Articles dans des revues avec comité de lecture (45)
12.
Marangoni, M., Smits, G., Ceysens, G., Costa, E., Coulon, R., Daelemans, C., De Coninck, C., Derisbourg, S., Gajewska, K., Garofalo, G., Gounongbe, C., Guizani, M., Holoye, A., Houba, C., Makhoul, J., Norgaard, C., Regnard, C., Romée, S., Soto, J., Stagel-Trabbia, A., Van Rysselberge, M., Vercoutere, A., Zaytouni, S., Bouri, S., D'Haene, N., D'Onle, D., Dugauquier, C., Racu, M.-L., Rocq, L., Segers, V., Verocq, C., Avni, E. F., Cassart, M., Massez, A., Blaumeiser, B., Brischoux-Boucher, E., Bulk, S., De Ravel, T., Debray, F.-G., Dimitrov, B., Janssens, S., Keymolen, K., Laterre, M., van Berkel, K., Van Maldergem, L., Vandernoot, I., Vilain, C., donner, C., Tecco, L., Thomas, D., Désir, J., Abramowicz, M., & Migeotte, I. (2021). Implementation of fetal clinical exome sequencing: Comparing prospective and retrospective cohorts. Genetics in medicine. doi:10.1016/j.gim.2021.09.01614.
Nakanishi, T. T., Pigazzini, S., Degenhardt, F., Cordioli, M., Butler-Laporte, G., Maya-Miles, D., Bujanda, L., Bouysran, Y., Niemi, M. E., Palom, A., Ellinghaus, D., Khan, A., Martínez-Bueno, M., Rolker, S., Amitrano, S., Roade Tato, L., Fava, F., Spinner, C. D., Prati, D., Bernardo, D., Garcia, F., Darcis, G., Fernandez-Cadenas, I., Holter, J. C., Banales, J. M., Frithiof, R., Kiryluk, K., Duga, S., Asselta, R., Pereira, A. C., Romero-Gómez, M., Nafría-Jiménez, B., Hov, J. R., Migeotte, I., Renieri, A., Planas, A. M., Ludwig, K. U., Buti, M., Rahmouni, S., Alarcón-Riquelme, M. M., Schulte, E. C., Franke, A., Karlsen, T. H., Valenti, L., Zeberg, H., Richards, J. B., & Ganna, A. (2021). Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. The Journal of clinical investigation. doi:10.1172/JCI15238615.
Dhooge, T., Van Damme, T., Syx, D., Mosquera, L. M., Nampoothiri, S., Radhakrishnan, A., Simsek-Kiper, P. Ö. P., Utine, G. E., Bonduelle, M., Migeotte, I., Essawi, O., Ceylaner, S., Al Kindy, A., Tinkle, B., Symoens, S., & Malfait, F. (2021). More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome. Human mutation. doi:10.1002/humu.2419916.
Khan, T., Rahman, M., Al Ali, F., Huang, S. S., Ata, M., Zhang, Q., Bastard, P., Liu, Z., Jouanguy, E., Beziat, V., Cobat, A., Nasrallah, G. K., Yassine, H. H., Smatti, M. M., Saeed, A., Vandernoot, I., Goffard, J.-C., Smits, G., Migeotte, I., Haerynck, F., Meyts, I., Abel, L., Casanova, J.-L., Hasan, M. R., & Marr, N. (2021). Distinct antibody repertoires against endemic human coronaviruses in children and adults. JCI insight. doi:10.1172/jci.insight.14449917.
Zhang, Q., Vandernoot, I., Goffard, J.-C., Smits, G., Migeotte, I., et al. (2020). Inborn errors of type I IFN immunity in patients with life-threatening COVID-19. Science (New York, N.Y.), 370(6515). doi:10.1126/science.abd457019.
Mathiah, N., Despin-Guitard, E., Stower, M., Nahaboo, W., Eski, S. E., Singh, S. P., Srinivas, S., & Migeotte, I. (2020). Asymmetry in the frequency and position of mitosis in the mouse embryo epiblast at gastrulation. EMBO reports, e50944. doi:10.15252/embr.20205094420.
Kyprianou, C., Christodoulou, N., Hamilton, R. S., Nahaboo, W., Suárez-Boomgaard, D., Amadei, G., Migeotte, I., & Zernicka-Goetz, M. (2020). Basement membrane remodelling regulates mouse embryogenesis. Nature (London), 582(7811), 253-258. doi:10.1038/s41586-020-2264-221.
Delavallée, L., Mathiah, N., Cabon, L., Mazeraud, A., Brunelle-Navas, M.-N., Lerner, L. L., Tannoury, M., Prola, A., Moreno-Loshuertos, R., Baritaud, M., Vela, L., Garbin, K., Garnier, D., Lemaire, C., Langa-Vives, F., Cohen-Salmon, M., Fernández-Silva, P., Chretien, F., Migeotte, I., & Susin, S. A. (2020). Mitochondrial AIF loss causes metabolic reprogramming, caspase-independent cell death blockade, embryonic lethality, and perinatal hydrocephalus. Molecular metabolism, 40, 101027. doi:10.1016/j.molmet.2020.10102722.
Meerschaut, I., De Coninck, S., Steyaert, W., Barnicoat, A., Bayat, A., Benedicenti, F., Berland, S., Blair, E. M., Breckpot, J., de Burca, A., Destrée, A., García-Miñaúr, S., Green, A. J., Hanna, B. C., Keymolen, K., Koopmans, M., Lederer, D., Lees, M., Longman, C., Lynch, S. A., Male, A. M., McKenzie, F., Migeotte, I., Mihci, E., Nur, B., Petit, F., Piard, J., Plasschaert, F. F., Rauch, A., Ribai A Nyam, P., Pacheco, I. S., Stanzial, F., Stolte-Dijkstra, I., Valenzuela, I., Varghese, V., Vasudevan, P. C., Wakeling, E. L., Wallgren-Pettersson, C., Coucke, P., De Paepe, A., De Wolf, D., Symoens, S., & Callewaert, B. (2019). A clinical scoring system for congenital contractural arachnodactyly. Genetics in medicine. doi:10.1038/s41436-019-0609-823.
Saykali, B., Nahaboo, W., Mathiah, N., Racu, M.-L., Defrance, M., & Migeotte, I. (2019). Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo. eLife, 8, e42434. doi:10.7554/eLife.42434.001