Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Cournu Rebeix, I."'
Publikováno v:
In Revue Neurologique 2011 167(11):791-801
Autor:
Patsopoulos, NA, Baranzini, SE, Santaniello, A, Shoostari, P, Cotsapas, C, Wong, G, Beecham, AH, James, T, Replogle, J, Vlachos, IS, McCabe, C, Pers, TH, Brandes, A, White, C, Keenan, B, Cimpean, M, Winn, P, Panteliadis, IP, Robbins, A, Andlauer, TFM, Zarzycki, O, Dubois, B, Goris, A, Sondergaard, HB, Sellebjerg, F, Sorensen, PS, Ullum, H, Thorner, LW, Saarela, J, Cournu-Rebeix, I, Damotte, V, Fontaine, B, Guillot-Noel, L, Lathrop, M, Vukusic, S, Berthele, A, Pongratz, V, Gasperi, C, Graetz, C, Grummel, V, Hemmer, B, Hoshi, M, Knier, B, Korn, T, Lill, CM, Luessi, F, Muhlau, M, Zipp, F, Dardiotis, E, Agliardi, C, Amoroso, A, Barizzone, N, Benedetti, MD, Bernardinelli, L, Cavalla, P, Clarelli, F, Comi, G, Cusi, D, Esposito, F, Ferre, L, Galimberti, D, Guaschino, C, Leone, MA, Martinelli, V, Moiola, L, Salvetti, M, Sorosina, M, Vecchio, D, Zauli, A, Santoro, S, Mancini, N, Zuccala, M, Mescheriakova, J, van Duijn, C, Bos, SD, Celius, EG, Spurkland, A, Comabella, M, Montalban, X, Alfredsson, L, Bomfim, IL, Gomez-Cabrero, D, Hillert, J, Jagodic, M, Linden, M, Piehl, F, Jelcic, I, Martin, R, Sospedra, M, Baker, A, Ban, M, Hawkins, C, Hysi, P, Kalra, S, Karpe, F, Khadake, J, Lachance, G, Molyneux, P, Neville, M, Thorpe, J, Bradshaw, E, Caillier, SJ, Calabresi, P, Cree, BAC, Cross, A, Davis, M, de Bakker, PWI, Delgado, S, Dembele, M, Edwards, K, Fitzgerald, K, Frohlich, IY, Gourraud, PA, Haines, JL, Hakonarson, H, Kimbrough, D, Isobe, N, Konidari, I, Lathi, E, Lee, MH, Li, T, An, D, Zimmer, A, Madireddy, L, Manrique, CP, Mitrovic, M, Olah, M, Patrick, E, Pericak-Vance, MA, Piccio, L, Schaefer, C, Weiner, H, Lage, K, Scott, RJ, Lechner-Scott, J, Leal, R, Moscato, P, Booth, DR, Stewart, GJ, Vucic, S, Pame, G, BamettO, M, Mason, D, GriffithS, L, Broadley, S, Tajouri, L, Baxter, A, Slee, M, Taylor, BV, Charlesworth, J, Kilpatrick, TJ, Rubio, J, Jokubaitis, V, Wiley, J, Butzkueven, H, Leslie, S, Motyer, A, Stankovich, J, Carroll, WM, Kermode, AG, Edrin, M, Barclay, M, Peyrin-Biroulet, L, Chamaillard, M, Colombe, JF, Cottone, M, Croft, A, D'Inca, R, Halfvarson, J, Hanigan, K, Henderson, P, Hugot, JP, Karban, A, Kennedy, NA, Khan, MA, Lemann, M, Levine, A, Massey, D, Milla, M, Motoey, GW, Ng, SME, Oikonomnou, J, Peeters, H, Proctor, DD, Rahier, JF, Roberts, R, Rutgeerts, P, Seibold, F, Stronati, L, Taylor, KM, Torkvist, L, Ublick, K, Van Limbergen, J, Van Gossum, A, Vatn, MH, Zhang, H, Zhang, W, Donnelly, P, Barroso, I, Blackwe, JM, Bramon, E, Brown, MA, Casas, JP, Corvin, A, Deloukas, P, Duncanson, A, Jankowski, J, Markus, HS, Mathew, CG, Palmer, CNA, Plomin, R, Rautanen, A, Sawcer, SJ, Trembath, RC, Viswanathan, AC, Wood, NW, Spencer, CCA, Band, G, Bellenguez, C, Freeman, C, Hellenthal, G, Giannoulatou, E, Pirinen, M, Pearson, R, Strange, A, Sul, Z, Vukcevic, DA, Langford, C, Hunt, SE, Edkins, S, Gwilliam, R, Blackburn, H, Bumpstead, SJ, Dronov, S, Gillman, M, Gray, E, Hammond, N, Jayakumar, A, McCann, OT, Liddle, J, Potter, SC, Ravindrarajah, R, Ricketts, M, Waller, M, Weston, P, Widaa, S, Whittaker, P, Compston, A, Hafler, D, Harbo, HF, Hauser, SL, Stewart, G, D'Alfonso, S, Hadjigeorgiou, G, Taylor, B, Barcellos, LF, Booth, D, Hintzen, R, Kockum, I, Martinelli-Boneschi, F, McCauley, JL, Oksenberg, JR, Oturai, A, Sawcer, S, Ivinson, AJ, Olsson, T, De Jager, PL
Publikováno v:
Science, 365(6460):eaav7188, 1417-+. American Association for the Advancement of Science
Science
Science
Genetic roots of multiple sclerosis The genetics underlying who develops multiple sclerosis (MS) have been difficult to work out. Examining more than 47,000 cases and 68,000 controls with multiple genome-wide association studies, the International Mu
Autor:
Cournu-Rebeix, I.1,2,3, Génin, E.4,5, Leray, E.6,7, Babron, M.-C.4,5, Cohen, J.1,2, Gout, C.1,2, Alizadeh, M.8, Perdry, H.4,5, Semana, G.8, Brassat, D.9, Clerget-Darpoux, F.4,5, Yaouanq, J.6,7, Edan, G.7, Rosenheim, M.10, Fontaine, B.1,2,3 bertrand.fontaine@psl.aphp.fr
Publikováno v:
Genes & Immunity. Sep2008, Vol. 9 Issue 6, p570-574. 5p. 4 Charts, 2 Graphs.
Autor:
Cournu-Rebeix, I.1, Génin, E.2, Lesca, G.1, Azoulay-Cayla, A.3, Tubridy, N.1, Noé, E.1, Clanet, M.4, Edan, G.5, Clerget-Darpoux, F.2, Sémana, C.6, Fontaine, B.1,3
Publikováno v:
Genes & Immunity. Oct2003, Vol. 4 Issue 7, p518. 6p.
Autor:
Lill, C., Schjeide, B., Graetz, C., Ban, M., Alcina, A., Ortiz, M., Perez, J., Damotte, V., Booth, D., de Lapuente, A., Broer, L., Schilling, M., Akkad, D., Aktas, O., Alloza, I., Antiguedad, A., Arroyo, R., Blaschke, P., Buttmann, M., Chan, A., Compston, A., Cournu-Rebeix, I., Dorner, T., Epplen, J., Fernandez, O., Gerdes, L., Guillot-Noel, L., Hartung, H., Hoffjan, S., Izquierdo, G., Kemppinen, A., Kroner, A., Kubisch, C., Kumpfel, T., Li, S., Lindenberger, U., Lohse, P., Lubetzki, C., Luessi, F., Malhotra, S., Mescheriakova, J., Montalban, X., Papeix, C., Paredes, L., Rieckmann, P., Steinhagen-Thiessen, E., Winkelmann, A., Zettl, U., Hintzen, R., Vandenbroeck, K., Stewart, G., Fontaine, B., Comabella, M., Urcelay, E., Matesanz, F., Sawcer, S., Bertram, L., Zipp, F., Genetics, I.
Publikováno v:
Brain, 136, 1778-1782. Oxford University Press
Brain
Brain
A recent genome-wide association study reported five loci for which there was strong, but sub-genome-wide significant evidence for association with multiple sclerosis risk. The aim of this study was to evaluate the role of these potential risk loci i
Autor:
Schrewe, L., Lill, C. M., Liu, T., Salmen, A., Gerdes, L. A., Guillot-Noel, L., Akkad, D. A., Blaschke, P., Graetz, C., Hoffjan, S., Kroner, A., Demir, S., Böhme, A., Rieckmann, P., Elali, A., Hagemann, N., Hermann, D. M., Cournu-Rebeix, I., Zipp, F., Kümpfel, T., Buttmann, M., Zettl, U. K., Fontaine, B., Bertram, L., Gold, R., Chan, A.
Publikováno v:
Journal of Neuroinflammation
Journal of Neuroinflammation, BioMed Central, 2015, 12 (1), pp.234. ⟨10.1186/s12974-015-0429-y⟩
Journal of Neuroinflammation, 2015, 12 (1), pp.234. ⟨10.1186/s12974-015-0429-y⟩
Journal of Neuroinflammation, BioMed Central, 2015, 12 (1), pp.234. ⟨10.1186/s12974-015-0429-y⟩
Journal of Neuroinflammation, 2015, 12 (1), pp.234. ⟨10.1186/s12974-015-0429-y⟩
Background Despite pleiotropic immunomodulatory effects of apolipoprotein E (apoE) in vitro, its effects on the clinical course of experimental autoimmune encephalomyelitis (EAE) and multiple sclerosis (MS) are still controversial. As sex hormones mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f2404a78baf2105c3ceba05eadaf748f
https://hal.sorbonne-universite.fr/hal-01250281/document
https://hal.sorbonne-universite.fr/hal-01250281/document
Autor:
Gilles Edan, Marie-Claude Babron, M. Rosenheim, Bertrand Fontaine, Hervé Perdry, Gout C, Mehdi Alizadeh, J. Yaouanq, Emmanuelle Leray, Gilbert Semana, Emmanuelle Génin, Françoise Clerget-Darpoux, David Brassat, Cournu-Rebeix I, Jérémie F. Cohen
Publikováno v:
Genes & Immunity. 9:570-574
Most of the published works so far have aimed at finding genes associated with multiple sclerosis (MS) susceptibility. Very few studies have attempted to correlate disease features with DNA variants. In a well-characterized sample (651 patients) repr
Autor:
Damotte, V, Guillot-Noel, L, Patsopoulos, N A, Madireddy, L, El Behi, M, De Jager, P L, Baranzini, S E, Cournu-Rebeix, I, Fontaine, B, Martin, R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1517ee9ae76f56d2d999446cd4b5568
https://doi.org/10.5167/uzh-95750
https://doi.org/10.5167/uzh-95750
Autor:
Games Collaborative Group, Ban, M, Booth, D, Heard, R, Stewart, G, Goris, A, Vandenbroeck, K, Dubois, B, Laaksonen, M, Ilonen,J, Alizadeh, M, Edan, G, Babron, MC, Brassat, D, Clanet, M, Cournu Rebeix, I, Fontaine, B, Semana, G, Goedde, R, Epplen, J, Weber, A, Infante Duarte, C, Zipp, F, Rajda, C, Bencsik, K, Vécsei, L, Heggarty, S, Graham, C, Hawkins, S, Liguori,M, Momigliano Richiardi,P, Caputo, D, Grimaldi, LM, Leone, M, Massacesi, L, Milanese, C, Salvetti, M, Trojano, M, Bielecki, B, Mycko, MP, Selmaj, K, Santos, M, Maciel,P, Pereira,C, Silva,A, Silva,BM, Coraddu,F, Marrosu,MG, Akesson,E, Hillert,J, Datta,P, Oturai, A, Harbo, HF, Spurkland,A, Goertsches,R, Villoslada, P, Eraksoy, M, Hensiek,A, Compston,A, Setakis,E, Gray,J, Yeo,TW, Sawcer, S., SAVETTIERI, Giovanni
By combining all the data available from the Genetic Analysis of Multiple sclerosis in EuropeanS (GAMES) project, we have been able to identify 17 microsatellite markers showing consistent evidence for apparent association. As might be expected five
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::28840ec8c3800159b133e4816b2d6ea5
http://hdl.handle.net/10447/55533
http://hdl.handle.net/10447/55533
Autor:
Beecham, AH, Patsopoulos, NA, Xifara, DK, Davis, MF, Kemppinen, A, Cotsapas, C, Shah, TS, Spencer, C, Booth, D, Goris, A, Oturai, A, Saarela, J, Fontaine, B, Hemmer, B, Martin, C, Zipp, F, D'Alfonso, S, Martinelli-Boneschi, F, Taylor, B, Harbo, HF, Kockum, I, Hillert, J, Olsson, T, Ban, M, Oksenberg, JR, Hintzen, R, Barcellos, LF, Agliardi, C, Alfredsson, L, Alizadeh, M, Anderson, C, Andrews, R, Søndergaard, HB, Baker, A, Band, G, Baranzini, SE, Barizzone, N, Barrett, J, Bellenguez, C, Bergamaschi, L, Bernardinelli, L, Berthele, A, Biberacher, V, Binder, TMC, Blackburn, H, Bomfim, IL, Brambilla, P, Broadley, S, Brochet, B, Brundin, L, Buck, D, Butzkueven, H, Caillier, SJ, Camu, W, Carpentier, W, Cavalla, P, Celius, EG, Coman, I, Comi, G, Corrado, L, Cosemans, L, Cournu-Rebeix, I, Cree, BAC, Cusi, D, Damotte, V, Defer, G, Delgado, SR, Deloukas, P, Di Sapio, A, Dilthey, AT, Donnelly, P, Dubois, B, Duddy, M, Edkins, S, Elovaara, I, Esposito, F, Evangelou, N, Fiddes, B, Field, J, Franke, A
Publikováno v:
Beecham, AH; Patsopoulos, NA; Xifara, DK; Davis, MF; Kemppinen, A; Cotsapas, C; et al.(2013). Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nature Genetics, 45(11), 1353-1362. doi: 10.1038/ng.2770. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/0tz6x2q0
Using the ImmunoChip custom genotyping array, we analyzed 14,498 subjects with multiple sclerosis and 24,091 healthy controls for 161,311 autosomal variants and identified 135 potentially associated regions (P < 1.0 × 10 -4). In a replication phase,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::3cbd226ce07622c6ab0f1afe7e90bad2
http://www.escholarship.org/uc/item/0tz6x2q0
http://www.escholarship.org/uc/item/0tz6x2q0