Energy-harnessing problem solving of primordial life: Modeling the emergence of catalytic host-nested parasite life cycles by Conrad, Bernard, Iseli, Christian, Pirovino, Magnus

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Gene duplication: a drive for phenotypic diversity and cause of human disease by Conrad, Bernard, Antonarakis, Stylianos E

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A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes by Sarfati, Julie, Guiochon-Mantel, Anne, Rondard, Philippe, Arnulf, Isabelle, Garcia-Piñero, Alfons, Wolczynski, Slawomir, Brailly-Tabard, Sylvie, Bidet, Maud, Ramos-Arroyo, Maria, Mathieu, Michèle, Lienhardt-Roussie, Anne, Morgan, Graeme, Turki, Zinet, Bremont, Catherine, Lespinasse, James, Du Boullay, Hélène, Chabbert-Buffet, Nathalie, Jacquemont, Sébastien, Reach, Gérard, De Talence, Nicole, Tonella, Paolo, Conrad, Bernard, Despert, Francois, Delobel, Bruno, Brue, Thierry, Bouvattier, Claire, Cabrol, Sylvie, Pugeat, Michel, Murat, Arnaud, Bouchard, Philippe, Hardelin, Jean-Pierre, Dodé, Catherine, Young, Jacques

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Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes by Loviglio, M N, Leleu, M, Männik, K, Passeggeri, M, Giannuzzi, G, van der Werf, I, Waszak, S M, Zazhytska, M, Roberts-Caldeira, I, Gheldof, N, Migliavacca, E, Alfaiz, A A, Hippolyte, L, Maillard, A M, Van Dijck, A, Kooy, R F, Sanlaville, D, Rosenfeld, J A, Shaffer, L G, Andrieux, J, Marshall, C, Scherer, S W, Shen, Y, Gusella, J F, Thorsteinsdottir, U, Thorleifsson, G, Dermitzakis, E T, Deplancke, B, Beckmann, J S, Rougemont, J, Jacquemont, S, Reymond, A

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Neuropsychological impairments and the impact of dystrophin mutations on general cognitive functioning of patients with Duchenne muscular dystrophy by Wingeier, Kevin, Giger, Elisabeth, Strozzi, Susi, Kreis, Roland, Joncourt, Franziska, Conrad, Bernard, Gallati, Sabina, Steinlin, Maja

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Potential Mechanisms of Interferon-α Induced Autoimmunity by Conrad, Bernard

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Epstein-Barr Virus Transactivates the Human Endogenous Retrovirus HERV-K18 that Encodes a Superantigen by Sutkowski, Natalie, Conrad, Bernard, Thorley-Lawson, David A, Huber, Brigitte T

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Interferon-α-Induced Endogenous Superantigen: A Model Linking Environment and Autoimmunity by Stauffer, Yves, Marguerat, Samuel, Meylan, Françoise, Ucla, Catherine, Sutkowski, Natalie, Huber, Brigitte, Pelet, Thierry, Conrad, Bernard

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Potential Mechanisms of Interferon- Induced Autoimmunity by Conrad, Bernard

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Novel procedures for high-throughput analysis of a frequent insertion-deletion polymorphism in the human T-cell receptor beta locus by Conrad, Bernard

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Potential mechanisms of interferon-α induced autoimmunity: The Role of IFN in Autoimmunity by CONRAD, Bernard

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Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease – Identification of Eight Novel Mutations in CYBB and NCF2 Genes by Martel, Cécile, Mollin, Michelle, Beaumel, Sylvain, Brion, Jean Paul, Coutton, Charles, Satre, Véronique, Vieville, Gaëlle, Callanan, Mary, Lefebvre, Christine, Salmon, Alexandra, Pagnier, Anne, Plantaz, Dominique, Bost-Bru, Cécile, Eitenschenck, Laurence, Durieu, Isabelle, Floret, Daniel, Galambrun, Claire, Chambost, Hervé, Michel, Gérard, Stephan, Jean-Louis, Hermine, Olivier, Blanche, Stéphane, Blot, Nathalie, Rubié, Hervé, Pouessel, Guillaume, Drillon-Haus, Stephanie, Conrad, Bernard, Posfay-Barbe, Klara M., Havlicekova, Zuzana, Voskresenky-Baricic, Tamara, Jadranka, Kelecic, Arriazu, Maria Cristina, Garcia, Luis Alberto, Mansour, Lamia Sfaihi Ben, Bordigoni, Pierre, Stasia, Marie José

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Negative thymocyte selection to HERV-K18 superantigens in humans by Meylan, Françoise, De Smedt, Magda, Leclercq, Georges, Plum, Jean, Leupin, Olivier, Marguerat, Samuel, Conrad, Bernard

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Evidence for superantigen involvement in insulin-dependent diabetes mellitus aetiology by Conrad, Bernard, Weidmann, Eckhart, Trucco, Giuliana, Rudert, William A, Behboo, Roubik, Ricordi, Camillo, Rodriquez-Rilo, Horacio, Finegold, David, Trucco, Massimo

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A Human Endogenous Retroviral Superantigen as Candidate Autoimmune Gene in Type I Diabetes by Conrad, Bernard, Weissmahr, Richard Nicolas, Böni, Jürg, Arcari, Rosanna, Schüpbach, Jörg, Mach, Bernard

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Späte Mutterschaft und Aufschub der Familiengründung by Moffat, Rebecca, Raggi, Anna, Sartorius, Gideon, Conrad, Bernard, Lapaire, Olav, De Geyter, Christian

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A de novo 1.1–1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features by Béna, Frédérique, Bottani, Armand, Marcelli, Fabienne, Sizonenko, Loredana D'Amato, Conrad, Bernard, Dahoun, Sophie

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Unilateral focal polymicrogyria in a patient with classical Aarskog–Scott syndrome due to a novel missense mutation in an evolutionary conserved RhoGEF domain of the faciogenital d... by Bottani, Armand, Orrico, Alfredo, Galli, Lucia, Karam, Olivier, Haenggeli, Charles‐André, Ferey, Solène, Conrad, Bernard

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Erratum to: Clinical, Functional and Genetic Analysis of Twenty-Four Patients with Chronic Granulomatous Disease—Identification of Eight Novel Mutations in CYBB and NCF2 Genes by Martel, Cécile, Mollin, Michelle, Beaumel, Sylvain, Brion, Jean Paul, Coutton, Charles, Satre, Véronique, Vieville, Gaëlle, Callanan, Mary, Lefebvre, Christine, Salmon, Alexandra, Pagnier, Anne, Plantaz, Dominique, Bost-Bru, Cécile, Eitenschenck, Laurence, Durieu, Isabelle, Floret, Daniel, Galambrun, Claire, Chambost, Hervé, Michel, Gérard, Stephan, Jean-Louis, Hermine, Olivier, Blanche, Stéphane, Blot, Nathalie, Rubié, Hervé, Pouessel, Guillaume, Drillon-Haus, Stephanie, Conrad, Bernard, Posfay-Barbe, Klara M., Havlicekova, Zuzana, Voskresenky-Baricic, Tamara, Jadranka, Kelecic, Arriazu, Maria Cristina, Garcia, Luis Alberto, Sfaihi, Lamia Ben Mansour, Bordigoni, Pierre, Stasia, Marie José

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Transcriptional activation by bidirectional RNA polymerase II elongation over a silent promoter by Leupin, Olivier, Attanasio, Catia, Marguerat, Samuel, Tapernoux, Myriam, Antonarakis, Stylianos E, Conrad, Bernard

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