LIBIOULLE, C., & BOURS, V. (2012). Les maladies complexes: l'importance de la genetique. Revue Médicale de Liège, 67 (5-6), 220-5. |
Libioulle, C., Louis, E., Hansoul, S., Sandor, C., Farnir, F., Franchimont, D., Vermeire, S., Dewit, O., de Vos, M., Dixon, A., Demarche, B., Gut, I., Heath, S., Foglio, M., Liang, L., Laukens, D., Mni, M., Zelenika, D., Van Gossum, A., ... Georges, M. (2007). Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. PLoS Genetics, 3 (4), 538-543. doi:10.1371/journal.pgen.0030058 |
Gernay, C., Brachet, C., Boros, E., Tenoutasse, S., Libioulle, C., & Heinrichs, C. (17 November 2022). Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty. Journal of the Endocrine Society, 7 (1), 168. doi:10.1210/jendso/bvac168 |
VALDES SOCIN, H. G., LIBIOULLE, C., DEBRAY, F.-G., DIDEBERG, V., BOURS, V., & BECKERS, A. (2018). Le Syndrome de Kallmann: un vieux syndrome revisité par la génétique. Urologic, 14, 1-7. |
VALDES SOCIN, H. G., Potorac, I., LIBIOULLE, C., Daly, A., & Beckers, A. (May 2017). La déficience en hormone lutéinisante: ses conséquences sur la reproduction. Urologic, 13 (1), 18-23. |
VALDES SOCIN, H. G., NECHIFOR, I., LIBIOULLE, C., Daly, A., & Beckers, A. (2017). Tekort aan luteïniserend hormoon : gevolgen voor de voortplanting. Bloedvaten, Hart, Longen, 22 (9). |
VALDES SOCIN, H. G., NECHIFOR, I., LIBIOULLE, C., Daly, A., & Beckers, A. (2017). La déficience en hormone lutéinisante (LH) : ses conséquences sur la reproduction. Vaisseaux, Coeur, Poumons, 22 (9). |
VALDES SOCIN, H. G., Pintiaux, A., Delbaere, A., Parent, A.-S., COPPENS, L., LIBIOULLE, C., & Beckers, A. (2017). La déficience en FSH : actualités cliniques et thérapeutiques. Urologic, 13 (3), 16-22. |
Momozawa, Y., Mni, M., Nakamura, K., Coppieters, W., Almer, S., Amininejad, L., Cleynen, I., Colombel, J.-F., de Rijk, P., Dewit, O., Finkel, Y., Gassull, M. A., Goossens, D., Laukens, D., Lemann, M., LIBIOULLE, C., O'Morain, C., Reenaers, C., Rutgeerts, P., ... Georges, M. (2011). Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease. Nature Genetics, 43 (1), 43-7. doi:10.1038/ng.733 |
Franke, A., McGovern, D. P. B., Barrett, J. C., Wang, K., Radford-Smith, G. L., Ahmad, T., Lees, C. W., Balschun, T., Lee, J., Roberts, R., Anderson, C. A., Bis, J. C., Bumpstead, S., Ellinghaus, D., Festen, E. M., Georges, M., Green, T., Haritunians, T., Jostins, L., ... Parkes, M. (2010). Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Nature Genetics, 42 (12), 1118-25. doi:10.1038/ng.717 |
Laukens, D., Georges, M., Libioulle, C., Sandor, C., Mni, M., Vander Cruyssen, B., Peeters, H., Elewaut, D., & Devos, M. (2010). Evidence for significant overlap between common risk variants for Crohn's disease and ankylosing spondylitis. PLoS ONE, 5 (11), 13795. doi:10.1371/journal.pone.0013795 |
Louis, E., Libioulle, C., Reenaers, C., Belaiche, J., & Georges, M. (October 2009). Génomique des maladies inflammatoires intestinales. Revue Médicale de Liège, 64, 24-28. |
Imielinski, M., Baldassano, R. N., Griffiths, A., Russell, R. K., Annese, V., Dubinsky, M., Kugathasan, S., Bradfield, J. P., Walters, T. D., Sleiman, P., Kim, C. E., Muise, A., Wang, K., Glessner, J. T., Saeed, S., Zhang, H., Frackelton, E. C., Hou, C., Flory, J. H., ... Georges, M. (Other coll.). (2009). Common variants at five new loci associated with early-onset inflammatory bowel disease. Nature Genetics, 41 (12), 1335-40. doi:10.1038/ng.489 |
Louis, E., Libioulle, C., Reenaers, C., Belaiche, J., & Georges, M. (2009). Genetics of ulcerative colitis: the come-back of interleukin 10. Gut, 58 (9), 1173-6. doi:10.1136/gut.2008.169235 |
Villani, A.-C., Lemire, M., Fortin, G., Louis, E., Silverberg, M. S., Collette, C., Baba, N., Libioulle, C., Belaiche, J., Bitton, A., Gaudet, D., Cohen, A., Langelier, D., Fortin, P. R., Wither, J. E., Sarfati, M., Rutgeerts, P., Rioux, J. D., Vermeire, S., ... Franchimont, D. (2009). Common variants in the NLRP3 region contribute to Crohn's disease susceptibility. Nature Genetics, 41 (1), 71-6. doi:10.1038/ng.285 |
Villani, A.-C., Lemire, M., Louis, E., Silverberg, M. S., Collette, C., Fortin, G., Nimmo, E. R., Renaud, Y., Brunet, S., Libioulle, C., Belaiche, J., Bitton, A., Gaudet, D., Cohen, A., Langelier, D., Rioux, J. D., Arnott, I. D. R., Wild, G. E., Rutgeerts, P., ... Franchimont, D. (2009). Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis. PLoS ONE, 4 (9), 7154. doi:10.1371/journal.pone.0007154 |
Dideberg, V., Kristjansdottir, G., Milani, L., Libioulle, C., Sigurdsson, S., Louis, E., Wiman, A. C., Vermeire, S., Rutgeerts, P., Belaiche, J., Franchimont, D., Van Gossum, A., Bours, V., & Syvanen, A. C. (15 December 2007). An insertion-deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases. Human Molecular Genetics, 16 (24), 3008-3016. doi:10.1093/hmg/ddm259 |
Feller, G., Lonhienne, T., Deroanne, C., Libioulle, C., Van Beeumen, J., & Gerday, C. (15 March 1992). Purification, Characterization, and Nucleotide Sequence of the Thermolabile Alpha-Amylase from the Antarctic Psychrotroph Alteromonas Haloplanctis A23. Journal of Biological Chemistry, 267 (8), 5217-21. |