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Elife|November 26, 2024
Estimating dispersal rates and locating genetic ancestors with genome-wide genealogiesMatthew Osmond, Graham Coop
Biotechnology and Bioengineering|October 25, 2016
Collagen and collagen-chondroitin sulfate scaffolds with uniaxially aligned pores for the biomimetic, three dimensional culture of trabecular meshwork cellsMatthew Osmond, Sarah M Bernier, Mina B Pantcheva, et al.
Microscopy and Microanalysis : the Official Journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada|March 12, 2019
Imaging and Analysis of Cellular Locations in Three-Dimensional Tissue ModelsWarren Colomb, Matthew Osmond, Charles Durfee, et al.
The Journal of Clinical Investigation|July 26, 2011
Prolactin increases SMN expression and survival in a mouse model of severe spinal muscular atrophy via the STAT5 pathwayFaraz Farooq, Francisco Abadía Molina, Jeremiah Hadwen, et al.
ACS Applied Bio Materials|February 15, 2022
Photopolymerized Zwitterionic Hydrogels with a Sustained Delivery of Cerium Oxide Nanoparticle-miR146a Conjugate Accelerate Diabetic Wound HealingMichael A Stager, James Bardill, Alexandra Raichart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare CanadaMatthew Osmond, Taila Hartley, David A Dyment, et al.
Biorxiv : the Preprint Server for Biology|September 25, 2023
Magnetically Powered Microwheel Thrombolysis of Occlusive Thrombi in ZebrafishM Hao Hao Pontius, Chia-Jui Ku, Matthew Osmond, et al.
Child Neurology Open|November 19, 2021
Neurophysiological Characteristics of Allgrove (Triple A) Syndrome: Case Report and Literature ReviewDaniel I Weiman, Meredith K Gillespie, Taila Hartley, et al.
Human Mutation|February 15, 2022
PhenomeCentral: 7 years of rare disease matchmakingMatthew Osmond, Taila Hartley, Brittney Johnstone, et al.
American Journal of Medical Genetics. Part A|November 4, 2022
The implementation of an enhanced clinical model to improve the diagnostic yield of exome sequencing for patients with a rare genetic disease: A Canadian experienceGrace Uwaila Ediae, Gabrielle Lemire, Caitlin Chisholm, et al.
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