Articles dans des revues avec comité de lecture (50)
12.
Chomette, L., Migeotte, I., Dewachter, C., Vachiery, J.-L., Smits, G., & Bondue, A. (2022). Early-onset and severe pulmonary arterial hypertension due to a novel compound heterozygous association of rare VHL mutations: A case report and review of existing data. Pulmonary circulation, 12(2), e12052. doi:10.1002/pul2.1205213.
Nahaboo, W., Eski, S. E., Despin-Guitard, E., Vermeersch, M., Versaevel, M., Saykali, B., Monteyne, D., Gabriele, S., Magin, T. M., Schwarz, N., Leube, R. E., Zwijsen, A., Perez-Morga, D., Singh, S. P., & Migeotte, I. (2022). Keratin filaments mediate the expansion of extra-embryonic membranes in the post-gastrulation mouse embryo. EMBO journal, 41(7), e108747. doi:10.15252/embj.202110874716.
Bourlard, L., Manigart, Y., donner, C., Smits, G., Désir, J., Migeotte, I., & Pichon, B. (2021). Rarity of fetal cells in exocervical samples for noninvasive prenatal diagnosis. Journal of perinatal medicine. doi:10.1515/jpm-2021-029117.
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.2021.09.01618.
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/JCI15238620.
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.2419921.
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.14449922.
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.abd4570