Cossette P - Search Results

1

The role of copy number variants in the genetic architecture of common familial epilepsies.

Epi4K Consortium. Epi4K Consortium. Epilepsia. 2024 Mar;65(3):792-804. doi: 10.1111/epi.17860. Epub 2024 Jan 20. Epilepsia. 2024. PMID: 38101940

2

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: cossette p. PLoS One. 2023 Sep 27;18(9):e0291935. doi: 10.1371/journal.pone.0291935. eCollection 2023. PLoS One. 2023. PMID: 37756314 Free PMC article.

3

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.

International League Against Epilepsy Consortium on Complex Epilepsies. International League Against Epilepsy Consortium on Complex Epilepsies. Nat Genet. 2023 Sep;55(9):1471-1482. doi: 10.1038/s41588-023-01485-w. Epub 2023 Aug 31. Nat Genet. 2023. PMID: 37653029 Free PMC article.

4

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.

Montanucci L, Lewis-Smith D, Collins RL, Niestroj LM, Parthasarathy S, Xian J, Ganesan S, Macnee M, Brünger T, Thomas RH, Talkowski M; Epi25 Collaborative; Helbig I, Leu C, Lal D. Montanucci L, et al. Nat Commun. 2023 Jul 20;14(1):4392. doi: 10.1038/s41467-023-39539-6. Nat Commun. 2023. PMID: 37474567 Free PMC article.

5

Does Cardiorespiratory Fitness Protect Memory from Sleep Deprivation?

Ayotte B, Cristini J, Lotlikar M, Parwanta Z, Cossette P, Gasparovic L, Yee-Wong M, He QY, Doyon J, Dal Maso F, Carrier J, Steib S, Robertson EM, Roig M. Ayotte B, et al. Among authors: cossette p. Med Sci Sports Exerc. 2023 Sep 1;55(9):1632-1640. doi: 10.1249/MSS.0000000000003200. Med Sci Sports Exerc. 2023. PMID: 37379255

6

Novel NALCN variant linked to temporal lobe epilepsy.

Nguyen E, Tétreault M, Toffa DH, Cossette P, Samarut É, Nguyen DK. Nguyen E, et al. Among authors: cossette p. Am J Med Genet A. 2023 Jul;191(7):1942-1947. doi: 10.1002/ajmg.a.63209. Epub 2023 Apr 12. Am J Med Genet A. 2023. PMID: 37046053

7

Assessment of burden and segregation profiles of CNVs in patients with epilepsy.

Moreau C, Tremblay F, Wolking S, Girard A, Laprise C, Hamdan FF, Michaud JL, Minassian BA, Cossette P, Girard SL. Moreau C, et al. Among authors: cossette p. Ann Clin Transl Neurol. 2022 Jul;9(7):1050-1058. doi: 10.1002/acn3.51598. Epub 2022 Jun 8. Ann Clin Transl Neurol. 2022. PMID: 35678011 Free PMC article.

8

Usage of Genetic Panels in an Adult Epilepsy Clinic.

Li J, Toffa DH, Lefèbvre M, Tétreault M, Cossette P, Samarut É, Nguyen DK. Li J, et al. Among authors: cossette p. Can J Neurol Sci. 2023 May;50(3):411-417. doi: 10.1017/cjn.2022.49. Epub 2022 Apr 28. Can J Neurol Sci. 2023. PMID: 35478072

9

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study.

Koko M, Motelow JE, Stanley KE, Bobbili DR, Dhindsa RS, May P; Canadian Epilepsy Network; Epi4K Consortium; Epilepsy Phenome/Genome Project; EpiPGX Consortium; EuroEPINOMICS-CoGIE Consortium. Koko M, et al. Epilepsia. 2022 Mar;63(3):723-735. doi: 10.1111/epi.17166. Epub 2022 Jan 15. Epilepsia. 2022. PMID: 35032048 Free PMC article.

10

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.

Epi25 Collaborative. Electronic address: jm4279@cumc.columbia.edu; Epi25 Collaborative. Epi25 Collaborative. Electronic address: jm4279@cumc.columbia.edu, et al. Am J Hum Genet. 2021 Oct 7;108(10):2024. doi: 10.1016/j.ajhg.2021.08.008. Am J Hum Genet. 2021. PMID: 34626584 Free PMC article. No abstract available.

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