A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD) von Giorgio, Elisa, Robyr, Daniel, Spielmann, Malte, Ferrero, Enza, Di Gregorio, Eleonora, Imperiale, Daniele, Vaula, Giovanna, Stamoulis, Georgios, Santoni, Federico, Atzori, Cristiana, Gasparini, Laura, Ferrera, Denise, Canale, Claudio, Guipponi, Michel, Pennacchio, Len A, Antonarakis, Stylianos E, Brussino, Alessandro, Brusco, Alfredo

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Microarray Deacetylation Maps Determine Genome-Wide Functions for Yeast Histone Deacetylases von Robyr, Daniel, Suka, Yuko, Xenarios, Ioannis, Kurdistani, Siavash K., Wang, Amy, Suka, Noriyuki, Grunstein, Michael

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Non-invasive prenatal testing leading to a maternal diagnosis of Charcot–Marie–Tooth neuropathy von Kumps, Camille, Niel Bütschi, Florence, Rapin, Blandine, Baud, David, Pescia, Graziano, Robyr, Daniel, Superti-Furga, Andrea, Unger, Sheila

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In vitro whole-genome analysis identifies a susceptibility locus for HIV-1 von Loeuillet, Corinne, Deutsch, Samuel, Ciuffi, Angela, Robyr, Daniel, Taffé, Patrick, Muñoz, Miguel, Beckmann, Jacques S, Antonarakis, Stylianos E, Telenti, Amalio

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A systematic enhancer screen using lentivector transgenesis identifies conserved and non-conserved functional elements at the Olig1 and Olig2 locus von Friedli, Marc, Barde, Isabelle, Arcangeli, Mélanie, Verp, Sonia, Quazzola, Alexandra, Zakany, Jozsef, Lin-Marq, Nathalie, Robyr, Daniel, Attanasio, Catia, Spitz, François, Duboule, Denis, Trono, Didier, Antonarakis, Stylianos E

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Chromosome conformation capture uncovers potential genome-wide interactions between human conserved non-coding sequences von Robyr, Daniel, Friedli, Marc, Gehrig, Corinne, Arcangeli, Mélanie, Marin, Marilyn, Guipponi, Michel, Farinelli, Laurent, Barde, Isabelle, Verp, Sonia, Trono, Didier, Antonarakis, Stylianos E

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Landscape of transcription in human cells von Djebali, Sarah, Davis, Carrie A., Merkel, Angelika, Dobin, Alex, Lassmann, Timo, Mortazavi, Ali, Tanzer, Andrea, Lagarde, Julien, Lin, Wei, Schlesinger, Felix, Xue, Chenghai, Marinov, Georgi K., Khatun, Jainab, Williams, Brian A., Zaleski, Chris, Rozowsky, Joel, Röder, Maik, Kokocinski, Felix, Abdelhamid, Rehab F., Alioto, Tyler, Antoshechkin, Igor, Baer, Michael T., Bar, Nadav S., Batut, Philippe, Bell, Kimberly, Bell, Ian, Chakrabortty, Sudipto, Chen, Xian, Chrast, Jacqueline, Curado, Joao, Derrien, Thomas, Drenkow, Jorg, Dumais, Erica, Dumais, Jacqueline, Duttagupta, Radha, Falconnet, Emilie, Fastuca, Meagan, Fejes-Toth, Kata, Ferreira, Pedro, Foissac, Sylvain, Fullwood, Melissa J., Gao, Hui, Gonzalez, David, Gordon, Assaf, Gunawardena, Harsha, Howald, Cedric, Jha, Sonali, Johnson, Rory, Kapranov, Philipp, King, Brandon, Kingswood, Colin, Luo, Oscar J., Park, Eddie, Persaud, Kimberly, Preall, Jonathan B., Ribeca, Paolo, Risk, Brian, Robyr, Daniel, Sammeth, Michael, Schaffer, Lorian, See, Lei-Hoon, Shahab, Atif, Skancke, Jorgen, Suzuki, Ana Maria, Takahashi, Hazuki, Tilgner, Hagen, Trout, Diane, Walters, Nathalie, Wang, Huaien, Wrobel, John, Yu, Yanbao, Ruan, Xiaoan, Hayashizaki, Yoshihide, Harrow, Jennifer, Gerstein, Mark, Hubbard, Tim, Reymond, Alexandre, Antonarakis, Stylianos E., Hannon, Gregory, Giddings, Morgan C., Ruan, Yijun, Wold, Barbara, Carninci, Piero, Guigó, Roderic, Gingeras, Thomas R.

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Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma von Nikolaev, Sergey I, Rimoldi, Donata, Iseli, Christian, Valsesia, Armand, Robyr, Daniel, Gehrig, Corinne, Harshman, Keith, Guipponi, Michel, Bukach, Olesya, Zoete, Vincent, Michielin, Olivier, Muehlethaler, Katja, Speiser, Daniel, Beckmann, Jacques S, Xenarios, Ioannis, Halazonetis, Thanos D, Jongeneel, C Victor, Stevenson, Brian J, Antonarakis, Stylianos E

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Detection of genomic variation by selection of a 9 mb DNA region and high throughput sequencing von Nikolaev, Sergey I, Iseli, Christian, Sharp, Andrew J, Robyr, Daniel, Rougemont, Jacques, Gehrig, Corinne, Farinelli, Laurent, Antonarakis, Stylianos E

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Analysis of Genome-Wide Histone Acetylation State and Enzyme Binding Using DNA Microarrays von Robyr, Daniel, Kurdistani, Siavash K, Grunstein, Michael

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Transcriptional Regulatory Patterns of the Myelin Basic Protein and Malic Enzyme Genes by the Thyroid Hormone Receptors α1 and β1 von Jeannin, Elisabeth, Robyr, Daniel, Desvergne, Béatrice

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Nuclear Hormone Receptor Coregulators In Action: Diversity For Shared Tasks von Robyr, Daniel, Wolffe, Alan P, Wahli, Walter

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Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster von Santoni, Federico A, Makrythanasis, Periklis, Nikolaev, Sergey, Guipponi, Michel, Robyr, Daniel, Bottani, Armand, Antonarakis, Stylianos E

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Genomewide analysis of nucleosome density histone acetylation and HDAC function in fission yeast von Wirén, Marianna, Silverstein, Rebecca A, Sinha, Indranil, Walfridsson, Julian, Lee, Hang-Mao, Laurenson, Patricia, Pillus, Lorraine, Robyr, Daniel, Grunstein, Michael, Ekwall, Karl

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A Single-Nucleotide Substitution Mutator Phenotype Revealed by Exome Sequencing of Human Colon Adenomas von NIKOLAEV, Sergey I, SOTIRIOU, Sotirios K, GORGOULIS, Vassilis G, ANTONARAKIS, Stylianos E, HALAZONETIS, Thanos D, PATERAS, Loannis S, SANTONI, Federico, SOUGIOULTZIS, Stavros, EDGREN, Henrik, ALMUSA, Henrikki, ROBYR, Daniel, GUIPPONI, Michel, SAARELA, Janna

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Genome wide analysis of nucleosome density histone acetylation and HDAC function in fission yeast von Wirén, Marianna, Silverstein, Rebecca A, Sinha, Indranil, Walfridsson, Julian, Lee, Hang-mao, Laurenson, Patricia, Pillus, Lorraine, Robyr, Daniel, Grunstein, Michael, Ekwall, Karl

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Domains of genome-wide gene expression dysregulation in Down’s syndrome von Letourneau, Audrey, Santoni, Federico A., Bonilla, Ximena, Sailani, M. Reza, Gonzalez, David, Kind, Jop, Chevalier, Claire, Thurman, Robert, Sandstrom, Richard S., Hibaoui, Youssef, Garieri, Marco, Popadin, Konstantin, Falconnet, Emilie, Gagnebin, Maryline, Gehrig, Corinne, Vannier, Anne, Guipponi, Michel, Farinelli, Laurent, Robyr, Daniel, Migliavacca, Eugenia, Borel, Christelle, Deutsch, Samuel, Feki, Anis, Stamatoyannopoulos, John A., Herault, Yann, van Steensel, Bas, Guigo, Roderic, Antonarakis, Stylianos E.

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Genomewide histone acetylation microarrays von Robyr, Daniel, Grunstein, Michael

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Corrigendum: Domains of genome-wide gene expression dysregulation in Down's syndrome von Letourneau, Audrey, Santoni, Federico A, Bonilla, Ximena, Sailani, M Reza, Gonzalez, David, Kind, Jop, Chevalier, Claire, Thurman, Robert, Sandstrom, Richard S, Hibaoui, Youssef, Garieri, Marco, Popadin, Konstantin, Falconnet, Emilie, Gagnebin, Maryline, Gehrig, Corinne, Vannier, Anne, Guipponi, Michel, Farinelli, Laurent, Robyr, Daniel, Migliavacca, Eugenia, Borel, Christelle, Deutsch, Samuel, Feki, Anis, Stamatoyannopoulos, John A, Herault, Yann, van Steensel, Bas, Guigo, Roderic, Antonarakis, Stylianos E

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Correction: Corrigendum: Domains of genome-wide gene expression dysregulation in Down’s syndrome von Letourneau, Audrey, Santoni, Federico A., Bonilla, Ximena, Reza Sailani, M., Gonzalez, David, Kind, Jop, Chevalier, Claire, Thurman, Robert, Sandstrom, Richard S., Hibaoui, Youssef, Garieri, Marco, Popadin, Konstantin, Falconnet, Emilie, Gagnebin, Maryline, Gehrig, Corinne, Vannier, Anne, Guipponi, Michel, Farinelli, Laurent, Robyr, Daniel, Migliavacca, Eugenia, Borel, Christelle, Deutsch, Samuel, Feki, Anis, Stamatoyannopoulos, John A., Herault, Yann, van Steensel, Bas, Guigo, Roderic, Antonarakis, Stylianos E.

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