Tauopathy in the young autistic brain: novel biomarker and therapeutic target by Grigg, Iris, Ivashko-Pachima, Yanina, Hait, Tom Aharon, Korenková, Vlasta, Touloumi, Olga, Lagoudaki, Roza, Van Dijck, Anke, Marusic, Zlatko, Anicic, Mirna, Vukovic, Jurica, Kooy, R. Frank, Grigoriadis, Nikolaos, Gozes, Illana

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Tracing the invisible mutant ADNP protein in Helsmoortel-Van der Aa syndrome patients by D’Incal, Claudio Peter, Cappuyns, Elisa, Choukri, Kaoutar, De Man, Kevin, Szrama, Kristy, Konings, Anthony, Bastini, Lina, Van Meel, Kim, Buys, Amber, Gabriele, Michele, Rizzuti, Ludovico, Vitriolo, Alessandro, Testa, Giuseppe, Mohn, Fabio, Bühler, Marc, Van der Aa, Nathalie, Van Dijck, Anke, Kooy, R. Frank, Berghe, Wim Vanden

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Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants by Smolen, Corrine, Jensen, Matthew, Dyer, Lisa, Pizzo, Lucilla, Tyryshkina, Anastasia, Banerjee, Deepro, Rohan, Laura, Huber, Emily, El Khattabi, Laila, Prontera, Paolo, Caberg, Jean-Hubert, Van Dijck, Anke, Schwartz, Charles, Faivre, Laurence, Callier, Patrick, Mosca-Boidron, Anne-Laure, Lefebvre, Mathilde, Pope, Kate, Snell, Penny, Lockhart, Paul J., Castiglia, Lucia, Galesi, Ornella, Avola, Emanuela, Mattina, Teresa, Fichera, Marco, Luana Mandarà, Giuseppa Maria, Bruccheri, Maria Grazia, Pichon, Olivier, Le Caignec, Cedric, Stoeva, Radka, Cuinat, Silvestre, Mercier, Sandra, Bénéteau, Claire, Blesson, Sophie, Nordsletten, Ashley, Martin-Coignard, Dominique, Sistermans, Erik, Kooy, R. Frank, Amor, David J., Romano, Corrado, Isidor, Bertrand, Juusola, Jane, Girirajan, Santhosh

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Chromatin remodeler Activity-Dependent Neuroprotective Protein (ADNP) contributes to syndromic autism by D'Incal, Claudio Peter, Van Rossem, Kirsten Esther, De Man, Kevin, Konings, Anthony, Van Dijck, Anke, Rizzuti, Ludovico, Vitriolo, Alessandro, Testa, Giuseppe, Gozes, Illana, Vanden Berghe, Wim, Kooy, R Frank

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De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms by Jansen, Sandra, van der Werf, Ilse M, Innes, A Micheil, Afenjar, Alexandra, Agrawal, Pankaj B, Anderson, Ilse J, Atwal, Paldeep S, van Binsbergen, Ellen, van den Boogaard, Marie-José, Castiglia, Lucia, Coban-Akdemir, Zeynep H, van Dijck, Anke, Doummar, Diane, van Eerde, Albertien M, van Essen, Anthonie J, van Gassen, Koen L, Guillen Sacoto, Maria J, van Haelst, Mieke M, Iossifov, Ivan, Jackson, Jessica L, Judd, Elizabeth, Kaiwar, Charu, Keren, Boris, Klee, Eric W, Klein Wassink-Ruiter, Jolien S, Meuwissen, Marije E, Monaghan, Kristin G, de Munnik, Sonja A, Nava, Caroline, Ockeloen, Charlotte W, Pettinato, Rosa, Racher, Hilary, Rinne, Tuula, Romano, Corrado, Sanders, Victoria R, Schnur, Rhonda E, Smeets, Eric J, Stegmann, Alexander P A, Stray-Pedersen, Asbjørg, Sweetser, David A, Terhal, Paulien A, Tveten, Kristian, VanNoy, Grace E, de Vries, Petra F, Waxler, Jessica L, Willing, Marcia, Pfundt, Rolph, Veltman, Joris A, Kooy, R Frank, Vissers, Lisenka E L M, de Vries, Bert B A

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A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome by Ligsay, Andrew, Van Dijck, Anke, Nguyen, Danh V, Lozano, Reymundo, Chen, Yanjun, Bickel, Erika S, Hessl, David, Schneider, Andrea, Angkustsiri, Kathleen, Tassone, Flora, Ceulemans, Berten, Kooy, R Frank, Hagerman, Randi J

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Correction to: ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van Der Aa syndrome autopsy case by D'Incal, Claudio, Dijck, Anke Van, Ibrahim, Joe, Man, Kevin De, Bastini, Lina, Konings, Anthony, Elinck, Ellen, Theys, Claudia, Gozes, Illana, Marusic, Zlatko, Anicic, Mirna, Vukovic, Jurica, Aa, Nathalie Van der, Mateiu, Ligia, Vanden Berghe, Wim, Kooy, R Frank

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Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disorders by van der Werf, Ilse M, Jansen, Sandra, de Vries, Petra F, Gerstmans, Amber, van de Vorst, Maartje, Van Dijck, Anke, de Vries, Bert B A, Gilissen, Christian, Hoischen, Alexander, Vissers, Lisenka E L M, Kooy, R Frank, Vandeweyer, Geert

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ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van der Aa syndrome autopsy case by D'Incal, Claudio, Van Dijck, Anke, Ibrahim, Joe, De Man, Kevin, Bastini, Lina, Konings, Anthony, Elinck, Ellen, Gozes, Lllana, Marusic, Zlatko, Anicic, Mirna, Vukovic, Jurica, Van der Aa, Nathalie, Mateiu, Ligia, Vanden Berghe, Wim, Kooy, R Frank

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Reduced serum levels of pro-inflammatory chemokines in fragile X syndrome by Van Dijck, Anke, Barbosa, Susana, Bermudez-Martin, Patricia, Khalfallah, Olfa, Gilet, Cyprien, Martinuzzi, Emanuela, Elinck, Ellen, Kooy, R Frank, Glaichenhaus, Nicolas, Davidovic, Laetitia

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The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings by Gozes, Illana, Patterson, Marc C, Van Dijck, Anke, Kooy, R Frank, Peeden, Joseph N, Eichenberger, Jacob A, Zawacki-Downing, Angela, Bedrosian-Sermone, Sandra

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The translational regulator FMRP controls lipid and glucose metabolism in mice and humans by Leboucher, Antoine, Pisani, Didier F., Martinez-Gili, Laura, Chilloux, Julien, Bermudez-Martin, Patricia, Van Dijck, Anke, Ganief, Tariq, Macek, Boris, Becker, Jérôme A.J., Le Merrer, Julie, Kooy, R. Frank, Amri, Ez-Zoubir, Khandjian, Edouard W., Dumas, Marc-Emmanuel, Davidovic, Laetitia

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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling by Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R.F., Venselaar, Hanka, Helsmoortel, Céline, Cho, Megan T., Hoischen, Alexander, Vissers, Lisenka E.L.M., Koemans, Tom S., Wissink-Lindhout, Willemijn, Eichler, Evan E., Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Oberndorff, Karin, van Bon, Bregje W.M., Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L., Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J., Henderson, Alex, Lynch, Sally A., Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, van Gassen, Koen L.I., Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L., Pediaditakis, Igor, Haas, Stefan A., Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G., Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C., Stein, Quinn, Strauss, Kevin A., Brigatti, Karlla W., Keating, Katherine, Burton, Barbara K., Kim, Katherine H., Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D., Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M., van Roozendaal, Kees, Brunner, Han, Chung, Wendy K., Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G., Katsanis, Nicholas, Kleefstra, Tjitske

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Gait deviations in rare genetic syndromes: is there a common denomitator for patients with Dravet, HVDAS and TSC? by Van De Walle, Patricia, Jansen, An, Schoonjans, An-Sofie, Van Dijck, Anke, Puts, Colette, van Hal, Iris, Weren, Marijn, Esra, Kinaci, Hallemans, Ann

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Diagnostic implications of genetic copy number variation in epilepsy plus by Coppola, Antonietta, Cellini, Elena, Stamberger, Hannah, Saarentaus, Elmo, Cetica, Valentina, Lal, Dennis, Djémié, Tania, Bartnik‐Glaska, Magdalena, Ceulemans, Berten, Helen Cross, J., Deconinck, Tine, Masi, Salvatore De, Dorn, Thomas, Guerrini, Renzo, Hoffman‐Zacharska, Dorotha, Kooy, Frank, Lagae, Lieven, Lench, Nicholas, Lemke, Johannes R., Lucenteforte, Ersilia, Madia, Francesca, Mefford, Heather C., Morrogh, Deborah, Nuernberg, Peter, Palotie, Aarno, Schoonjans, An‐Sofie, Striano, Pasquale, Szczepanik, Elzbieta, Tostevin, Anna, Vermeesch, Joris R., Van Esch, Hilde, Van Paesschen, Wim, Waters, Jonathan J, Weckhuysen, Sarah, Zara, Federico, De Jonghe, Peter, Sisodiya, Sanjay M., Marini, Carla, Lehesjioki, Anna‐Elina, Craiu, Dana, Talvik, Tiina, Caglayan, Hande, Serratosa, Jose, Sterbova, Katalin, Møller, Rikke S., Hjalgrim, Helle, Lerche, Holger, Weber, Yvonne, Helbig, Ingo, Spiczak, Sarah, Barba, Carmen, Bogaerts, Anneleen, Boni, Antonella, Galizia, Elisabeth Caruana, Chiari, Sara, Gacomo, Gianpiero, Ferrari, Annarita, Guarducci, Silvia, Giglio, Sabrina, Holmgren, Philip, Leu, Costin, Melani, Federico, Novara, Francesca, Pantaleo, Marilena, Peeters, Elke, Pisano, Tiziana, Rosati, Anna, Sander, Josemir, Schoeler, Natasha, Stankiewicz, Pawel, Striano, Salvatore, Suls, Arvid, Traverso, Monica, Vandeweyer, Geert, Dijck, Anke, Zuffardi, Orsetta

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Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging by Flex, Elisabetta, Martinelli, Simone, Van Dijck, Anke, Ciolfi, Andrea, Cecchetti, Serena, Coluzzi, Elisa, Pannone, Luca, Andreoli, Cristina, Radio, Francesca Clementina, Pizzi, Simone, Carpentieri, Giovanna, Bruselles, Alessandro, Catanzaro, Giuseppina, Pedace, Lucia, Miele, Evelina, Carcarino, Elena, Ge, Xiaoyan, Chijiwa, Chieko, Lewis, M.E. Suzanne, Meuwissen, Marije, Kenis, Sandra, Van der Aa, Nathalie, Larson, Austin, Brown, Kathleen, Wasserstein, Melissa P., Skotko, Brian G., Begtrup, Amber, Person, Richard, Karayiorgou, Maria, Roos, J. Louw, Van Gassen, Koen L., Koopmans, Marije, Bijlsma, Emilia K., Santen, Gijs W.E., Barge-Schaapveld, Daniela Q.C.M., Ruivenkamp, Claudia A.L., Hoffer, Mariette J.V., Lalani, Seema R., Streff, Haley, Craigen, William J., Graham, Brett H., van den Elzen, Annette P.M., Kamphuis, Daan J., Õunap, Katrin, Reinson, Karit, Pajusalu, Sander, Wojcik, Monica H., Viberti, Clara, Di Gaetano, Cornelia, Bertini, Enrico, Petrucci, Simona, De Luca, Alessandro, Rota, Rossella, Ferretti, Elisabetta, Matullo, Giuseppe, Dallapiccola, Bruno, Sgura, Antonella, Walkiewicz, Magdalena, Kooy, R. Frank, Tartaglia, Marco

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The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism by Vandeweyer, Geert, Helsmoortel, Céline, Van Dijck, Anke, Vulto-van Silfhout, Anneke T., Coe, Bradley P., Bernier, Raphael, Gerdts, Jennifer, Rooms, Liesbeth, van den Ende, Jenneke, Bakshi, Madhura, Wilson, Meredith, Nordgren, Ann, Hendon, Laura G., Abdulrahman, Omar A., Romano, Corrado, de Vries, Bert B.A., Kleefstra, Tjitske, Eichler, Evan E., Van der Aa, Nathalie, Kooy, R. Frank

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Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability by van der Werf, Ilse M., Van Dijck, Anke, Reyniers, Edwin, Helsmoortel, Céline, Kumar, Ajay Anand, Kalscheuer, Vera M., de Brouwer, Arjan PM, Kleefstra, Tjitske, van Bokhoven, Hans, Mortier, Geert, Janssens, Sandra, Vandeweyer, Geert, Kooy, R. Frank

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F75THE TRUE CONTRIBUTION OF THE 15Q11.2 BP1-BP2 DELETION TO NEURODEVELOPMENTAL SYMPTOMS by Jønch, Aia, Douard, Elise, Moreau, Clara, Van Dijck, Anke, Kooy, Frank, Sanlaville, Damien, Brasch-Andersen, Charlotte, Lemyre, Emmanuelle, Ousager, Lilian B., Jacquemont, Sébastien

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A mouse model for intellectual disability caused by mutations in the X-linked 2′‑O‑methyltransferase Ftsj1 gene by Jensen, Lars R., Garrett, Lillian, Hölter, Sabine M., Rathkolb, Birgit, Rácz, Ildikó, Adler, Thure, Prehn, Cornelia, Hans, Wolfgang, Rozman, Jan, Becker, Lore, Aguilar-Pimentel, Juan Antonio, Puk, Oliver, Moreth, Kristin, Dopatka, Monika, Walther, Diego J., von Bohlen und Halbach, Viola, Rath, Matthias, Delatycki, Martin, Bert, Bettina, Fink, Heidrun, Blümlein, Katharina, Ralser, Markus, Van Dijck, Anke, Kooy, Frank, Stark, Zornitza, Müller, Sabine, Scherthan, Harry, Gecz, Jozef, Wurst, Wolfgang, Wolf, Eckhard, Zimmer, Andreas, Klingenspor, Martin, Graw, Jochen, Klopstock, Thomas, Busch, Dirk, Adamski, Jerzy, Fuchs, Helmut, Gailus-Durner, Valérie, de Angelis, Martin Hrabě, von Bohlen und Halbach, Oliver, Ropers, Hans-Hilger, Kuss, Andreas W.

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