iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells von Mouka, Aurélie, Arkoun, Brahim, Moison, Pauline, Drévillon, Loïc, Jarray, Rafika, Brisset, Sophie, Mayeur, Anne, Bouligand, Jérôme, Boland-Auge, Anne, Deleuze, Jean-François, Yates, Frank, Lemonnier, Thomas, Callier, Patrick, Duffourd, Yannis, Nitschke, Patrick, Ollivier, Emmanuelle, Bourdin, Arnaud, De Vos, John, Livera, Gabriel, Tachdjian, Gérard, Maouche-Chrétien, Leïla, Tosca, Lucie

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Co-lethality studied as an asset against viral drug escape: the HIV protease case von Brouillet, Sophie, Valere, Thomas, Ollivier, Emmanuelle, Marsan, Laurent, Vanet, Anne

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16p13.11p11.2 triplication syndrome: a new recognizable genomic disorder characterized by optical genome mapping and whole genome sequencing von Nicolle, Romain, Siquier-Pernet, Karine, Rio, Marlène, Guimier, Anne, Ollivier, Emmanuelle, Nitschke, Patrick, Bole-Feysot, Christine, Romana, Serge, Hastie, Alex, Cantagrel, Vincent, Malan, Valérie

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NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal–Hreidarsson syndrome von Benyelles, Maname, O’Donohue, Marie-Françoise, Kermasson, Laëtitia, Lainey, Elodie, Borie, Raphael, Lagresle-Peyrou, Chantal, Nunes, Hilario, Cazelles, Clarisse, Fourrage, Cécile, Ollivier, Emmanuelle, Marcais, Ambroise, Gamez, Anne-Sophie, Morice-Picard, Fanny, Caillaud, Denis, Pottier, Nicolas, Ménard, Christelle, Ba, Ibrahima, Fernandes, Alicia, Crestani, Bruno, de Villartay, Jean-Pierre, Gleizes, Pierre-Emmanuel, Callebaut, Isabelle, Kannengiesser, Caroline, Revy, Patrick

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Hunting for the genetic basis of Susac syndrome von David, Clemence, Papo, Thomas, Ba, Ibrahima, Ollivier, Emmanuelle, Boileau, Catherine, Dieudé, Philippe, Keren, Boris, Kannengiesser, Caroline, Sacre, Karim

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Increased diagnostic yield in complex dystonia through exome sequencing von Wirth, Thomas, Tranchant, Christine, Drouot, Nathalie, Keren, Boris, Mignot, Cyril, Cif, Laura, Lefaucheur, Romain, Lion-François, Laurence, Méneret, Aurélie, Gras, Domitille, Roze, Emmanuel, Laroche, Cécile, Burbaud, Pierre, Bannier, Stéphanie, Lagha-Boukbiza, Ouhaid, Spitz, Marie-Aude, Laugel, Vincent, Bereau, Matthieu, Ollivier, Emmanuelle, Nitschke, Patrick, Doummar, Diane, Rudolf, Gabrielle, Anheim, Mathieu, Chelly, Jamel

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Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism von Wirth, Thomas, Mariani, Louise Laure, Bergant, Gaber, Baulac, Michel, Habert, Marie‐Odile, Drouot, Nathalie, Ollivier, Emmanuelle, Hodžić, Alenka, Rudolf, Gorazd, Nitschke, Patrick, Rudolf, Gabrielle, Chelly, Jamel, Tranchant, Christine, Anheim, Mathieu, Roze, Emmanuel

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Exome sequencing in 57 patients with self-limited focal epilepsies of childhood with typical or atypical presentations suggests novel candidate genes von Rudolf, Gabrielle, de Bellescize, Julitta, de Saint Martin, Anne, Arzimanoglou, Alexis, Valenti Hirsch, Maria Paola, Labalme, Audrey, Boulay, Clotilde, Simonet, Thomas, Boland, Anne, Deleuze, Jean François, Nitschké, Patrick, Ollivier, Emmanuelle, Sanlaville, Damien, Hirsch, Edouard, Chelly, Jamel, Lesca, Gaetan

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NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal–Hreidarsson syndrome von Benyelles, Maname, O’donohue, Marie-Françoise, Kermasson, Laëtitia, Lainey, Elodie, Borie, Raphael, Lagresle-Peyrou, Chantal, Nunes, Hilario, Cazelles, Clarisse, Fourrage, Cécile, Ollivier, Emmanuelle, Marcais, Ambroise, Gamez, Anne-Sophie, Morice-Picard, Fanny, Caillaud, Denis, Pottier, Nicolas, Ménard, Christelle, Ba, Ibrahima, Fernandes, Alicia, Crestani, Bruno, de Villartay, Jean-Pierre, Gleizes, Pierre-Emmanuel, Callebaut, Isabelle, Kannengiesser, Caroline, Revy, Patrick

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Co-lethality studied as an asset against viral drug escape: the HIV protease case von Brouillet, Sophie, Valere, Thomas, Ollivier, Emmanuelle, Marsan, Laurent, Vanet, Anne

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Identification of genomic features using microsyntenies of domains: domain teams von Pasek, Sophie, Bergeron, Anne, Risler, Jean-Loup, Louis, Alexandra, Ollivier, Emmanuelle, Raffinot, Mathieu

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Massive Sequence Comparisons as a Help in Annotating Genomic Sequences von Louis, A.

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Codon usage as a tool to predict the cellular location of eukaryotic ribosomal proteins and aminoacyl-tRNA synthetases von Chiapello, Hélène, Ollivier, Emmanuelle, Landès-Devauchelle, Claudine, Nitschké, Patrick, Risler, Jean-Loup

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Massive sequence comparisons as a help in annotating genomic sequences von Louis, A, Ollivier, E, Aude, J C, Risler, J L

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A scale-independent signal processing method for sequence analysis von Viarl, Alain, Soldano, Henry, Ollivier, Emmanuelle

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'Multifrequency' location and clustering of sequence patterns from proteins von Ollivier, E, Soldano, H, Viari, A

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Method for identifying combinations of motifs that do not mutate simultaneously in a set of viral polypeptide sequences comprising a putative drug binding site von BROUILLET SOPHIE, VALERE THOMAS, OLLIVIER EMMANUELLE, MULLER-TRUTWIN MICHAELA, VANET ANNE, MARSAN LAURENT

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Method for identifying combinations of motifs that do not mutate simultaneously in a set of viral polypeptide sequences comprising a putative drug binding site von Vanet, Anne, Muller-Trutwin, Michaela, Valère, Thomas, Brouillet, Sophie, Ollivier, Emmanuelle, Marsan, Laurent

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Higher eucaryotic cdc25 proteins are structurally related to phosphoseryl/threonyl protein phosphatases von Belle´, Robert, Ollivier, Emmanuelle, Guerrucci, Marie-Anne

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Method for identifying motifs and/or combinations of motifs having a boolean state of predetermined mutation in a set of sequences and its applications von BROUILLET SOPHIE, VALERE THOMAS, OLLIVIER EMMANUELLE, MULLER-TRUTWIN MICHAELA, VANET ANNE, MARSAN LAURENT

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