper, S. Thibodeau, 2012, Modern Pathology.

Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history

Aung Ko Win, J. Emery, J. Potter, 2018, bioRxiv.

PIK3CA Activating Mutation in Colorectal Carcinoma: Associations with Molecular Features and Survival

Aung Ko Win, D. English, G. Giles, 2013, PloS one.

Prediction of overall survival in stage II and III colon cancer beyond TNM system: a retrospective, pooled biomarker study

D. Sargent, M. Delorenzi, R. Lothe, 2017, Annals of oncology : official journal of the European Society for Medical Oncology.

Germline MBD4 deficiency causes a multi-tumor predisposition syndrome

M. Christie, D. Wedge, N. López-Bigas, 2022, American journal of human genetics.

PMS2 monoallelic mutation carriers: the known unknown

Aung Ko Win, C. Boland, S. Thibodeau, 2015, Genetics in Medicine.

Evaluating multiple next-generation sequencing derived tumor features to accurately predict DNA mismatch repair status

Aung Ko Win, P. Gibbs, O. Sieber, 2022, medRxiv.

Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis

M. Woods, J. Hopper, M. Jenkins, 2009, Familial Cancer.

Colonic Transit Time and IBS Symptoms: What's the Link?

Aung Ko Win, M. Woods, J. Hopper, 2012, The American Journal of Gastroenterology.

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

M. Woods, J. Hopper, A. de la Chapelle, 2010, International Journal of Colorectal Disease.

Recurrent and founder mutations in the PMS2 gene

J. Hopper, S. Liyanarachchi, M. Jenkins, 2013, Clinical genetics.

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.

W. Foulkes, G. Capellá, I. Tomlinson, 2019, Cancer cell.

Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures

J. Manson, Peter T Campbell, T. Hudson, 2022, Nature Communications.

Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort

S. Gruber, N. Lindor, C. Rosty, 2017, Oncotarget.

Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for lynch syndrome

S. Thibodeau, P. Goodfellow, A. de la Chapelle, 2009, Familial Cancer.

Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndrome

Aung Ko Win, G. Giles, J. Hopper, 2015, Genes & cancer.

RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers

B. Leggett, V. Whitehall, C. Rosty, 2017, Familial Cancer.

Long‐range PCR facilitates the identification of PMS2‐specific mutations

A. de la Chapelle, A. Lindblom, Janet C Lockman, 2006, Human mutation.

Lack of evidence for germline RNF43 mutations in patients with serrated polyposis syndrome from a large multinational study

S. Gallinger, M. Jenkins, C. Rosty, 2016, Gut.

Café‐au‐lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2

A. Pollett, S. Gallinger, K. Boycott, 2008, Pediatric blood & cancer.

Multifocal anaplastic astrocytoma in a patient with hereditary colorectal cancer, transcobalamin II deficiency, agenesis of the corpus callosum, mental retardation, and inherited PMS2 mutation.

W. Frankel, J. Eastwood, H. Friedman, 2008, Neuro-oncology.

High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry

Aung Ko Win, J. Hopper, S. Thibodeau, 2014, Familial Cancer.

Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer.

Aung Ko Win, G. Giles, J. Hopper, 2013, Cancer epidemiology.

Germline HOXB 13 p . Gly 84 Glu Mutation and Risk of Colorectal Cancer

Aung Ko Win, G. Giles, J. Hopper, 2013 .

Phenotype and Polyp Landscape in Serrated Polyposis Syndrome: A Series of 100 Patients From Genetics Clinics

Aung Ko Win, J. Hopper, W. Frankel, 2012, The American journal of surgical pathology.

A Multifactorial Likelihood Model for MMR Gene Variant Classification Incorporating Probabilities Based on Sequence Bioinformatics and Tumor Characteristics: A Report from the Colon Cancer Family Registry

Steven Gallinger, John L Hopper, Sean V Tavtigian, 2013, Human mutation.

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

Aung Ko Win, M. Woods, J. Hopper, 2010, International Journal of Colorectal Disease.

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.

W. Frankel, A. de la Chapelle, H. Nakagawa, 2006, Cancer research.

Reply to J. Moline et al.

Alexander M. Metcalf, A. Spurdle, F. Lose, 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Body Mass Index, sex, non-steroidal anti-inflammatory drug medications, smoking and alcohol are differentially associated with World Health Organisation criteria and colorectal cancer risk in people with Serrated Polyposis Syndrome: an Australian case-control study

Aung Ko Win, J. Hopper, M. Jenkins, 2022, BMC Gastroenterology.

Hepatic adenomas caused by somatic HNF1A mutations in children with biallelic mismatch repair gene mutations.

A. Pollett, S. Gallinger, K. Boycott, 2011, Gastroenterology.

Expression of MUC2, MUC5AC, MUC5B, and MUC6 mucins in colorectal cancers and their association with the CpG island methylator phenotype

Aung Ko Win, D. English, G. Giles, 2013, Modern Pathology.

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

Rodney J Scott, John-Paul Plazzer, Finlay Macrae, 2013, Nature Genetics.

Risk of colorectal cancer for carriers of a germline mutation in POLE or POLD1

Aung Ko Win, J. Hopper, M. Southey, 2017, Genetics in Medicine.

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

Aung Ko Win, J. Potter, G. Giles, 2016, Cancer Epidemiology, Biomarkers & Prevention.

Genomic Characterization of Upper-Tract Urothelial Carcinoma in Patients With Lynch Syndrome

B. Taylor, J. Hopper, J. Coleman, 2018, JCO precision oncology.

Rare germline variants in the AXIN2 gene in families with colonic polyposis and colorectal cancer

M. Jenkins, C. Rosty, D. Buchanan, 2021, Familial Cancer.

Alcohol Consumption and the Risk of Colorectal Cancer for Mismatch Repair Gene Mutation Carriers

Aung Ko Win, J. Potter, G. Giles, 2016, Cancer Epidemiology, Biomarkers & Prevention.

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.

J. Potter, J. Hopper, S. Thibodeau, 2008, Gastroenterology.

Cancer Risks for PMS2-Associated Lynch Syndrome.

Aung Ko Win, M. von Knebel Doeberitz, P. Møller, 2018, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Risk of colorectal cancer for carriers of a germline mutation in POLE or POLD1

Aung Ko Win, J. Hopper, M. Southey, 2017, Genetics in Medicine.

Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.

Aung Ko Win, G. Giles, J. Hopper, 2014, Gastroenterology.

Germline and Tumor Sequencing as a Diagnostic Tool to Resolve Suspected Lynch Syndrome.

Aung Ko Win, J. Hopper, A. Spurdle, 2020, The Journal of molecular diagnostics : JMD.

Germline and Tumor Whole Genome Sequencing as a Diagnostic Tool to Resolve Suspected Lynch Syndrome

Aung Ko Win, J. Hopper, A. Spurdle, 2020 .

Colorectal carcinomas with KRAS mutation are associated with distinctive morphological and molecular features

Aung Ko Win, D. English, G. Giles, 2013, Modern Pathology.

Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study.

Aung Ko Win, G. Giles, J. Hopper, 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry

J. Potter, J. Hopper, S. Thibodeau, 2010, Clinical Cancer Research.

SNP rs16906252C>T Is an Expression and Methylation Quantitative Trait Locus Associated with an Increased Risk of Developing MGMT-Methylated Colorectal Cancer

Aung Ko Win, J. Hopper, M. Southey, 2016, Clinical Cancer Research.

Association of the Colorectal CpG Island Methylator Phenotype with Molecular Features, Risk Factors, and Family History

Peter W. Laird, Kimberly D. Siegmund, Loic Le Marchand, 2015, Cancer Epidemiology, Biomarkers & Prevention.

Family History of Colorectal Cancer in BRAF p.V600E-Mutated Colorectal Cancer Cases

Aung Ko Win, J. Potter, G. Giles, 2013, Cancer Epidemiology, Biomarkers & Prevention.

Germline miRNA DNA variants and the risk of colorectal cancer by subtype

Aung Ko Win, J. Potter, E. Goode, 2016, Genes, chromosomes & cancer.

Prediction of overall survival in stage II and III colon cancer beyond TNM system: a retrospective, pooled biomarker study

D. Sargent, M. Delorenzi, R. Lothe, 2017, Annals of oncology : official journal of the European Society for Medical Oncology.

Should the grading of colorectal adenocarcinoma include microsatellite instability status?

Aung Ko Win, D. English, G. Giles, 2014, Human pathology.

Informed choice and attitudes regarding a genomic test to predict risk of colorectal cancer in general practice.

J. Emery, M. Jenkins, D. Buchanan, 2021, Patient education and counseling.

Origins and prevalence of the American Founder Mutation of MSH2.

Shuying Sun, S. Thibodeau, S. Liyanarachchi, 2008, Cancer research.

Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)

J. Potter, D. Duggan, J. Hopper, 2010, Familial Cancer.

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome

A. de la Chapelle, A. Lindblom, D. Buchanan, 2008, Journal of Medical Genetics.

Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.

K. Kinzler, B. Vogelstein, N. Papadopoulos, 2007, Journal of the National Cancer Institute.

Association between hypermethylation of DNA repetitive elements in white blood cell DNA and early-onset colorectal cancer

Aung Ko Win, D. English, G. Giles, 2013, Epigenetics.

Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients.

W. Frankel, A. de la Chapelle, H. Nakagawa, 2007, Cancer research.

DNA Methylation Signatures and the Contribution of Age-Associated Methylomic Drift to Carcinogenesis in Early-Onset Colorectal Cancer

Aung Ko Win, D. English, G. Giles, 2021, medRxiv.

Substantial unexplained variation in cancer risks for MLH1 and MSH2 mutation carriers

Aung Ko Win, G. Giles, J. Hopper, 2012, Human mutation.

Feasibility of screening for Lynch syndrome among patients with colorectal cancer.

Heather Hampel, Wendy L Frankel, W. Frankel, 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

BRAFV600E Immunohistochemistry Facilitates Universal Screening of Colorectal Cancers for Lynch Syndrome

Aung Ko Win, J. Hopper, A. von Deimling, 2013, The American journal of surgical pathology.

Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study.

Katherine M. Tucker, Aung Ko Win, Swati G. Patel, 2021, The Lancet. Oncology.

Female Hormonal Factors and the Risk of Endometrial Cancer in Lynch Syndrome.

Aung Ko Win, J. Potter, J. Hopper, 2015, JAMA.

Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts

Aung Ko Win, D. English, G. Giles, 2017, Journal of gastroenterology and hepatology.

A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome

Aung Ko Win, M. Clendenning, M. Wilding, 2023, Journal of Translational Medicine.

Assessment of a Polygenic Risk Score for Colorectal Cancer to Predict Risk of Lynch Syndrome Colorectal Cancer

Aung Ko Win, R. Hayes, J. Hopper, 2021, JNCI cancer spectrum.

Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survival

Peter T Campbell, J. Chang-Claude, M. Hoffmeister, 2023, medRxiv.

Evaluating the utility of tumour mutational signatures for identifying hereditary colorectal cancer and polyposis syndrome carriers

Aung Ko Win, J. Hopper, M. Jenkins, 2019, Gut.

Associations of alcohol intake, smoking, physical activity and obesity with survival following colorectal cancer diagnosis by stage, anatomic site and tumor molecular subtype

D. English, G. Giles, J. Hopper, 2018, International journal of cancer.

Multivitamin, calcium and folic acid supplements and the risk of colorectal cancer in Lynch syndrome.

Aung Ko Win, J. Potter, G. Giles, 2016, International journal of epidemiology.

Quantifying the utility of single nucleotide polymorphisms to guide colorectal cancer screening.

Aung Ko Win, J. Hopper, J. Dowty, 2016, Future oncology.

Colorectal Cancer ) among Endometrial Cancer Patients Screening for Lynch Syndrome ( Hereditary Nonpolyposis

W. Frankel, H. Nakagawa, Janet C Lockman, 2006 .

Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome.

Aung Ko Win, L. Lipton, G. Giles, 2012, Journal of the National Cancer Institute.

Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome.

Aung Ko Win, J. Potter, G. Giles, 2015, Journal of the National Cancer Institute.

Estimation of probabilities in favour of pathogenicity for missense substitutions for use in clinical evaluation of mismatch repair gene variants

Brian Thompson, C. Paterson, M. Clendenning, 2012, Hereditary Cancer in Clinical Practice.

Estimation of probabilities in favour of pathogenicity for missense substitutions for use in clinical evaluation of mismatch repair gene variants

A. Spurdle, C. Paterson, B. Thompson, 2012, Hereditary Cancer in Clinical Practice.

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease

A. de la Chapelle, A. Pollett, P. Parfrey, 2010, Gut.

Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins

J. Hopper, M. Cummings, M. Jenkins, 2013, Modern Pathology.

Risk Factors for Colorectal Cancer in Patients with Multiple Serrated Polyps: A Cross-Sectional Case Series from Genetics Clinics

Aung Ko Win, D. English, J. Potter, 2010, PloS one.

Do serrated neoplasms of the small intestine represent a distinct entity? Pathological findings and molecular alterations in a series of 13 cases

C. Rosty, D. Buchanan, M. Clendenning, 2015, Histopathology.

Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives

Aung Ko Win, J. Potter, G. Giles, 2014, Gut.

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

Aung Ko Win, G. Giles, J. Hopper, 2011, Journal of Medical Genetics.

Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort

Aung Ko Win, J. Potter, J. Hopper, 2016, BMJ Open.

Multiplicity and Molecular Heterogeneity of Colorectal Carcinomas in Individuals With Serrated Polyposis

Aung Ko Win, J. Hopper, W. Frankel, 2013, The American journal of surgical pathology.

Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH

Aung Ko Win, J. Hopper, S. Thibodeau, 2016, International journal of cancer.

Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome

Aung Ko Win, J. Hopper, S. Gallinger, 2013, PloS one.

New Haplotype and Genealogical Data Give Important Implications for the Origins and Prevalence of the American Founder Mutation of MSH 2

M. Clendenning, K. Walsh, H. Hampel, 2007 .

Methylation of Breast Cancer Predisposition Genes in Early-Onset Breast Cancer: Australian Breast Cancer Family Registry

G. Giles, J. Hopper, M. Southey, 2016, PloS one.

Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 (vol 20, pg 890, 2018)

Aung Ko Win, J. Hopper, M. Southey, 2018 .

Reducing the polyp burden in serrated polyposis by serial colonoscopy: the impact of nationally coordinated community surveillance.

Aung Ko Win, Joanne P Young, C. Rosty, 2017, The New Zealand medical journal.

Lifetime alcohol intake is associated with an increased risk of KRAS+ and BRAF‐/KRAS‐ but not BRAF+ colorectal cancer

D. English, G. Giles, J. Hopper, 2016, International journal of cancer.

Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene

Katherine M. Tucker, Aung Ko Win, J. Hopper, 2015, Familial Cancer.

Identifying primary and secondary MLH1 epimutation carriers displaying low-level constitutional MLH1 methylation using droplet digital PCR and genome-wide DNA methylation profiling of colorectal cancers

M. Jenkins, J. Kirk, A. Dobrovic, 2023, Clinical Epigenetics.

Assessing the ProMCol classifier as a prognostic marker for non-metastatic colorectal cancer within the Melbourne Collaborative Cohort Study

D. English, G. Giles, J. Hopper, 2018, Gut.

Mismatch repair gene pathogenic germline variants in a population-based cohort of breast cancer

Daniel J. Park, G. Giles, J. Hopper, 2020, Familial Cancer.

Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes

Aung Ko Win, Y. Asmann, E. Goode, 2017, Molecular genetics & genomic medicine.

Germline loss-of-function variants in the base-excision repair gene MBD4 cause a Mendelian recessive syndrome of adenomatous colorectal polyposis and acute myeloid leukaemia

M. Christie, D. Wedge, N. López-Bigas, 2021, bioRxiv.

Tumor mutational signatures in sebaceous skin lesions from individuals with Lynch syndrome

M. Jenkins, D. Buchanan, M. Clendenning, 2019, Molecular genetics & genomic medicine.

High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry

Aung Ko Win, J. Hopper, S. Thibodeau, 2014, Familial Cancer.

Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?

J. Potter, J. Hopper, S. Thibodeau, 2013, Familial Cancer.

Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?

J. Potter, J. Hopper, S. Thibodeau, 2013, Familial Cancer.

Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas

Aung Ko Win, D. English, G. Giles, 2017, Familial Cancer.

Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene

Aung Ko Win, J. Hopper, S. Thibodeau, 2015, Familial Cancer.

Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history

Aung Ko Win, J. Emery, J. Potter, 2018, bioRxiv.

Identification of nine new susceptibility loci for endometrial cancer

M. Beckmann, P. Fasching, C. Vachon, 2018 .

Cancer risks for relatives of patients with serrated polyposis.

Aung Ko Win, M. Woods, J. Hopper, 2012, The American journal of gastroenterology.

Identification of nine new susceptibility loci for endometrial cancer

M. Beckmann, P. Fasching, C. Vachon, 2018, Nature Communications.

Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency ( suspected Lynch syndrome )

Aung Ko Win, A. Spurdle, C. Rosty, 2014 .

Absence of PMS2 mutations in colon‐CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression

S. Gallinger, C. Rosty, M. Clendenning, 2013, Clinical Genetics.

Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency ( suspected Lynch syndrome )

Aung Ko Win, A. Spurdle, C. Rosty, 2014 .

Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing

D. Schaid, D. Serie, Y. Asmann, 2013, Cancer Epidemiology, Biomarkers & Prevention.

Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history

Aung Ko Win, J. Emery, J. Potter, 2018, Familial Cancer.

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

Aung Ko Win, J. Potter, G. Giles, 2016, Cancer Epidemiology, Biomarkers & Prevention.

Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome.

Aung Ko Win, L. Lipton, G. Giles, 2012, Journal of the National Cancer Institute.

Title: Evaluating the utility of tumour mutational signatures for identifying hereditary colorectal cancer and polyposis syndrome carriers

Aung Ko Win, O. Sieber, S. Gallinger, 2019 .

Alcohol Consumption and the Risk of Colorectal Cancer for Mismatch Repair Gene Mutation Carriers

Aung Ko Win, J. Potter, G. Giles, 2016, Cancer Epidemiology, Biomarkers & Prevention.

DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands

C. Rosty, N. Pachter, M. Clendenning, 2023, medRxiv.

A study of cancer risks in relatives of patients with serrated polyposis

C. Rosty, M. Clendenning, K. Sweet, 2012, Hereditary Cancer in Clinical Practice.

Should the grading of colorectal adenocarcinoma include microsatellite instability status?

Aung Ko Win, D. English, G. Giles, 2014, Human pathology.

PIK3CA Activating Mutation in Colorectal Carcinoma: Associations with Molecular Features and Survival

Aung Ko Win, D. English, G. Giles, 2013, PloS one.

Intratumoral presence of the genotoxic gut bacteria pks+ E. coli, Enterotoxigenic Bacteroides fragilis, and Fusobacterium nucleatum and their association with clinicopathological and molecular features of colorectal cancer

M. Southey, R. Milne, C. Rosty, 2024, British journal of cancer.

The Effect of a Target Date Based Utilization Review Program on Length of Stay

L J Shuman, H Wolfe, L. Shuman, 1976, Medical care.

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease

M. Clendenning, S. Stuckless, A. Chapelle, 2010, Gut.