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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1965 1
1966 1
1969 3
1970 3
1973 1
1974 3
1977 3
1978 1
1979 1
1982 1
1990 1
1991 1
1995 1
1997 1
2000 1
2004 1
2008 1
2010 3
2012 3
2013 1
2014 6
2015 3
2016 5
2017 6
2018 2
2019 5
2020 3
2021 6
2022 3
2023 7
2024 2

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77 results

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Page 1
Familial aggregation of seizure outcomes in four familial epilepsy cohorts.
Ellis CA, Tu D, Oliver KL, Mefford HC, Hauser WA, Buchhalter J, Epstein MP, Cao Q; EPGP Consortium; Epi4K Consortium; Berkovic SF, Ottman R. Ellis CA, et al. Among authors: oliver kl. Epilepsia. 2024 May 13. doi: 10.1111/epi.18004. Online ahead of print. Epilepsia. 2024. PMID: 38738647
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic Architecture.
Harris RV, Oliver KL, Perucca P, Striano P, Labate A, Riva A, Grinton BE, Reid J, Hutton J, Todaro M, O'Brien TJ, Kwan P, Sadleir LG, Mullen SA, Dazzo E, Crompton DE, Scheffer IE, Bahlo M, Nobile C, Gambardella A, Berkovic SF. Harris RV, et al. Among authors: oliver kl. Ann Neurol. 2023 Nov;94(5):825-835. doi: 10.1002/ana.26765. Epub 2023 Aug 31. Ann Neurol. 2023. PMID: 37597255 Free PMC article.
Recognition and epileptology of protracted CLN3 disease.
Cameron JM, Damiano JA, Grinton B, Carney PW, McKelvie P, Silbert P, Lawn N, Scheffer IE, Oliver KL, Hildebrand MS, Berkovic SF. Cameron JM, et al. Among authors: oliver kl. Epilepsia. 2023 Jul;64(7):1833-1841. doi: 10.1111/epi.17616. Epub 2023 Apr 27. Epilepsia. 2023. PMID: 37039534 Free PMC article.
IRF2BPL: A new genotype for progressive myoclonus epilepsies.
Costa C, Oliver KL, Calvello C, Cameron JM, Imperatore V, Tonelli L, Colavito D, Franceschetti S, Canafoglia L, Berkovic SF, Prontera P. Costa C, et al. Among authors: oliver kl. Epilepsia. 2023 Aug;64(8):e164-e169. doi: 10.1111/epi.17557. Epub 2023 Mar 9. Epilepsia. 2023. PMID: 36810721
Genes4Epilepsy: An epilepsy gene resource.
Oliver KL, Scheffer IE, Bennett MF, Grinton BE, Bahlo M, Berkovic SF. Oliver KL, et al. Epilepsia. 2023 May;64(5):1368-1375. doi: 10.1111/epi.17547. Epub 2023 Mar 9. Epilepsia. 2023. PMID: 36808730 Free PMC article.
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk.
Oliver KL, Trivisano M, Mandelstam SA, De Dominicis A, Francis DI, Green TE, Muir AM, Chowdhary A, Hertzberg C, Goldhahn K, Metreau J, Prager C, Pinner J, Cardamone M, Myers KA, Leventer RJ, Lesca G, Bahlo M, Hildebrand MS, Mefford HC, Kaindl AM, Specchio N, Scheffer IE. Oliver KL, et al. Epilepsia. 2023 May;64(5):1351-1367. doi: 10.1111/epi.17542. Epub 2023 Mar 11. Epilepsia. 2023. PMID: 36779245 Free PMC article.
Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability.
Francis DI, Stark Z, Scheffer IE, Tan TY, Murali K, Gallacher L, Amor DJ, Goel H, Downie L, Stutterd CA, Krzesinski EI, Vasudevan A, Oertel R, Petrovic V, Boys A, Wei V, Burgess T, Dun K, Oliver KL, Baxter A, Hackett A, Ayres S, Lunke S, Kalitsis P, Wall M. Francis DI, et al. Among authors: oliver kl. Eur J Hum Genet. 2023 May;31(5):521-525. doi: 10.1038/s41431-022-01232-5. Epub 2022 Nov 29. Eur J Hum Genet. 2023. PMID: 36446895 Free PMC article.
A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure.
Grinton BE, Robertson E, Fearnley LG, Scheffer IE, Marson AG, O'Brien TJ, Pickrell WO, Rees MI, Sisodiya SM, Balding DJ, Bennett MF, Bahlo M, Berkovic SF, Oliver KL. Grinton BE, et al. Among authors: oliver kl. Am J Hum Genet. 2022 Nov 3;109(11):2080-2087. doi: 10.1016/j.ajhg.2022.10.004. Epub 2022 Oct 25. Am J Hum Genet. 2022. PMID: 36288729 Free PMC article.
77 results