Finlay A Macrae


Ontology type: schema:Person     


Person Info

NAME

Finlay A

SURNAME

Macrae

Publications in SciGraph latest 50 shown

  • 2018-12 The use of a risk assessment and decision support tool (CRISP) compared with usual care in general practice to increase risk-stratified colorectal cancer screening: study protocol for a randomised controlled trial in TRIALS
  • 2018-10 Correction: Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 in GENETICS IN MEDICINE
  • 2018-08 Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 in GENETICS IN MEDICINE
  • 2018-07 An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review in FAMILIAL CANCER
  • 2018-01 Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas in FAMILIAL CANCER
  • 2018 The InSiGHT Database: An Example LOVD System in HEREDITARY COLORECTAL CANCER
  • 2017-12 Improving adherence to colorectal cancer surveillance guidelines: results of a randomised controlled trial in BMC CANCER
  • 2017-12 Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2017-01 Exploring clinicians’ attitudes about using aspirin for risk reduction in people with Lynch Syndrome with no personal diagnosis of colorectal cancer in FAMILIAL CANCER
  • 2016-12 Harmonizing the interpretation of genetic variants across the world: the Malaysian experience in BMC RESEARCH NOTES
  • 2016-12 Experiences of colorectal cancer patients in the 2-years post-diagnosis and patient factors predicting poor outcome in SUPPORTIVE CARE IN CANCER
  • 2016-02 Knowledge and Uptake of Genetic Counseling and Colonoscopic Screening Among Individuals at Increased Risk for Lynch Syndrome and their Endoscopists from the Family Health Promotion Project in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2016-01 PMS2 monoallelic mutation carriers: the known unknown in GENETICS IN MEDICINE
  • 2015-12 Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene in FAMILIAL CANCER
  • 2015-11 The Human Variome Project: ensuring the quality of DNA variant databases in inherited renal disease in PEDIATRIC NEPHROLOGY
  • 2014-12 Little evidence for association between the TGFBR1*6A variant and colorectal cancer: a family-based association study on non-syndromic family members from Australia and Spain in BMC CANCER
  • 2014-02 Perceived Versus Predicted Risks of Colorectal Cancer and Self-Reported Colonoscopies by Members of Mismatch Repair Gene Mutation-Carrying Families Who Have Declined Genetic Testing in JOURNAL OF GENETIC COUNSELING
  • 2014-02 Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database in NATURE GENETICS
  • 2014 DNA Variant Databases: Current State and Future Directions in CLINICAL BIOINFORMATICS
  • 2013-12 An association between the PTGS2 rs5275 polymorphism and colorectal cancer risk in families with inherited non-syndromic predisposition in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-12 A population-based cross-sectional study of colorectal cancer screening practices of first-degree relatives of colorectal cancer patients in BMC CANCER
  • 2013-12 Individual- and provider-level factors associated with colorectal cancer screening in accordance with guideline recommendation: a community-level perspective across varying levels of risk in BMC PUBLIC HEALTH
  • 2013-07 Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins in MODERN PATHOLOGY
  • 2013-06 Risk of Metachronous Colon Cancer Following Surgery for Rectal Cancer in Mismatch Repair Gene Mutation Carriers in ANNALS OF SURGICAL ONCOLOGY
  • 2012-12 Factors associated with consultation behaviour for primary symptoms potentially indicating colorectal cancer: A cross-sectional study on response to symptoms in BMC GASTROENTEROLOGY
  • 2012-12 Improving adherence to surveillance and screening recommendations for people with colorectal cancer and their first degree relatives: a randomized controlled trial in BMC CANCER
  • 2012-12 Colorectal cancer risk assessment and screening recommendation: a community survey of healthcare providers' practice from a patient perspective in BMC FAMILY PRACTICE
  • 2012-06 Management of duodenal adenomatosis in FAP: single centre experience in FAMILIAL CANCER
  • 2012-01 Evidence of linkage to chromosomes 10p15.3–p15.1, 14q24.3–q31.1 and 9q33.3–q34.3 in non-syndromic colorectal cancer families in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-12 Metachronous colorectal cancer risk for mismatch repair gene mutation carriers – the advantage of more extensive surgery in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2011-12 Mutation (variation) databases and registries: a rationale for coordination of efforts in NATURE REVIEWS GENETICS
  • 2011-12 Time and motion study of familial bowel and breast cancer gene mutational analysis in Victoria, Australia in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2011-12 InSiGHT leads in the implementation of the Human Variome Project in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2011-12 Hyperplastic Polyposis and the smoking paradox in females in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2011-06 Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome) in FAMILIAL CANCER
  • 2010-12 Erratum to: Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study in INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
  • 2010-12 Surveillance of FAP: a prospective blinded comparison of capsule endoscopy and other GI imaging to detect small bowel polyps in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2010-12 Magnetic resonance colonography for colorectal cancer screening in patients with Lynch syndrome gene mutation in FAMILIAL CANCER
  • 2010-12 Report of the Combined Meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldorf, Germany, 24 June 2009 in FAMILIAL CANCER
  • 2010-06 Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study in INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
  • 2010 Genetic Counselling Across Culture and Health Systems: Australia in HEREDITARY COLORECTAL CANCER
  • 2009-12 Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis in FAMILIAL CANCER
  • 2009-12 Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project in GENETICS IN MEDICINE
  • 2008-04-11 Suggested actions from the Melbourne HVP Information Seminar in NATURE PRECEDINGS
  • 2007-09 Impact of Familial Adenomatous Polyposis on Young Adults: Quality of Life Outcomes in DISEASES OF THE COLON & RECTUM
  • 2006-11 Impact of familial adenomatous polyposis on young adults: Attitudes toward genetic testing, support, and information needs in GENETICS IN MEDICINE
  • 2006-09 Familial adenomatous polyposis: the practical applications of clinical and molecular screening in FAMILIAL CANCER
  • 2005-12 Survey of HNPCC Management Analysis of Responses from 18 International Cancer Centres in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2003-02 Two mismatch repair gene mutations found in a colon cancer patient – which one is pathogenic? in HUMAN GENETICS
  • 1990 Managing Surveillance for Colorectal Cancer: The Importance of Microcomputers in HEREDITARY COLORECTAL CANCER
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