Search Results - Feingold, Josué

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  1. 1
    Identifying modifier genes of monogenic disease: strategies and difficulties

    Identifying modifier genes of monogenic disease: strategies and difficulties by Genin, Emmanuelle, Feingold, Josué, Clerget-Darpoux, Françoise

    Published 2008
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  2. 2
    Long-term outcome of presymptomatic testing in Huntington disease

    Long-term outcome of presymptomatic testing in Huntington disease by Gargiulo, Marcela, Lejeune, Séverine, Tanguy, Marie-Laure, Lahlou-Laforêt, Khadija, Faudet, Anne, Cohen, David, Feingold, Josué, Durr, Alexandra

    Published 2009
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  3. 3
    Involvement of the Modifier Gene of a Human Mendelian Disorder in a Negative Selection Process

    Involvement of the Modifier Gene of a Human Mendelian Disorder in a Negative Selection Process by Jéru, Isabelle, Hayrapetyan, Hasmik, Duquesnoy, Philippe, Cochet, Emmanuelle, Serre, Jean-Louis, Feingold, Josué, Grateau, Gilles, Sarkisian, Tamara, Jeanpierre, Marc, Amselem, Serge

    Published 2009
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  4. 4
    Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France

    Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France by Rey, Françoise, Berthelon, Monique, Caillaud, Catherine, Lyonnet, Stanislas, Abadie, Véronique, Blandin-Savoja, Félicienne, Feingold, Josué, Saudubray, Jean-Marie, Frézal, Jean, Munnich, Arnold, Rey, Jean

    Published 1988
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  5. 5
    Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis

    Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis by Corvol, Harriet, Nathan, Nadia, Charlier, Celine, Chadelat, Katarina, Le Rouzic, Philippe, Tabary, Olivier, Fauroux, Brigitte, Henrion-Caude, Alexandra, Feingold, Josue, Boelle, Pierre-Yves, Clement, Annick

    Published 2007
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  6. 6
    Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients

    Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients by Lorenz, Delia, Klebe, Stephan, Stevanin, Giovanni, Thier, Sandra, Nebel, Almut, Feingold, Josué, Frederiksen, Henrik, Denis, Elodie, Christensen, Kaare, Schreiber, Stefan, Brice, Alexis, Deuschl, Günther, Dürr, Alexandra

    Published 2009
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  7. 7
    Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression

    Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression by Mochel, Fanny, Charles, Perrine, Seguin, François, Barritault, Julie, Coussieu, Christiane, Perin, Laurence, Le Bouc, Yves, Gervais, Christiane, Carcelain, Guislaine, Vassault, Anne, Feingold, Josué, Rabier, Daniel, Durr, Alexandra

    Published 2007
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  8. 8
    rs5888 Variant of SCARB1 Gene Is a Possible Susceptibility Factor for Age-Related Macular Degeneration

    rs5888 Variant of SCARB1 Gene Is a Possible Susceptibility Factor for Age-Related Macular Degeneration by Zerbib, Jennyfer, Seddon, Johanna M., Richard, Florence, Reynolds, Robyn, Leveziel, Nicolas, Benlian, Pascale, Borel, Patrick, Feingold, Josué, Munnich, Arnold, Soubrane, Gisèle, Kaplan, Josseline, Rozet, Jean-Michel, Souied, Eric H.

    Published 2009
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  9. 9
    Genetic association study of mitochondrial polymorphisms in neovascular age-related macular degeneration

    Genetic association study of mitochondrial polymorphisms in neovascular age-related macular degeneration by Tilleul, Julien, Richard, Florence, Puche, Nathalie, Zerbib, Jennyfer, Leveziel, Nicolas, Sahel, Jose Alain, Cohen, Salomon Yves, Korobelnik, Jean-Francois, Feingold, Josue, Munnich, Arnold, Kaplan, Josseline, Rozet, Jean-Michel, Souied, Eric H.

    Published 2013
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  10. 10
    Segregation of mtDNA Throughout Human Embryofetal Development: m.3243A > G as a Model System

    Segregation of mtDNA Throughout Human Embryofetal Development: m.3243A > G as a Model System by Monnot, Sophie, Gigarel, Nadine, Samuels, David C, Burlet, Philippe, Hesters, Laetitia, Frydman, Nelly, Frydman, René, Kerbrat, Violaine, Funalot, Benoit, Martinovic, Jelena, Benachi, Alexandra, Feingold, Josué, Munnich, Arnold, Bonnefont, Jean-Paul, Steffann, Julie

    Published 2011
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  11. 11
    Poor Correlations in the Levels of Pathogenic Mitochondrial DNA Mutations in Polar Bodies versus Oocytes and Blastomeres in Humans

    Poor Correlations in the Levels of Pathogenic Mitochondrial DNA Mutations in Polar Bodies versus Oocytes and Blastomeres in Humans by Gigarel, Nadine, Hesters, Laetitia, Samuels, David C., Monnot, Sophie, Burlet, Philippe, Kerbrat, Violaine, Lamazou, Frédéric, Benachi, Alexandra, Frydman, René, Feingold, Josué, Rotig, Agnes, Munnich, Arnold, Bonnefont, Jean-Paul, Frydman, Nelly, Steffann, Julie

    Published 2011
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  12. 12
    Anonymous Marker Loci within 400 kb of HLA-A Generate Haplotypes in Linkage Disequilibrium with the Hemochromatosis Gene (HFE)

    Anonymous Marker Loci within 400 kb of HLA-A Generate Haplotypes in Linkage Disequilibrium with the Hemochromatosis Gene (HFE) by Yaouanq, Jacqueline, Perichon, Muriel, Chorney, Michael, Pontarotti, Pierre, Le Treut, André, El Kahloun, Abdel, Mauvieux, Valérie, Blayau, Martine, Jouanolle, Anne Marie, Chauvel, Bruno, Moirand, Romain, Nouel, Olivier, Le Gall, Jean Yves, Feingold, Josué, David, Véronique

    Published 1994
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  13. 13
    Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy

    Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy by Cartault, François, Munier, Patrick, Benko, Edgar, Desguerre, Isabelle, Hanein, Sylvain, Boddaert, Nathalie, Bandiera, Simonetta, Vellayoudom, Jeanine, Krejbich-Trotot, Pascale, Bintner, Marc, Hoarau, Jean-Jacques, Girard, Muriel, Génin, Emmanuelle, de Lonlay, Pascale, Fourmaintraux, Alain, Naville, Magali, Rodriguez, Diana, Feingold, Josué, Renouil, Michel, Munnich, Arnold, Westhof, Eric, Fähling, Michael, Lyonnet, Stanislas, Henrion-Caude, Alexandra

    Published 2012
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