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Author Details

Jacqueline Yaouanq
1986
51
24
PMIDPaper TitleJournal TitlePublished Year
28934989Small-area distribution of multiple sclerosis incidence in western France: in search of environmental triggers.International Journal of Health Geographics2017
25515927Ten-year prognosis in multiple sclerosis: a better outcome in relapsing-remitting patients but not in primary progressive patients.European Journal of Neurology2015
25313028Register-based incidence of multiple sclerosis in Brittany (north-western France), 2000-2001.Acta Neurologica Scandinavica2015
22859724'Clinically definite benign multiple sclerosis', an unwarranted conceptual hodgepodge: evidence from a 30-year observational study.Multiple Sclerosis Journal2013
21833088Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.Nature2011
21618648REEP1 mutations in SPG31: frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction.Hum Mutat2011
20117844MGAT5 alters the severity of multiple sclerosis.Journal of Neuroimmunology2010
20423930Evidence for a two-stage disability progression in multiple sclerosis.Brain2010
18354419IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.Genes Immun2008
18615093HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis.Genes Immun2008
17881399Long-term survival of patients with multiple sclerosis in West France.Multiple Sclerosis Journal2007
15095853NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype- phenotype analysis.European Journal of Gastroenterology and Hepatology2004
15494893A second-generation genomic screen for multiple sclerosis.Am J Hum Genet2004
14595552Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study.Neurogenetics2004
14575918Genetic analysis of multiple sclerosis in Europeans: French data.Journal of Neuroimmunology2003
12838528Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients.Annals of Neurology2003
14510831FOunder effect in patients with Unverricht-Lundborg disease on reunion island.Epilepsia2003
10331690Familial factors influence disability in MS multiplex families. French Multiple Sclerosis Genetics Group.Neurology1999
10371284Positive association of the HLA DMB1*0101-0101 genotype with rheumatoid arthritis.Rheumatology1999
10674165[French Society for Human Genetics. "Genetics in Practice" Commission. Core scientific data of use in genetic counseling. Hemochromatosis].1999
9832046Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosis.Journal of Medical Genetics1998
9341868A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.Human Genetics1997
9040586Interleukin-1 receptor antagonist gene in multiple sclerosis.Lancet, The1997
9380912[Should we screen for hemochromatosis? Critical analysis of the literature].Revue d'Epidemiologie et de Sante Publique1997
9164339Haemochromatosis Cys282Tyr mutation in pyridoxine-responsive sideroblastic anaemia.Lancet, The1997
9157540Evidence for linkage disequilibrium between HLA-DRB1 gene and multiple sclerosis. The French Research Group on Genetic Susceptibility to MS.Science1997
9219791Significance of interleukin-1beta and interleukin-1 receptor antagonist genetic polymorphism in inflammatory bowel diseases.Am J Gastroenterol1997
8557248Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE).Human Genetics1996
8896550Haemochromatosis and HLA-H.Nature Genetics1996
9157088The role of HLA-DR-DR and HLA-DR-DP interactions in genetic susceptibility to rheumatoid arthritis.Human Immunology1996
8586148Diabetes and haemochromatosis: current concepts, management and prevention.1995
8304342Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE)Am J Hum Genet1994
7972774Hemochromatosis: diagnosis and quantification of liver iron with gradient-echo MR imaging.Radiology1994
8419246Primary liver cancer in genetic hemochromatosis: a clinical, pathological, and pathogenetic study of 54 cases.Gastroenterology1993
8353773[Molecular genetics of hemochromatosis].Bull Acad Natl Med1993
8117056[Molecular genetics of hemochromatosis].Ann Gastroenterol Hepatol (Paris)1993
1349563Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis.Hum Genet1992
1349923Familial screening for genetic haemochromatosis by means of DNA markers.J Med Genet1992
2363427Percent transferrin saturation in segregating hemochromatosis.American Journal of Medical Genetics1990
1975556HLA class I gene polymorphism in genetic hemochromatosis.Human Genetics1990
2393027Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLA.American Journal of Human Genetics1990
2147432Renal scintigraphy in insulin-dependent diabetes mellitus: early glomerular and urologic dysfunction.1990
2365376Serum ferritin as a marker of affection for genetic hemochromatosis.Human Heredity1990
2563249Ferritin H gene polymorphism in idiopathic hemochromatosis.Human Genetics1989
2488506[Heredity and genetics of hemochromatosis].Revue de Medecine Interne1989
2596531Genetic hemochromatosis: distribution analysis of six laboratory measures of iron metabolism.American Journal of Medical Genetics1989
2773939Segregation of genetic hemochromatosis indexed by latent capacity of transferrin.American Journal of Human Genetics1989
3291675Genetics of hemochromatosis: HLA association and mode of inheritance.Annals of the New York Academy of Sciences1988
3226462HLA alleles, hemochromatosis allele, and serum ferritin in hemodialysis patients.Nephron1988
3475981A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA associatAmerican Journal of Human Genetics1987
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Massachusetts General Hospital and Harvard Medical School
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