List of works - Finlay Macrae

Celecoxib for the prevention of sporadic colorectal adenomas

scientific article (publication date: 31 August 2006)

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

scientific article published on 27 October 2011

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

scientific article

Risks of Lynch syndrome cancers for MSH6 mutation carriers

scientific article

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

scientific article published on 13 February 2012

Crohn's disease management after intestinal resection: a randomised trial

scientific article published on 24 December 2014

Five-year efficacy and safety analysis of the Adenoma Prevention with Celecoxib Trial

scientific article

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

scientific article published on 9 December 2015

Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome

scientific article

Use of Molecular Tumor Characteristics to Prioritize Mismatch Repair Gene Testing in Early-Onset Colorectal Cancer

article

Cancer risks for MLH1 and MSH2 mutation carriers

scientific article

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

scientific article

Functional Significance and Clinical Phenotype of Nontruncating Mismatch Repair Variants of MLH1

scientific article published in August 2005

Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome

scientific article

Measurement of fecal calprotectin improves monitoring and detection of recurrence of Crohn's disease after surgery

scientific article published on 22 January 2015

Cancer Risks For Mismatch Repair Gene Mutation Carriers: A Population-Based Early Onset Case-Family Study

article

Hyperplastic polyposis syndrome: phenotypic presentations and the role of MBD4 and MYH.

scientific article

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

scientific article published on 28 July 2017

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

scientific article published on 17 January 2014

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry

scientific article published on 9 March 2010

Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinics

scientific article

A review of juvenile polyposis syndrome

scientific article

Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers

scientific article

Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome

scientific article published on 5 February 2013

Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein

scientific article published on 22 August 2006

Relationship between disease severity and quality of life and assessment of health care utilization and cost for ulcerative colitis in Australia: a cross-sectional, observational study.

scientific article published on 15 December 2013

Combining wheat bran with resistant starch has more beneficial effects on fecal indexes than does wheat bran alone

scientific article

How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.

scientific article

Planning the human variome project: the Spain report

scientific article published in April 2009

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

scientific article

Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project

scientific article

Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

scientific article published on 17 August 2015

Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

article

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

scientific article

GENETICS. The Human Variome Project

scientific article

Is uptake of genetic testing for colorectal cancer influenced by knowledge of insurance implications?

scientific article published on 01 September 2009

Germ line mutations of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients with small bowel cancer: International Society for Gastrointestinal Hereditary Tumours Collaborative Study

scientific article published in June 2006

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

scientific article published on 3 June 2016

Colorectal cancer and inherited mutations in base-excision repair

scientific article published in October 2004

Family history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases

scientific article

Familial adenomatous polyposis: The practical applications of clinical and molecular screening

scientific article published on January 2006

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

scientific article

Applicability of next generation sequencing technology in microsatellite instability testing

scientific article

Microsatellite Instability Markers for Identifying Early-Onset Colorectal Cancers Caused by Germ-Line Mutations in DNA Mismatch Repair Genes

article

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

scientific article published on 24 July 2019

PMS2 monoallelic mutation carriers: the known unknown

scientific article

AfterhMSH2 andhMLH1?what next? Analysis of three-generational, population-based, early-onset colorectal cancer families

article

Evaluation of CADD Scores in Curated Mismatch Repair Gene Variants Yields a Model for Clinical Validation and Prioritization

scientific article

Two mismatch repair gene mutations found in a colon cancer patient--which one is pathogenic?

scientific article

Relationship between disease severity, quality of life and health-care resource use in a cross-section of Australian patients with Crohn's disease

scientific article published on 07 June 2007

List of works by Finlay Macrae

Celecoxib for the prevention of sporadic colorectal adenomas

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

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

Risks of Lynch syndrome cancers for MSH6 mutation carriers

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

Crohn's disease management after intestinal resection: a randomised trial

Five-year efficacy and safety analysis of the Adenoma Prevention with Celecoxib Trial

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome

Use of Molecular Tumor Characteristics to Prioritize Mismatch Repair Gene Testing in Early-Onset Colorectal Cancer

Cancer risks for MLH1 and MSH2 mutation carriers

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

Functional Significance and Clinical Phenotype of Nontruncating Mismatch Repair Variants of MLH1

Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome

Measurement of fecal calprotectin improves monitoring and detection of recurrence of Crohn's disease after surgery

Cancer Risks For Mismatch Repair Gene Mutation Carriers: A Population-Based Early Onset Case-Family Study

Hyperplastic polyposis syndrome: phenotypic presentations and the role of MBD4 and MYH.

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

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

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry

Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinics

A review of juvenile polyposis syndrome

Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers

Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome

Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein

Relationship between disease severity and quality of life and assessment of health care utilization and cost for ulcerative colitis in Australia: a cross-sectional, observational study.

Combining wheat bran with resistant starch has more beneficial effects on fecal indexes than does wheat bran alone

How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.

Planning the human variome project: the Spain report

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

Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project

Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

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

GENETICS. The Human Variome Project

Is uptake of genetic testing for colorectal cancer influenced by knowledge of insurance implications?

Germ line mutations of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients with small bowel cancer: International Society for Gastrointestinal Hereditary Tumours Collaborative Study

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

Colorectal cancer and inherited mutations in base-excision repair

Family history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases

Familial adenomatous polyposis: The practical applications of clinical and molecular screening

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

Applicability of next generation sequencing technology in microsatellite instability testing

Microsatellite Instability Markers for Identifying Early-Onset Colorectal Cancers Caused by Germ-Line Mutations in DNA Mismatch Repair Genes

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

PMS2 monoallelic mutation carriers: the known unknown

AfterhMSH2 andhMLH1?what next? Analysis of three-generational, population-based, early-onset colorectal cancer families

Evaluation of CADD Scores in Curated Mismatch Repair Gene Variants Yields a Model for Clinical Validation and Prioritization

Two mismatch repair gene mutations found in a colon cancer patient--which one is pathogenic?

Relationship between disease severity, quality of life and health-care resource use in a cross-section of Australian patients with Crohn's disease