Ouvrages publiés en collaboration (1)
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Thanassekos, Y., Danblon, E., Javeau, C., Dan, B., Abramowicz, M., de Biseau D'Hauteville, J.-C., Van der Dungen, P., Roviello, A. M., Schreiber, J.-P., & Haarscher, G. (2009). Les Lumières contre elles-mêmes. Avatars de la modernité. Paris: Kimé. Parties d'ouvrages collectifs (2)
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Naeije, G., Van den Berge, D., Vokaer, M., Fery, P., Vilain, C., Abramowicz, M., van den broeck, M., Van Broeckhoven, C., & Bier, J. C. (2011). Focal cortical presentations genetically proven Alzheimer disease. In S. De La Monte (Ed.), The Clinical Spectrum of Alzheimer's Disease -The Charge Toward Comprehensive Diagnostic and Therapeutic Strategies (1 ed., pp. 63-74). InTech, an Open Access Publisher, Inc.(Alzheimer's Disease).2.
Dan, B., & Abramowicz, M. (2009). Le statut du discours scientifique. In Y. Thanassekos, E. Danblon, C. Javeau, B. Dan, M. Abramowicz, J.-C. de Biseau D'Hauteville, P. Van Den Dungen, A. M. Roviello, J.-P. Schreiber, & G. Haarscher (Eds.), Les Lumières contre elles-mêmes: avatars de la modernité. Paris: Éditions Kimé. Articles dans des revues avec comité de lecture (148)
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Al-Thani, M., Goodwin-Trotman, M., Bell, S., Patel, K., Fleming, L. L., Vilain, C., Abramowicz, M., Allan, S. M. R. S., Wang, T., Cader, Z. M., Horsburgh, K., van Agtmael, T., Sinha, S., Markus, H. S., & Granata, A. (2023). A novel human iPSC model of COL4A1/A2 small vessel disease unveils a key pathogenic role of matrix metalloproteinases. Stem Cell Reports, 18(12), 2386-2399. doi:10.1016/j.stemcr.2023.10.0142.
Massart, A., Danger, R., Olsen, C., Emond, M., Viklicky, O., Jacquemin, V., Soblet, J., Duerinckx, S., Croes, D., Perazzolo, C., Hruba, P., Daneels, D., Caljon, B., Sever, M. S., Pascual, J., Miglinas, M., Pirson, I., Ghisdal, L., Smits, G., Giral, M., Abramowicz, D., Abramowicz, M., & Brouard, S. (2023). An exome-wide study of renal operational tolerance. Frontiers in medicine, 9. doi:10.3389/fmed.2022.9762483.
Becker, A., Felici, C., Lambert, L., de Saint Martin, A., Abi‐Warde, M., Schaefer, E., Zix, C., Zamani, M., Sadeghian, S., Zeighami, J., Seifi, T., Azizimalamiri, R., Shariati, G., Galehdari, H., Selig, M., Ding, C., Duerinckx, S., Pirson, I., Abramowicz, M., Clément, G., Leheup, B., Jonveaux, P., Lefort, G., Bronner, M., Renaud, M., & Bonnet, C. (2023). Putative founder effect of Arg338* AP4M1 ( SPG50 ) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three families. Clinical genetics, 103(3), 346-351. doi:10.1111/cge.142644.
Jacquemin, V., Versbraegen, N., Duerinckx, S., Massart, A., Soblet, J., Perazzolo, C., Deconinck, N., Brischoux-Boucher, E., De Leener, A., Revencu, N., Janssens, S., Moorgat, S., Blaumeiser, B., Avela, K., Touraine, R., Abou Jaoude, I., Keymolen, K., Saugier-Veber, P., Lenaerts, T., Abramowicz, M., & Pirson, I. (2023). Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance. Human genomics, 17(1), 16. doi:10.1186/s40246-023-00464-w5.
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:10.1080/13816810.2022.20511916.
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.2021.09.0167.
Duerinckx, S., Désir, J., Perazzolo, C., Badoer, C., Jacquemin, V., Soblet, J., Maystadt, I., Tunca, Y., Blaumeiser, B., Ceulemans, B., Courtens, W., Debray, F.-G., Donckier De Donceel, A., Devriendt, K., Jansen, A. C. M. A., Keymolen, K., Lederer, D., Loeys, B., Meuwissen, M. E. C., Moortgat, S., Mortier, G., Nassogne, M.-C., Sekhara, T., Van Coster, R., Van Den Ende, J., Van Der Aa, N., Van Esch, H., Vanakker, O., Verhelst, H., Vilain, C., Weckhuysen, S., Passemard, S., Verloes, A., Aeby, A., Deconinck, N., Van Bogaert, P., Pirson, I., & Abramowicz, M. (2021). Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy. Molecular genetics & genomic medicine. doi:10.1002/mgg3.17688.
Sassi, A., Désir, J., Duerinckx, S., Soblet, J., Van Dooren, S., Bonduelle, M., Abramowicz, M., & Delbaere, A. (2021). Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea. Molecular genetics & genomic medicine. doi:10.1002/mgg3.17769.
Chomette, L., Caravita, S., Dewachter, C., Abramowicz, M., Vachiery, J.-L., & Bondue, A. (2021). Pulmonary arterial hypertension-associated genetic variants in combined post-capillary and pre-capillary pulmonary hypertension: a case report. Pulmonary circulation, 11(1), PMID: 33738094. doi:10.1177/2045894021996571