This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a Memorial University of Newfoundland directory, so their courses may be missing. Find their university profile.
Research
Latest papers
Barriers to reducing preoperative testing for low-risk surgical procedures: A qualitative assessment guided by the Theoretical Domains Framework.
PloS one · 2022
Changing Health-Related Behaviours 5: On Interventions to Change Physician Behaviours.
Methods in molecular biology (Clifton, N.J.) · 2021
Changing Health-Related Behaviors 3: Lessons from Implementation Science.
Methods in molecular biology (Clifton, N.J.) · 2021
Latest funding
- $4,884,436
Newfoundland and Labrador SUPPORT Unit -Phase II Funding Application
CIHR · 2020 · Principal investigator
9 publications.
Barriers to reducing preoperative testing for low-risk surgical procedures: A qualitative assessment guided by the Theoretical Domains Framework.
Hall A, Pike A, Patey A, Mortazhejri S, Inwood S, Ruzycki S, Kirkham K, Mahoney K, Grimshaw J
Changing Health-Related Behaviours 5: On Interventions to Change Physician Behaviours.
Etchegary C, Taylor L, Mahoney K, Parfrey O, Hall A
Changing Health-Related Behaviors 3: Lessons from Implementation Science.
Hall A, Richmond H, Mahoney K, Matthews J
Protocol for assessing the determinants of preoperative test-ordering behaviour for low-risk surgical procedures using a theoretically driven, qualitative design.
Pike A, Mahoney K, Patey AM, Inwood S, Mortazhejri S, Lawrence R, Hall A, De-implementing Wisely Research Group
Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.
Fernandez BA, Green JS, Bursey F, Barrett B, MacMillan A, McColl S, Fernandez S, Rahman P, Mahoney K, Pereira SL, Scherer SW, Boycott KM, Woods MO, FORGE Canada Consortium
A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features.
Fernandez BA, Fox G, Bhatia R, Sala E, Noble B, Denic N, Fernandez D, Duguid N, Dohey A, Kamel F, Edwards L, Mahoney K, Stuckless S, Parfrey PS, Woods MO
Inherited deleterious variants in GALNT12 are associated with CRC susceptibility.
Clarke E, Green RC, Green JS, Mahoney K, Parfrey PS, Younghusband HB, Woods MO
High incidence of pediatric idiopathic epilepsy is associated with familial and autosomal dominant disease in Eastern Newfoundland.
Mahoney K, Buckley D, Alam M, Penney S, Young TL, Parfrey P, Moore SJ
Variable neurologic phenotype in a GEFS+ family with a novel mutation in SCN1A.
Mahoney K, Moore SJ, Buckley D, Alam M, Parfrey P, Penney S, Merner N, Hodgkinson K, Young TL
Newfoundland and Labrador SUPPORT Unit -Phase II Funding Application
Principal investigators: Barrett, Brendan J; McKenna, Andrea; Senior, Dorothy M; Warren, Mike; Aubrey-Bassler, Kris; Etchegary, Holly; Mahoney, Krista; Parfrey, Patrick S; Street, Catherine A; Taylor, Lynn; Wilson, Robert C
Keywords: Health System Improvement; Implementatation Science; Patient Engagement; Patient Oriented Research; Research Support
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Medicine
- Family Medicine
- Department of Medicine
- Genetics
Co-authors at Memorial University of Newfoundland, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Amanda Hall
Family Medicine
4 shared papers, latest 2022
Patrick Parfrey
Medicine
2 shared papers, latest 2012
Lynn Taylor
Medicine
1 shared papers, latest 2021
Amanda Dohey
Family Medicine
1 shared papers, latest 2012
Jeremy Grimshaw
Department of Medicine
1 shared papers, latest 2022
Proton Rahman
Genetics
1 shared papers, latest 2012
Brendan Barrett
Medicine
1 shared papers, latest 2012
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