Publications
- Chaudhari K, Zhang K, Yam P T, Zang Y, Kramer D A, Gagnon S, Schlienger S, Calabretta S Michaud J-F, Collins M, Wang J, Srour M, Chen B, Charron F, & Bashaw G J. A human DCC variant causing mirror movement disorder reveals that the WAVE regulatory complex mediates axon guidance by netrin-1-DCC. Sci. Signal.17, eadk2345(2024). DOI:10.1126/scisignal.adk2345
- Hutchinson M L C, St-Onge J, Schlienger S, Boudrahem-Addour N, Mougharbel ., Michaud J F, Lloyd C, Bruneau E, Roux C, Sahly A N, Osterman B, Myers K A, Rouleau G A, Jimenez Cruz D A, Rivière J B, Accogli A, Charron F, & Srour M. (2024). Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals. Movement Disorders: official journal of the Movement Disorder Society, 39(2), 400–410. https://doi.org/10.1002/mds.29669
- Accogli A, Hutchinson M L C, Krochmalnek E, St-Onge J, Boudrahem-Addour N, Rivière J-B, Joober R, Srour M, Trakadis Y. Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing. Psychiatry Research Case Reports. 2023 Oct 20; 100189. https://doi.org/10.1016/j.psycr.2023.100189
- Collins M, Krochmalnek E, Alsubhi S, Srour M. Teaching NeuroImages: CLOVES Syndrome. Neurology. 2021 Mar 9;96(10):e1487-e1488. doi: 10.1212/WNL.0000000000010856. Epub 2020 Dec 1. PMID: 33262231; PMCID: PMC8055316.
- Collins M, Miranda V, Rousseau J, Kratz LE, Campeau PM. A homozygous variant in the Lamin B receptor gene LBR results in a non-lethal skeletal dysplasia without Pelger-Huët anomaly. Bone. 2020 Dec;141:115601. doi: 10.1016/j.bone.2020.115601. Epub 2020 Aug 19. PMID: 32827848.
Professional Meeting & Conferences/Abstracts Presented
- Collins M, Wang M, Guyot M-C, St-Onge J, Boudrahem-Addour N, Kibar Z, Srour M. “Genetics and Mechanisms of Congenital Mirror Movements." Poster presented at: Congrès provincial de la recherche Mère-Enfant (Quebec Provincial Mother-Child Research Conference); May 17, 2019; Montréal, QC, Canada.