This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a Université Laval directory, so their courses and email address may be missing. Find their university profile.
Research
Latest papers
Expansion of non-invasive prenatal screening to the screening of 10 types of chromosomal anomalies: a cost-effectiveness analysis.
BMJ open · 2023
Decision impact studies, evidence of clinical utility for genomic assays in cancer: A scoping review.
PloS one · 2023
Non-invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta-analysis of diagnostic test accuracy studies.
Molecular genetics & genomic medicine · 2021
Latest funding
- $599,003
L'inversion de la pyramide des soins anténataux pour améliorer l'accès aux soins et la santé des mères et des enfants vivant en région éloignée (PROJET PYRAMIDE)
CIHR · 2024 · Co-investigator
- $2,801,102
PEGASUS-2 - PErsonalized Genomics for prenatal Abnormalities Screening USing maternal blood : Towards First Tier Screening and Beyond
CIHR · 2017 · Nominated PI
- $199,888
Analytical mobile application to support shared decision making for pregnant women
CIHR · 2017 · Co-investigator
9 publications.
Expansion of non-invasive prenatal screening to the screening of 10 types of chromosomal anomalies: a cost-effectiveness analysis.
Soukkhaphone B, Baradaran M, Nguyen BD, Nshimyumukiza L, Little J, Rousseau F, Audibert F, Langlois S, Reinharz D
Decision impact studies, evidence of clinical utility for genomic assays in cancer: A scoping review.
Parker G, Hunter S, Ghazi S, Hayeems RZ, Rousseau F, Miller FA
Non-invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta-analysis of diagnostic test accuracy studies.
Soukkhaphone B, Lindsay C, Langlois S, Little J, Rousseau F, Reinharz D
Web-Based Training for Nurses on Shared Decision Making and Prenatal Screening for Down Syndrome: Protocol for a Randomized Controlled Trial.
Poulin Herron A, Agbadje TT, Cote M, Djade CD, Roch G, Rousseau F, Légaré F
Toward harmonization of clinical molecular diagnostic reports: findings of an international survey.
Payne DA, Baluchova K, Russomando G, Ahmad-Nejad P, Mamotte C, Rousseau F, van Schaik RHN, Marriott K, Maekawa M, Chan KCA, IFCC Committee on Molecular Diagnostics
Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma.
Rivera B, Di Iorio M, Frankum J, Nadaf J, Fahiminiya S, Arcand SL, Burk DL, Grapton D, Tomiak E, Hastings V, Hamel N, Wagener R, Aleynikova O, Giroux S, Hamdan FF, Dionne-Laporte A, Zogopoulos G, Rousseau F, Berghuis AM, Provencher D, Rouleau GA, Michaud JL, Mes-Masson AM, Majewski J, Bens S, Siebert R, Narod SA, Akbari MR, Lord CJ, Tonin PN, Orthwein A, Foulkes WD
Germline RECQL mutations are associated with breast cancer susceptibility.
Cybulski C, Carrot-Zhang J, Kluźniak W, Rivera B, Kashyap A, Wokołorczyk D, Giroux S, Nadaf J, Hamel N, Zhang S, Huzarski T, Gronwald J, Byrski T, Szwiec M, Jakubowska A, Rudnicka H, Lener M, Masojć B, Tonin PN, Rousseau F, Górski B, Dębniak T, Majewski J, Lubiński J, Foulkes WD, Narod SA, Akbari MR
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project.
Beaulieu CL, Majewski J, Schwartzentruber J, Samuels ME, Fernandez BA, Bernier FP, Brudno M, Knoppers B, Marcadier J, Dyment D, Adam S, Bulman DE, Jones SJ, Avard D, Nguyen MT, Rousseau F, Marshall C, Wintle RF, Shen Y, Scherer SW, FORGE Canada Consortium, Friedman JM, Michaud JL, Boycott KM
Autonomy and the patient's right 'not to know' in clinical whole-genomic sequencing.
Townsend A, Rousseau F, Friedman J, Adam S, Lohn Z, Birch P
L'inversion de la pyramide des soins anténataux pour améliorer l'accès aux soins et la santé des mères et des enfants vivant en région éloignée (PROJET PYRAMIDE)
Principal investigators: Bujold, Emmanuel; Guilbeault, Nathalie; Boutin, Amélie; Piché, Marie-Ève
Keywords: Biomarqueurs; Essai Clinique; Grossesse; Naissance; Placenta; Prématurité; Prééclampsie; Échographie
PEGASUS-2 - PErsonalized Genomics for prenatal Abnormalities Screening USing maternal blood : Towards First Tier Screening and Beyond
Principal investigators: Rousseau, François
Keywords: Real-World Comparative Effectiveness
Analytical mobile application to support shared decision making for pregnant women
Principal investigators: Légaré, France
Keywords: Decision Aid; Down Syndrome; E-Health And Mhealth; Knowledge Translation; Mobile Applications; Multiple Criteria Decision Analysis Model; Pregnant Women; Prenatal Screening; Shared Decision Making; Technologies
Diagnostic Test Accuracy Review : Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.
Principal investigators: Forest, Jean-Claude; Langlois, Sylvie F; Légaré, France; Turgeon, Alexis F; Rousseau, François
Keywords: Chromosomal Aneuploidy; Diagnostic Test Accuracy Review; Genomic-Based Fetal Testing; Next-Generation Sequencing; Non-Invasive Prenatal Testing
Clinical outcomes and predictors of PITuitary disorders in patients with moderate and severe Traumatic Brain Injury: the PIT-TBI prospective multicenter pilot cohort study.
Principal investigators: Lauzier, François
Keywords: Critical Care; Outcome Research; Patient Oriented Research; Pituitary Disorders; Risk Factors; Traumatic Brain Injury
Simulating cost-effectiveness of screening strategies for preeclampsia risk in pregnant women
Principal investigators: Giguere, Yves; Reinharz, Daniel
Keywords: Cost-Effectiveness; Preeclampsia; Screening Strategies; Simulation
PEGASUS: PErsonalized Genomics for prenatal Aneuploidy Screening USing maternal blood
Principal investigators: Rousseau, François
Keywords: Evidence-Based Laboratory Medicine; Ge3ls; Health Services Research; Non-Invasive Prenatal Testing; Real-World Comparative Effectiveness
Validating and refining genome-wide signals for genetic determinants of bone mineral density in pre and post-menopausal women.
Principal investigators: Rousseau, François
Keywords: Bone Metabolism; Human Genetics; Laboratory Medicine; Osteoporosis; Peak Bone Mass; Translational Research
Validation of genetic determinants of peak bone mass and post-menopausal bone density in women using SNPs and CNVs.
Principal investigators: Rousseau, François
Keywords: Bone Metabolism; Human Genetics; Laboratory Medicine; Osteoporosis; Peak Bone Mass; Translational Research
Simulating the Cost/Effectiveness of Screening Strategies for Cystic Fibrosis
Principal investigators: Reinharz, Daniel; Daigneault, Patrick
Keywords: Cost/Effectiveness; Cost/Utility; Cystic Fibrosis; Screening Strategies; Simulation
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
- Human Genetics
- School of Epidemiology and Public Health
- Medicine
- Department of Medicine
- Medical Genetics
- Computer Science
- Other
Co-authors at Université Laval, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Jacek Majewski
Human Genetics
3 shared papers, latest 2017
Daniel Reinharz
Faculty
2 shared papers, latest 2023
Julian Little
School of Epidemiology and Public Health
2 shared papers, latest 2023
Bartha Knoppers
Human Genetics
1 shared papers, latest 2014
Jan Friedman
Medical Genetics
1 shared papers, latest 2014
Eva Tomiak
Department of Medicine
1 shared papers, latest 2017
Michael Brudno
Computer Science
1 shared papers, latest 2014
Anne-Marie Mes-Masson
Medicine
1 shared papers, latest 2017
Alexandre Orthwein
Faculty
1 shared papers, latest 2017
Denise Avard
Human Genetics
1 shared papers, latest 2014
David Dyment
Faculty
1 shared papers, latest 2014
A short, specific email works best. This draft uses one of their recent papers; replace the parts in brackets with your own details before sending.