1. I. Cournu-Rebeix, E. Genin, E. Leray, M. C. Babron, J. Cohen, C. Gout, M. Alizadeh, H. Perdry, G. Semana, D. Brassat, F. Clerget-Darpoux, J. Yaouanq, G. Edan, M. Rosenheim, and B. Fontaine. HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis. Genes Immun, 9(6):570-4, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW]



2. P. Richard, K. Gaudon, H. Haddad, A. B. Ammar, E. Genin, S. Bauche, M. Paturneau-Jouas, J. S. Muller, H. Lochmuller, D. Grid, A. Hamri, S. Nouioua, M. Tazir, M. Mayer, C. Desnuelle, A. Barois, B. Chabrol, J. Pouget, J. Koenig, N. Gouider-Khouja, F. Hentati, B. Eymard, and D. Hantai. The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa. Neurology, 71(24):1967-72, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Africa, Northern/ethnology, Cholinesterase Inhibitors/pharmacology, DNA Mutational Analysis, Female, Founder Effect, Gene Frequency, Genetic Counseling/standards, Genetic Markers/genetics, Genetic Predisposition to Disease/*genetics, Genetic Screening, Genotype, Haplotypes, Heterozygote, Humans, Male, Molecular Biology/standards, Mutation/*genetics, Myasthenic Syndromes, Congenital/ethnology/*genetics/physiopathology, Receptors, Nicotinic/*genetics.



3. S. Mace, E. Cousin, S. Ricard, E. Genin, E. Spanakis, C. Lafargue-Soubigou, B. Genin, R. Fournel, S. Roche, G. Haussy, F. Massey, S. Soubigou, G. Brefort, P. Benoit, A. Brice, D. Campion, M. Hollis, L. Pradier, J. Benavides, and J. F. Deleuze. ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease. Neurobiol Dis, 18(1):119-25, 2005. Note: Journal ArticleUnited States. [WWW] Keyword(s): ATP-Binding Cassette Transporters/*genetics/metabolism, Age of Onset, Aged, Alzheimer Disease/epidemiology/*genetics/metabolism, Apolipoprotein E4, Apolipoproteins E/genetics, Brain/metabolism/physiopathology, Case-Control Studies, Cholesterol/*metabolism, DNA Mutational Analysis, European Continental Ancestry Group/genetics, Female, France/epidemiology, Gene Frequency, Genetic Markers/genetics, Genetic Predisposition to Disease/*genetics, Genetic Screening, Genotype, Humans, Male, Middle Aged, Mutation/*genetics, Odds Ratio, Polymorphism, Single Nucleotide/*genetics, Risk Factors, Sex Factors, Variation (Genetics)/genetics.



4. 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.



5. C. Verny, N. Ravise, A. L. Leutenegger, F. Pouplard, O. Dubourg, S. Tardieu, F. Dubas, A. Brice, E. Genin, and E. LeGuern. Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single family. Neurology, 63(8):1527-9, 2004. Note: Case ReportsJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Charcot-Marie-Tooth Disease/*genetics, *Chromosome Aberrations, Chromosomes, Human, Pair 17/*genetics, DNA Mutational Analysis, Disease Progression, Family Health, Female, Genes, Recessive/genetics, Genetic Predisposition to Disease/*genetics, Genetic Screening, Humans, Inheritance Patterns/*genetics, Male, Muscle Weakness/genetics/pathology/physiopathology, Mutation/*genetics, Nerve Fibers, Myelinated/pathology, Pedigree, Peripheral Nerves/pathology/physiopathology, Protein-Tyrosine-Phosphatase/genetics.



6. 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.



7. 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.



8. 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.



9. E. Cousin, D. Hannequin, S. Mace, B. Dubois, S. Ricard, E. Genin, C. Brun, C. Chansac, L. Pradier, T. Frebourg, A. Brice, D. Campion, and J. F. Deleuze. No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease. Neurosci Lett, 353(2):153-5, 2003. Note: Comparative StudyJournal ArticleIreland. [WWW] Keyword(s): Age of Onset, Aged, Alzheimer Disease/*genetics, Amyloid Precursor Protein Secretases, Apolipoprotein E4, Apolipoproteins E/genetics, France, Gene Frequency, Genotype, Haplotypes, Humans, Membrane Glycoproteins/*genetics, Middle Aged, Polymerase Chain Reaction, Polymorphism, Single Nucleotide.



10. E. Cousin, D. Hannequin, S. Ricard, S. Mace, E. Genin, C. Chansac, A. Brice, B. Dubois, T. Frebourg, L. Mercken, J. Benavides, L. Pradier, D. Campion, and J. F. Deleuze. A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism. Neurosci Lett, 342(1-2):5-8, 2003. Note: Journal ArticleIreland. [WWW] Keyword(s): Age Factors, Age of Onset, Aged, Aged, 80 and over, Alleles, Alzheimer Disease/epidemiology/*genetics, Case-Control Studies, Female, Genotype, Humans, *Introns, Male, Middle Aged, Nerve Tissue Proteins/*genetics, Nuclear Proteins/*genetics, *Polymorphism, Genetic, Risk Factors, Sex Factors.

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