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Page 1
Antiepileptic Drug Teratogenicity and De Novo Genetic Variation Load.
Perucca P, Anderson A, Jazayeri D, Hitchcock A, Graham J, Todaro M, Tomson T, Battino D, Perucca E, Ferri MM, Rochtus A, Lagae L, Canevini MP, Zambrelli E, Campbell E, Koeleman BPC, Scheffer IE, Berkovic SF, Kwan P, Sisodiya SM, Goldstein DB, Petrovski S, Craig J, Vajda FJE, O'Brien TJ; EpiPGX and EPIGEN Consortia. Perucca P, et al. Among authors: sisodiya sm. Ann Neurol. 2020 Jun;87(6):897-906. doi: 10.1002/ana.25724. Epub 2020 Apr 15. Ann Neurol. 2020. PMID: 32215971
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: sisodiya sm. Ann Neurol. 2003 May;53(5):658-63. doi: 10.1002/ana.10576. Ann Neurol. 2003. PMID: 12731001
Genetics of drug resistance in epilepsy.
Sisodiya SM. Sisodiya SM. Curr Neurol Neurosci Rep. 2005 Jul;5(4):307-11. doi: 10.1007/s11910-005-0076-2. Curr Neurol Neurosci Rep. 2005. PMID: 15987615 Review.
A pharmacogenetic exploration of vigabatrin-induced visual field constriction.
Kinirons P, Cavalleri GL, Singh R, Shahwan A, Acheson JF, Wood NW, Goldstein DB, Sisodiya SM, Doherty CP, Delanty N. Kinirons P, et al. Among authors: sisodiya sm. Epilepsy Res. 2006 Aug;70(2-3):144-52. doi: 10.1016/j.eplepsyres.2006.03.012. Epub 2006 May 3. Epilepsy Res. 2006. PMID: 16675198
Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutation.
Sisodiya SM, Thompson PJ, Need A, Harris SE, Weale ME, Wilkie SE, Michaelides M, Free SL, Walley N, Gumbs C, Gerrelli D, Ruddle P, Whalley LJ, Starr JM, Hunt DM, Goldstein DB, Deary IJ, Moore AT. Sisodiya SM, et al. J Med Genet. 2007 Jun;44(6):373-80. doi: 10.1136/jmg.2006.047407. Epub 2007 Jan 19. J Med Genet. 2007. PMID: 17237123 Free PMC article. Clinical Trial.
398 results