Depondt C - Search Results

1

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping.

Weale ME, Depondt C, Macdonald SJ, Smith A, Lai PS, Shorvon SD, Wood NW, Goldstein DB. Weale ME, et al. Among authors: depondt c. Am J Hum Genet. 2003 Sep;73(3):551-65. doi: 10.1086/378098. Epub 2003 Jul 29. Am J Hum Genet. 2003. PMID: 12900796 Free PMC article.

2

Diagnostic and therapeutic approaches in refractory insular epilepsy.

Feys O, Goldman S, Lolli V, Depondt C, Legros B, Gaspard N, Schuind S, De Tiège X, Rikir E. Feys O, et al. Among authors: depondt c. Epilepsia. 2023 Jun;64(6):1409-1423. doi: 10.1111/epi.17571. Epub 2023 Mar 30. Epilepsia. 2023. PMID: 36869701 Review.

3

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. Among authors: depondt c. 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.

4

The -1021C->T DBH gene variant is not associated with epilepsy or antiepileptic drug response.

Depondt C, Cock HR, Healy DG, Burley MW, Weinshenker D, Wood NW, Goldstein DB, Sisodiya SM. Depondt C, et al. Neurology. 2004 Oct 26;63(8):1497-9. doi: 10.1212/01.wnl.0000142092.16719.ad. Neurology. 2004. PMID: 15505174

5

Commentary on "A genome wide linkage disequilibrium screen in Parkinson's disease" by Foltynie et al. in J Neurol (2005) 252:597-602.

Wood NW, Healy DG, Depondt C, Abou-Sleiman PM. Wood NW, et al. Among authors: depondt c. J Neurol. 2005 May;252(5):603-4. doi: 10.1007/s00415-005-0707-1. Epub 2005 Mar 7. J Neurol. 2005. PMID: 15742113 No abstract available.

6

Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin.

Tate SK, Depondt C, Sisodiya SM, Cavalleri GL, Schorge S, Soranzo N, Thom M, Sen A, Shorvon SD, Sander JW, Wood NW, Goldstein DB. Tate SK, et al. Among authors: depondt c. Proc Natl Acad Sci U S A. 2005 Apr 12;102(15):5507-12. doi: 10.1073/pnas.0407346102. Epub 2005 Apr 1. Proc Natl Acad Sci U S A. 2005. PMID: 15805193 Free PMC article.

7

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. Among authors: depondt c. Brain. 2005 Aug;128(Pt 8):1832-40. doi: 10.1093/brain/awh524. Epub 2005 May 11. Brain. 2005. PMID: 15888540

8

Genetic association studies in epilepsy pharmacogenomics: lessons learnt and potential applications.

Depondt C, Shorvon SD. Depondt C, et al. Pharmacogenomics. 2006 Jul;7(5):731-45. doi: 10.2217/14622416.7.5.731. Pharmacogenomics. 2006. PMID: 16886898 Review.

9

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. Among authors: depondt c. Pharmacogenet Genomics. 2006 Oct;16(10):721-6. doi: 10.1097/01.fpc.0000230114.41828.73. Pharmacogenet Genomics. 2006. PMID: 17001291

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. Among authors: depondt c. 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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