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Bi-allelic variants in MYH3 cause recessively-inherited arthrogryposis.
Morali B, Miranda V, Raelson J, Grimard G, Glavas P, Audibert F, Dumont NA, Barone J, Bamshad M, Lemyre E, Campeau PM. Morali B, et al. Among authors: grimard g. Clin Genet. 2024 Oct;106(4):483-487. doi: 10.1111/cge.14570. Epub 2024 Jun 10. Clin Genet. 2024. PMID: 38856159
Convolutional Neural Networks for Automatic Risser Stage Assessment.
Kaddioui H, Duong L, Joncas J, Bellefleur C, Nahle I, Chémaly O, Nault ML, Parent S, Grimard G, Labelle H. Kaddioui H, et al. Among authors: grimard g. Radiol Artif Intell. 2020 May 27;2(3):e180063. doi: 10.1148/ryai.2020180063. eCollection 2020 May. Radiol Artif Intell. 2020. PMID: 33937822 Free PMC article.
A Differential Hypofunctionality of Gαi Proteins Occurs in Adolescent Idiopathic Scoliosis and Correlates with the Risk of Disease Progression.
Akoume MY, Elbakry M, Veillette M, Franco A, Nada D, Labelle H, Mac-Thiong JM, Grimard G, Ouellet J, Parent S, Rivard CH, Lombardi G, Colombini A, Banfi G, Brayda-Bruno M, Gorman KF, Moreau A. Akoume MY, et al. Among authors: grimard g. Sci Rep. 2019 Jul 11;9(1):10074. doi: 10.1038/s41598-019-46325-2. Sci Rep. 2019. PMID: 31296888 Free PMC article.
72 results