Assessment of parental mosaicism rates in neurodevelopmental disorders caused by apparent de novo pathogenic variants using deep sequencing by Lecoquierre, François, Cassinari, Kévin, Drouot, Nathalie, May, Angèle, Fourneaux, Steeve, Charbonnier, Francoise, Derambure, Celine, Coutant, Sophie, Saugier-Veber, Pascale, Hoischen, Alexander, Charbonnier, Camille, Nicolas, Gaël

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Glucocorticoids paradoxically promote steroid resistance in B cell acute lymphoblastic leukemia through CXCR4/PLC signaling by Abdoul-Azize, Souleymane, Hami, Rihab, Riou, Gaetan, Derambure, Céline, Charbonnier, Camille, Vannier, Jean-Pierre, Guzman, Monica L, Schneider, Pascale, Boyer, Olivier

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Knowledge, attitudes and practices of French university students towards COVID-19 prevention—are health students better? by Alessandri-Gradt, Elodie, Charbonnier, Camille, Plantier, Jean-Christophe, Marini, Hélène, Costa, Damien, Gueit, Isabelle, Etienne, Manuel, Caron, François, Frebourg, Noëlle, Unal, Guillemette, Favennec, Loïc, Merle, Véronique

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Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers by Nicolas, Gaël, Charbonnier, Camille, de Lemos, Roberta Rodrigues, Richard, Anne-Claire, Guillin, Olivier, Wallon, David, Legati, Andrea, Geschwind, Daniel, Coppola, Giovanni, Frebourg, Thierry, Campion, Dominique, de Oliveira, João Ricardo Mendes, Hannequin, Didier

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A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in Drosophila by Feuillette, Sébastien, Charbonnier, Camille, Frebourg, Thierry, Campion, Dominique, Lecourtois, Magalie

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Haploinsufficiency of the Primary Familial Brain Calcification Gene SLC20A2 Mediated by Disruption of a Regulatory Element by Cassinari, Kévin, Rovelet‐Lecrux, Anne, Tury, Sandrine, Quenez, Olivier, Richard, Anne‐Claire, Charbonnier, Camille, Olaso, Robert, Boland, Anne, Deleuze, Jean‐François, Besancenot, Jean‐François, Delpont, Benoit, Pouliquen, Dorothée, Lecoquierre, François, Chambon, Pascal, Thauvin‐Robinet, Christel, Campion, Dominique, Frebourg, Thierry, Battini, Jean‐Luc, Nicolas, Gaël

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Publisher Correction: Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes by Schramm, Catherine, Charbonnier, Camille, Zaréa, Aline, Lacour, Morgane, Wallon, David, Boland, Anne, Deleuze, Jean-François, Olaso, Robert, Alarcon, Flora, Campion, Dominique, Nuel, Grégory, Nicolas, Gaël

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Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing by Husson, Thomas, Duboc, Jean-Baptiste, Quenez, Olivier, Charbonnier, Camille, Rotharmel, Maud, Cuenca, Macarena, Jegouzo, Xavier, Richard, Anne-Claire, Frebourg, Thierry, Deleuze, Jean-François, Boland, Anne, Genin, Emmanuelle, Debette, Stéphanie, Tzourio, Christophe, Campion, Dominique, Nicolas, Gaël, Guillin, Olivier

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SORL1 genetic variants and Alzheimer disease risk: a literature review and meta-analysis of sequencing data by Campion, Dominique, Charbonnier, Camille, Nicolas, Gaël

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Estimation of minimal disease prevalence from population genomic data: Application to primary familial brain calcification by Nicolas, Gaël, Charbonnier, Camille, Campion, Dominique, Veltman, Joris A.

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Large‐scale comparative evaluation of user‐friendly tools for predicting variant‐induced alterations of splicing regulatory elements by Tubeuf, Hélène, Charbonnier, Camille, Soukarieh, Omar, Blavier, André, Lefebvre, Arnaud, Dauchel, Hélène, Frebourg, Thierry, Gaildrat, Pascaline, Martins, Alexandra

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Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy by Colin, Estelle, Daniel, Jens, Ziegler, Alban, Wakim, Jamal, Scrivo, Aurora, Haack, Tobias B., Khiati, Salim, Denommé, Anne-Sophie, Amati-Bonneau, Patrizia, Charif, Majida, Procaccio, Vincent, Reynier, Pascal, Aleck, Kyrieckos A., Botto, Lorenzo D., Herper, Claudia Lena, Kaiser, Charlotte Sophia, Nabbout, Rima, N’Guyen, Sylvie, Mora-Lorca, José Antonio, Assmann, Birgit, Christ, Stine, Meitinger, Thomas, Strom, Tim M., Prokisch, Holger, Génin, Emmanuelle, Campion, Dominique, Dartigues, Jean-François, Deleuze, Jean-François, Lambert, Jean-Charles, Redon, Richard, Ludwig, Thomas, Grenier-Boley, Benjamin, Letort, Sébastien, Lindenbaum, Pierre, Meyer, Vincent, Quenez, Olivier, Dina, Christian, Bellenguez, Céline, -Le Clézio, Camille Charbonnier, Giemza, Joanna, Chatel, Stéphanie, Férec, Claude, Le Marec, Hervé, Letenneur, Luc, Nicolas, Gaël, Rouault, Karen, Bacq, Delphine, Boland, Anne, Lechner, Doris, Miranda-Vizuete, Antonio, Hoffmann, Georg F., Lenaers, Guy, Bomont, Pascale, Liebau, Eva, Bonneau, Dominique

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A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in Drosophila by Feuillette, Sébastien, Charbonnier, Camille, Frebourg, Thierry, Campion, Dominique, Lecourtois, Magalie

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From Common to Rare Variants: The Genetic Component of Alzheimer Disease by Nicolas, Gaël, Charbonnier, Camille, Campion, Dominique

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Contribution of genotoxic anticancer treatments to the development of multiple primary tumours in the context of germline TP53 mutations by Kasper, Edwige, Angot, Emilie, Colasse, Elodie, Nicol, Lionel, Sabourin, Jean-Christophe, Adriouch, Sahil, Lacoume, Yann, Charbonnier, Camille, Raad, Sabine, Frebourg, Thierry, Flaman, Jean-Michel, Bougeard, Gaëlle

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Penetrance estimation of SORL1 loss‐of‐function variants adjusted on APOE genotypes suggest a non‐monogenic inheritance by Schramm, Catherine, Charbonnier, Camille, Zarea, Aline, Wallon, David, Lacour, Morgane, Alarcon, Flora, Génin, Emmanuelle, Campion, Dominique, Nuel, Grégory, Nicolas, Gaël

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Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluation by Quenez, Olivier, Cassinari, Kevin, Coutant, Sophie, Lecoquierre, François, Le Guennec, Kilan, Rousseau, Stéphane, Richard, Anne-Claire, Vasseur, Stéphanie, Bouvignies, Emilie, Bou, Jacqueline, Lienard, Gwendoline, Manase, Sandrine, Fourneaux, Steeve, Drouot, Nathalie, Nguyen-Viet, Virginie, Vezain, Myriam, Chambon, Pascal, Joly-Helas, Géraldine, Le Meur, Nathalie, Castelain, Mathieu, Boland, Anne, Deleuze, Jean-François, Tournier, Isabelle, Charbonnier, Françoise, Kasper, Edwige, Bougeard, Gaëlle, Frebourg, Thierry, Saugier-Veber, Pascale, Baert-Desurmont, Stéphanie, Campion, Dominique, Rovelet-Lecrux, Anne, Nicolas, Gaël

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Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification by NICOLAS, Gaël, POTTIER, Cyril, MARTINAUD, Olivier, LEFAUCHEUR, Romain, GUILLIN, Olivier, WALLON, David, CHAUMETTE, Boris, RONDEPIERRE, Philippe, DERACHE, Nathalie, FROMAGER, Guillaume, SCHAEFFER, Stéphane, KRYSTKOWIAK, Pierre, CHARBONNIER, Camille, VERNY, Christophe, JURICI, Snejana, SAUVEE, Mathilde, VERIN, Marc, LEBOUVIER, Thibaud, ROUAUD, Olivier, THAUVIN-ROBINET, Christel, ROUSSEAU, Stéphane, ROVELET-LECRUX, Anne, FREBOURG, Thierry, GUYANT-MARECHAL, Lucie, CAMPION, Dominique, HANNEQUIN, Didier, LE BER, Isabelle, PARIENTE, Jérémie, LABAUGE, Pierre, AYRIGNAC, Xavier, DEFEBVRE, Luc, MALTETE, David

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Heritable defects in telomere and mitotic function selectively predispose to sarcomas by Ballinger, Mandy L, Pattnaik, Swetansu, Zaheed, Milita, Rath, Emma, Priestley, Peter, Baber, Jonathan, Isambert, Nicholas, van der Graaf, Winette T A, Puri, Ajay, Duffaud, Florence, Chandrasekar, Coonoor, Brohl, Andrew S, James, Paul A, Kurtz, Jean-Emmanuel, Penel, Nicolas, Myklebost, Ola, Meza-Zepeda, Leonardo A, Kansara, Maya, Kondrashova, Olga, Barbour, Andrew P, Li, Shuai, Nguyen, Tuong L, Graham, Robert M, Giannoulatou, Eleni, Green, Melissa J, Kaplan, Warren, Ravishankar, Shyamsundar, Copty, Joseph, Cuppen, Edwin, van Eijk, Kristel, Veldink, Jan, Tucker, Kathy, Ludwig, Thomas, Deleuze, Jean-Francois, Haber, Michelle, Marshall, Glenn, Cairns, Murray J, Thomas, David M, Neuhaus, Susan, Lewis, Craig, Dickinson, Ian, Thorne, Heather, Ray-Coquard, Isabelle, Blay, Jean-Yves, Cassier, Philippe, Duffaud, Florence, Isambert, Nicolas, Kurtz, Jean-Emmanuel, Sarin, Rajiv, Ahn, Jin-Hee, Kim, Jeong Eun, Judson, Ian, Chandrasekar, Coonoor, Rickar, Rory, Hennig, Ivo, Schiffman, Joshua, Randall, R Lor, Silvestri, Audrey, Zaratzian, Anaiis, Tayao, Michael, Walwyn, Kelly, Niedermayr, Eveline, Mang, Denia, Clark, Richard, MacDonald, Jessica, Riddell, Kim, Mar, Jasmine, Fennelly, Vicki, Wicht, Allison, Zielony, Belinda, Galligan, Emma, Glavich, Genna, Williams, Lynda, Djandjgava, Lana, Buettner, Iwona, Osinki, Carla, Stephens, Sonya, Girodet, Magali, Charreton, Amandine, Fayet, Yohan, Crasto, Saniya, Sandupatla, Bhanupriya, Yoon, Yeon, Je, Noda, Thompson, Liz, Johnson, Bella, Petrikova, Galina, Hutchins, Angela, Bottero, Diego, Stokes-Denson, Jo, Campion, Dominique, Deleuze, Jean-François, Lambert, Jean-Charles, Grenier-Boley, Benjamin, Lindenbaum, Pierre, Quenez, Olivier, Le Clézio, Camille Charbonnier, Giemza, Joanna, Férec, Claude, Nicolas, Gaël

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Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype by Grangeon, Lou, Wallon, David, Charbonnier, Camille, Quenez, Olivier, Richard, Anne-Claire, Rousseau, Stéphane, Budowski, Clara, Lebouvier, Thibaud, Corbille, Anne-Gaëlle, Vidailhet, Marie, Méneret, Aurélie, Roze, Emmanuel, Anheim, Mathieu, Tranchant, Christine, Favrole, Pascal, Antoine, Jean-Christophe, Defebvre, Luc, Ayrignac, Xavier, Labauge, Pierre, Pariente, Jérémie, Clanet, Michel, Maltête, David, Rovelet-Lecrux, Anne, Boland, Anne, Deleuze, Jean-François, Frebourg, Thierry, Hannequin, Didier, Campion, Dominique, Nicolas, Gaël

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