Pleuropulmonary blastoma in children and adolescents: The EXPeRT/PARTNER diagnostic and therapeutic recommendations von Bisogno, Gianni, Sarnacki, Sabine, Stachowicz‐Stencel, Teresa, Minard Colin, V., Ferrari, Andrea, Godzinski, Jan, Gauthier Villars, Marion, Bien, Ewa, Hameury, Frederic, Helfre, Sylvie, Schneider, Dominik T., Reguerre, Yves, Lopez Almaraz, Ricardo, Janic, Dragana, Cesen, Maja, Kolenova, Alexandra, Rascon, Jelena, Martinova, Kata, Cosnarovici, Rodica, Pourtsidis, Apostolos, Ben Ami, Tal, Roganovic, Jelena, Koscielniak, Ewa, Schultz, Kris Ann P., Brecht, Ines B., Orbach, Daniel

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Hereditary cancer predispositions: Comparison of multigene panel sequencing on fresh‐frozen breast/ovarian tumor versus blood von Schwartz, Mathias, Moncoutier, Virginie, Peytral, Adrien, Le Gall, Jessica, Suybeng, Voreak, Pagès, Mélanie, Masliah‐Planchon, Julien, Trabelsi‐Grati, Olfa, Melaabi, Samia, Callens, Céline, Bièche, Ivan, Delhomelle, Hélène, De Pauw, Antoine, Saule, Claire, Mouret‐Fourme, Emmanuelle, Gauthier‐Villars, Marion, Buecher, Bruno, Colas, Chrystelle, Stoppa‐Lyonnet, Dominique, Golmard, Lisa

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Craniofacial second primary tumors in patients with germline retinoblastoma previously treated with external beam radiotherapy: A retrospective institutional analysis von Jiménez, Irene, Laé, Marick, Tanguy, Marie‐Laure, Savignoni, Alexia, Gauthier‐Villars, Marion, Desjardins, Laurence, Cassoux, Nathalie, Dendale, Rémi, Rodriguez, Joseph, Doz, François, Brisse, Hervé J., Aerts, Isabelle

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Gene‐ and pathway‐level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility von 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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Evaluation of in silico splice tools for decision-making in molecular diagnosis von Houdayer, Claude, Dehainault, Catherine, Mattler, Christophe, Michaux, Dorothée, Caux-Moncoutier, Virginie, Pagès-Berhouet, Sabine, d'Enghien, Catherine Dubois, Laugé, Anthony, Castera, Laurent, Gauthier-Villars, Marion, Stoppa-Lyonnet, Dominique

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Rhabdomyosarcoma and rhabdomyoma associated with nevoid basal cell carcinoma syndrome: Local treatment strategy von Kerbrat, Adeline, Beaufrere, Aurelie, Neiva‐Vaz, Cecilia, Galmiche, Louis, Belhous, Kahina, Orbach, Daniel, Gauthier‐Villars, Marion, Picard, Arnaud, Kadlub, Natacha

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Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers von Bougeard, Gaëlle, Renaux-Petel, Mariette, Flaman, Jean-Michel, Charbonnier, Camille, Fermey, Pierre, Belotti, Muriel, Gauthier-Villars, Marion, Stoppa-Lyonnet, Dominique, Consolino, Emilie, Brugières, Laurence, Caron, Olivier, Benusiglio, Patrick R, Bressac-de Paillerets, Brigitte, Bonadona, Valérie, Bonaïti-Pellié, Catherine, Tinat, Julie, Baert-Desurmont, Stéphanie, Frebourg, Thierry

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The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling von Bouassida, Malek, Molina‐Gomes, Denise, Koraichi, Fairouz, Hervé, Bérénice, Lhuilier, Morgane, Duvillier, Clémence, Le Gall, Jessica, Gauthier‐Villars, Marion, Serazin, Valérie, Quibel, Thibaud, Dard, Rodolphe, Vialard, François

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Osteosarcoma without prior retinoblastoma related to RB1 low‐penetrance germline pathogenic variants: A novel type of RB1‐related hereditary predisposition syndrome? von Imbert‐Bouteille, Marion, Gauthier‐Villars, Marion, Leroux, Dominique, Meunier, Isabelle, Aerts, Isabelle, Lumbroso‐Le Rouic, Livia, Lejeune, Sophie, Delnatte, Capucine, Abadie, Caroline, Pujol, Pascal, Houdayer, Claude, Corsini, Carole

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Predisposition to cancer in children and adolescents von Kratz, Christian P, Jongmans, Marjolijn C, Cavé, Hélène, Wimmer, Katharina, Behjati, Sam, Guerrini-Rousseau, Lea, Milde, Till, Pajtler, Kristian W, Golmard, Lisa, Gauthier-Villars, Marion, Jewell, Rosalyn, Duncan, Catriona, Maher, Eamonn R, Brugieres, Laurence, Pritchard-Jones, Kathy, Bourdeaut, Franck

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Long response to immune checkpoint inhibitors in metastatic NSCLC despite EGFR germline mutation. A case report von Trabelsi Grati, Olfa, Zemoura, Leila, Nhy, Caroline, Daniel, Catherine, Melaabi, Samia, Callens, Céline, Gauthier Villars, Marion, Bièche, Ivan, Girard, Nicolas

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Mosaicism in clinical practice exemplified by prenatal diagnosis in retinoblastoma von Castéra, Laurent, Gauthier-Villars, Marion, Dehainault, Catherine, Michaux, Dorothée, Benachi, Alexandra, Rouic, Livia Lumbroso-Le, Stoppa-Lyonnet, Dominique, Houdayer, Claude

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Mutiple DICER1‐related lesions associated with a germline deep intronic mutation von Verrier, Florian, Dubois d'Enghien, Catherine, Gauthier‐Villars, Marion, Bonadona, Valérie, Faure‐Conter, Cécile, Dijoud, Frédérique, Stoppa‐Lyonnet, Dominique, Houdayer, Claude, Golmard, Lisa

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Neonatal cancer von Orbach, Daniel, MD, Sarnacki, Sabine, Prof, Brisse, Hervé J, MD, Gauthier-Villars, Marion, MD, Jarreau, Pierre-Henri, Prof, Tsatsaris, Vassilis, Prof, Baruchel, André, Prof, Zerah, Michel, Prof, Seigneur, Etienne, MD, Peuchmaur, Michel, Prof, Doz, François, Prof

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A Parent-of-Origin Effect Impacts the Phenotype in Low Penetrance Retinoblastoma Families Segregating the c.1981C>T/p.Arg661Trp Mutation of RB1 von Eloy, Philippine, Dehainault, Catherine, Sefta, Meriem, Aerts, Isabelle, Doz, François, Cassoux, Nathalie, Lumbroso le Rouic, Livia, Stoppa-Lyonnet, Dominique, Radvanyi, François, Millot, Gaël A, Gauthier-Villars, Marion, Houdayer, Claude

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Results of a Multicenter Prospective Study on the Postoperative Treatment of Unilateral Retinoblastoma After Primary Enucleation von Aerts, Isabelle, Sastre-Garau, Xavier, Savignoni, Alexia, Lumbroso-Le Rouic, Livia, Thebaud-Leculée, Estelle, Frappaz, Didier, Coze, Carole, Thomas, Caroline, Gauthier-Villars, Marion, Lévy-Gabriel, Christine, Brisse, Hervé J, Desjardins, Laurence, Doz, François

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Extensive Variation in the Mutation Rate Between and Within Human Genes Associated with Mendelian Disease von Smith, Thomas, Ho, Gladys, Christodoulou, John, Price, Elizabeth Ann, Onadim, Zerrin, Gauthier-Villars, Marion, Dehainault, Catherine, Houdayer, Claude, Parfait, Beatrice, van Minkelen, Rick, Lohman, Dietmar, Eyre-Walker, Adam

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Retinoblastoma von Aerts, Isabelle, Lumbroso-Le Rouic, Livia, Gauthier-Villars, Marion, Brisse, Hervé, Doz, François, Desjardins, Laurence

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Pregnancies, Breast-Feeding, and Breast Cancer Risk in the International BRCA1/2 Carrier Cohort Study (IBCCS) von Andrieu, Nadine, Goldgar, David E., Easton, Douglas F., Rookus, Matti, Brohet, Richard, Antoniou, Antonis C., Peock, Susan, Evans, Gareth, Eccles, Diana, Douglas, Fiona, Noguès, Catherine, Gauthier-Villars, Marion, Chompret, Agnès, Van Leeuwen, Flora E., Kluijt, Irma, Benitez, Javier, Arver, Brita, Olah, Edith, Chang-Claude, Jenny

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Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2 von Blein, Sophie, Barjhoux, Laure, Damiola, Francesca, Dondon, Marie-Gabrielle, Eon-Marchais, Séverine, Marcou, Morgane, Caron, Olivier, Lortholary, Alain, Buecher, Bruno, Vennin, Philippe, Berthet, Pascaline, Noguès, Catherine, Lasset, Christine, Gauthier-Villars, Marion, Mazoyer, Sylvie, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Thomas, Gilles, Sinilnikova, Olga M, Cox, David G

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