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F

François P. Bernier

university of calgary

56H-index
237Paper Count
1.0WCitation Count
Published Papers 80
Publication Date
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Shared genetic basis and structure of syndromic and normal facial variation
errAmerican Journal of Human Genetics
IF8.1
err2026-08-21
err0
PREAI
errJ. David Aponte; Cassidy Da Silva; Hanne Hoskens; Seppe Goovaerts; Michiel Vanneste; Jay Devine; Katherine Caine; Alexander Buchner Beaudet; H. Artee Luchman; Seth M. Weinberg; Hilde Peeters; Ophir D. Klein; Ralph S. Marcucio; A. Micheil Innes; Peter Claes; Richard A. Spritz; Francois P. Bernier; Benedikt Hallgrímsson
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Clinical Utility of Exome Sequencing: Post-Exome Testing Decision Changes in the Management of Children with Suspected Rare Genetic Disease
errGenetics in Medicine
IF6.2
err2026-06-11
err0
errOAAI
errToni Tagimacruz; Trevor Adam Seeger; Koen Degeling; Katharine Fooks; Viji Venkataramanan; Francois P. Bernier; Kym M. Boycott; Roberto Mendoza-Londono; Taila Hartley; Robin Hayeems; Deborah A. Marshall
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A comprehensive approach to evaluating the clinical utility of genome sequencing in rare disease: A large prospective Canadian cohort
errGenetics in Medicine
IF6.2
err2026-01-10
err0
errOAAI
errSalma Shickh; Katharine Fooks; Viji Venkataramanan; Meryl Acker; Karen V. MacDonald; Trevor A. Seeger; Meredith Gillespie; Taila Hartley; Kym M. Boycott; Francois Bernier; Deborah A. Marshall; Robin Z. Hayeems
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To test or not to test? Study protocol for a best-worst scaling to understand decision-making and preferences for genetic testing in moderate-risk individuals
errPLoS One
IF2.6
err2025-12-29
err0
PREAI
errOedingen, Carina; Hua, Nicolle; MacDonald, Karen V.; Marcadier, Julien; Perrier, Renee; Tuer, Lindsay; McInnes, Brenda; Bernier, Francois; Marshall, Deborah A.
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Is next generation sequencing for the diagnosis of rare diseases worth its cost? A user-based approach to valuation
errThe European Journal of Health Economics
IF0
err2025-11-12
err0
PREAI
errKaren V. MacDonald; Sebastian Heidenreich; Nicolas Krucien; Kym M. Boycott; Francois P. Bernier; Mandy Ryan; Deborah A. Marshall
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errSave
A roadmap for navigating child health research data sharing across Canada and beyond – building on UCAN CAN-DU
errPediatric Rheumatology
IF2.3
err2025-10-02
err0
errOAAI
errBrittany Gerber; Gillian R. Currie; Alexander Mosoiu; Alexander Bernier; Francois P. Bernier; Kym M. Boycott; Guillermo Fiebelkorn; Kristien Hens; Bartha M. Knoppers; Claire LeBlanc; Stephen W. Scherer; David Shaw; Chris Viney; Carl Virtanen; Susanne M. Benseler; Rae S. M. Yeung; Deborah A. Marshall
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Genome Sequencing Identifies a Heterozygous Deletion of RBFOX2 in a Family With Congenital Heart Disease: A Case Report
errAmerican Journal of Medical Genetics Part A
IF1.7
err2025-10-01
err0
PREAI
errJean, Francesca; Stuart, Amanda; Marcadier, Julien; Bernier, Francois P.; Lamont, Ryan E.
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Mainstreaming of clinical genetic testing: A conceptual framework
errGenetics in Medicine
IF6.2
err2025-05-22
err0
errOAAI
errMichael P. Mackley; Julie Richer; Andrea Guerin; Oana Caluseriu; Linlea Armstrong; Katherine A. Blood; Francois Bernier; Christie Boswell-Patterson; Marisa Chard; Gregory Costain; David Dyment; Alison Eaton; Hanna Faghfoury; Patrick Frosk; Meredith K. Gillespie; Elaine S. Goh; Robin Z. Hayeems; Bita Hashemi; A. Micheil Innes; Molly Jackson; Kym M. Boycott
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Exome Sequencing in the Diagnostic Pathway for Suspected Rare Genetic Diseases: Does the Order of Testing Affect its Cost-Effectiveness?
errAPPLIED HEALTH ECONOMICS AND HEALTH POLICY
IF3.3
err2024-12-30
err0
PREAI
errDegeling, Koen; Tagimacruz, Toni; MacDonald, Karen, V; Seeger, Trevor A.; Fooks, Katharine; Venkataramanan, Viji; Boycott, Kym M.; Bernier, Francois P.; Mendoza-Londono, Roberto; Hartley, Taila; Hayeems, Robin Z.; Marshall, Deborah A.
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errSave
Ectomycorrhizal exploration type could be a functional trait explaining the spatial distribution of tree symbiotic fungi as a function of forest humus forms
errMYCORRHIZA
IF3.8
err2024-05-03
err1
PREAI
errKhalfallah, F.; Bon, L.; El Mazlouzi, M.; Bakker, M. R.; Fanin, N.; Bellanger, R.; Bernier, F.; De Schrijver, A.; Ducatillon, C.; Fotelli, M. N.; Gateble, G.; Gundale, M. J.; Larsson, M.; Legout, A.; Mason, W. l.; Nordin, A.; Smolander, A.; Spyroglou, G.; Vanguelova, E. I.; Verheyen, K.; Vesterdal, L.; Zeller, B.; Augusto, L.; Derrien, D.; Buee, M.
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An interactive atlas of three-dimensional syndromic facial morphology
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2024-01-01
err0
errOAAI
errAponte, J. David; Bannister, Jordan J.; Hoskens, Hanne; Matthews, Harold; Katsura, Kaitlin; Da Silva, Cassidy; Cruz, Tim; Pilz, Julie H. M.; Spritz, Richard A.; Forkert, Nils D.; Claes, Peter; Bernier, Francois P.; Klein, Ophir D.; Katz, David C.; Hallgrimsson, Benedikt
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Probiotic Bifidobacterium breve MCC1274 Protects against Oxidative Stress and Neuronal Lipid Droplet Formation via PLIN4 Gene Regulation
errMICROORGANISMS
IF4.2
err2023-03-20
err13
errOAAI
errBernier, Francois; Kuhara, Tatsuya; Xiao, Jinzhong
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Comparing 2D and 3D representations for face-based genetic syndrome diagnosis
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2023-02-07
err4
PREAI
errBannister, Jordan J.; Wilms, Matthias; Aponte, J. David; Katz, David C.; Klein, Ophir D.; Bernier, Francois P.; Spritz, Richard A.; Hallgrimsson, Benedikt; Forkert, Nils D.
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Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2022-11-01
err22
errOAAI
errBoycott, Kym M.; Hartley, Taila; Kernohan, Kristin D.; Dyment, David A.; Howley, Heather; Innes, A. Micheil; Bernier, Francois P.; Brudno, Michael
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A Deep Invertible 3-D Facial Shape Model for Interpretable Genetic Syndrome Diagnosis
errIEEE JOURNAL OF BIOMEDICAL AND HEALTH INFORMATICS
IF6.8
err2022-07-01
err6
errOAAI
errBannister, Jordan J.; Wilms, Matthias; Aponte, J. David; Katz, David C.; Klein, Ophir D.; Bernier, Francois P. J.; Spritz, Richard A.; Hallgrimsson, Benedikt; Forkert, Nils D.
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Effect of Probiotic Bifidobacterium breve in Improving Cognitive Function and Preventing Brain Atrophy in Older Patients with Suspected Mild Cognitive Impairment: Results of a 24-Week Randomized, Double-Blind, Placebo-Controlled Trial
errJOURNAL OF ALZHEIMERS DISEASE
IF3.1
err2022-06-28
err75
errOAAI
errAsaoka, Daisuke; Xiao, Jinzhong; Takeda, Tsutomu; Yanagisawa, Naotake; Yamazaki, Takahiro; Matsubara, Yoichiro; Sugiyama, Hideki; Endo, Noemi; Higa, Motoyuki; Kasanuki, Koji; Ichimiya, Yosuke; Koido, Shigeo; Ohno, Kazuya; Bernier, Francois; Katsumata, Noriko; Nagahara, Akihito; Arai, Heii; Ohkusa, Toshifumi; Sato, Nobuhiro
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The complexity of diagnosing rare disease: An organizing framework for outcomes research and health economics based on real-world evidence
errGENETICS IN MEDICINE
IF6.2
err2022-03-01
err6
errOAAI
errHayeems, Robin Z.; Michaels-Igbokwe, Christine; Venkataramanan, Viji; Hartley, Taila; Acker, Meryl; Gillespie, Meredith; Ungar, Wendy J.; Mendoza-Londona, Roberto; Bernier, Francois P.; Boycott, Kym M.; Marshall, Deborah A.
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Association of Plasma Hemoglobin A1c with Improvement of Cognitive Functions by Probiotic Bifidobacterium breve Supplementation in Healthy Adults with Mild Cognitive Impairment
errJOURNAL OF ALZHEIMERS DISEASE
IF3.1
err2021-05-18
err15
errOAAI
errBernier, Francois; Ohno, Kazuya; Katsumata, Noriko; Shimizu, Takashi; Xiao, Jinzhong
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Effects of prenatal exposure and co-exposure to metallic or metalloid elements on early infant neurodevelopmental outcomes in areas with small-scale gold mining activities in Northern Tanzania
errENVIRONMENT INTERNATIONAL
IF9.7
err2021-04-01
err30
errOAAI
errNyanza, Elias C.; Bernier, Francois P.; Martin, Jonathan W.; Manyama, Mange; Hatfield, Jennifer; Dewey, Deborah
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(Un)standardized testing: the diagnostic odyssey of children with rare genetic disorders in Alberta, Canada
errGENETICS IN MEDICINE
IF6.2
err2021-02-01
err21
errOAAI
errMichaels-Igbokwe, Christine; McInnes, Brenda; MacDonald, Karen V.; Currie, Gillian R.; Omar, Fadya; Shewchuk, Brittany; Bernier, Francois P.; Marshall, Deborah A.
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Research Directions

No research directions
Co-authors
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