Andree J. Macmillan

St. John's, NL, Canada

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications

Suboptimal Adherence to Hereditary Cancer Risk Management Guidelines: A Cohort Study of High-Risk Individuals in Newfoundland and Labrador, Canada.

Suboptimal Adherence to Hereditary Cancer Risk Management Guidelines: A Cohort Study of High-Risk Individuals in Newfoundland and Labrador, Canada.

Journal: Current oncology (Toronto, Ont.)
Published: February 05, 2026

Canadian consensus for the assessment and testing of Lynch syndrome.

Canadian consensus for the assessment and testing of Lynch syndrome.

Journal: Journal of medical genetics
Published: October 28, 2024

Safety of topical administration of nasal decongestants and vasoconstrictors in paediatric nasal surgery - A systematic review.

Safety of topical administration of nasal decongestants and vasoconstrictors in paediatric nasal surgery - A systematic review.

Journal: International journal of pediatric otorhinolaryngology
Published: September 08, 2021

Group plus "mini" individual pre-test genetic counselling sessions for hereditary cancer shorten provider time and improve patient satisfaction.

Group plus "mini" individual pre-test genetic counselling sessions for hereditary cancer shorten provider time and improve patient satisfaction.

Journal: Hereditary cancer in clinical practice
Published: August 25, 2019

A dominant RAD51C pathogenic splicing variant predisposes to breast and ovarian cancer in the Newfoundland population due to founder effect.

A dominant RAD51C pathogenic splicing variant predisposes to breast and ovarian cancer in the Newfoundland population due to founder effect.

Journal: Molecular genetics & genomic medicine
Published: March 29, 2019

Universal tumor screening for Lynch syndrome: Perceptions of Canadian pathologists and genetic counselors of barriers and facilitators.

Universal tumor screening for Lynch syndrome: Perceptions of Canadian pathologists and genetic counselors of barriers and facilitators.

Journal: Cancer medicine
Published: January 30, 2019

Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap.

Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap.

Journal: Journal of medical genetics
Published: May 04, 2018

Universal tumor screening for Lynch syndrome: perspectives of Canadian pathologists and genetic counselors.

Universal tumor screening for Lynch syndrome: perspectives of Canadian pathologists and genetic counselors.

Journal: Journal of community genetics
Published: April 09, 2018

Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11.

Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11.

Journal: Human mutation
Published: June 19, 2017

Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond.

Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond.

Journal: JAMA oncology
Published: July 17, 2015

Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.

Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.

Journal: BMC medical genetics
Published: July 03, 2012
Showing 1-11 of 11

Last Updated: 09/26/2026