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Page 1
The role of common genetic variation in presumed monogenic epilepsies.
Campbell C, Leu C, Feng YA, Wolking S, Moreau C, Ellis C, Ganesan S, Martins H, Oliver K, Boothman I, Benson K, Molloy A, Brody L; Epi4K Collaborative; Genomics England Research Consortium; Michaud JL, Hamdan FF, Minassian BA, Lerche H, Scheffer IE, Sisodiya S, Girard S, Cosette P, Delanty N, Lal D, Cavalleri GL; Epi25 Collaborative. Campbell C, et al. Among authors: moreau c. EBioMedicine. 2022 Jul;81:104098. doi: 10.1016/j.ebiom.2022.104098. Epub 2022 Jun 6. EBioMedicine. 2022. PMID: 35679801 Free PMC article.
Testing association of rare genetic variants with resistance to three common antiseizure medications.
Wolking S, Moreau C, Nies AT, Schaeffeler E, McCormack M, Auce P, Avbersek A, Becker F, Krenn M, Møller RS, Nikanorova M, Weber YG, Weckhuysen S, Cavalleri GL, Delanty N, Depondt C, Johnson MR, Koeleman BPC, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Schwab M, Krause R, Sisodiya SM, Cossette P, Girard SL, Lerche H; EpiPGX Consortium. Wolking S, et al. Among authors: moreau c. Epilepsia. 2020 Apr;61(4):657-666. doi: 10.1111/epi.16467. Epub 2020 Mar 6. Epilepsia. 2020. PMID: 32141622 Free article.
Polygenic risk scores of several subtypes of epilepsies in a founder population.
Moreau C, Rébillard RM, Wolking S, Michaud J, Tremblay F, Girard A, Bouchard J, Minassian B, Laprise C, Cossette P, Girard SL. Moreau C, et al. Neurol Genet. 2020 Mar 27;6(3):e416. doi: 10.1212/NXG.0000000000000416. eCollection 2020 Jun. Neurol Genet. 2020. PMID: 32337343 Free PMC article.
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy.
Wolking S, Moreau C, McCormack M, Krause R, Krenn M; EpiPGx Consortium; Berkovic S, Cavalleri GL, Delanty N, Depondt C, Johnson MR, Koeleman BPC, Kunz WS, Lerche H, Marson AG, O'Brien TJ, Petrovski S, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Sisodiya SM, Girard SL, Cossette P. Wolking S, et al. Among authors: moreau c. Ann Clin Transl Neurol. 2021 Jul;8(7):1376-1387. doi: 10.1002/acn3.51374. Epub 2021 May 21. Ann Clin Transl Neurol. 2021. PMID: 34018700 Free PMC article.
Unraveling the role of non-coding rare variants in epilepsy.
Girard A, Moreau C, Michaud JL, Minassian B, Cossette P, Girard SL. Girard A, et al. Among authors: moreau c. PLoS One. 2023 Sep 27;18(9):e0291935. doi: 10.1371/journal.pone.0291935. eCollection 2023. PLoS One. 2023. PMID: 37756314 Free PMC article.
Fine-scale genetic structure and rare variant frequencies.
Gagnon L, Moreau C, Laprise C, Girard SL. Gagnon L, et al. Among authors: moreau c. PLoS One. 2024 Nov 5;19(11):e0313133. doi: 10.1371/journal.pone.0313133. eCollection 2024. PLoS One. 2024. PMID: 39499706 Free PMC article.
[Founder effects and genetic variability in Quebec].
Moreau C, Vézina H, Labuda D. Moreau C, et al. Med Sci (Paris). 2007 Nov;23(11):1008-13. doi: 10.1051/medsci/200723111008. Med Sci (Paris). 2007. PMID: 18021716 Free article. French.
1,087 results