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  2. 2. Depondt, C. (2009). Pharmacogenetics in Neurological Diseases. In M. Ritsner (Ed.), Neuropsychiatric Biomarkers, Endophenotypes, and Genes. Willey Sciences.
  3. 3. Depondt, C. (2008). Pharmacogenomics applications in epilepsy. In N. Cohen (Ed.), Pharmacogenomics and Personalized Medicine. Humana Press.
  4. 4. Depondt, C. (2008). Epilepsies due to monogenic disorders of metabolism. In S. Shorvon & T. Pedley (Eds.), The Epilepsies. Elsevier.(Blue Books of Neurology).
  5. 5. Pandolfo, M., & Depondt, C. (2007). Friedreich's Ataxia and Related DNA Loss-of-Function Disorders. In Molecular Neurology (pp. 277-294). Elsevier Inc. doi:10.1016/B978-012369509-3.50020-2
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  6. 1. Taylor, C., Tudur‐Smith, C., Dixon, P., Linehan, C., Gunko, A., Christensen, J., Pearson, M., Tomson, T., Marson, A. G., Trinka, E., Visee, H., Depondt, C., Santos, S. F., Van Dycke, A., Van Paesschen, W., Conway, C., O’Rourke, G., Flynn, C., McCarthy, A., Cunningham, D., Wakai, A., Petricevic, M., Costello, D., Zelano, J., Al‐Jasami, F., Melin, S., Berglund, M., Bergstrom, L., Vall, V., Rouhl, R. R., Dingli, N., Rheims, S., Tazarourte, K., Tyvaert, L., Derambure, P., Girot, M., Marchal, C., Kolstad, E., Jahr, S. H., Bo, S. H., Samsonsen, C., Kalvianen, R., Mazurkiewicz‐Beldzinska, M., Kaymovskiy, I., Ryvlin, P., Wisiewski, I., Bader, C., Podewils, F. V., Knake, S., Menzler, K., Hirsch, M., Brich, J., Surges, R., Dague, K. O., Wehner, T., Strzelczyk, A., Kay, L., Miklic, L., Kimiskidis, V., Spilioti, M., Afrantou, T., Terzoudi, A., Kazis, D., Markoula, S., Markou, K., Papacostas, S., & Christou, Y. P. (2022). Care in Europe after presenting to the emergency department with a seizure; position paper and insights from the European Audit of Seizure Management in Hospitals. European journal of neurology, 29(7), 1873-1884. doi:10.1111/ene.15336
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  8. 3. Koko, M., Depondt, C., et al. (2022). Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. Epilepsia, 63(3), 723-735. doi:10.1111/epi.17166
  9. 4. Stanley, K., Hostyk, J., Tran, L. T., Amengual‐Gual, M., Dugan, P., Clark, J., Choi, H., Tchapyjnikov, D., Perucca, P., Fernandes, C., Andrade, D., Devinsky, O. I., Cavalleri, G. L., Depondt, C., Sen, A., O'Brien, T., Heinzen, E., Loddenkemper, T., Goldstein, D. B., Mikati, M. A., & Delanty, N. (2022). Genomic analysis of “microphenotypes” in epilepsy. American journal of medical genetics. Part A, 188(1), 138-146. doi:10.1002/ajmg.a.62505
  10. 5. Damien, C., Cissé, F. A., Depondt, C., Rikir, E., Legros, B., & Gaspard, N. (2021). Duration of nonconvulsive seizures in critically ill patients. Epilepsy & behavior, 124, 108312. doi:10.1016/j.yebeh.2021.108312
  11. 6. Motelow, J. E., & Depondt, C. (2021). Correction: Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals. American journal of human genetics, 108(10), 2024. doi:10.1016/j.ajhg.2021.08.008
  12. 7. Koko, M., Depondt, C., et al. (2021). Distinct gene-set burden patterns underlie common generalized and focal epilepsies. EBioMedicine, 72, 103588. doi:10.1016/j.ebiom.2021.103588
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