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Role of SOX2 mutations in human hippocampal malformations and epilepsy.
Sisodiya SM, Ragge NK, Cavalleri GL, Hever A, Lorenz B, Schneider A, Williamson KA, Stevens JM, Free SL, Thompson PJ, van Heyningen V, Fitzpatrick DR. Sisodiya SM, et al. Among authors: stevens jm. Epilepsia. 2006 Mar;47(3):534-42. doi: 10.1111/j.1528-1167.2006.00464.x. Epilepsia. 2006. PMID: 16529618 Free article.
Polymicrogyria and absence of pineal gland due to PAX6 mutation.
Mitchell TN, Free SL, Williamson KA, Stevens JM, Churchill AJ, Hanson IM, Shorvon SD, Moore AT, van Heyningen V, Sisodiya SM. Mitchell TN, et al. Among authors: stevens jm. Ann Neurol. 2003 May;53(5):658-63. doi: 10.1002/ana.10576. Ann Neurol. 2003. PMID: 12731001
Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32.
Angelicheva D, Tournev I, Guergueltcheva V, Mihaylova V, Azmanov DN, Morar B, Radionova M, Smith SJ, Zlatareva D, Stevens JM, Kaneva R, Bojinova V, Carter K, Brown M, Jablensky A, Kalaydjieva L, Sander JW. Angelicheva D, et al. Among authors: stevens jm. Epilepsia. 2009 Jul;50(7):1679-88. doi: 10.1111/j.1528-1167.2009.02066.x. Epub 2009 Mar 23. Epilepsia. 2009. PMID: 19400876 Free article.
How broad is the phenotype of Hallervorden-Spatz disease?
Hickman SJ, Ward NS, Surtees RA, Stevens JM, Farmer SF. Hickman SJ, et al. Among authors: stevens jm. Acta Neurol Scand. 2001 Mar;103(3):201-3. doi: 10.1034/j.1600-0404.2001.103003201.x. Acta Neurol Scand. 2001. PMID: 11240570
Identifying general reaction conditions by bandit optimization.
Wang JY, Stevens JM, Kariofillis SK, Tom MJ, Golden DL, Li J, Tabora JE, Parasram M, Shields BJ, Primer DN, Hao B, Del Valle D, DiSomma S, Furman A, Zipp GG, Melnikov S, Paulson J, Doyle AG. Wang JY, et al. Among authors: stevens jm. Nature. 2024 Feb;626(8001):1025-1033. doi: 10.1038/s41586-024-07021-y. Epub 2024 Feb 28. Nature. 2024. PMID: 38418912
368 results