Neurofilament light chain: a biomarker for genetic frontotemporal dementia von Meeter, Lieke H., Dopper, Elise G., Jiskoot, Lize C., Sanchez‐Valle, Raquel, Graff, Caroline, Benussi, Luisa, Ghidoni, Roberta, Pijnenburg, Yolande A., Borroni, Barbara, Galimberti, Daniela, Laforce, Robert Jr, Masellis, Mario, Vandenberghe, Rik, Ber, Isabelle Le, Otto, Markus, Minkelen, Rick, Papma, Janne M., Rombouts, Serge A., Balasa, Mircea, Öijerstedt, Linn, Jelic, Vesna, Dick, Katrina M., Cash, David M., Harding, Sophie R., Jorge Cardoso, M., Ourselin, Sebastien, Rossor, Martin N., Padovani, Alessandro, Scarpini, Elio, Fenoglio, Chiara, Tartaglia, Maria C., Lamari, Foudil, Barro, Christian, Kuhle, Jens, Rohrer, Jonathan D., Teunissen, Charlotte E., Swieten, John C.

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New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers von Viodé, Arthur, Fournier, Clémence, Camuzat, Agnès, Fenaille, François, Latouche, Morwena, Elahi, Fanny, Le Ber, Isabelle, Junot, Christophe, Lamari, Foudil, Anquetil, Vincent, Becher, François

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Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia von Ber, Isabelle Le, Guedj, Eric, Gabelle, Audrey, Verpillat, Patrice, Volteau, Magali, Thomas-Anterion, Catherine, Decousus, Marielle, Hannequin, Didier, Véra, Pierre, Lacomblez, Lucette, Camuzat, Agnès, Didic, Mira, Puel, Michèle, Lotterie, Jean-Albert, Golfier, Véronique, Bernard, Anne-Marie, Vercelletto, Martine, Magne, Christine, Sellal, François, Namer, Izzie, Michel, Bernard-François, Pasquier, Jacques, Salachas, François, Bochet, Jean, Brice, Alexis, Habert, Marie-Odile, Dubois, Bruno

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Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis von Ciura, Sorana, Lattante, Serena, Le Ber, Isabelle, Latouche, Morwena, Tostivint, Hervé, Brice, Alexis, Kabashi, Edor

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Frontotemporal dementia subtypes based on behavioral inhibition deficits von Godefroy, Valérie, Tanguy, Delphine, Bouzigues, Arabella, Sezer, Idil, Ferrand‐Verdejo, Johan, Azuar, Carole, Bendetowicz, David, Carle, Guilhem, Rametti‐Lacroux, Armelle, Bombois, Stéphanie, Cognat, Emmanuel, Jannin, Pierre, Morandi, Xavier, Ber, Isabelle Le, Levy, Richard, Batrancourt, Bénédicte, Migliaccio, Raffaella

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A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia von Coutelier, Marie, Blesneac, Iulia, Monteil, Arnaud, Monin, Marie-Lorraine, Ando, Kunie, Mundwiller, Emeline, Brusco, Alfredo, Le Ber, Isabelle, Anheim, Mathieu, Castrioto, Anna, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra, Lory, Philippe, Stevanin, Giovanni

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Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms von Huin, Vincent, Barbier, Mathieu, Bottani, Armand, Lobrinus, Johannes Alexander, Clot, Fabienne, Lamari, Foudil, Chat, Laureen, Rucheton, Benoit, Fluchere, Frederique, Auvin, Stephane, Myers, Peter, Gelot, Antoinette, Camuzat, Agnes, Caillaud, Catherine, Jornea, Ludmila, Forlani, Sylvie, Saracino, Dario, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra, Le Ber, Isabelle

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A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement von BANNWARTH, Sylvie, AIT-EL-MKADEM, Samira, VERSCHUEREN, Annie, ROUZIER, Cecile, LE BER, Isabelle, AUGE, Gaëlle, COCHAUD, Charlotte, LESPINASSE, Françoise, N'GUYEN, Karine, DE SEPTENVILLE, Anne, BRICE, Alexis, YU-WAI-MAN, Patrick, CHAUSSENOT, Annabelle, SESAKI, Hiromi, POUGET, Jean, PAQUIS-FLUCKLINGER, Véronique, GENIN, Emmanuelle C, LACAS-GERVAIS, Sandra, FRAGAKI, Konstantina, BERG-ALONSO, Laetitia, KAGEYAMA, Yusuke, SERRE, Valérie, MOORE, David G

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Questioning the causality of HTT CAG-repeat expansions in FTD/ALS von Thomas, Quentin, Coarelli, Giulia, Heinzmann, Anna, Le Ber, Isabelle, Amador, Maria del Mar, Durr, Alexandra

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Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging study von Querin, Giorgia, Bede, Peter, El Mendili, Mohamed Mounir, Li, Menghan, Pélégrini‐Issac, Mélanie, Rinaldi, Daisy, Catala, Martin, Saracino, Dario, Salachas, François, Camuzat, Agnes, Marchand‐Pauvert, Véronique, Cohen‐Adad, Julien, Colliot, Olivier, Le Ber, Isabelle, Pradat, Pierre‐François

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Homozygous TREM2 mutation in a family with atypical frontotemporal dementia von Le Ber, Isabelle, De Septenville, Anne, Guerreiro, Rita, Bras, José, Camuzat, Agnès, Caroppo, Paola, Lattante, Serena, Couarch, Philippe, Kabashi, Edor, Bouya-Ahmed, Kawtar, Dubois, Bruno, Brice, Alexis

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Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification von NICOLAS, Gaël, POTTIER, Cyril, MARTINAUD, Olivier, DEFEBVRE, Luc, KRYSTKOWIAK, Pierre, PARIENTE, Jérémie, CLANET, Michel, LABAUGE, Pierre, AYRIGNAC, Xavier, LEFAUCHEUR, Romain, LE BER, Isabelle, FREBOURG, Thierry, MALTETE, David, HANNEQUIN, Didier, CAMPION, Dominique, COUTANT, Sophie, ROVELET-LECRUX, Anne, LEGALLIC, Solenn, ROUSSEAU, Stéphane, VASCHALDE, Yvan, GUYANT-MARECHAL, Lucie, AUGUSTIN, Jérôme

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Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxias von Chan, Ellis, Charles, Perrine, Ribai, Pascale, Goizet, Cyril, Marelli, Cecilia, Vincitorio, Carlo-Maria, Bayon, Alice Le, Guyant-Maréchal, Lucie, Vandenberghe, Nadia, Anheim, Mathieu, Devos, David, Freeman, Leorah, Ber, Isabelle Le, N'Guyen, Karine, Tchikviladzé, Maya, Labauge, Pierre, Hannequin, Didier, Brice, Alexis, Durr, Alexandra, du Montcel, Sophie Tezenas

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Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients von Chaussenot, Annabelle, Le Ber, Isabelle, Ait-El-Mkadem, Samira, Camuzat, Agnès, de Septenville, Anne, Bannwarth, Sylvie, Genin, Emmanuelle C, Serre, Valérie, Augé, Gaëlle, Brice, Alexis, Pouget, Jean, Paquis-Flucklinger, Véronique

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C9orf72 repeat expansions are a rare genetic cause of parkinsonism von LESAGE, Suzanne, LE BER, Isabelle, ROULEAU, Guy A, DÜRR, Alexandra, BRICE, Alexis, CONDROYER, Christel, BROUSSOLLE, Emmanuel, GABELLE, Audrey, THOBOIS, Stéphane, PASQUIER, Florence, MONDON, Karl, DION, Patrick A, ROCHEFORT, Daniel

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Disease Progression Score Estimation From Multimodal Imaging and MicroRNA Data Using Supervised Variational Autoencoders von Kmetzsch, Virgilio, Becker, Emmanuelle, Saracino, Dario, Rinaldi, Daisy, Camuzat, Agnes, Le Ber, Isabelle, Colliot, Olivier

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TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration von Benajiba, Lina, Le Ber, Isabelle, Camuzat, Agnès, Lacoste, Mathieu, Thomas-Anterion, Catherine, Couratier, Philippe, Legallic, Solenn, Salachas, François, Hannequin, Didier, Decousus, Marielle, Lacomblez, Lucette, Guedj, Eric, Golfier, Véronique, Camu, William, Dubois, Bruno, Campion, Dominique, Meininger, Vincent, Brice, Alexis

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SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease von Nicolas, G, Charbonnier, C, Wallon, D, Quenez, O, Bellenguez, C, Grenier-Boley, B, Rousseau, S, Richard, A-C, Rovelet-Lecrux, A, Le Guennec, K, Bacq, D, Garnier, J-G, Olaso, R, Boland, A, Meyer, V, Deleuze, J-F, Amouyel, P, Munter, H M, Bourque, G, Lathrop, M, Frebourg, T, Redon, R, Letenneur, L, Dartigues, J-F, Génin, E, Lambert, J-C, Hannequin, D, Campion, D

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Integrative genetic analysis illuminates ALS heritability and identifies risk genes von Megat, Salim, Mora, Natalia, Sanogo, Jason, Roman, Olga, Catanese, Alberto, Alami, Najwa Ouali, Freischmidt, Axel, Mingaj, Xhuljana, De Calbiac, Hortense, Muratet, François, Dirrig-Grosch, Sylvie, Dieterle, Stéphane, Van Bakel, Nick, Müller, Kathrin, Sieverding, Kirsten, Weishaupt, Jochen, Andersen, Peter Munch, Weber, Markus, Neuwirth, Christoph, Margelisch, Markus, Sommacal, Andreas, Van Eijk, Kristel R., Veldink, Jan H., Lautrette, Géraldine, Couratier, Philippe, Camuzat, Agnès, Le Ber, Isabelle, Grassano, Maurizio, Chio, Adriano, Boeckers, Tobias, Ludolph, Albert C., Roselli, Francesco, Yilmazer-Hanke, Deniz, Millecamps, Stéphanie, Kabashi, Edor, Storkebaum, Erik, Sellier, Chantal, Dupuis, Luc

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CSF sTREM2 is elevated in a subset in GRN-related frontotemporal dementia von van der Ende, Emma L., Morenas-Rodriguez, Estrella, McMillan, Corey, Grossman, Murray, Irwin, David, Sanchez-Valle, Raquel, Graff, Caroline, Vandenberghe, Rik, Pijnenburg, Yolande A.L., Laforce, Robert, Ber, Isabelle Le, Lleo, Alberto, Haass, Christian, Suarez-Calvet, Marc, van Swieten, John C., Seelaar, Harro

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