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LIBIOULLE Cécile

Unilab > Unité de laboratoire - prénatal, néonatal

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ORCID
0000-0002-3550-2954
Main Referenced Co-authors
Valdes-Socin, Hernan  (24)
Beckers, Albert  (19)
Bours, Vincent  (17)
Debray, François-Guillaume  (17)
Dideberg, Vinciane  (13)
Main Referenced Keywords
Humans (8); Crohn Disease/genetics (5); Genetic Predisposition to Disease (5); Genome-Wide Association Study (4); Animals (3);
Main Referenced Unit & Research Centers
Service d'Endocrinologie (1)
Service d'Endocrinologie. CHU de Liège (1)
Main Referenced Disciplines
Endocrinology, metabolism & nutrition (21)
Genetics & genetic processes (17)
Gastroenterology & hepatology (9)
Biochemistry, biophysics & molecular biology (6)
Anatomy (cytology, histology, embryology...) & physiology (2)

Publications (total 51)

The most downloaded
3569 downloads
LIBIOULLE, C., & BOURS, V. (2012). Les maladies complexes: l'importance de la genetique. Revue Médicale de Liège, 67 (5-6), 220-5. https://hdl.handle.net/2268/142675

The most cited

2237 citations (Scopus®)

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 https://hdl.handle.net/2268/4413

Articles in scientific journals as first or last author

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

Articles in scientific journals as co-author

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., 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).

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).

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
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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

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

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

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.
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