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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ADAM33, a new candidate for psoriasis susceptibility von Lesueur, Fabienne, Oudot, Tiphaine, Heath, Simon, Foglio, Mario, Lathrop, Mark, Prud'homme, Jean-François, Fischer, Judith

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Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3 von Lefèvre, Caroline, Bouadjar, Bakar, Ferrand, Véronique, Tadini, Gianluca, Mégarbané, André, Lathrop, Mark, Prud'homme, Jean-François, Fischer, Judith

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First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene von Baulac, Stéphanie, Huberfeld, Gilles, Gourfinkel-An, Isabelle, Mitropoulou, Georgia, Beranger, Alexandre, Prud'homme, Jean-François, Baulac, Michel, Brice, Alexis, Bruzzone, Roberto, LeGuern, Eric

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Exploration of the Genetic Architecture of Idiopathic Generalized Epilepsies von Hempelmann, Anne, Taylor, Kirsten P., Heils, Armin, Lorenz, Susanne, Prud'Homme, Jean‐Francois, Nabbout, Rima, Dulac, Olivier, Rudolf, Gabrielle, Zara, Federico, Bianchi, Amedeo, Robinson, Robert, Gardiner, R. Mark, Covanis, Athanasios, Lindhout, Dick, Stephani, Ulrich, Elger, Christian E., Weber, Yvonne G., Lerche, Holger, Nürnberg, Peter, Kron, Katherine L., Scheffer, Ingrid E., Mulley, John C., Berkovic, Samuel F., Sander, Thomas

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Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families von Lesueur, Fabienne, Lefèvre, Caroline, Has, Cristina, Guilloud-Bataille, Michel, Oudot, Tiphaine, Mahé, Emmanuel, Lahfa, Morad, Mansouri, Samira, Mosharraf-Olmolk, Haydeh, Sobel, Eric, Heath, Simon, Lathrop, Mark, Dizier, Marie-Hélène, Prud'Homme, Jean-François, Fischer, Judith

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Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis von Lefèvre, Caroline, Bouadjar, Bakar, Karaduman, Aysen, Jobard, Florence, Saker, Safa, Özguc, Meral, Lathrop, Mark, Prud'homme, Jean-François, Fischer, Judith

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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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Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome von Jobard, Florence, Bouadjar, Bakar, Caux, Frédéric, Hadj-Rabia, Smail, Has, Christina, Matsuda, Fumi, Weissenbach, Jean, Lathrop, Mark, Prud'homme, Jean-François, Fischer, Judith

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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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l-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1 von Topçu, Meral, Jobard, Florence, Halliez, Sophie, Coskun, Turgay, Yalçinkayal, Cengiz, Gerceker, Filiz Ozbas, Wanders, Ronald J.A., Prud'homme, Jean-François, Lathrop, Mark, Özguc, Meral, 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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Genome search for susceptibility loci of common idiopathic generalised epilepsies von SANDER, T, SCHULZ, H, VILLE, D, CIEUTA, C, PICARD, F, PRUD'HOMME, J.-F, BATE, L, SUNDQUIST, A, GARDINER, R. M, JANSSEN, G. A. M. A. J, DE HAAN, G.-J, KASTELEIJN-NOLST-TRENITE, D. G. A, SAAR, K, BADER, A, LINDHOUT, D, RIESS, O, WIENKER, T. F, JANZ, D, REIS, A, GENNARO, E, RIGGIO, M. C, BIANCHI, A, ZARA, F, LUNA, D, BULTEAU, C, KAMINSKA, A

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An Association Study of 22 Candidate Genes in Psoriasis Families Reveals Shared Genetic Factors with Other Autoimmune and Skin Disorders von Oudot, Tiphaine, Lesueur, Fabienne, Guedj, Mickaël, de Cid, Rafael, McGinn, Steven, Heath, Simon, Foglio, Mario, Prum, Bernard, Lathrop, Mark, Prud'homme, Jean-François, Fischer, Judith

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Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31 von Baulac, Stéphanie, Picard, Fabienne, Herman, Alexandra, Feingold, Josué, Genin, Emmanuelle, Hirsch, Edouard, Prud'Homme, Jean-François, Baulac, Michel, Brice, Alexis, LeGuern, Eric

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PARTIDOS Y SISTEMA DE PARTIDOS EN LAS ELECCIONES MEXICANAS DE 2018 von Prud’homme, Jean-François

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A locus for simple pure febrile seizures maps to chromosome 6q22–q24 von Nabbout, Rima, Prud’homme, Jean‐François, Herman, Alexandra, Feingold, Josué, Brice, Alexis, Dulac, Olivier, LeGuern, Eric

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Linkage Analysis and Disease Models in Benign Familial Infantile Seizures: A Study of 16 Families von Striano, Pasquale, Lispi, Maria Luisa, Gennaro, Elena, Madia, Francesca, Traverso, Monica, Bordo, Laura, Aridon, Paolo, Boneschi, Filippo Martinelli, Barone, Baldassare, Bernardina, Bernardo dalla, Bianchi, Amedeo, Capovilla, Giuseppe, De Marco, Pasquale, Dulac, Olivier, Gaggero, Roberto, Gambardella, Antonio, Nabbout, Rima, Prud'homme, Jean‐François, Day, Ruth, Vanadia, Francesca, Vecchi, Marilena, Veggiotti, Pierangelo, Vigevano, Federico, Viri, Maurizio, Minetti, Carlo, Zara, Federico

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Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1 von Jobard, Florence, Lefèvre, Caroline, Karaduman, Aysen, Blanchet-Bardon, Claudine, Emre, Serap, Weissenbach, Jean, Ozgüc, Meral, Lathrop, Mark, Prud'homme, Jean-François, Fischer, Judith

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Novel Mutations in the Gene Encoding Secreted Lymphocyte Antigen-6/Urokinase-type Plasminogen Activator Receptor-related Protein-1 (SLURP-1) and Description of Five Ancestral Haplo... von Marrakchi, Slaheddine, Zahaf, Abdelmadjid, Turki, Hamida, Audebert, Stéphanie, Bouadjar, Bakar, Has, Christina, Lefèvre, Caroline, Munro, Colin, Cure, Susan, Jobard, Florence, Morlot, Susanne, Hohl, Daniel, Prud'homme, Jean-François, Fischer, Judith

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