Articles dans des revues avec comité de lecture (112)
  1. 32. Niestroj, L.-M., Depondt, C., Epi25 Collaborative,, et al. (2020). Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects. Brain.
  2. 33. Wolking, S., Moreau, C., Nies, A. A., Schaeffeler, E., McCormack, M., Auce, P., Avbersek, A., Becker, F., Krenn, M., Møller, R. S., Nikanorova, M., Weber, Y. Y., Weckhuysen, S., Cavalleri, G., Delanty, N., Depondt, C., Johnson, M., Koeleman, B., Kunz, W. W., Marson, A. G., Sander, L. J., Sills, G., Striano, P., Zara, F., Zimprich, F., Schwab, M., Krause, R., Sisodiya, S., Cossette, P., Girard, S. S., & Lerche, H. (2020). Testing association of rare genetic variants with resistance to three common antiseizure medications. Epilepsia, 61(4), 657-666. doi:10.1111/epi.16467
  3. 34. Wolking, S., Schulz, H., Nies, A. A., McCormack, M., Schaeffeler, E., Auce, P., Avbersek, A., Becker, F., Klein, K. M., Krenn, M., Møller, R. S., Nikanorova, M., Weckhuysen, S., Consortium, E. P., Cavalleri, G., Delanty, N., Depondt, C., Johnson, M., Koeleman, B., Kunz, W. W., Marson, A. G., Sander, J. W., Sills, G., Striano, P., Zara, F., Zimprich, F., Weber, Y. Y., Krause, R., Sisodiya, S., Schwab, M., Sander, T., & Lerche, H. (2020). Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study. Pharmacogenomics, 21(5), 325-335. doi:10.2217/pgs-2019-0179
  4. 35. Grasby, K., Depondt, C., & et, A. (2020). The genetic architecture of the human cerebral cortex. Science, 367.
  5. 36. Thorpe, J., Ashby, S., Hallab, A., Ding, D., Andraus, M., Dugan, P., Perucca, P., Costello, D., French, J. J., O'Brien, T. J., Depondt, C., Andrade, D., Sengupta, R., Delanty, N., Jette, N., Newton, C. C., Brodie, M. J., Devinsky, O. I., Helen Cross, J., Sander, J. W., Hanna, J., & Sen, A. (2020). Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study. Epilepsy & behavior., 107658. doi:10.1016/j.yebeh.2020.107658
  6. 37. Leu, C., Depondt, C., Epi25 Collaborative,, et al. (2019). Polygenic burden in focal and generalized epilepsies. Brain.
  7. 38. Satizabal, C., Depondt, C., et al. (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. Nature genetics.
  8. 39. Silvennoinen, K., Depondt, C., Brodie, M. J., Chinthapalli, K., de Haan, G. J., Doherty, C. P., Heavin, S., McCormack, M., Petrovski, S., Sargsyan, N., Slattery, L., & Willis, J. (2019). Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy. Epilepsia Open, 4(3), 420-430. doi:10.1002/epi4.12349
  9. 40. Heavin, S., McCormack, M., Wolking, S., Slattery, L., Walley, N., Avbersek, A., Novy, J., Sinha, S. S., Radtke, R., Doherty, C. P., Auce, P., Craig, J., Johnson, M., Koeleman, B., Krause, R., Kunz, W. W., Marson, A. G., O'Brien, T. J., Sander, J. W., Sills, G., Stefansson, H., Striano, P., Zara, F., Depondt, C., Sisodiya, S., Goldstein, D., Lerche, H., Cavalleri, G., & Delanty, N. (2019). Genomic and clinical predictors of lacosamide response in refractory epilepsies. Epilepsia Open. doi:10.1002/epi4.12360
  10. 41. Conte, F., Van Paesschen, W., Legros, B., & Depondt, C. (2019). The Epilepsy Surgery Grading Scale: Validation in an independent population with drug-resistant focal epilepsy. Epilepsia, 60(8), e78-e82. doi:10.1111/epi.16096
  11. 42. Epi25 Collaborative,, Depondt, C., et al. (2019). Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals. American journal of human genetics.
  12. 43. Berghuis, B., Stapleton, C., Sonsma, A. A., Hulst, J., de Haan, G. J., Lindhout, D., Demurtas, R., Krause, R., Depondt, C., Kunz, W. W., Zara, F., Striano, P., Craig, J., Auce, P., Marson, A. G., Stefansson, H., O'Brien, T. J., Johnson, M., Sills, G., Wolking, S., Lerche, H., Sisodiya, S., Sander, L. J., Cavalleri, G., Koeleman, B. B., & McCormack, M. (2019). A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Epilepsia Open, 4(1), 102-109. doi:10.1002/epi4.12297
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