Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia von Kulis, Marta, Heath, Simon, Bibikova, Marina, Queirós, Ana C, Navarro, Alba, Clot, Guillem, Martínez-Trillos, Alejandra, Castellano, Giancarlo, Brun-Heath, Isabelle, Pinyol, Magda, Barberán-Soler, Sergio, Papasaikas, Panagiotis, Jares, Pedro, Beà, Sílvia, Rico, Daniel, Ecker, Simone, Rubio, Miriam, Royo, Romina, Ho, Vincent, Klotzle, Brandy, Hernández, Lluis, Conde, Laura, López-Guerra, Mónica, Colomer, Dolors, Villamor, Neus, Aymerich, Marta, Rozman, María, Bayes, Mónica, Gut, Marta, Gelpí, Josep L, Orozco, Modesto, Fan, Jian-Bing, Quesada, Víctor, Puente, Xose S, Pisano, David G, Valencia, Alfonso, López-Guillermo, Armando, Gut, Ivo, López-Otín, Carlos, Campo, Elías, Martín-Subero, José I

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Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder von Ramos-Quiroga, Josep-Antoni, Sánchez-Mora, Cristina, Casas, Miguel, Garcia-Martínez, Iris, Bosch, Rosa, Nogueira, Mariana, Corrales, Montse, Palomar, Gloria, Vidal, Raquel, Coll-Tané, Mireia, Bayés, Mònica, Cormand, Bru, Ribasés, Marta

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Mutational Mechanisms of Williams-Beuren Syndrome Deletions von Bayés, Mònica, Magano, Luis F., Rivera, Núria, Flores, Raquel, A. Pérez Jurado, Luis

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Design and evaluation of a panel of single-nucleotide polymorphisms in microRNA genomic regions for association studies in human disease von Muiños-Gimeno, Margarita, Montfort, Magda, Bayés, Mònica, Estivill, Xavier, Espinosa-Parrilla, Yolanda

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Association Study of 10 Genes Encoding Neurotrophic Factors and Their Receptors in Adult and Child Attention-Deficit/Hyperactivity Disorder von Ribasés, Marta, Hervás, Amaia, Ramos-Quiroga, Josep Antoni, Bosch, Rosa, Bielsa, Anna, Gastaminza, Xavier, Fernández-Anguiano, Mònica, Nogueira, Mariana, Gómez-Barros, Núria, Valero, Sergi, Gratacòs, Mònica, Estivill, Xavier, Casas, Miquel, Cormand, Bru, Bayés, Mònica

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Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion von Cuscó, Ivon, Corominas, Roser, Bayés, Mònica, Flores, Raquel, Rivera-Brugués, Núria, Campuzano, Victoria, Pérez-Jurado, Luis A

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Low Exchangeability of Selenocysteine, the 21st Amino Acid, in Vertebrate Proteins von Castellano, Sergi, Andrés, Aida M., Bosch, Elena, Bayes, Mònica, Guigó, Roderic, Clark, Andrew G.

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A Brain-Derived Neurotrophic Factor Haplotype Is Associated with Therapeutic Response in Obsessive-Compulsive Disorder von Real, Eva, Gratacòs, Mònica, Soria, Virginia, Escaramís, Geòrgia, Alonso, Pino, Segalàs, Cinto, Bayés, Mònica, de Cid, Rafael, Menchón, José M, Estivill, Xavier

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Evolution of Robustness to Protein Mistranslation by Accelerated Protein Turnover von Kalapis, Dorottya, Bezerra, Ana R, Farkas, Zoltán, Horvath, Peter, Bódi, Zoltán, Daraba, Andreea, Szamecz, Béla, Gut, Ivo, Bayes, Mónica, Santos, Manuel A S, Pál, Csaba

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Ectodysplasin Is a Collagenous Trimeric Type II Membrane Protein with a Tumor Necrosis Factor-Like Domain and Co-Localizes With Cytoskeletal Structures at Lateral and Apical Surfac... von Ezer, Sini, Bayés, Mònica, OutiElomaa, Schlessinger, David, Kere, Juha

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Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred von Cuenca-León, Ester, Corominas, Roser, Montfort, Magda, Artigas, Josep, Roig, Manuel, Bayés, Mònica, Cormand, Bru, Macaya, Alfons

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Systemic Inflammation in Preclinical Ulcerative Colitis von Bergemalm, Daniel, Andersson, Erik, Hultdin, Johan, Eriksson, Carl, Rush, Stephen T., Kalla, Rahul, Adams, Alex T., Keita, Åsa V., D’Amato, Mauro, Gomollon, Fernando, Jahnsen, Jørgen, Arnott, Ian D., Bayes, Monica, Bonfiglio, Ferdinando, Boyapati, Ray K., Carstens, Adam, Casén, Christina, Ciemniejewska, Ewa, Dahl, Fredrik A., Detlie, Trond Espen, Drummond, Hazel E., Ekeland, Gunn S., Ekman, Daniel, Frengen, Anna B., Gullberg, Mats, Gut, Ivo G., Gut, Marta, Heath, Simon C., Hjelm, Fredrik, Hjortswang, Henrik, Ho, Gwo-Tzer, Jonkers, Daisy, Söderholm, Johan, Kennedy, Nicholas A., Lees, Charles W., Lindahl, Torbjørn, Lindqvist, Mårten, Merkel, Angelika, Modig, Eddie, Moen, Aina E.F., Nilsen, Hilde, Nimmo, Elaine R., Noble, Colin L., Nordberg, Niklas, O’Leary, Kate R., Ocklind, Anette, Olbjørn, Christine, Pettersson, Erik, Pierik, Marieke, Dominique, Ricanek, Petr, Satsangi, Jack, Repsilber, Dirk, Karling, Pontus, Halfvarson, Jonas

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Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease von Ventham, N. T., Kennedy, N. A., Adams, A. T., Kalla, R., Heath, S., O'Leary, K. R., Drummond, H., Wilson, D. C., Gut, I. G., Nimmo, E. R., Satsangi, J.

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Spinal Muscular Atrophy Associated with Progressive Myoclonic Epilepsy Is Caused by Mutations in ASAH1 von Zhou, Jie, Tawk, Marcel, Tiziano, Francesco Danilo, Veillet, Julien, Bayes, Monica, Nolent, Flora, Garcia, Virginie, Servidei, Serenella, Bertini, Enrico, Castro-Giner, Francesc, Renda, Yavuz, Carpentier, Stéphane, Andrieu-Abadie, Nathalie, Gut, Ivo, Levade, Thierry, Topaloglu, Haluk, Melki, Judith

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The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons von Simões, João, Bezerra, Ana R, Moura, Gabriela R, Araújo, Hugo, Gut, Ivo, Bayes, Mónica, Santos, Manuel A S

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DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders von Reif, Andreas, Nguyen, T Trang, Weißflog, Lena, Jacob, Christian P, Romanos, Marcel, Renner, Tobias J, Buttenschon, Henriette N, Kittel-schneider, Sarah, Gessner, Alexandra, Weber, Heike, Neuner, Maria, Gross-lesch, Silke, Zamzow, Karin, Kreiker, Susanne, Walitza, Susanne, Meyer, Jobst, Freitag, Christine M, Bosch, Rosa, Casas, Miquel, Gómez, Nuria, Ribasès, Marta, Bayès, Mónica, Buitelaar, Jan K, Kiemeney, Lambertus Alm, Kooij, Jj Sandra, Kan, Cees C, Hoogman, Martine, Johansson, Stefan, Jacobsen, Kaya K, Knappskog, Per M, Fasmer, Ole B, Asherson, Phil, Warnke, Andreas, Grabe, Hans-jörgen, Mahler, Jessie, Teumer, Alexander, Völzke, Henry, Mors, Ole N, Schäfer, Helmut

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Characterization of alternatively spliced products and tissue-specific isoforms of USP28 and USP25 von Valero, R, Bayés, M, Francisca Sánchez-Font, M, González-Angulo, O, Gonzàlez-Duarte, R, Marfany, G

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The involvement of serotonin polymorphisms in autistic spectrum symptomatology von Hervás, Amaia, Toma, Claudio, Romarís, Patricia, Ribasés, Marta, Salgado, Marta, Bayes, Mònica, Balmaña, Noemí, Cormand, Bru, Maristany, Marta, Guijarro, Silvina, Arranz, María J

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Reversion of a fungal genetic code alteration links proteome instability with genomic and phenotypic diversification von Bezerra, Ana R., Simões, João, Lee, Wanseon, Rung, Johan, Weil, Tobias, Gut, Ivo G., Gut, Marta, Bayés, Mónica, Rizzetto, Lisa, Cavalieri, Duccio, Giovannini, Gloria, Bozza, Silvia, Romani, Luigina, Kapushesky, Misha, Moura, Gabriela R., Santos, Manuel A. S.

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Analysis of Systemic Epigenetic Alterations in Inflammatory Bowel Disease: Defining Geographical, Genetic and Immune-Inflammatory influences on the Circulating Methylome von Kalla, Rahul, Adams, Alex T, Nowak, Jan K, Bergemalm, Daniel, Vatn, Simen, Ventham, Nicholas T, Kennedy, Nicholas A, Ricanek, Petr, Lindstrom, Jonas, Söderholm, Johan, Pierik, Marie, D'Amato, Mauro, Gomollón, Fernando, Olbjørn, Christine, Richmond, Rebecca, Relton, Caroline, Jahnsen, Jørgen, Vatn, Morten H, Halfvarson, Jonas, Satsangi, Jack

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