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  1. No Access

    Article

    HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis

    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...

    I Cournu-Rebeix, E Génin, E Leray, M-C Babron, J Cohen, C Gout… in Genes & Immunity (2008)

  2. No Access

    Article

    IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations

    Multiple sclerosis (MS) is the most common chronic inflammatory neurologic disorder diagnosed in young adults and, due to its chronic course, is responsible for a substantial economic burden. MS is considered ...

    F Weber, B Fontaine, I Cournu-Rebeix, A Kroner, M Knop, S Lutz… in Genes & Immunity (2008)

  3. No Access

    Article

    Response

    F. Clot, C. Gianfrani, M.-C. Babron, F. Bouguerra, S. Southwood… in Immunogenetics (2000)

  4. No Access

    Article

    Chromosome 17q22–q24 and multiple sclerosis genetic susceptibility

    Recently, genome-wide searches for multiple sclerosis (MS) susceptibility genes have suggested that the chromosome 17q22–q24 region might contain susceptibility genes in two sets of families of different ethni...

    B Fontaine, I Cournu, I Arnaud, M-C Babron, S Eichenbaum-Voline… in Genes & Immunity (1999)

  5. No Access

    Chapter and Conference Paper

    Family Studies of Affective Disorders with 11p15.5 DNA Markers

    Family, twin, and adoption studies suggest the involvement of genetic factors in manic-depressive illness (MDI) but the mode of inheritance remains elusive. The remarkable success with which the classical loga...

    J. Mallet, A. Malafosse, M. Leboyer, T. d’Amato… in Genetic Research in Psychiatry (1992)

  6. No Access

    Chapter and Conference Paper

    Genetic Epidemiology of Retinoblastoma

    The retinoblastoma story provides a very good example of a case where mechanisms assessed by genetic epidemiology were confirmed several years later by molecular genetics. There are still some questions raised...

    C. Bonaïti-Pellié, F. Clerget-Darpoux… in Recent Progress in the Genetic Epidemiolog… (1991)

  7. No Access

    Article

    Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q

    PROXIMAL spinal muscular atrophies represent the second most common fatal, autosomal recessive disorder after cystic fibrosis1. The childhood form is classically subdivided into three groups: acute Werdnig-Hoffm...

    J. Melki, S. Abdelhak, Peter Sheth, M. F. Bachelot, Peter Burlet, Alun Marcadet… in Nature (1990)