Aurora A kinase activity is required to maintain an active spindle assembly checkpoint during prometaphase von Courtheoux, Thibault, Diallo, Alghassimou, Damodaran, Arun Prasath, Reboutier, David, Watrin, Erwan, Prigent, Claude

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The cohesin complex is required for the DNA damage-induced G2/M checkpoint in mammalian cells von Watrin, Erwan, Peters, Jan-Michael

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Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy von Guénantin, Anne-Claire, Jebeniani, Imen, Leschik, Julia, Watrin, Erwan, Bonne, Gisèle, Vignier, Nicolas, Pucéat, Michel

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Sororin pre-mRNA splicing is required for proper sister chromatid cohesion in human cells von Watrin, Erwan, Demidova, Maria, Watrin, Tanguy, Hu, Zheng, Prigent, Claude

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Sororin Is Required for Stable Binding of Cohesin to Chromatin and for Sister Chromatid Cohesion in Interphase von Schmitz, Julia, Watrin, Erwan, Lénárt, Péter, Mechtler, Karl, Peters, Jan-Michael

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Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes von Parenti, Ilaria, Teresa-Rodrigo, María E., Pozojevic, Jelena, Ruiz Gil, Sara, Bader, Ingrid, Braunholz, Diana, Bramswig, Nuria C., Gervasini, Cristina, Larizza, Lidia, Pfeiffer, Lutz, Ozkinay, Ferda, Ramos, Feliciano, Reiz, Benedikt, Rittinger, Olaf, Strom, Tim M., Watrin, Erwan, Wendt, Kerstin, Wieczorek, Dagmar, Wollnik, Bernd, Baquero-Montoya, Carolina, Pié, Juan, Deardorff, Matthew A., Gillessen-Kaesbach, Gabriele, Kaiser, Frank J.

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Overarching control of autophagy and DNA damage response by CHD6 revealed by modeling a rare human pathology von Kargapolova, Yulia, Rehimi, Rizwan, Kayserili, Hülya, Brühl, Joanna, Sofiadis, Konstantinos, Zirkel, Anne, Palikyras, Spiros, Mizi, Athanasia, Li, Yun, Yigit, Gökhan, Hoischen, Alexander, Frank, Stefan, Russ, Nicole, Trautwein, Jonathan, van Bon, Bregje, Gilissen, Christian, Laugsch, Magdalena, Gusmao, Eduardo Gade, Josipovic, Natasa, Altmüller, Janine, Nürnberg, Peter, Längst, Gernot, Kaiser, Frank J., Watrin, Erwan, Brunner, Han, Rada-Iglesias, Alvaro, Kurian, Leo, Wollnik, Bernd, Bouazoune, Karim, Papantonis, Argyris

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Human Scc4 Is Required for Cohesin Binding to Chromatin, Sister-Chromatid Cohesion, and Mitotic Progression von Watrin, Erwan, Schleiffer, Alexander, Tanaka, Koichi, Eisenhaber, Frank, Nasmyth, Kim, Peters, Jan-Michael

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The cohesin ATPase cycle is mediated by specific conformational dynamics and interface plasticity of SMC1A and SMC3 ATPase domains von Vitoria Gomes, Marina, Landwerlin, Pauline, Diebold-Durand, Marie-Laure, Shaik, Tajith B., Durand, Alexandre, Troesch, Edouard, Weber, Chantal, Brillet, Karl, Lemée, Marianne Victoria, Decroos, Christophe, Dulac, Ludivine, Antony, Pierre, Watrin, Erwan, Ennifar, Eric, Golzio, Christelle, Romier, Christophe

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Regulation of the cohesin-loading factor NIPBL: Role of the lncRNA NIPBL-AS1 and identification of a distal enhancer element von Zuin, Jessica, Casa, Valentina, Pozojevic, Jelena, Kolovos, Petros, van den Hout, Mirjam C G N, van Ijcken, Wilfred F J, Parenti, Ilaria, Braunholz, Diana, Baron, Yorann, Watrin, Erwan, Kaiser, Frank J, Wendt, Kerstin S

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Contribution of hCAP-D2, a Non-SMC Subunit of Condensin I, to Chromosome and Chromosomal Protein Dynamics during Mitosis von Watrin, Erwan, Legagneux, Vincent

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Hidden Mutations in Cornelia de Lange Syndrome Limitations of Sanger Sequencing in Molecular Diagnostics von Braunholz, Diana, Obieglo, Carolin, Parenti, Ilaria, Pozojevic, Jelena, Eckhold, Juliane, Reiz, Benedikt, Brænne, Ingrid, Wendt, Kerstin S., Watrin, Erwan, Vodopiutz, Julia, Rieder, Harald, Gillessen-Kaesbach, Gabriele, Kaiser, Frank J.

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Gene regulation and chromatin organization: relevance of cohesin mutations to human disease von Watrin, Erwan, Kaiser, Frank J, Wendt, Kerstin S

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The histone methyltransferase NSD3 contributes to sister chromatid cohesion and to cohesin loading at mitotic exit von Eot-Houllier, Grégory, Magnaghi-Jaulin, Laura, Bourgine, Gaëlle, Smagulova, Fatima, Giet, Régis, Watrin, Erwan, Jaulin, Christian

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Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly von Kim, Artem, Savary, Clara, Dubourg, Christèle, Carré, Wilfrid, Mouden, Charlotte, Hamdi-Rozé, Houda, Guyodo, Hélène, Douce, Jerome Le, Pasquier, Laurent, Flori, Elisabeth, Gonzales, Marie, Bénéteau, Claire, Boute, Odile, Attié-Bitach, Tania, Roume, Joelle, Goujon, Louise, Akloul, Linda, Odent, Sylvie, Watrin, Erwan, Dupé, Valérie, de Tayrac, Marie, David, Véronique

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Alteration of SC35 localization by transfection reagents von Damodaran, Arun Prasath, Courthéoux, Thibault, Watrin, Erwan, Prigent, Claude

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Multiple roles of Condensins: a complex story von Legagneux, Vincent, Cubizolles, Fabien, Watrin, Erwan

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HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle von Deardorff, Matthew A., Bando, Masashige, Nakato, Ryuichiro, Watrin, Erwan, Itoh, Takehiko, Minamino, Masashi, Saitoh, Katsuya, Komata, Makiko, Katou, Yuki, Clark, Dinah, Cole, Kathryn E., De Baere, Elfride, Decroos, Christophe, Di Donato, Nataliya, Ernst, Sarah, Francey, Lauren J., Gyftodimou, Yolanda, Hirashima, Kyotaro, Hullings, Melanie, Ishikawa, Yuuichi, Jaulin, Christian, Kaur, Maninder, Kiyono, Tohru, Lombardi, Patrick M., Magnaghi-Jaulin, Laura, Mortier, Geert R., Nozaki, Naohito, Petersen, Michael B., Seimiya, Hiroyuki, Siu, Victoria M., Suzuki, Yutaka, Takagaki, Kentaro, Wilde, Jonathan J., Willems, Patrick J., Prigent, Claude, Gillessen-Kaesbach, Gabriele, Christianson, David W., Kaiser, Frank J., Jackson, Laird G., Hirota, Toru, Krantz, Ian D., Shirahige, Katsuhiko

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Proteomic study identifies Aurora-A–mediated regulation of alternative splicing through multiple splicing factors von Damodaran, Arun Prasath, Gavard, Olivia, Gagné, Jean-Philippe, Rogalska, Malgorzata Ewa, Behera, Amit K., Mancini, Estefania, Bertolin, Giulia, Courtheoux, Thibault, Kumari, Bandana, Cailloce, Justine, Mereau, Agnès, Poirier, Guy G., Valcárcel, Juan, Gonatopoulos-Pournatzis, Thomas, Watrin, Erwan, Prigent, Claude

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How silence shapes the brain: synonymous variants alter codon usage and translation of Sonic Hedgehog in holoprosencephaly von Kim, Artem, Le Douce, Jérôme, Diab, Farah, Ferorova, Monika, Dubourg, Christèle, Odent, Sylvie, Dupe, Valerie, David, Véronique, Diambra, Luis, Watrin, Erwan, de Tayrac, Marie

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