Clinical Associate Professor of Neurology
[email protected]
Available to mentor
Simon M Glynn, MD
Clinical Associate Professor
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Epi4K Consortium . Epilepsia, 2024 Mar; 65 (3): 792 - 804.Journal ArticleThe role of copy number variants in the genetic architecture of common familial epilepsies.
DOI:10.1111/epi.17860 PMID: 38101940 -
Pellinen J, Pardoe H, Sillau S, Barnard S, French J, Knowlton R, Lowenstein D, Cascino GD, Glynn S, Jackson G, Szaflarski J, Morrison C, Meador KJ, Kuzniecky R, Human Epilepsy Project Investigators . Epilepsia, 2023 Oct; 64 (10): 2761 - 2770.Journal ArticleLater onset focal epilepsy with roots in childhood: Evidence from early learning difficulty and brain volumes in the Human Epilepsy Project.
DOI:10.1111/epi.17727 PMID: 37517050 -
Kanner AM, Saporta AS, Kim DH, Barry JJ, Altalib H, Omotola H, Jette N, O'Brien TJ, Nadkarni S, Winawer MR, Sperling M, French JA, Abou-Khalil B, Alldredge B, Bebin M, Cascino GD, Cole AJ, Cook MJ, Detyniecki K, Devinsky O, Dlugos D, Faught E, Ficker D, Fields M, Gidal B, Gelfand M, Glynn S, Halford JJ, Haut S, Hegde M, Holmes MG, Kalviainen R, Kang J, Klein P, Knowlton RC, Krishnamurthy K, Kuzniecky R, Kwan P, Lowenstein DH, Marcuse L, Meador KJ, Mintzer S, Pardoe HR, Park K, Penovich P, Singh RK, Somerville E, Szabo CA, Szaflarski JP, Lin Thio KL, Trinka E, Burneo JG, Human Epilepsy Project . Neurology, 2023 Mar 14; 100 (11): e1123 - e1134.Journal ArticleMood and Anxiety Disorders and Suicidality in Patients With Newly Diagnosed Focal Epilepsy: An Analysis of a Complex Comorbidity.
DOI:10.1212/WNL.0000000000201671 PMID: 36539302 -
Terman SW, O'Kula SS, Asmar MM, Davis KA, Gazzola DM, Lesanu R, George L, Selwa LM, Glynn SM, Hill CE. Epilepsy Behav, 2022 Dec; 137 (Pt A): 108947Journal ArticleInpatient long-term video-electroencephalographic monitoring event capture audiovisual diagnostic quality.
DOI:10.1016/j.yebeh.2022.108947 PMID: 36274332 -
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 . Epilepsia, 2022 Mar; 63 (3): 723 - 735.Journal ArticleAssociation of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study.
DOI:10.1111/epi.17166 PMID: 35032048 -
Stovall T, Hunt B, Glynn S, Stacey WC, Gliske SV. Brain Commun, 2021 3 (3): fcab188Journal ArticleInterictal high frequency background activity as a biomarker of epileptogenic tissue.
DOI:10.1093/braincomms/fcab188 PMID: 34704026 -
Epilepsy Phenome/Genome Project, Epi4K Consortium . Epilepsia, 2021 Apr; 62 (4): 973 - 983.Journal ArticleDiverse genetic causes of polymicrogyria with epilepsy.
DOI:10.1111/epi.16854 PMID: 33818783 -
Project EPG, Consortium E. Epilepsia, 2021 Apr 1; 64 (4): 973 - 983.Journal ArticleDiverse genetic causes of polymicrogyria with epilepsy
