Finlay A Macrae


Ontology type: schema:Person     


Person Info

NAME

Finlay A

SURNAME

Macrae

Publications in SciGraph latest 50 shown

  • 2021-09-08 Commentary: Pivoting during a pandemic: developing a new recruitment model for a randomised controlled trial in response to COVID-19 in TRIALS
  • 2021-07-15 An RCT of a decision aid to support informed choices about taking aspirin to prevent colorectal cancer and other chronic diseases: a study protocol for the SITA (Should I Take Aspirin?) trial in TRIALS
  • 2021-04-09 Impact of national guidelines on use of BRCA1/2 germline testing, risk management advice given to women with pathogenic BRCA1/2 variants and uptake of advice in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2020-12-01 Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report in GENETICS IN MEDICINE
  • 2020-07-20 Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database in GENETICS IN MEDICINE
  • 2020-07-01 Medically actionable pathogenic variants in a population of 13,131 healthy elderly individuals in GENETICS IN MEDICINE
  • 2020-05-09 Evaluation of implementation of risk management guidelines for carriers of pathogenic variants in mismatch repair genes: a nationwide audit of familial cancer clinics in FAMILIAL CANCER
  • 2019-10-14 Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2019-09-25 Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome in BRITISH JOURNAL OF CANCER
  • 2019-08-16 Outcomes of screening and surveillance in people with two parents affected by colorectal cancers: experiences from the Familial Bowel Cancer Service in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2019-07-24 Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database in GENETICS IN MEDICINE
  • 2019-06-20 Comparing theory and non-theory based implementation approaches to improving referral practices in cancer genetics: a cluster randomised trial protocol in TRIALS
  • 2019-06-17 Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history in FAMILIAL CANCER
  • 2019-01-22 Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene in FAMILIAL CANCER
  • 2018-07-25 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
  • 2018-05-05 The InSiGHT Database: An Example LOVD System in HEREDITARY COLORECTAL CANCER
  • 2018-02-28 Heritable DNA methylation marks associated with susceptibility to breast cancer in NATURE COMMUNICATIONS
  • 2018-02-01 Correction: Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1 in GENETICS IN MEDICINE
  • 2017-11-09 Risk of colorectal cancer for carriers of a germline mutation in POLE or POLD1 in GENETICS IN MEDICINE
  • 2017-10-10 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
  • 2017-09-12 An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review in FAMILIAL CANCER
  • 2017-06-14 Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas in FAMILIAL CANCER
  • 2017-02-06 Improving adherence to colorectal cancer surveillance guidelines: results of a randomised controlled trial in BMC CANCER
  • 2016-09-27 Exploring clinicians’ attitudes about using aspirin for risk reduction in people with Lynch Syndrome with no personal diagnosis of colorectal cancer in FAMILIAL CANCER
  • 2016-07-16 Experiences of colorectal cancer patients in the 2-years post-diagnosis and patient factors predicting poor outcome in SUPPORTIVE CARE IN CANCER
  • 2016-02-26 Harmonizing the interpretation of genetic variants across the world: the Malaysian experience in BMC RESEARCH NOTES
  • 2016-02-09 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
  • 2015-07-23 Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene in FAMILIAL CANCER
  • 2015-04-09 PMS2 monoallelic mutation carriers: the known unknown in GENETICS IN MEDICINE
  • 2014-11-11 The Human Variome Project: ensuring the quality of DNA variant databases in inherited renal disease in PEDIATRIC NEPHROLOGY
  • 2014-07-01 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
  • 2014-05-09 DNA Variant Databases: Current State and Future Directions in CLINICAL BIOINFORMATICS
  • 2014-02-08 Capsule endoscopy versus magnetic resonance enterography for the detection of small bowel polyps in Peutz–Jeghers syndrome in FAMILIAL CANCER
  • 2013-03-27 An association between the PTGS2 rs5275 polymorphism and colorectal cancer risk in families with inherited non-syndromic predisposition in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-03-20 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
  • 2013-02-27 The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome in FAMILIAL CANCER
  • 2013-02-01 Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins in MODERN PATHOLOGY
  • 2013-01-29 Risk of Metachronous Colon Cancer Following Surgery for Rectal Cancer in Mismatch Repair Gene Mutation Carriers in ANNALS OF SURGICAL ONCOLOGY
  • 2013-01-10 A population-based cross-sectional study of colorectal cancer screening practices of first-degree relatives of colorectal cancer patients in BMC CANCER
  • 2012-08-03 Factors associated with consultation behaviour for primary symptoms potentially indicating colorectal cancer: A cross-sectional study on response to symptoms in BMC GASTROENTEROLOGY
  • 2012-04-12 Metachronous colon cancer risk following surgery for first primary rectal cancer in Lynch syndrome in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-04-12 Audit of routine immunohistochemistry testing for mismatch repair proteins at diagnosis of colorectal cancer under the age of 50 in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-04-12 When is it best to test? Attitudes of health professionals regarding genetic testing for Familial Adenomatous Polyposis (FAP) in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-04-12 Polyposis syndromes– what to do when genotyping seems not informative in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-04-12 Substantial unexplained variation in cancer risks for MLH1 and MSH2 mutation carriers in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-03-14 Colorectal cancer risk assessment and screening recommendation: a community survey of healthcare providers' practice from a patient perspective in BMC FAMILY PRACTICE
  • 2012-02-08 Improving adherence to surveillance and screening recommendations for people with colorectal cancer and their first degree relatives: a randomized controlled trial in BMC CANCER
  • 2011-12-01 Management of duodenal adenomatosis in FAP: single centre experience in FAMILIAL CANCER
  • 2011-10-25 Mutation (variation) databases and registries: a rationale for coordination of efforts in NATURE REVIEWS GENETICS
  • 2011-08-10 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
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