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Postictal Psychosis in Epilepsy: A Clinicogenetic Study.
Ann Neurol. 2021 Sep;90(3):464-476. doi: 10.1002/ana.26174. Epub 2021 Aug 3.
Ann Neurol. 2021.
PMID: 34288049
Free PMC article.
Complex epilepsy: it's all in the history.
Silvennoinen K, Martins Custodio H, Balestrini S, Rugg-Gunn F, England Research Consortium G, Sisodiya SM.
Silvennoinen K, et al. Among authors: martins custodio h.
Pract Neurol. 2020 Oct 17:practneurol-2020-002522. doi: 10.1136/practneurol-2020-002522. Online ahead of print.
Pract Neurol. 2020.
PMID: 33070112
No abstract available.
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Climate change and epilepsy: Insights from clinical and basic science studies.
Gulcebi MI, Bartolini E, Lee O, Lisgaras CP, Onat F, Mifsud J, Striano P, Vezzani A, Hildebrand MS, Jimenez-Jimenez D, Junck L, Lewis-Smith D, Scheffer IE, Thijs RD, Zuberi SM, Blenkinsop S, Fowler HJ, Foley A; Epilepsy Climate Change Consortium; Sisodiya SM.
Gulcebi MI, et al.
Epilepsy Behav. 2021 Mar;116:107791. doi: 10.1016/j.yebeh.2021.107791. Epub 2021 Feb 10.
Epilepsy Behav. 2021.
PMID: 33578223
Free PMC article.
Review.
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Late diagnoses of Dravet syndrome: How many individuals are we missing?
Silvennoinen K, Puvirajasinghe C, Hudgell K, Sidhu MK, Martins Custodio H; Genomics England Research Consortium; Jones WD, Balestrini S, Sisodiya SM.
Silvennoinen K, et al. Among authors: martins custodio h.
Epilepsia Open. 2021 Dec;6(4):770-776. doi: 10.1002/epi4.12525. Epub 2021 Aug 5.
Epilepsia Open. 2021.
PMID: 34268891
Free PMC article.
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SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility.
Silvennoinen K, Gawel K, Tsortouktzidis D, Pitsch J, Alhusaini S, van Loo KMJ, Picardo R, Michalak Z, Pagni S, Martins Custodio H, Mills J, Whelan CD, de Zubicaray GI, McMahon KL, van der Ent W, Kirstein-Smardzewska KJ, Tiraboschi E, Mudge JM, Frankish A, Thom M, Wright MJ, Thompson PM, Schoch S, Becker AJ, Esguerra CV, Sisodiya SM.
Silvennoinen K, et al. Among authors: martins custodio h.
Acta Neuropathol. 2022 Jul;144(1):107-127. doi: 10.1007/s00401-022-02429-0. Epub 2022 May 12.
Acta Neuropathol. 2022.
PMID: 35551471
Free PMC article.
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Risk-conferring HLA variants in an epilepsy cohort: benefits of multifaceted use of whole genome sequencing in clinical practice.
Vakrinou A, Bellampalli R, Gulcebi MI, Martins Custodio H, Research Consortium GE, Balestrini S, Sisodiya SM.
Vakrinou A, et al. Among authors: martins custodio h.
J Neurol Neurosurg Psychiatry. 2023 Nov;94(11):887-892. doi: 10.1136/jnnp-2023-331419. Epub 2023 Jun 26.
J Neurol Neurosurg Psychiatry. 2023.
PMID: 37364985
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Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition.
Martins Custodio H, Clayton LM, Bellampalli R, Pagni S, Silvennoinen K, Caswell R; Genomics England Research Consortium; Brunklaus A, Guerrini R, Koeleman BPC, Lemke JR, Møller RS, Scheffer IE, Weckhuysen S, Zara F, Zuberi S, Kuchenbaecker K, Balestrini S, Mills JD, Sisodiya SM.
Martins Custodio H, et al.
Brain. 2023 Sep 1;146(9):3885-3897. doi: 10.1093/brain/awad111.
Brain. 2023.
PMID: 37006128
Free PMC article.
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