Cavalleri G - Search Results

1

Postictal Psychosis in Epilepsy: A Clinicogenetic Study.

Braatz V, Martins Custodio H, Leu C, Agrò L, Wang B, Calafato S, Rayner G, Doyle MG, Hengsbach C, Bisulli F, Weber YG, Gambardella A, Delanty N, Cavalleri G, Foong J, Scheffer IE, Berkovic SF, Bramon E, Balestrini S, Sisodiya SM. Braatz V, et al. Among authors: cavalleri g. 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.

2

Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene.

Soranzo N, Cavalleri GL, Weale ME, Wood NW, Depondt C, Marguerie R, Sisodiya SM, Goldstein DB. Soranzo N, et al. Genome Res. 2004 Jul;14(7):1333-44. doi: 10.1101/gr.1965304. Epub 2004 Jun 14. Genome Res. 2004. PMID: 15197162 Free PMC article.

3

Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?

Cavalleri GL, Lynch JM, Depondt C, Burley MW, Wood NW, Sisodiya SM, Goldstein DB. Cavalleri GL, et al. Brain. 2005 Aug;128(Pt 8):1832-40. doi: 10.1093/brain/awh524. Epub 2005 May 11. Brain. 2005. PMID: 15888540

4

Vigabatrin retinopathy in an Irish cohort: lack of correlation with dose.

Kinirons P, Cavalleri GL, O'Rourke D, Doherty CP, Reid I, Logan P, Liggan B, Delanty N. Kinirons P, et al. Epilepsia. 2006 Feb;47(2):311-7. doi: 10.1111/j.1528-1167.2006.00422.x. Epilepsia. 2006. PMID: 16499754 Free article.

5

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. Epilepsia. 2006 Mar;47(3):534-42. doi: 10.1111/j.1528-1167.2006.00464.x. Epilepsia. 2006. PMID: 16529618 Free article.

6

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. 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

7

Examining the role of common genetic variation in the gamma2 subunit of the GABA(A) receptor in epilepsy using tagging SNPs.

Kinirons P, Cavalleri GL, Shahwan A, Wood NW, Goldstein DB, Sisodiya SM, Delanty N, Doherty CP. Kinirons P, et al. Epilepsy Res. 2006 Aug;70(2-3):229-38. doi: 10.1016/j.eplepsyres.2006.05.009. Epub 2006 Jun 27. Epilepsy Res. 2006. PMID: 16806831

8

A common polymorphism in the SCN1A gene associates with phenytoin serum levels at maintenance dose.

Tate SK, Singh R, Hung CC, Tai JJ, Depondt C, Cavalleri GL, Sisodiya SM, Goldstein DB, Liou HH. Tate SK, et al. Pharmacogenet Genomics. 2006 Oct;16(10):721-6. doi: 10.1097/01.fpc.0000230114.41828.73. Pharmacogenet Genomics. 2006. PMID: 17001291

9

The controversial association of ABCB1 polymorphisms in refractory epilepsy: an analysis of multiple SNPs in an Irish population.

Shahwan A, Murphy K, Doherty C, Cavalleri GL, Muckian C, Dicker P, McCarthy M, Kinirons P, Goldstein D, Delanty N. Shahwan A, et al. Epilepsy Res. 2007 Feb;73(2):192-8. doi: 10.1016/j.eplepsyres.2006.10.004. Epub 2006 Nov 27. Epilepsy Res. 2007. PMID: 17125969

10

A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy.

Cavalleri GL, Walley NM, Soranzo N, Mulley J, Doherty CP, Kapoor A, Depondt C, Lynch JM, Scheffer IE, Heils A, Gehrmann A, Kinirons P, Gandhi S, Satishchandra P, Wood NW, Anand A, Sander T, Berkovic SF, Delanty N, Goldstein DB, Sisodiya SM. Cavalleri GL, et al. Epilepsia. 2007 Apr;48(4):706-12. doi: 10.1111/j.1528-1167.2007.00977.x. Epilepsia. 2007. PMID: 17437413 Free article.

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