Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing by Bruel, Ange-Line, Nambot, Sophie, Quéré, Virginie, Vitobello, Antonio, Thevenon, Julien, Assoum, Mirna, Moutton, Sébastien, Houcinat, Nada, Lehalle, Daphné, Jean-Marçais, Nolwenn, Chevarin, Martin, Jouan, Thibaud, Poë, Charlotte, Callier, Patrick, Tisserand, Emilie, Philippe, Christophe, Them, Frédéric Tran Mau, Duffourd, Yannis, Faivre, Laurence, Thauvin-Robinet, Christel

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Clinical and molecular characterization of patients with YWHAG‐related epilepsy by Cetica, Valentina, Pisano, Tiziana, Lesca, Gaetan, Marafi, Dana, Licchetta, Laura, Riccardi, Florence, Mei, Davide, Chung, Hon‐yin B., Bayat, Allan, Balasubramanian, Meena, Lowenstein, Daniel H., Endzinienė, Milda, Alotaibi, Maha, Villeneuve, Nathalie, Jacobs, Julia, Isidor, Bertrand, Solazzi, Roberta, Hollander, Nicolette S., Marjanovic, Dragan, Rougeot‐Jung, Christelle, Jung, Julien, Lesieur‐Sebellin, Marion, Accogli, Andrea, Salpietro, Vincenzo, Saadi, Nebal W., Panagiotakaki, Eleni, Foiadelli, Thomas, Redon, Sylvia, Tsai, Meng‐Han, Bisulli, Francesca, Hammer, Trine B., Lupski, James R., Parrini, Elena, Guerrini, Renzo, Alotaibi, Lena, Ambrosetti, Irene, Bellanger, Séverine A., Castellotti, Barbara, Cavallin, Mara, Chan, Joshua C. K., Chatron, Nicolas, Chavany, Julie, Cogne, Benjamin, Fung, Jasmine L. F., Gjerulfsen, Cathrine E., Granata, Tiziana, Guimier, Anne, Herman, Isabella, Ho, Chen‐Jui, Mandorlini, Claudia, Milh, Mathieu, Minardi, Raffaella, Montanari, Francesca, Rosenfeld, Jill A., Moller, Rikke S., Operto, Francesca F., Posey, Jennifer E., Ruivenkamp, Claudia A. L., Sacaze, Elise, Santi, Viola, Savasta, Salvatore, Touraine, Renaud, Tumiene, Birute, Uguen, Kevin, Villard, Laurent

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An unusual diagnosis of alpha‐mannosidosis with ocular anomalies: Behind the scenes of a hidden copy number variation by Uguen, Kevin, Redon, Sylvia, Rouault, Karen, Pensec, Marine, Benech, Caroline, Schutz, Sacha, Zanlonghi, Xavier, Nadjar, Yann, Le Maréchal, Cédric, Férec, Claude, Audebert‐Bellanger, Séverine

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Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility by Lonjou, Christine, Eon‐Marchais, Séverine, Truong, Thérèse, Dondon, Marie‐Gabrielle, Karimi, Mojgan, Jiao, Yue, Damiola, Francesca, Barjhoux, Laure, Le Gal, Dorothée, Beauvallet, Juana, Mebirouk, Noura, Cavaciuti, Eve, Chiesa, Jean, Floquet, Anne, Audebert‐Bellanger, Séverine, Giraud, Sophie, Frebourg, Thierry, Limacher, Jean‐Marc, Gladieff, Laurence, Mortemousque, Isabelle, Dreyfus, Hélène, Lejeune‐Dumoulin, Sophie, Lasset, Christine, Venat‐Bouvet, Laurence, Bignon, Yves‐Jean, Pujol, Pascal, Maugard, Christine M., Luporsi, Elisabeth, Bonadona, Valérie, Noguès, Catherine, Berthet, Pascaline, Delnatte, Capucine, Gesta, Paul, Lortholary, Alain, Faivre, Laurence, Buecher, Bruno, Caron, Olivier, Gauthier‐Villars, Marion, Coupier, Isabelle, Mazoyer, Sylvie, Monraz, Luis‐Cristobal, Kondratova, Maria, Kuperstein, Inna, Guénel, Pascal, Barillot, Emmanuel, Stoppa‐Lyonnet, Dominique, Andrieu, Nadine, Lesueur, Fabienne

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A new case of Kaufman Oculocerebrofacial syndrome caused by two splicing variants in UBE3B and review of the literature by Couloigner, Loïc, Planes, Marc, Ka, Chandran, Audebert‐Bellanger, Séverine, Redon, Sylvia, Benech, Caroline, Rouault, Karen, Küry, Sebastien, Peudenier, Sylviane, Autret, Sandrine, Gourlaouen, Isabelle, Bonneau, Dominique, Odent, Sylvie, Bézieau, Stéphane, Gilbert‐Dussardier, Brigitte, Toutain, Annick, Boland, Anne, Deleuze, Jean‐François, Le Marechal, Cédric, Le Gac, Gérald, Ferec, Claude, Uguen, Kevin

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Orbital angular momentum beams generation from 61 channels coherent beam combining femtosecond digital laser by Veinhard, Matthieu, Bellanger, Séverine, Daniault, Louis, Fsaifes, Ihsan, Bourderionnet, Jérôme, Larat, Christian, Lallier, Eric, Brignon, Arnaud, Chanteloup, Jean-Christophe

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Heterozygous HMGB1 loss‐of‐function variants are associated with developmental delay and microcephaly by Uguen, Kévin, Krysiak, Kilannin, Audebert‐Bellanger, Séverine, Redon, Sylvia, Benech, Caroline, Viora‐Dupont, Eléonore, Tran Mau‐Them, Frederic, Rondeau, Sophie, Elsharkawi, Ibrahim, Granadillo, Jorge L., Neidich, Julie, Soares, Celia Azevedo, Tkachenko, Natáliya, M. Amudhavalli, Shivarajan, Engleman, Kendra, Boland, Anne, Deleuze, Jean‐François, Bezieau, Stéphane, Odent, Sylvie, Toutain, Annick, Bonneau, Dominique, Gilbert‐Dussardier, Brigitte, Faivre, Laurence, Rio, Marlène, Le Marechal, Cedric, Ferec, Claude, Repnikova, Elena, Cao, Yang

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Functional Characterization of Splice Variants in the Diagnosis of Albinism by Diallo, Modibo, Courdier, Cécile, Mercier, Elina, Sequeira, Angèle, Defay-Stinat, Alicia, Plaisant, Claudio, Mesdaghi, Shahram, Rigden, Daniel, Javerzat, Sophie, Lasseaux, Eulalie, Bourgeade, Laetitia, Audebert-Bellanger, Séverine, Dollfus, Hélène, Hadj-Rabia, Smail, Morice-Picard, Fanny, Philibert, Manon, Sidibé, Mohamed Kole, Smirnov, Vasily, Sylla, Ousmane, Michaud, Vincent, Arveiler, Benoit

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Complete mitochondrial exploration of Echinococcus multilocularis from French alveolar echinococcosis patients by Bohard, Louis, Lallemand, Séverine, Borne, Romain, Courquet, Sandra, Bresson-Hadni, Solange, Richou, Carine, Millon, Laurence, Bellanger, Anne-Pauline, Knapp, Jenny

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3q29 duplications: A cohort of 46 patients and a literature review by Massier, Marie, Doco‐Fenzy, Martine, Egloff, Matthieu, Le Guillou, Xavier, Le Guyader, Gwenaël, Redon, Sylvia, Benech, Caroline, Le Millier, Karine, Uguen, Kevin, Ropars, Juliette, Sacaze, Elise, Audebert‐Bellanger, Séverine, Apetrei, Andreea, Molin, Arnaud, Gruchy, Nicolas, Vincent‐Devulder, Aline, Spodenkiewicz, Marta, Jacquin, Clémence, Loron, Gauthier, Thibaud, Marie, Delplancq, Geoffroy, Brisset, Sophie, Lesieur‐Sebellin, Marion, Malan, Valérie, Romana, Serge, Rio, Marlène, Marlin, Sandrine, Amiel, Jeanne, Marquet, Valentine, Dauriat, Benjamin, Moradkhani, Kamran, Mercier, Sandra, Isidor, Bertrand, Arpin, Stéphanie, Pujalte, Mathilde, Jedraszak, Guillaume, Pebrel‐Richard, Céline, Salaun, Gaëlle, Laffargue, Fanny, Boudjarane, John, Missirian, Chantal, Chelloug, Nora, Toutain, Annick, Chiesa, Jean, Keren, Boris, Mignot, Cyril, Gouy, Evan, Jaillard, Sylvie, Landais, Emilie, Poirsier, Céline

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Far field energy distribution control using a coherent beam combining femtosecond digital laser by Fsaifes, Ihsan, Ranély-Vergé-Dépré, Claude-Alban, Veinhard, Matthieu, Bellanger, Séverine, Chanteloup, Jean-Christophe

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Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation by Ribeiro Guerra, Maximiliano, Coignard, Juliette, Eon-Marchais, Séverine, Dondon, Marie-Gabrielle, Le Gal, Dorothée, Beauvallet, Juana, Mebirouk, Noura, Belotti, Muriel, Caron, Olivier, Gauthier-Villars, Marion, Coupier, Isabelle, Buecher, Bruno, Lortholary, Alain, Fricker, Jean-Pierre, Gesta, Paul, Noguès, Catherine, Faivre, Laurence, Berthet, Pascaline, Luporsi, Elisabeth, Delnatte, Capucine, Bonadona, Valérie, Maugard, Christine M, Pujol, Pascal, Lasset, Christine, Longy, Michel, Bignon, Yves-Jean, Adenis-Lavignasse, Claude, Venat-Bouvet, Laurence, Dreyfus, Hélène, Gladieff, Laurence, Mortemousque, Isabelle, Audebert-Bellanger, Séverine, Soubrier, Florent, Giraud, Sophie, Lejeune-Dumoulin, Sophie, Limacher, Jean-Marc, Chiesa, Jean, Fajac, Anne, Floquet, Anne, Eisinger, François, Tinat, Julie, Fert-Ferrer, Sandra, Colas, Chrystelle, Frebourg, Thierry, Damiola, Francesca, Barjhoux, Laure, Cavaciuti, Eve, Mazoyer, Sylvie, Tardivon, Anne, Lesueur, Fabienne, Stoppa-Lyonnet, Dominique, Andrieu, Nadine

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Correction to: Effectiveness of cleaning of workplace cytotoxic surface by Lê, Laetitia Minh Mai, Jolivot, Pierre Alain, Yayé, Hassane Sadou, Rieutord, André, Bellanger, Agnès, Pradeau, Dominique, Barbault-Foucher, Séverine, Caudron, Eric

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Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects by Kermasson, Laëtitia, Churikov, Dmitri, Awad, Aya, Smoom, Riham, Lainey, Elodie, Touzot, Fabien, Audebert-Bellanger, Séverine, Haro, Sophie, Roger, Lauréline, Costa, Emilia, Mouf, Maload, Bottero, Adriana, Oleastro, Matias, Abdo, Chrystelle, de Villartay, Jean-Pierre, Géli, Vincent, Tzfati, Yehuda, Callebaut, Isabelle, Danielian, Silvia, Soares, Gabriela, Kannengiesser, Caroline, Revy, Patrick

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Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants by Marguet, Florent, Vezain, Myriam, Marcorelles, Pascale, Audebert-Bellanger, Séverine, Cassinari, Kévin, Drouot, Nathalie, Chambon, Pascal, Gonzalez, Bruno J, Horowitz, Arie, Laquerriere, Annie, Saugier-Veber, Pascale

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Coherent beam combining of seven fiber chirped-pulse amplifiers using an interferometric phase measurement by Heilmann, Anke, Le Dortz, Jérémy, Daniault, Louis, Fsaifes, Ihsan, Bellanger, Séverine, Bourderionnet, Jérôme, Larat, Christian, Lallier, Eric, Antier, Marie, Durand, Eric, Simon-Boisson, Christophe, Brignon, Arnaud, Chanteloup, Jean-Christophe

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Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing by Girard, Elodie, Eon‐Marchais, Séverine, Olaso, Robert, Renault, Anne‐Laure, Damiola, Francesca, Dondon, Marie‐Gabrielle, Barjhoux, Laure, Goidin, Didier, Meyer, Vincent, Le Gal, Dorothée, Beauvallet, Juana, Mebirouk, Noura, Lonjou, Christine, Coignard, Juliette, Marcou, Morgane, Cavaciuti, Eve, Baulard, Céline, Bihoreau, Marie‐Thérèse, Cohen‐Haguenauer, Odile, Leroux, Dominique, Penet, Clotilde, Fert‐Ferrer, Sandra, Colas, Chrystelle, Frebourg, Thierry, Eisinger, François, Adenis, Claude, Fajac, Anne, Gladieff, Laurence, Tinat, Julie, Floquet, Anne, Chiesa, Jean, Giraud, Sophie, Mortemousque, Isabelle, Soubrier, Florent, Audebert‐Bellanger, Séverine, Limacher, Jean‐Marc, Lasset, Christine, Lejeune‐Dumoulin, Sophie, Dreyfus, Hélène, Bignon, Yves‐Jean, Longy, Michel, Pujol, Pascal, Venat‐Bouvet, Laurence, Bonadona, Valérie, Berthet, Pascaline, Luporsi, Elisabeth, Maugard, Christine M., Noguès, Catherine, Delnatte, Capucine, Fricker, Jean‐Pierre, Gesta, Paul, Faivre, Laurence, Lortholary, Alain, Buecher, Bruno, Caron, Olivier, Gauthier‐Villars, Marion, Coupier, Isabelle, Servant, Nicolas, Boland, Anne, Mazoyer, Sylvie, Deleuze, Jean‐François, Stoppa‐Lyonnet, Dominique, Andrieu, Nadine, Lesueur, Fabienne

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Deficiency of the minor spliceosome component U4atac snRNA secondarily results in ciliary defects in human and zebrafish by Khatri, Deepak, Putoux, Audrey, Cologne, Audric, Kaltenbach, Sophie, Besson, Alicia, Bertiaux, Eloïse, Guguin, Justine, Fendler, Adèle, Dupont, Marie A, Benoit-Pilven, Clara, Qebibo, Leila, Ahmed-Elie, Samira, Audebert-Bellanger, Séverine, Blanc, Pierre, Rambaud, Thomas, Castelle, Martin, Cornen, Gaëlle, Grotto, Sarah, Guët, Agnès, Guibaud, Laurent, Michot, Caroline, Odent, Sylvie, Ruaud, Lyse, Sacaze, Elise, Hamel, Virginie, Bordonné, Rémy, Leutenegger, Anne-Louise, Edery, Patrick, Burglen, Lydie, Attié-Bitach, Tania, Mazoyer, Sylvie, Delous, Marion

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Challenging the phylogenetic relationships among Echinococcus multilocularis isolates from main endemic areas by Lallemand, Séverine, Oyhenart, Jorge, Valot, Benoit, Borne, Romain, Bohard, Louis, Umhang, Gérald, Karamon, Jacek, Konyaev, Sergey, Rönnberg, Caroline, Gottstein, Bruno, Weil-Verhoeven, Delphine, Richou, Carine, Bresson-Hadni, Solange, Millon, Laurence, Bellanger, Anne-Pauline, Knapp, Jenny

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Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly by Herbst, Charlotte, Bothe, Viktoria, Wegler, Meret, Axer-Schaefer, Susanne, Audebert-Bellanger, Séverine, Gecz, Jozef, Cogne, Benjamin, Feldman, Hagit Baris, Horn, Anselm H. C., Hurst, Anna C. E., Kelly, Melissa A., Kruer, Michael C., Kurolap, Alina, Laquerriere, Annie, Li, Megan, Mark, Paul R., Morawski, Markus, Nizon, Mathilde, Pastinen, Tomi, Polster, Tilman, Saugier-Veber, Pascale, SeSong, Jang, Sticht, Heinrich, Stieler, Jens T., Thifffault, Isabelle, van Eyk, Clare L., Marcorelles, Pascale, Vezain-Mouchard, Myriam, Abou Jamra, Rami, Oppermann, Henry

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