Articles dans des revues avec comité de lecture (110)
  1. 68. Depondt, C. (2013). Pharmacogénétique de l'épilepsie - Science ou fiction ? MS. Médecine sciences, 29(2), 189-193. doi:10.1051/medsci/2013292017
  2. 69. Kasperavičiūtė, D., Pandolfo, M., Depondt, C., et al. (2013). Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Brain, 136, 2040-2050. doi:10.1093/brain/awt233
  3. 70. Hitomi, Y., Heinzen, E. L., Donatello, S., Dahl, H.-H., Damiano, J. A., McMahon, J. M., Berkovic, S. F., Scheffer, I. E., Legros, B., Rai, M., Weckhuysen, S., Suls, A., de Jonghe, P., Pandolfo, M., Goldstein, D. B., Van Bogaert, P., & Depondt, C. (2013). Mutations in TNK2 in severe autosomal recessive infantile-onset epilepsy. Annals of neurology, 74(3), 496-501. doi:10.1002/ana.23934
  4. 71. Chinthapalli, K., Bartolini, E., Novy, J., Suttie, M., Marini, C., Falchi, M., Fox, Z., Clayton, L. M. S., Sander, J. W., Guerrini, R., Depondt, C., Hennekam, R., Hammond, P., & Sisodiya, S. M. (2012). Atypical face shape and genomic structural variants in epilepsy. Brain, 135(Pt 10), 3101-3114. doi:10.1093/brain/aws232
  5. 72. Heinzen, E., Depondt, C., Cavalleri, G. L., Ruzzo, E. K., Walley, N. M., Need, A. C., Ge, D., He, M., Cirulli, E. T., Zhao, Q., Cronin, K. D., Gumbs, C. E., Campbell, C. R., Hong, L. K., Maia, J. M., Shianna, K. V., McCormack, M., Radtke, R. A., O'Conner, G. D., Mikati, M. A., Gallentine, W. B., Husain, A. M., Sinha, S. R., Chinthapalli, K., Puranam, R. S., McNamara, J. O., Ottman, R., Sisodiya, S. M., Delanty, N., & Goldstein, D. B. (2012). Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy. American journal of human genetics, 91(2), 293-302. doi:10.1016/j.ajhg.2012.06.016
  6. 73. Pandolfo, M., Depondt, C., & Huppke, P. (2012). Periventricular heterotopia: Identifying homogeneity among heterogeneity. Neurology. doi:10.1212/WNL.0b013e31826aad7d
  7. 74. Stein, J. L., Pandolfo, M., Depondt, C., et al. (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature genetics, 44, 552–561. doi:10.1038/ng.2250
  8. 75. McCormack, M., Urban, T. J., Shianna, K. V., Walley, N., Pandolfo, M., Depondt, C., Chaila, E., O'Conner, G. D., Kasperavičiūtė, D., Radtke, R. A., Heinzen, E., Sisodiya, S. M., Delanty, N., & Cavalleri, G. L. (2012). Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions. Pharmacogenomics, 13(4), 399-405. doi:10.2217/pgs.11.165
  9. 76. Naeije, G., Gaspard, N., Depondt, C., Pepersack, T., & Legros, B. (2012). Acute confusional state of unknown cause in the elderly: a study with continuous EEG monitoring. Epilepsy & behavior, 23(3), 330-334. doi:10.1016/j.yebeh.2012.01.023
  10. 77. Cirulli, E. T., Urban, T. J., Marino, S. E., Linney, K. N., Birnbaum, A. K., Depondt, C., Attix, D. K., Radtke, R. A., & Goldstein, D. B. (2012). Genetic and environmental correlates of topiramate-induced cognitive impairment. Epilepsia, 53(1), e5-e8. doi:10.1111/j.1528-1167.2011.03322.x
  11. 78. Cnop, M., Igoillo Esteve, M., Rai, M., Begu, A., Serroukh, Y., Depondt, C., Musuaya, A., Marhfour, I., Ladrière, L., Moles Lopez, X., Lefkaditis, D., Moore, F., Brion, J. P., Cooper, M. J., Schapira, A. H., Clark, A., Koeppen, A., Marchetti, P., Pandolfo, M., Eizirik, D. L., & Fery, F. (2012). Central role and mechanisms of beta-cell dysfunction and death in Friedreich ataxia- associated diabetes. Annals of neurology, 72(6), 971-982. doi:10.1002/ana.23698
  12. 79. Depondt, C., Godard, P., Sens Espel, R., Lopes Da Cruz, A., Lienard, P., & Pandolfo, M. (2011). A candidate gene study of antiepileptic drug tolerability and efficacy identifies an association of CYP2C9 variants with phenytoin toxicity. European journal of neurology, 18(9), 1159-1164. doi:10.1111/j.1468-1331.2011.03361.x
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