1. N. Collongues, R. Marignier, H. Zephir, C. Papeix, F. Blanc, C. Ritleng, M. Tchikviladze, O. Outteryck, S. Vukusic, M. Fleury, B. Fontaine, D. Brassat, M. Clanet, M. Milh, J. Pelletier, B. Audoin, A. Ruet, C. Lebrun-Frenay, E. Thouvenot, W. Camu, M. Debouverie, A. Creange, T. Moreau, P. Labauge, G. Castelnovo, G. Edan, E. Le Page, G. Defer, B. Barroso, O. Heinzlef, O. Gout, D. Rodriguez, S. Wiertlewski, D. Laplaud, F. Borgel, P. Tourniaire, J. Grimaud, B. Brochet, P. Vermersch, C. Confavreux, and J. de Seze. Neuromyelitis optica in France: A multicenter study of 125 patients. Neurology, 74(9):736-42, 2010. Note: Journal ArticleUnited States. [WWW]



2. N. Couturier, P. A. Gourraud, I. Cournu-Rebeix, C. Gout, F. Bucciarelli, G. Edan, M. C. Babron, F. Clerget-Darpoux, M. Clanet, B. Fontaine, and D. Brassat. IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients. Eur J Hum Genet, 17(6):844-7, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglandEjhg. [WWW]



3. M. Jagodic, C. Colacios, R. Nohra, A. S. Dejean, A. D. Beyeen, M. Khademi, A. Casemayou, L. Lamouroux, C. Duthoit, O. Papapietro, L. Sjoholm, I. Bernard, D. Lagrange, I. Dahlman, F. Lundmark, A. B. Oturai, H. B. Soendergaard, A. Kemppinen, J. Saarela, P. J. Tienari, H. F. Harbo, A. Spurkland, S. V. Ramagopalan, D. A. Sadovnick, G. C. Ebers, M. Seddighzadeh, L. Klareskog, L. Alfredsson, L. Padyukov, J. Hillert, M. Clanet, G. Edan, B. Fontaine, G. J. Fournie, I. Kockum, A. Saoudi, and T. Olsson. A role for VAV1 in experimental autoimmune encephalomyelitis and multiple sclerosis. Sci Transl Med, 1(10):10ra21, 2009. Note: Journal ArticleUnited States. [WWW]



4. P. Labauge, B. Fontaine, J. P. Neau, F. Bergametti, F. Riant, A. Blecon, F. Marchelli, M. Arnoult, A. Lannuzel, M. Clanet, S. Olschwang, C. Denier, and E. Tournier-Lasserve. Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutations. Neurology, 72(23):2044-6, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



5. M. Y. Frederic, F. Clot, L. Cif, A. Blanchard, A. Durr, I. Vuillaume, G. Lesca, A. Kreisler, C. Davin, T. Besnard, F. Rousset, D. Thorel, C. Saquet, D. Mechin, L. Ozelius, Y. Agid, B. Barroso, B. Chabrol, V. Chan, M. Clanet, C. Coubes, A. Destee, K. Nguyen, C. Vial, M. Vidailhet, J. Xie, B. Sablonniere, A. Calender, A. Brice, A. Roubertie, P. Coubes, M. Claustres, S. Tuffery-Giraud, and G. Collod-Beroud. Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?. Neurogenetics, 9(2):143-50, 2008. Note: Journal ArticleUnited States. [WWW]



6. F. Weber, B. Fontaine, I. Cournu-Rebeix, A. Kroner, M. Knop, S. Lutz, F. Muller-Sarnowski, M. Uhr, T. Bettecken, M. Kohli, S. Ripke, M. Ising, P. Rieckmann, D. Brassat, G. Semana, M. C. Babron, S. Mrejen, C. Gout, O. Lyon-Caen, J. Yaouanq, G. Edan, M. Clanet, F. Holsboer, F. Clerget-Darpoux, and B. Muller-Myhsok. IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations. Genes Immun, 9(3):259-63, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW]



7. C. Renoux, S. Vukusic, Y. Mikaeloff, G. Edan, M. Clanet, B. Dubois, M. Debouverie, B. Brochet, C. Lebrun-Frenay, J. Pelletier, T. Moreau, C. Lubetzki, P. Vermersch, E. Roullet, L. Magy, M. Tardieu, S. Suissa, and C. Confavreux. Natural history of multiple sclerosis with childhood onset. N Engl J Med, 356(25):2603-13, 2007. Note: Adult Neurology Departments KIDMUS Study GroupComparative StudyJournal ArticleMulticenter StudyResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Adult, *Age of Onset, Child, Child, Preschool, Cohort Studies, Disease Progression, Female, Humans, Infant, Kaplan-Meiers Estimate, Male, *Multiple Sclerosis, Observation, Prognosis.



8. E. Le Page, E. Leray, B. Brochet, M. Clanet, P. Clavelou, C. Confavreux, M. Debouverie, C. Lebrun, C. Lubetzki, M. Madigand, J. Pelletier, E. Roullet, L. Rumbach, D. Brassat, and G. Edan. Long-term safety profile of mitoxantrone in a French cohort of 802 multiple sclerosis patients: final report. Mult Scler, 12:S211-S211, 2006. Note: Suppl. 1. [WWW]



9. C. Renoux, S. Vukusic, Y. Mikaeloff, G. Edan, M. Clanet, B. Dubois, M. Debouverie, B. Brochet, C. Lebrun-Frenay, J. Pelletier, T. Moreau, C. Lubetzki, P. Vermersch, E. Roullet, L. Magy, M. Tardieu, S. Suissa, and C. Confavreux. Childhood onset multiple sclerosis (the KIDMUS study): course and prognosis as compared to adult onset multiple sclerosis. Mult Scler, 12:S130-S131, 2006. Note: Suppl. 1. [WWW]



10. B. Stankoff, I. Arnulf, F. Viala, S. T. du Montcel, R. Assouad, L. Mallet, M. Tiberge, C. Papeix, B. Fontaine, A. Tourbah, O. L. Caen, C. Lubetzki, and M. Clanet. Disorders of excessive daytime sleepiness in MS patients with abnormal fatigue. Mult Scler, 12:S152-S152, 2006. Note: Suppl. 1. [WWW]



11. B. Stankoff, E. Waubant, C. Confavreux, G. Edan, M. Debouverie, L. Rumbach, T. Moreau, J. Pelletier, C. Lubetzki, and M. Clanet. Modafinil for fatigue in MS: a randomized placebo-controlled double-blind study. Neurology, 64(7):1139-43, 2005. Note: French Modafinil Study GroupJournal ArticleMulticenter StudyRandomized Controlled TrialResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adult, Benzhydryl Compounds/*administration & dosage/adverse effects, Central Nervous System Stimulants/*administration & dosage/adverse effects, Double-Blind Method, Fatigue/*drug therapy/etiology/prevention & control, Female, Gastrointestinal Diseases/chemically induced, Humans, Male, Middle Aged, Multiple Sclerosis/*complications, Placebos, Sleep Initiation and Maintenance Disorders/chemically induced, Treatment Outcome.



12. H. Coppin, M. T. Ribouchon, B. Fontaine, G. Edan, M. Clanet, and M. P. Roth. A vulnerability locus to multiple sclerosis maps to 7p15 in a region syntenic to an EAE locus in the rat. Genes Immun, 5(1):72-5, 2004. Note: French Multiple Sclerosis Genetics GroupJournal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Alleles, Animals, Chromosomes, Encephalomyelitis, Autoimmune, Experimental/*genetics, Female, France, Genetic Markers, *Genetic Predisposition to Disease, Great Britain, HLA-DQ Antigens/*genetics, HLA-DR Antigens/*genetics, Humans, Male, Microsatellite Repeats, Multiple Sclerosis/etiology/*genetics, Rats.



13. S. J. Kenealy, M. C. Babron, Y. Bradford, N. Schnetz-Boutaud, J. L. Haines, J. B. Rimmler, S. Schmidt, M. A. Pericak-Vance, L. F. Barcellos, R. R. Lincoln, J. R. Oksenberg, S. L. Hauser, M. Clanet, D. Brassat, G. Edan, J. Yaouanq, G. Semana, I. Cournu-Rebeix, O. Lyon-Caen, and B. Fontaine. A second-generation genomic screen for multiple sclerosis. Am J Hum Genet, 75(6):1070-8, 2004. Note: American-French Multiple Sclerosis Genetics GroupNs26799/ns/nindsNs32830/ns/nindsJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.United States. [WWW] Keyword(s): *Chromosome Mapping, Chromosomes, Human, Pair 13/genetics, Chromosomes, Human, Pair 16/genetics, Chromosomes, Human, Pair 2/genetics, Chromosomes, Human, Pair 6/genetics, France, Gene Frequency, Genetic Screening/*methods, *Genome, Human, HLA-DR2 Antigen/genetics, Humans, Lod Score, Microsatellite Repeats/genetics, Models, Genetic, Multiple Sclerosis/*genetics, United States.



14. M. A. Pericak-Vance, J. B. Rimmler, J. L. Haines, M. E. Garcia, J. R. Oksenberg, L. F. Barcellos, R. Lincoln, S. L. Hauser, I. Cournu-Rebeix, A. Azoulay-Cayla, O. Lyon-Caen, B. Fontaine, E. Duhamel, H. Coppin, D. Brassat, M. P. Roth, M. Clanet, M. Alizadeh, J. Yaouanq, E. Quelvennec, G. Semana, G. Edan, M. C. Babron, E. Genin, and F. Clerget-Darpoux. Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study. Neurogenetics, 5(1):45-8, 2004. Note: Ns26799/ns/nindsNs32830/ns/nindsJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.United States. [WWW] Keyword(s): Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 19, Chromosomes, Human, Pair 3, Cooperative Behavior, France, Genetic Predisposition to Disease, HLA-DR Antigens/genetics, Humans, Linkage (Genetics)/*genetics, Multiple Sclerosis/*genetics, United States.



15. M. Alizadeh, M. C. Babron, B. Birebent, F. Matsuda, E. Quelvennec, R. Liblau, I. Cournu-Rebeix, P. Momigliano-Richiardi, J. Sequeiros, J. Yaouanq, E. Genin, A. Vasilescu, H. Bougerie, M. Trojano, B. Martins Silva, P. Maciel, F. Clerget-Darpoux, M. Clanet, G. Edan, B. Fontaine, and G. Semana. Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients. Ann Neurol, 54(1):119-22, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tReviewUnited States. [WWW] Keyword(s): Antigens, CD, Antigens, Differentiation/*genetics, Cohort Studies, DNA Primers/genetics, Genetic Predisposition to Disease, HLA-DR Antigens/*genetics, Humans, Immunoblotting, *Immunoconjugates, Multiple Sclerosis/*genetics, Polymerase Chain Reaction, Polymorphism, Genetic/genetics, Promoter Regions (Genetics)/genetics.



16. M. Alizadeh, E. Genin, M. C. Babron, B. Birebent, I. Cournu-Rebeix, J. Yaouanq, S. Dreano, S. Sawcer, A. Compston, M. Clanet, G. Edan, B. Fontaine, F. Clerget-Darpoux, and G. Semana. Genetic analysis of multiple sclerosis in Europeans: French data. J Neuroimmunol, 143(1-2):74-8, 2003. Note: French Multiple Sclerosis Genetics GroupJournal ArticleMulticenter StudyResearch Support, Non-U.S. Gov'tValidation StudiesNetherlands. [WWW] Keyword(s): Alleles, Case-Control Studies, France/epidemiology, Gene Frequency, Genetic Screening/*methods/statistics & numerical data, Genome, Human, Genotype, Humans, International Cooperation, Linkage Disequilibrium, Microsatellite Repeats, Multiple Sclerosis/epidemiology/*genetics, Prospective Studies.



17. I. Cournu-Rebeix, E. Genin, G. Lesca, A. Azoulay-Cayla, N. Tubridy, E. Noe, M. Clanet, G. Edan, F. Clerget-Darpoux, G. Semana, and B. Fontaine. Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis. Genes Immun, 4(7):518-23, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Age of Onset, Alleles, Female, France/epidemiology, Gene Frequency, Genetic Predisposition to Disease, HLA-DR Antigens/genetics/immunology, *Haplotypes, Heterozygote, Humans, Intercellular Adhesion Molecule-1/*genetics, Male, Microsatellite Repeats, Multiple Sclerosis/*genetics, Polymerase Chain Reaction, Polymorphism, Single Nucleotide.

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