Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans von Radner, Franz P W, Marrakchi, Slaheddine, Kirchmeier, Peter, Kim, Gwang-Jin, Ribierre, Florence, Kamoun, Bourane, Abid, Leila, Leipoldt, Michael, Turki, Hamida, Schempp, Werner, Heilig, Roland, Lathrop, Mark, Fischer, Judith

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DNA replication origin interference increases the spacing between initiation events in human cells von Lebofsky, Ronald, Heilig, Roland, Sonnleitner, Max, Weissenbach, Jean, Bensimon, Aaron

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Genome-enabled phylogenetic and functional reconstruction of an araphid pennate diatom Plagiostriata sp. CCMP470, previously assigned as a radial centric diatom, and its bacterial... von Sato, Shinya, Nanjappa, Deepak, Dorrell, Richard G., Vieira, Fabio Rocha Jimenez, Kazamia, Elena, Tirichine, Leila, Veluchamy, Alaguraj, Heilig, Roland, Aury, Jean-Marc, Jaillon, Olivier, Wincker, Patrick, Fussy, Zoltan, Obornik, Miroslav, Muñoz-Gómez, Sergio A., Mann, David G., Bowler, Chris, Zingone, Adriana

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Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome von Lefèvre, Caroline, Jobard, Florence, Caux, Frédéric, Bouadjar, Bakar, Karaduman, Aysen, Heilig, Roland, Lakhdar, Hakima, Wollenberg, Andreas, Verret, Jean-Luc, Weissenbach, Jean, Özgüc, Meral, Lathrop, Mark, Prud'homme, Jean-François, Fischer, Judith

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia von Heilig, Roland, Dürr, Alexandra, Brottier, Philippe, Fontaine, Bertrand, Weissenbach, Jean, Burgunder, Jean-Marc, Paternotte, Caroline, Fonknechten, Nùria, Samson, Delphine, Cruaud, Corinne, Wincker, Patrick, Davoine, Claire-Sophie, Brice, Alexis, Hazan, Jamilé, Cattolico, Laurence, Mavel, Delphine, Artiguenave, François, Barbe, Valérie, Prud'homme, Jean-François

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An integrated analysis of the genome of the hyperthermophilic archaeon Pyrococcus abyssi von Cohen, Georges N., Barbe, Valérie, Flament, Didier, Galperin, Michael, Heilig, Roland, Lecompte, Odile, Poch, Olivier, Prieur, Daniel, Quérellou, Joël, Ripp, Raymond, Thierry, Jean‐Claude, Van der Oost, John, Weissenbach, Jean, Zivanovic, Yvan, Forterre, Patrick

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A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family von Cruaud, Corinne, Leibovici, Michel, Compain, Sylvie, Lacombe, Didier, Bitner-Glindzicz, Maria, Vigneron, Jacqueline, Boven, Katia, Petit, Christine, Charachon, Robert, Francis, Mary, Weil, Dominique, Regemorter, Nicole Van, Samson, Delphine, Weissenbach, Jean, Bedbeder, Philippe, Heilig, Roland, Sahly, Iman, Abdelhak, Sonia, Kalatzis, Vasiliki, Vincent, Christophe

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Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans von Radner, Franz P. W., Marrakchi, Slaheddine, Kirchmeier, Peter, Kim, Gwang-Jin, Ribierre, Florence, Kamoun, Bourane, Abid, Leila, Leipoldt, Michael, Turki, Hamida, Schempp, Werner, Heilig, Roland, Lathrop, Mark, Fischer, Judith

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Characterization of the NPHP1 Locus: Mutational Mechanism Involved in Deletions in Familial Juvenile Nephronophthisis von Saunier, Sophie, Calado, Joaquim, Benessy, France, Silbermann, Flora, Heilig, Roland, Weissenbach, Jean, Antignac, Corinne

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Continuum of overlapping clones spanning the entire human chromosome 21q von Chumakov, Ilya, Rigault, Philippe, Guillou, Sophie, Ougen, Pierre, Billaut, Alain, Guasconi, Ghislaine, Gervy, Patricia, LeGall, Isabelle, Soularue, Pascal, Grinas, Laurent, Bougueleret, Lydie, Bellanné-Chantelot, Christine, Lacroix, Bruno, Barillot, Emmanuel, Gesnouin, Philippe, Pook, Stuart, Vaysseix, Guy, Frelat, Gerard, Schmitz, Annette, Sambucy, Jean-Luc, Bosch, Assumpcio, Estivill, Xavier, Weissenbach, Jean, Vignal, Alain, Riethman, Harold, Cox, David, Patterson, David, Gardiner, Kathleen, Hattori, Masahira, Sakaki, Yoshiyuki, Ichikawa, Hitoshi, Ohki, Misao, Paslier, Denis Le, Heilig, Roland, Antonarakis, Stylianos, Cohen, Daniel

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Expanding the Mutation Spectrum Affecting alpha IIb beta 3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort von Nurden, Alan T, Pillois, Xavier, Fiore, Mathieu, Alessi, Marie-Christine, Bonduel, Mariana, Dreyfus, Marie, Goudemand, Jenny, Gruel, Yves, Benabdallah-Guerida, Scheherazade, Latger-Cannard, Veronique, Negrier, Claude, Nugent, Diane, Oiron, Roseline d, Rand, Margaret L, Sie, Pierre, Trossaert, Marc, Alberio, Lorenzo, Martins, Nathalie, Sirvain-Trukniewicz, Peggy, Couloux, Arnaud, Canault, Mathias, Fronthroth, Juan Pablo, Fretigny, Mathilde, Nurden, Paquita, Heilig, Roland, Vinciguerra, Christine

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Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort von Nurden, Alan T., Pillois, Xavier, Fiore, Mathieu, Alessi, Marie-Christine, Bonduel, Mariana, Dreyfus, Marie, Goudemand, Jenny, Gruel, Yves, Benabdallah-Guerida, Schéhérazade, Latger-Cannard, Véronique, Négrier, Claude, Nugent, Diane, Oiron, Roseline d, Rand, Margaret L., Sié, Pierre, Trossaert, Marc, Alberio, Lorenzo, Martins, Nathalie, Sirvain-Trukniewicz, Peggy, Couloux, Arnaud, Canault, Mathias, Fronthroth, Juan Pablo, Fretigny, Mathilde, Nurden, Paquita, Heilig, Roland, Vinciguerra, Christine

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Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2 von Lefèvre, Caroline, Audebert, Stéphanie, Jobard, Florence, Bouadjar, Bakar, Lakhdar, Hakima, Boughdene-Stambouli, Omar, Blanchet-Bardon, Claudine, Heilig, Roland, Foglio, Mario, Weissenbach, Jean, Lathrop, Mark, Prud'homme, Jean-François, Fischer, Judith

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A candidate gene for familial Mediterranean fever von The French FMF Consortium, Bernot, Alain, Clepet, Christian, Dasilva, Corinne, Devaud, Catherine, Petit, Jean-Louis, Caloustian, Christophe, Cruaud, Corinne, Samson, Delphine, Pulcini, Françoise, Weissenbach, Jean, Heilig, Roland, Notanicola, Cécile, Domingo, Cécile, Rozenbaum, Michael, Benchetrit, Eldad, Topaloglu, Rezzan, Dewalle, Marie, Dross, Christiane, Hadjari, Philippe, Dupont, Madeleine, Demaille, Jacques, Touitou, Isabelle, Smaoui, Nizar, Nedelec, Brigitte, Méry, Jean-Philippe, Chaabouni, Habiba, Delpech, Marc, Grateau, Gilles

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The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis von Chambaud, I, Heilig, R, Ferris, S, Barbe, V, Samson, D, Galisson, F, Moszer, I, Dybvig, K, Wróblewski, H, Viari, A, Rocha, E P, Blanchard, A

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Bacterial Mode of Replication with Eukaryotic-Like Machinery in a Hyperthermophilic Archaeon von Myllykallio, Hannu, Lopez, Philippe, López-García, Purificación, Heilig, Roland, Saurin, William, Zivanovic, Yvan, Philippe, Hervé, Forterre, Patrick

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Mutations in the gene encoding SLURP-1 in Mal de Meleda von FISCHER, Judith, BOUADJAR, Bakar, LATHROP, Mark, HOHL, Daniel, PRUD-HOMME, Jean-Francois, HEILIG, Roland, HUBER, Marcel, LEFEVRE, Caroline, JOBARD, Florence, MACARI, Francoise, BAKIJA-KONSUO, Ana, ALT-BELKACEM, Farid, WEISSENBACH, Jean

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Expanding the Mutation Spectrum Affecting [alpha]IIb[beta]3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International Cohort von Nurden, Alan T, Pillois, Xavier, Fiore, Mathieu, Alessi, Marie-Christine, Bonduel, Mariana, Dreyfus, Marie, Goudemand, Jenny, Gruel, Yves, Benabdallah-Guerida, Schéhérazade, Latger-Cannard, Véronique, Negrier, Claude, Nugent, Diane, Oiron, Roseline d, Rand, Margaret L, Sie, Pierre, Trossaert, Marc, Alberio, Lorenzo, Martins, Nathalie, Sirvain-Trukniewicz, Peggy, Couloux, Arnaud, Canault, Mathias, Fronthroth, Juan Pablo, Fretigny, Mathilde, Nurden, Paquita, Heilig, Roland, Vinciguerra, Christine

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Correction: Mutations in Cause Autosomal Recessive Congenital Ichthyosis in Humans von Franz P. W. Radner, Slaheddine Marrakchi, Peter Kirchmeier, Gwang-Jin Kim, Florence Ribierre, Bourane Kamoun, Leila Abid, Michael Leipoldt, Hamida Turki, Werner Schempp, Roland Heilig, Mark Lathrop, Judith Fischer

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Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans: e1003536 von Radner, Franz PW, Marrakchi, Slaheddine, Kirchmeier, Peter, Kim, Gwang-Jin, Ribierre, Florence, Kamoun, Bourane, Abid, Leila, Leipoldt, Michael, Turki, Hamida, Schempp, Werner, Heilig, Roland, Lathrop, Mark, Fischer, Judith

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