DDX3X syndrome: From clinical phenotypes to biological insights von Mueffling, Alexa, Garcia‐Forn, Marta, De Rubeis, Silvia

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Control of heterochromatin localization and silencing by the nuclear membrane protein Lem2 von Barrales, Ramón Ramos, Forn, Marta, Georgescu, Paula Raluca, Sarkadi, Zsuzsa, Braun, Sigurd

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Neuron type‐specific increase in lamin B1 contributes to nuclear dysfunction in Huntington’s disease von Alcalá‐Vida, Rafael, Garcia‐Forn, Marta, Castany‐Pladevall, Carla, Creus‐Muncunill, Jordi, Ito, Yoko, Blanco, Enrique, Golbano, Arantxa, Crespí‐Vázquez, Kilian, Parry, Aled, Slater, Guy, Samarajiwa, Shamith, Peiró, Sandra, Di Croce, Luciano, Narita, Masashi, Pérez‐Navarro, Esther

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Pharmacogenetic modulation of STEP improves motor and cognitive function in a mouse model of Huntington's disease von García-Forn, Marta, Martínez-Torres, Sara, García-Díaz Barriga, Gerardo, Alberch, Jordi, Milà, Montse, Azkona, Garikoitz, Pérez-Navarro, Esther

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Deconstruction of DNA Methylation Patterns During Myogenesis Reveals Specific Epigenetic Events in the Establishment of the Skeletal Muscle Lineage von carrió, Elvira, Díez‐Villanueva, Anna, Lois, Sergi, Mallona, Izaskun, Cases, Ildefonso, Forn, Marta, Peinado, Miguel A., Suelves, Mònica

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Lamin B1 and nuclear morphology in peripheral cells as new potential biomarkers to follow treatment response in Huntington's disease von Garcia‐Forn, Marta, Castany‐Pladevall, Carla, Golbano, Arantxa, Pérez‐Pérez, Jesús, Brito, Verónica, Kulisevsky, Jaime, Pérez‐Navarro, Esther

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Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex von Salamon, Iva, Park, Yongkyu, Miškić, Terezija, Kopić, Janja, Matteson, Paul, Page, Nicholas F., Roque, Alfonso, McAuliffe, Geoffrey W., Favate, John, Garcia-Forn, Marta, Shah, Premal, Judaš, Miloš, Millonig, James H., Kostović, Ivica, De Rubeis, Silvia, Hart, Ronald P., Krsnik, Željka, Rasin, Mladen-Roko

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Overlapping DNA methylation dynamics in mouse intestinal cell differentiation and early stages of malignant progression von Forn, Marta, Díez-Villanueva, Anna, Merlos-Suárez, Anna, Muñoz, Mar, Lois, Sergi, Carriò, Elvira, Jordà, Mireia, Bigas, Anna, Batlle, Eduard, Peinado, Miguel A

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RTP801/REDD1 Is Involved in Neuroinflammation and Modulates Cognitive Dysfunction in Huntington's Disease von Pérez-Sisqués, Leticia, Solana-Balaguer, Júlia, Campoy-Campos, Genís, Martín-Flores, Núria, Sancho-Balsells, Anna, Vives-Isern, Marcel, Soler-Palazón, Ferran, Garcia-Forn, Marta, Masana, Mercè, Alberch, Jordi, Pérez-Navarro, Esther, Giralt, Albert, Malagelada, Cristina

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Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome von Boitnott, Andrea, Garcia-Forn, Marta, Ung, Devina C., Niblo, Kristi, Mendonca, Danielle, Park, Yeaji, Flores, Michael, Maxwell, Sylvia, Ellegood, Jacob, Qiu, Lily R., Grice, Dorothy E., Lerch, Jason P., Rasin, Mladen-Roko, Buxbaum, Joseph D., Drapeau, Elodie, De Rubeis, Silvia

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Linking Autism Risk Genes to Disruption of Cortical Development von Garcia-Forn, Marta, Boitnott, Andrea, Akpinar, Zeynep, De Rubeis, Silvia

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Changes in the pattern of DNA methylation associate with twin discordance in systemic lupus erythematosus von Javierre, Biola M, Fernandez, Agustin F, Richter, Julia, Al-Shahrour, Fatima, Martin-Subero, J Ignacio, Rodriguez-Ubreva, Javier, Berdasco, Maria, Fraga, Mario F, O'Hanlon, Terrance P, Rider, Lisa G, Jacinto, Filipe V, Lopez-Longo, F Javier, Dopazo, Joaquin, Forn, Marta, Peinado, Miguel A, Carreño, Luis, Sawalha, Amr H, Harley, John B, Siebert, Reiner, Esteller, Manel, Miller, Frederick W, Ballestar, Esteban

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Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4 von Campisi, Laura, Chizari, Shahab, Ho, Jessica S. Y., Gromova, Anastasia, Arnold, Frederick J., Mosca, Lorena, Mei, Xueyan, Fstkchyan, Yesai, Torre, Denis, Beharry, Cindy, Garcia-Forn, Marta, Jiménez-Alcázar, Miguel, Korobeynikov, Vladislav A., Prazich, Jack, Fayad, Zahi A., Seldin, Marcus M., De Rubeis, Silvia, Bennett, Craig L., Ostrow, Lyle W., Lunetta, Christian, Squatrito, Massimo, Byun, Minji, Shneider, Neil A., Jiang, Ning, La Spada, Albert R., Marazzi, Ivan

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Increased translation as a novel pathogenic mechanism in Huntington's disease von Creus-Muncunill, Jordi, Badillos-Rodríguez, Raquel, Garcia-Forn, Marta, Masana, Mercè, Garcia-Díaz Barriga, Gerardo, Guisado-Corcoll, Anna, Alberch, Jordi, Malagelada, Cristina, Delgado-García, José M, Gruart, Agnès, Pérez-Navarro, Esther

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Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome von Boitnott, Andrea, Garcia-Forn, Marta, Ung, Dévina C., Niblo, Kristi, Mendonca, Danielle, Park, Yeaji, Flores, Michael, Maxwell, Sylvia, Ellegood, Jacob, Qiu, Lily R., Grice, Dorothy E., Lerch, Jason P., Rasin, Mladen-Roko, Buxbaum, Joseph D., Drapeau, Elodie, De Rubeis, Silvia

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Neuronal diversity and stereotypy at multiple scales through whole brain morphometry von Liu, Yufeng, Jiang, Shengdian, Li, Yingxin, Zhao, Sujun, Yun, Zhixi, Zhao, Zuo-Han, Zhang, Lingli, Wang, Gaoyu, Chen, Xin, Manubens-Gil, Linus, Hang, Yuning, Gong, Qiaobo, Li, Yuanyuan, Qian, Penghao, Qu, Lei, Garcia-Forn, Marta, Wang, Wei, De Rubeis, Silvia, Wu, Zhuhao, Osten, Pavel, Gong, Hui, Hawrylycz, Michael, Mitra, Partha, Dong, Hongwei, Luo, Qingming, Ascoli, Giorgio A., Zeng, Hongkui, Liu, Lijuan, Peng, Hanchuan

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Shelterin and subtelomeric DNA sequences control nucleosome maintenance and genome stability von van Emden, Thomas S, Forn, Marta, Forné, Ignasi, Sarkadi, Zsuzsa, Capella, Matías, Martín Caballero, Lucía, Fischer‐Burkart, Sabine, Brönner, Cornelia, Simonetta, Marco, Toczyski, David, Halic, Mario, Imhof, Axel, Braun, Sigurd

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Lack of Annexin A6 Exacerbates Liver Dysfunction and Reduces Lifespan of Niemann-Pick Type C Protein–Deficient Mice von Meneses-Salas, Elsa, Garcia-Forn, Marta, Castany-Pladevall, Carla, Lu, Albert, Fajardo, Alba, Jose, Jaimy, Wahba, Mohamed, Bosch, Marta, Pol, Albert, Tebar, Francesc, Klein, Andrés D., Zanlungo, Silvana, Pérez-Navarro, Esther, Grewal, Thomas, Enrich, Carlos, Rentero, Carles

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Lack of Annexin A6 exacerbates liver dysfunction and reduces lifespan of Niemann-Pick type C protein-deficient mice von Meneses Salas, Elsa, Garcia-Forn, Marta, Castany Pladevall, Carla, Lu, Albert, Fajardo, Alba, Jose, Jaimy, Wahba, Mohamed, Bosch i Rodríguez, Marta, Pol i Sorolla, Albert, Tebar Ramon, Francesc, Klein, Andrés D, Zanlungo, Silvana, Pérez Navarro, Esther, Grewal, Thomas, Enrich Bastús, Carles, Rentero Alfonso, Carles

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Author Correction: Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4 von Campisi, Laura, Chizari, Shahab, Ho, Jessica S. Y., Gromova, Anastasia, Arnold, Frederick J., Mosca, Lorena, Mei, Xueyan, Fstkchyan, Yesai, Torre, Denis, Beharry, Cindy, Garcia-Forn, Marta, Jiménez-Alcázar, Miguel, Korobeynikov, Vladislav A., Prazich, Jack, Fayad, Zahi A., Seldin, Marcus M., De Rubeis, Silvia, Bennett, Craig L., Ostrow, Lyle W., Lunetta, Christian, Squatrito, Massimo, Byun, Minji, Shneider, Neil A., Jiang, Ning, La Spada, Albert R., Marazzi, Ivan

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