Golgipathies in Neurodevelopment: A New View of Old Defects von Rasika, Sowmyalakshmi, Passemard, Sandrine, Verloes, Alain, Gressens, Pierre, El Ghouzzi, Vincent

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ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects von Izumi, Kosuke, Brett, Maggie, Nishi, Eriko, Drunat, Séverine, Tan, Ee-Shien, Fujiki, Katsunori, Lebon, Sophie, Cham, Breana, Masuda, Koji, Arakawa, Michiko, Jacquinet, Adeline, Yamazumi, Yusuke, Chen, Shu-Ting, Verloes, Alain, Okada, Yuki, Katou, Yuki, Nakamura, Tomohiko, Akiyama, Tetsu, Gressens, Pierre, Foo, Roger, Passemard, Sandrine, Tan, Ene-Choo, El Ghouzzi, Vincent, Shirahige, Katsuhiko

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Endoplasmic reticulum and Golgi stress in microcephaly von Passemard, Sandrine, Perez, Franck, Gressens, Pierre, El Ghouzzi, Vincent

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ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly and p53 von Ghouzzi, Vincent El, Bianchi, Federico T, Molineris, Ivan, Mounce, Bryan C, Berto, Gaia E, Rak, Malgorzata, Lebon, Sophie, Aubry, Laetitia, Tocco, Chiara, Gai, Marta, Chiotto, Alessandra MA, Sgrò, Francesco, Pallavicini, Gianmarco, Simon-Loriere, Etienne, Passemard, Sandrine, Vignuzzi, Marco, Gressens, Pierre, Di Cunto, Ferdinando

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Golgipathies reveal the critical role of the sorting machinery in brain and skeletal development von El Ghouzzi, Vincent, Boncompain, Gaelle

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Cortical Organoids to Model Microcephaly von Farcy, Sarah, Albert, Alexandra, Gressens, Pierre, Baffet, Alexandre D, El Ghouzzi, Vincent

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Golgi Dysfunctions in Ciliopathies von Masson, Justine, El Ghouzzi, Vincent

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Golgi trafficking defects in postnatal microcephaly: The evidence for "Golgipathies" von Passemard, Sandrine, Perez, Franck, Colin-Lemesre, Emilie, Rasika, Sowmyalakshmi, Gressens, Pierre, El Ghouzzi, Vincent

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Stem cell therapy for neonatal brain injury: Perspectives and Challenges von Titomanlio, Luigi, Kavelaars, Annemieke, Dalous, Jeremie, Mani, Shyamala, El Ghouzzi, Vincent, Heijnen, Cobi, Baud, Olivier, Gressens, Pierre

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Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons von Harding, Brian N., Moccia, Amanda, Drunat, Séverine, Soukarieh, Omar, Tubeuf, Hélène, Chitty, Lyn S., Verloes, Alain, Gressens, Pierre, El Ghouzzi, Vincent, Joriot, Sylvie, Di Cunto, Ferdinando, Martins, Alexandra, Passemard, Sandrine, Bielas, Stephanie L.

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Vulnerability of white matter towards antenatal hypoxia is linked to a species-dependent regulation of glutamate receptor subunits von Fontaine, Romain H, Olivier, Paul, Massonneau, Véronique, Leroux, Philippe, Degos, Vincent, Lebon, Sophie, El Ghouzzi, Vincent, Lelièvre, Vincent, Gressens, Pierre, Baud, Olivier

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STIL balancing primary microcephaly and cancer von Patwardhan, Dhruti, Mani, Shyamala, Passemard, Sandrine, Gressens, Pierre, El Ghouzzi, Vincent

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Saethre-Chotzen mutations cause TWIST protein degradation or impaired nuclear location von EL GHOUZZI, V, LEGEAI-MALLET, L, ARESTA, S, BENOIST, C, MUNNICH, A, DE GUNZBURG, J, BONAVENTURE, J

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Neurological outcome in WDR62 primary microcephaly von Ruaud, Lyse, Drunat, Séverine, Elmaleh‐Bergès, Monique, Ernault, Anais, Guilmin Crepon, Sophie, El Ghouzzi, Vincent, Auvin, Stéphane, Verloes, Alain, Passemard, Sandrine, Van Maldergem, Lionel, Engel, Camille, Altuzarra, Cecilia, Lamidieu, Charlie, Bayat, Allan, Moortgat, Stéphanie, Pelc, Karine, Maystadt, Isabelle, Abramowicz, Marc, Pirson, Isabelle, Duerinckx, Sarah, Rostomashvili, Nino, Zweier, Christiane, Abou Jamra, Rami, Lorenz, Imke, Haye, Damien, Zaafrane‐Khachnaoui, Khaoula, Vaessen, Sandrine, Capri, Yline, Servais, Laurent, Di Maria, Emilio, Kohlhase, Jürgen, Bast, Thomas, Miladi, Najoua, Dali, Selma

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Trans-Modulation of the Somatostatin Type 2A Receptor Trafficking by Insulin-Regulated Aminopeptidase Decreases Limbic Seizures von De Bundel, Dimitri, Fafouri, Assia, Csaba, Zsolt, Loyens, Ellen, Lebon, Sophie, El Ghouzzi, Vincent, Peineau, Stéphane, Vodjdani, Guilan, Kiagiadaki, Foteini, Aourz, Najat, Coppens, Jessica, Walrave, Laura, Portelli, Jeanelle, Vanderheyden, Patrick, Chai, Siew Yeen, Thermos, Kyriaki, Bernard, Véronique, Collingridge, Graham, Auvin, Stéphane, Gressens, Pierre, Smolders, Ilse, Dournaud, Pascal

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Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome von LAJEUNIE, Elisabeth, HEUERTZ, Solange, EL GHOUZZI, Vincent, MARTINOVIC, Jelena, RENIER, Dominique, LE MERRER, Martine, BONAVENTURE, Jacky

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Mitochondrial succinate is instrumental for HIF1α nuclear translocation in SDHA-mutant fibroblasts under normoxic conditions von Brière, Jean-Jacques, Favier, Judith, Bénit, Paule, Ghouzzi, Vincent El, Lorenzato, Annalisa, Rabier, Daniel, Di Renzo, Maria Flavia, Gimenez-Roqueplo, Anne-Paule, Rustin, Pierre

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Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory von Passemard, Sandrine, Verloes, Alain, Billette de Villemeur, Thierry, Boespflug-Tanguy, Odile, Hernandez, Karen, Laurent, Marion, Isidor, Bertrand, Alberti, Corinne, Pouvreau, Nathalie, Drunat, Séverine, Gérard, Bénédicte, El Ghouzzi, Vincent, Gallego, Jorge, Elmaleh-Bergès, Monique, Huttner, Wieland B., Eliez, Stephan, Gressens, Pierre, Schaer, Marie

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Correction to: ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly von El Ghouzzi, Vincent, Bianchi, Federico T., Molineris, Ivan, Mounce, Bryan C., Berto, Gaia E., Rak, Malgorzata, Lebon, Sophie, Aubry, Laetitia, Tocco, Chiara, Gai, Marta, Chiotto, Alessandra M. A., Sgrò, Francesco, Pallavicini, Gianmarco, Simon-Loriere, Etienne, Passemard, Sandrine, Vignuzzi, Marco, Gressens, Pierre, Di Cunto, Ferdinando

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Apoptosis-Inducing Factor Deficiency Induces Early Mitochondrial Degeneration in Brain Followed by Progressive Multifocal Neuropathology von El Ghouzzi, Vincent, Csaba, Zsolt, Olivier, Paul, Lelouvier, Benjamin, Schwendimann, Leslie, Dournaud, Pascal, Verney, Catherine, Rustin, Pierre, Gressens, Pierre

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