  | LIBIOULLE, C., & BOURS, V. (2012). Les maladies complexes: l'importance de la genetique. Revue Médicale de Liège, 67 (5-6), 220-5.  Peer reviewed |
 | 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 Peer Reviewed verified by ORBi |
Libioulle, C., Corbesier, L., & Gilles, R. (2001). Changes in major intracellular osmolytes in L-929 cells following rapid and slow application of hyperosmotic media. Comparative Biochemistry and Physiology. Part A, Molecular and Integrative Physiology, 130 (3), 461-70. doi:10.1016/S1095-6433(01)00415-9 Peer Reviewed verified by ORBi |
Libioulle, C., Llabres, G., & Gilles, R. (1996). Protein patterns, osmolytes, and aldose reductase of L-929 cells exposed to hyperosmotic media. Journal of Cellular Physiology, 168/1, 147-154. doi:10.1002/(SICI)1097-4652(199607)168:1<147::AID-JCP18>3.0.CO;2-4 Peer Reviewed verified by ORBi |
 | 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 Peer Reviewed verified by ORBi |
  | Lausberg, E., Gießelmann, S., Dewulf, J. P., Wiame, E., Holz, A., Salvarinova, R., van Karnebeek, C. D., Klemm, P., Ohl, K., Mull, M., Braunschweig, T., Weis, J., Sommer, C. J., Demuth, S., Haase, C., Stollbrink-Peschgens, C., DEBRAY, F.-G., LIBIOULLE, C., Choukair, D., ... Kraft, F. (2021). C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation. The Journal of clinical investigation, 131 (12). doi:10.1172/JCI143078 Peer reviewed |
 | 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). 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. |
 | 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). |
 | Sharma, M., Ioannidis, J. P. A., Aasly, J. O., Annesi, G., Brice, A., Bertram, L., Bozi, M., Barcikowska, M., Crosiers, D., Clarke, C. E., Facheris, M. F., Farrer, M., Garraux, G., Gispert, S., Auburger, G., Vilarino-Guell, C., Hadjigeorgiou, G. M., Hicks, A. A., Hattori, N., ... Kruger, R. (2012). A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics, 49 (11), 721-6. doi:10.1136/jmedgenet-2012-101155 Peer Reviewed verified by ORBi |
 | Anderson, C. A., Boucher, G., Lees, C. W., Franke, A., D'Amato, M., Taylor, K. D., Lee, J. C., Goyette, P., Imielinski, M., Latiano, A., Lagace, C., Scott, R., Amininejad, L., Bumpstead, S., Baidoo, L., Baldassano, R. N., Barclay, M., Bayless, T. M., Brand, S., ... Rioux, J. D. (February 2011). Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nature Genetics, 43 (3), 246-52. doi:10.1038/ng.764 Peer Reviewed verified by ORBi |
 | BOEMER, F., Cornet, Y., LIBIOULLE, C., SEGERS, K., Bours, V., & SCHOOS, R. (2011). 3-years experience review of neonatal screening for hemoglobin disorders using tandem mass spectrometry. Clinica Chimica Acta, 412 (15-16), 1476-9. doi:10.1016/j.cca.2011.04.031 Peer Reviewed verified by ORBi |
 | 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 Peer Reviewed verified by ORBi |
 | 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 Peer Reviewed verified by ORBi |
 | 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 Peer Reviewed verified by ORBi |
 | Louis, E., Libioulle, C., Reenaers, C., Belaiche, J., & Georges, M. (October 2009). Génomique des maladies inflammatoires intestinales. Revue Médicale de Liège, 64, 24-28. Peer reviewed |
 | 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 Peer Reviewed verified by ORBi |
 | 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 Peer Reviewed verified by ORBi |
 | 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 Peer Reviewed verified by ORBi |
 | 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 Peer Reviewed verified by ORBi |
 | Barrett, J. C., Hansoul, S., Nicolae, D. L., Cho, J. H., Duerr, R. H., Rioux, J. D., Brant, S. R., Silverberg, M. S., Taylor, K. D., Barmada, M. M., Bitton, A., Dassopoulos, T., Wu Datta, L., Green, T., Griffiths, A. M., Kistner, E. O., Murtha, M. T., Regueiro, M. D., Rotter, J. I., ... Daly, M. J. (2008). Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nature Genetics, 40 (8), 955-62. doi:10.1038/ng.175 Peer Reviewed verified by ORBi |
 | 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 Peer Reviewed verified by ORBi |
 | De Jager, P. L., Franchimont, D., Waliszewska, A., Bitton, A., Cohen, A., Langelier, D., Belaiche, J., Vermeire, S., Farwell, L., Goris, A., Libioulle, C., Jani, N., Dassopoulos, T., Bromfield, G. P., Dubois, B., Cho, J. H., Brant, S. R., Duerr, R. H., Yang, H., ... Rioux, J. D. (July 2007). The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases. Genes and Immunity, 8 (5), 387-397. doi:10.1038/sj.gene.6364398 Peer Reviewed verified by ORBi |
 | Gilles, R., Belkhir, M., Compère, P., Libioulle, C., & Thiry, M. (1995). Effect of high osmolarity acclimation on tolerance to hyperosmotic shocks in L929 cultured cells. Tissue and Cell, 27 (6), 679-687. doi:10.1016/S0040-8166(05)80023-0 Peer Reviewed verified by ORBi |
 | 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. Peer Reviewed verified by ORBi |
