Suicide attempts by jumping and length of stay in general hospital von Todorov, L., Vulser, H., Follin, A., Thauvin, I., Radtchenko, A., Vidal, J., Guigui, P., Limosin, F., Lemogne, C.

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Standardized screening of alcohol misuse in emergency wards: The experience of a systematic use of the FACE scale in the European Georges-Pompidou Hospital von Hinfray, S, Airagnes, G, Le Faou, A-L, Ducoutumany, G, Louville, P, Lemogne, C, Thauvin, I, Juvin, P, Limosin, F

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High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease von Pottier, C, Hannequin, D, Coutant, S, Rovelet-Lecrux, A, Wallon, D, Rousseau, S, Legallic, S, Paquet, C, Bombois, S, Pariente, J, Thomas-Anterion, C, Michon, A, Croisile, B, Etcharry-Bouyx, F, Berr, C, Dartigues, J-F, Amouyel, P, Dauchel, H, Boutoleau-Bretonnière, C, Thauvin, C, Frebourg, T, Lambert, J-C, Campion, D

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De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease von Rovelet-Lecrux, A, Charbonnier, C, Wallon, D, Nicolas, G, Seaman, M N J, Pottier, C, Breusegem, S Y, Mathur, P P, Jenardhanan, P, Le Guennec, K, Mukadam, A S, Quenez, O, Coutant, S, Rousseau, S, Richard, A-C, Boland, A, Deleuze, J-F, Frebourg, T, Hannequin, D, Campion, D

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Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases von Zurek, Birte, Ellwanger, Kornelia, Vissers, Lisenka E L M, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, de Voer, Richarda M, Laurie, Steven, Matalonga, Leslie, Gilissen, Christian, Ossowski, Stephan, 't Hoen, Peter A C, Vitobello, Antonio, Schulze-Hentrich, Julia M, Riess, Olaf, Brunner, Han G, Brookes, Anthony J, Rath, Ana, Bonne, Gisèle, Gumus, Gulcin, Verloes, Alain, Hoogerbrugge, Nicoline, Evangelista, Teresinha, Harmuth, Tina, Swertz, Morris, Spalding, Dylan, Hoischen, Alexander, Beltran, Sergi, Graessner, Holm

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Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls von Bellenguez, Céline, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Le Guennec, Kilan, Nicolas, Gaël, Chauhan, Ganesh, Wallon, David, Rousseau, Stéphane, Richard, Anne Claire, Boland, Anne, Bourque, Guillaume, Munter, Hans Markus, Olaso, Robert, Meyer, Vincent, Rollin-Sillaire, Adeline, Pasquier, Florence, Letenneur, Luc, Redon, Richard, Dartigues, Jean-François, Tzourio, Christophe, Frebourg, Thierry, Lathrop, Mark, Deleuze, Jean-François, Hannequin, Didier, Genin, Emmanuelle, Amouyel, Philippe, Debette, Stéphanie, Lambert, Jean-Charles, Campion, Dominique, Hannequin, Didier, Campion, Dominique, Wallon, David, Martinaud, Olivier, Zarea, Aline, Nicolas, Gaël, Rollin-Sillaire, Adeline, Bombois, Stéphanie, Mackowiak, Marie-Anne, Deramecourt, Vincent, Pasquier, Florence, Michon, Agnès, Le Ber, Isabelle, Dubois, Bruno, Godefroy, Olivier, Etcharry-Bouyx, Frédérique, Chauviré, Valérie, Chamard, Ludivine, Berger, Eric, Magnin, Eloi, Dartigues, Jean-Francois, Auriacombe, Sophie, Tison, François, Sayette, Vincent de la, Castan, Dominique, Dionet, Elsa, Sellal, Francois, Rouaud, Olivier, Thauvin, Christel, Moreaud, Olivier, Sauvée, Mathilde, Formaglio, Maïté, Mollion, Hélène, Roullet-Solignac, Isabelle, Vighetto, Alain, Croisile, Bernard, Didic, Mira, Félician, Olivier, Koric, Lejla, Ceccaldi, Mathieu, Gabelle, Audrey, Marelli, Cecilia, Labauge, Pierre, Jonveaux, Thérèse, Vercelletto, Martine, Boutoleau-Bretonnière, Claire, Castelnovo, Giovanni, Paquet, Claire, Dumurgier, Julien, Hugon, Jacques, De Boisgueheneuc, Foucauld, Belliard, Serge, Bakchine, Serge, Sarazin, Marie, Barrellon, Marie-Odile, Laurent, Bernard, Blanc, Frédéric, Pariente, Jérémie, Jurici, Snejana

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Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification von 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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Identification of potential common genetic modifiers of neurofibromas: a genome-wide association study in 1333 patients with neurofibromatosis type 1 von Pacot, Laurence, Sabbagh, Audrey, Sohier, Pierre, Hadjadj, Djihad, Ye, Manuela, Boland-Auge, Anne, Bacq-Daian, Delphine, Laurendeau, Ingrid, Briand-Suleau, Audrey, Deleuze, Jean-François, Margueron, Raphaël, Vidaud, Michel, Ferkal, Salah, Parfait, Béatrice, Vidaud, Dominique, Pasmant, Eric, Wolkenstein, Pierre

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Valuing genetic and genomic testing in France: current challenges and latest evidence von Lejeune, Catherine, Amado, Ines F.

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Trends in incidence, prevalence, and survival of breast cancer in the United Kingdom from 2000 to 2021 von Barclay, Nicola L., Burn, Edward, Delmestri, Antonella, Duarte-Salles, Talita, Golozar, Asieh, Man, Wai Yi, Tan, Eng Hooi, Tietzova, Ilona, Prieto-Alhambra, Daniel, Newby, Danielle

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Primary progressive aphasias associated with C9orf72 expansions: Another side of the story von Saracino, Dario, Géraudie, Amandine, Remes, Anne M., Ferrieux, Sophie, Noguès-Lassiaille, Marie, Bottani, Simona, Cipriano, Lorenzo, Houot, Marion, Funkiewiez, Aurélie, Camuzat, Agnès, Rinaldi, Daisy, Teichmann, Marc, Pariente, Jérémie, Couratier, Philippe, Boutoleau-Bretonnière, Claire, Auriacombe, Sophie, Etcharry-Bouyx, Frédérique, Levy, Richard, Migliaccio, Raffaella, Solje, Eino, Le Ber, Isabelle, Auriacombe, Sophie, Belliard, Serge, Blanc, Frédéric, Benchetrit, Eve, Bertin, Hugo, Boutoleau-Bretonnière, Claire, Bertrand, Anne, Bissery, Anne, Bombois, Stéphanie, Boncoeur, Marie-Paule, Brice, Alexis, Ceccaldi, Mathieu, Chastan, Mathieu, Chen, Yaohua, Chupin, Marie, Colliot, Olivier, Couratier, Philippe, Delbeuck, Xavier, Delmaire, Christine, Deramecourt, Vincent, Didic, Mira, Duyckaerts, Charles, Etcharry-Bouyx, Frédérique, Formaglio, Maïté, Gerardin, Emmanuel, Golfier, Véronique, Habert, Marie-Odile, idier Hannequin, Lacomblez, Lucette, Lagarde, Julien, Lautrette, Géraldine, Le Ber, Isabelle, Le Toullec, Benjamin, Mackowiak, Marie-Anne, Martinaud, Olivier, Michel, Bernard-François, Monteil, Jacques, Oya, Assi-Hervé, Pariente, Jérémie, Pasquier, Florence, Petyt, Grégory, Rinaldi, Daisy, Rollin-Sillaire, Adeline, Roué-Jagot, Carole, Sayah, Sabrina, Sarazin, Marie, Thauvin-Robinet, Christel, Thomas-Anterion, Catherine, Sellal, François, Vercelletto, Martine, Wallon, David

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A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis von de Boer, Elke, Ockeloen, Charlotte W, Matalonga, Leslie, Horvath, Rita, Rodenburg, Richard J, Coenen, Marieke J H, Janssen, Mirian, Henssen, Dylan, Gilissen, Christian, Steyaert, Wouter, Paramonov, Ida, Trimouille, Aurélien, Kleefstra, Tjitske, Verloes, Alain, Vissers, Lisenka E L M

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Solving unsolved rare neurological diseases-a Solve-RD viewpoint von Schüle, Rebecca, Timmann, Dagmar, Erasmus, Corrie E, Reichbauer, Jennifer, Wayand, Melanie, van de Warrenburg, Bart, Schöls, Ludger, Wilke, Carlo, Bevot, Andrea, Zuchner, Stephan, Beltran, Sergi, Laurie, Steven, Matalonga, Leslie, Graessner, Holm, Synofzik, Matthis

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Role of Noncoding RNA ANRIL in Genesis of Plexiform Neurofibromas in Neurofibromatosis Type 1 von Pasmant, Eric, Sabbagh, Audrey, Masliah-Planchon, Julien, Ortonne, Nicolas, Laurendeau, Ingrid, Melin, Lucie, Ferkal, Salah, Hernandez, Lucie, Leroy, Karen, Valeyrie-Allanore, Laurence, Parfait, Béatrice, Vidaud, Dominique, Bièche, Ivan, Lantieri, Laurent, Wolkenstein, Pierre, Vidaud, Michel

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Twist exome capture allows for lower average sequence coverage in clinical exome sequencing von Yaldiz, Burcu, Kucuk, Erdi, Hampstead, Juliet, Hofste, Tom, Pfundt, Rolph, Corominas Galbany, Jordi, Rinne, Tuula, Yntema, Helger G, Hoischen, Alexander, Nelen, Marcel, Gilissen, Christian

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Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy von Sanson, Benoît, Stalens, Caroline, Guien, Céline, Villa, Luisa, Eng, Catherine, Rabarimeriarijaona, Sitraka, Bernard, Rafaëlle, Cintas, Pascal, Solé, Guilhem, Tiffreau, Vincent, Echaniz-Laguna, Andoni, Magot, Armelle, Juntas Morales, Raul, Boyer, François Constant, Nadaj-Pakleza, Aleksandra, Jacquin-Piques, Agnès, Béroud, Christophe, Sacconi, Sabrina

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Identification of three clinical neurofibromatosis 1 subtypes: Latent class analysis of a series of 1351 patients von Bergqvist, C., Fertitta, L., Ezzedine, K., Jannic, A., Zehou, O., Ferkal, S., Combemale, P., Barbarot, S., Mazereeuw‐Hautier, J., Sbidian, E., Wolkenstein, P., Adamski, Henri, Baumann‐Morel, Clarisse, Bellanné, Christine, Bieth, Eric, Bousquet, Pascal, Brandt, Christian, Balguerie, Xavier, Castelnau, Pierre, Chaix, Yves, Chevrant‐Breton, Jacqueline, Collet, Evelyne, Cuny, Jean‐François, Chastagner, Pascal, Chandeclerc, Marie‐Lorraine, Cheuret, Emmanuel, Cintas, Pascal, Dollfus, Helene, Derancourt, Christian, Drouin‐Garraud, Valérie, d'Incan, Michel, De Leersnyder, Hélène, Dereure, Olivier, Doumar, Diane, Fabre, Nicolas, Ferraro, Vincenza, Francannet, Christine, Faivre, Laurence, Fellmann, Florence, Feugier, Nathalie, Gaillard, Dominique, Goldenberg, Alice, Guyant‐Marechal, Lucie, Guillot, Bernard, Guillamo, Jean‐Sebastien, Hadj‐Rabia, Smaïl, Hamel‐Teillac, Dominique, Kemlin, Isabelle, Lacour, Jean‐Philippe, Laithier, Veronique, Lesavre, Nathalie, Lyonnet, Stanislas, Maincent, Kim, Maradeix, Sophie, Machet, Laurent, Mansat, Eva, Meyer, Nicolas, Mozelle, Monique, Celine Moret, Jean Christophe Moreno, Puzenat, Eric, Parfait, Béatrice, Pinson, Stéphane, Pasmant, Eric, Rodriguez, Diana, Stalder, Jean‐François, Schweitzer, Elisabeth, Thalamas, Claire, Thauvin, Christel, Vidaud, Dominique, Vidaud, Michel, Verloes, Alain, Zeller, Jacques

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Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis von de Boer, Elke, Ockeloen, Charlotte W, Matalonga, Leslie, Horvath, Rita, Rodenburg, Richard J, Coenen, Marieke J H, Janssen, Mirian, Henssen, Dylan, Gilissen, Christian, Steyaert, Wouter, Paramonov, Ida, Trimouille, Aurélien, Kleefstra, Tjitske, Verloes, Alain, Vissers, Lisenka E L M

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Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1 von Sabbagh, Audrey, Pasmant, Eric, Laurendeau, Ingrid, Parfait, Béatrice, Barbarot, Sébastien, Guillot, Bernard, Combemale, Patrick, Ferkal, Salah, Vidaud, Michel, Aubourg, Patrick, Vidaud, Dominique, Wolkenstein, Pierre

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Medical factors associated with early IVF discontinuation von Troude, Pénélope, Guibert, Juliette, Bouyer, Jean, de La Rochebrochard, Elise

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