Patrick Cossette
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| Girard A, Moreau C, Michaud JL, et al. (2023) Unraveling the role of non-coding rare variants in epilepsy. Plos One. 18: e0291935 |
| Nguyen E, Tétreault M, Toffa DH, et al. (2023) Novel NALCN variant linked to temporal lobe epilepsy. American Journal of Medical Genetics. Part A |
| Cadieux-Dion M, Meneghini S, Villa C, et al. (2020) Variants in and identified in patients with insular epilepsy. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 1-25 |
| Mohamed IS, Toffa DH, Robert M, et al. (2020) Utility of magnetic source imaging in nonlesional focal epilepsy: a prospective study. Neurosurgical Focus. 48: E16 |
| Wolking S, Moreau C, Nies AT, et al. (2020) Testing association of rare genetic variants with resistance to three common antiseizure medications. Epilepsia |
| Jedličková I, Cadieux-Dion M, Přistoupilová A, et al. (2020) Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencing. European Journal of Human Genetics : Ejhg |
| Liao M, Kundap U, Rosch RE, et al. (2019) Targeted knockout of GABA receptor gamma 2 subunit provokes transient light-induced reflex seizures in zebrafish larvae. Disease Models & Mechanisms |
| Paradis C, Cadieux-Dion M, Meloche C, et al. (2019) TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia. Journal of Clinical Immunology |
| Samarut É, Swaminathan A, Riché R, et al. (2018) γ-Aminobutyric acid receptor alpha 1 subunit loss of function causes genetic generalized epilepsy by impairing inhibitory network neurodevelopment. Epilepsia |
| Monlong J, Cossette P, Meloche C, et al. (2018) Human copy number variants are enriched in regions of low mappability. Nucleic Acids Research. 46: 7236-7249 |