Parties d'ouvrages collectifs (1)
  1. 1. Gosse, C., Zhao, X., Migeotte, I., Suárez-Boomgaard, D., Hue, I., Degrelle, S., Perea-Gomez, A., & Mazari, E. (2017). The use of electroporation in developmental biology. In Handbook of Electroporation (pp. 1375-1409). Springer International Publishing. doi:10.1007/978-3-319-32886-7_139
    2.   Articles dans des revues avec comité de lecture (50)
  2. 1. Neuens, S., Soblet, J., Penninckx, A., Detry, C., Badoer, C., Desmyter, L., Peyrassol, X., Wilkin, F., Busson, A., Bruneau, M., Grenet, M.-L., Le Morillon, A., Aeby, A., Deconinck, N., Prigogine, C., Monier, A., Juvené, E., Balfroid, T., Van Hecke, A., Christiaens, F., Depondt, C., Brachet, C., Delvenne, V., Lufin, N., Bouysran, Y., Kammoun, M., Daneels, D., Caljon, B., Croes, D., Olsen, C., Van Dooren, S., Migeotte, I., Vandernoot, I., Marangoni, M., Coppens, S., Smits, G., & Vilain, C. (2025). Diagnostic yield of clinical exome sequencing in 868 children with neurodevelopmental disorders. European journal of medical genetics, 105030. doi:10.1016/j.ejmg.2025.105030
  3. 2. Nehme, E., Panda, A., Migeotte, I., & Pasque, V. (2025). Extra-embryonic mesoderm during development and in in vitro models. Development, 152(5), dev204624. doi:10.1242/dev.204624
  4. 3. Despin-Guitard, E., Rosa, V. S., Plunder, S., Mathiah, N., Van Schoor, K., Nehme, E., Merino-Aceituno, S., Egea, J., Shahbazi, M. N., Theveneau, E., & Migeotte, I. (2024). Non-apical mitoses contribute to cell delamination during mouse gastrulation. Nature communications, 15(1), 7364. doi:10.1038/s41467-024-51638-6
  5. 4. Van Schoor, K., Bruet, E., Jones, E. A. V., & Migeotte, I. (2024). Origin and flow-mediated remodeling of the murine and human extraembryonic circulation systems. Frontiers in physiology, 15, 1395006. doi:10.3389/fphys.2024.1395006
  6. 5. Matuozzo, D., Migeotte, I., Dauby, N., Goffard, J.-C., Vandernoot, I., et al. (2023). Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Genome medicine, 15(1), 22. doi:10.1186/s13073-023-01173-8
  7. 6. Masahiro, K., Migeotte, I., Tiembe, N., Goffard, J.-C., et al. (2023). A second update on mapping the human genetic architecture of COVID-19. Nature (London), 621(7977), 7-26. doi:10.1038/s41586-023-06355-3
  8. 7. Llucià-Carol, L., Muiño, E., Cullell, N., Cárcel-Márquez, J., Lledós, M., Gallego-Fabrega, C., Martin-Campos, J., Martí-Fàbregas, J., Aguilera-Simón, A., Planas, A. M., DeDiego, M. M., de Felipe Mimbrera, A., Masjuan, J., García-Madrona, S., Segura, T., González-Villar, E., Serrano-Heras, G., Domínguez Mayoral, A., Menéndez-Valladares, P., Montaner, J., Migeotte, I., Rahmouni, S., Darcis, G., Bernardo, D., Rojo, S., Schulte, E. C., Protzer, U., Fricke, L., Winter, C., Niemi, M. E. K., Cordioli, M., Delgado, P., & Fernández-Cadenas, I. (2023). Genetic Architecture of Ischaemic Strokes after COVID-19 Shows Similarities with Large Vessel Strokes. International journal of molecular sciences, 24(17). doi:10.3390/ijms241713452
  9. 8. Despin-Guitard, E., Quenec’Hdu, R., Nahaboo, W., Schwarz, N., Leube, R. E., Chazaud, C., & Migeotte, I. (2022). Regionally specific levels and patterns of keratin 8 expression in the mouse embryo visceral endoderm emerge upon anterior-posterior axis determination. Frontiers in Cell and Developmental Biology, 10. doi:10.3389/fcell.2022.1037041
  10. 9. Campbell, T. M., Liu, Z., Zhang, Q., Moncada-Velez, M., Covill, L. L., Zhang, P., Darazam, I. A., Bastard, P., Bizien, L., Bucciol, G., Enoksson, S. L., Jouanguy, E., Karabela, Ş. N., Khan, T., Kendir-Demirkol, Y., Arias, A. A., Mansouri, D., Marits, P., Marr, N., Migeotte, I., Moens, L., Ozcelik, T., Pellier, I., Sendel, A., Shahrooei, M., Edvard Smith, C. I. E. C., Vandernoot, I., Willekens, K., Bergman, P., Abel, L., Cobat, A., Casanova, J.-L., Meyts, I., & Bryceson, Y. T. (2022). Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency. The Journal of experimental medicine, 219(7), e20220202. doi:10.1084/jem.20220202
  11. 10. Meunier, A., Zanlonghi, X., Roux, A. F., Fils, J. F., Caspers, L., Migeotte, I., Abramowicz, M., & Meunier, I. (2022). Natural history of Usher type 2 with the c.2299delG mutation of USH2A in a large cohort. Ophthalmic genetics. doi:10.1080/13816810.2022.2051191
  12. 11. Cruz, R., Bouysran, Y., Migeotte, I., et al. (2022). Novel genes and sex differences in COVID-19 severity. Human molecular genetics, 1-18. doi:10.1093/hmg/ddac132
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