Participations à des congrès et colloques internationaux (21)
2.
Lenaerts, T., Gazzo, A., Daneels, D., Cilia, E., Bonduelle, M., Abramowicz, M., Van Dooren, S., & Smits, G. (2016). Exploring the variant combinations in the digenic diseases database DIDA. Proceedings of the European Conference on Computational Biology Abstract session presented at uropean Conference on Computational Biology(3-7 September 2016: Den Hague, the Netherlands)4.
Fumagalli, D., Gacquer, D., Rothé, F., Lefort, A., Libert, F., Brown, D. N., Kheddoumi, N., Shlien, A., Konopka, T., Salgado, R., Larsimont, D., Polyak, K., Willard-Gallo, K., Desmedt, C., Piccart-Gebhart, M., Abramowicz, M., Campbell, P. J., Detours, V., & Sotiriou, C. (2014). Principles governing A-to-I RNA editing in breast cancer transcriptome. SABCS online Ressources 2014 Abstract session presented at San Antonio Breast Cancer Symposium 2014(37th: Dec. 9-13, 2014: San Antonio, Tx, USA)5.
Fumagalli, D., Gacquer, D., Rothé, F., Lefort, A., Libert, F., Brown, D. N., Kheddoumi, N., Shlien, A., Konopka, T., Salgado, R., Larsimont, D., Polyak, K., Willard-Gallo, K., Desmedt, C., Piccart-Gebhart, M., Abramowicz, M., Campbell, P. J., Detours, V., & Sotiriou, C. (2014). Principles governing A-to-I RNA editing in breast cancer transcriptome. Paper session presented at San Antonio Breast Cancer Symposium (December 11, 2014: San Antonio, Tx, USA).6.
De Wilde, V., Spilleboudt, C., Racapé, J., Lewalle, P., Bron, D., Cohen, J., Maury, S., Abramowicz, M., & Le Moine, A. (2014). Long (GT)n repeat in the promoter region of heme oxygenase-1 is associated with severe graft-versus-host disease. Poster présenté à la conférence 29th General Annual Meeting Belgian Hematological Society (29: 2014).7.
Igoillo Esteve, M., Genin, A., Lambert, N., Désir, J., Pirson, I., Abdulkarim, B., Simonis, N., Drielsma, A., Marselli, L., Marchetti, P., Vanderhaeghen, P., Eizirik, D. L., Wuyts, W., Julier, C., Chakera, A. J., Ellard, S., Hattersley, A. T., & Abramowicz, M. (2013). Loss-of-function of TRMT10A causes young onset diabetes and microcephaly. Paper session presented at 23rd Meeting of the Belgian Endocrine Society (2013: Ghent, Belgium).8.
Igoillo Esteve, M., Genin, A., Lambert, N., Désir, J., Pirson, I., Abdulkarim, B., Simonis, N., Drielsma, A., Marselli, L., Marchetti, P., Vanderhaeghen, P., Eizirik, D. L., Wuyts, W., Julier, C., Chakera, A. J., Ellard, S., Hattersley, A. T., & Abramowicz, M. (2013). tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans. Paper session presented at Belgian Medical Genomics Initiative (BeMGI) Kickoff Meeting (2013: Leuven, Belgium).9.
Lemaire, A., Trepo, E., Ouziel, R., Gustot, T., Moreno, C., Degré, D., Minsart, C., De Wilde, V., Le Moine, O., Devière, J., Abramowicz, M., Le Moine, A., & Lemmers, A. (2013). (GT)N repeat genetic variant in the promoter of HO-1 is not associated to alcoholic liver disease. Paper session presented at Belgian Week of Gastroenterology (28/02/2013: Anvers).10.
Lemaire, A., Trepo, E., Ouziel, R., Gustot, T., Moreno, C., Degré, D., Minsart, C., Quertinmont, E., Vercruysse, V., De Wilde, V., Le Moine, O., Devière, J., Abramowicz, M., Le Moine, A., & Lemmers, A. (2012). (GT)n repeat genetic variant in the promoter of heme oxygenase-1 is not associated to alcoholic liver disease severity. Poster présenté à la conférence United European Gastroenterology Week (2012: Amsterdam).11.
Remiche, G., Kadhim, H., Abramowicz, M., Mavroudakis, N., Monnier, N., & Lunardi, J. (2012). A Novel Large Rearrangement in Ryanodine Receptor 1 (RYR1) gene Associated with Adolescence-Onset Recessive Core Myopathy. Poster présenté à la conférence Xèmes Journées annuelles de la Société Française de Myologie (SFM) : Myopathies congénitales et calcium (10: 14-16 novembre 2012: Grenoble).12.
Aeby, A., Vilain, C., Balériaux, D., Van Coster, R., Abramowicz, M., & Van Bogaert, P. (2009). Isolated brain stem lesions in complex 1 deficiency: report of two cases. Paper session presented at 8th Congress of the European Pediatric Neurology Society (30/09-03/10/2009: Harrogate, United Kingdo).13.
Englert, Y., Zengbe, V., Vannin, A.-S., Place, I., Bostan, A., Emiliani, S., Liesnard, C., Goffard, J.-C., Abramowicz, M., & Gonzales-Merino, E. (2008). Préimplantation genetic diagnosis in an HIV serodiscordant couple carrier for sickle cell disease: lessons from a case report. Paper session presented at 13th International annual conference- EFSS (16-17 October 2008: Le Caire, Egypte).