Canlyniadau Chwilio - Feingold, Josué

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn

Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Dopamine receptor D3 gene and essential tremor in large series of German, Danish and French patients gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Early Energy Deficit in Huntington Disease: Identification of a Plasma Biomarker Traceable during Disease Progression gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Genetic association study of mitochondrial polymorphisms in neovascular age-related macular degeneration gan 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.

Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Poor Correlations in the Levels of Pathogenic Mitochondrial DNA Mutations in Polar Bodies versus Oocytes and Blastomeres in Humans gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

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

Cael y testun llawn Cael y testun llawn

Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn