This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a Queen's University directory, so their courses and email address may be missing. Find their university profile.
Latest papers
Evaluation of the determinants of FVIII/FIX levels, bleeding score, and health-related quality of life in the Canadian hemophilia carriers (CHiC) study
Journal of Thrombosis and Haemostasis · 2026
Genomic testing for bleeding disorders (GT4BD): protocol for a randomised controlled trial evaluating the introduction of whole genome sequencing early in the diagnostic pathway for patients with inherited bleeding disorders as compared with standard of care.
BMJ open · 2025
Evaluating the impact of the self-BAT screening tool on patient outcomes: Results of the let's talk period project.
Haemophilia : the official journal of the World Federation of Hemophilia · 2024
Latest funding
- $1,374,999
Early genomic testing for inherited bleeding disorders in patients without a diagnosis after first-line testing: a randomized controlled trial
CIHR · 2023 · Principal investigator
5 publications.
Evaluation of the determinants of FVIII/FIX levels, bleeding score, and health-related quality of life in the Canadian hemophilia carriers (CHiC) study
Swystun LL, Grabell J, Hinds M, Avgeropoulos M, Bowman M, Chaigneau M, de Repentigny K, Belletrutti M, Hopman W, Iorio A
Genomic testing for bleeding disorders (GT4BD): protocol for a randomised controlled trial evaluating the introduction of whole genome sequencing early in the diagnostic pathway for patients with inherited bleeding disorders as compared with standard of care.
Chaigneau M, Bowman M, Grabell J, Conboy M, Johnson A, Thorpe K, Guerin A, Dinchong R, Paterson A, Good D, Mahar A, Callum J, Wheaton L, Leung J, Khalife R, Sholzberg M, Lillicrap D, James PD
Evaluating the impact of the self-BAT screening tool on patient outcomes: Results of the let's talk period project.
McDonald L, Grabell J, Leung J, Hopman W, James P
New and emerging therapies for women, girls, and people with the potential to menstruate with VWD.
Casari C, Leung J, James PD
Commentary on Laffan et al expert consensus for equitable care for VWD.
Leung J, James P
Early genomic testing for inherited bleeding disorders in patients without a diagnosis after first-line testing: a randomized controlled trial
Principal investigators: James, Paula D; Leung, Jennifer; Lillicrap, David P; Sholzberg, Michelle
Keywords: Diagnosis; Genetic Testing; Inherited Bleeding Disorders
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
- Pathology and Molecular Medicine
- Health Research Methods, Evidence, and Impact
- Public Health Sciences
- Surgery
- Other
Co-authors at Queen's University, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Paula James
Faculty
2 shared papers, latest 2024
David Lillicrap
Pathology and Molecular Medicine
1 shared papers, latest 2025
Ana Johnson
Public Health Sciences
1 shared papers, latest 2025
Alfonso Iorio
Health Research Methods, Evidence, and Impact
1 shared papers, latest 2026
Alyson Mahar
Faculty
1 shared papers, latest 2025
Jeannie Callum
Pathology and Molecular Medicine
1 shared papers, latest 2025
Kevin Thorpe
Surgery
1 shared papers, latest 2025
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