Excitatory/inhibitory balance in epilepsies and neurodevelopmental disorders: Depolarizing γ‐aminobutyric acid as a common mechanism von van Hugte, Eline J. H., Schubert, Dirk, Nadif Kasri, Nael

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m.3243A > G-Induced Mitochondrial Dysfunction Impairs Human Neuronal Development and Reduces Neuronal Network Activity and Synchronicity von Klein Gunnewiek, Teun M., Van Hugte, Eline J.H., Frega, Monica, Guardia, Gemma Solé, Foreman, Katharina, Panneman, Daan, Mossink, Britt, Linda, Katrin, Keller, Jason M., Schubert, Dirk, Cassiman, David, Rodenburg, Richard, Vidal Folch, Noemi, Oglesbee, Devin, Perales-Clemente, Ester, Nelson, Timothy J., Morava, Eva, Nadif Kasri, Nael, Kozicz, Tamas

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The OTUD7A-Ankyrin pathway: a newly identified disease mechanism for the 15q13.3 microdeletion disorder von Scheefhals, Nicky, Ciptasari, Ummi, van Hugte, Eline J. H., Nadif Kasri, Nael

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Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks von Mossink, Britt, van Rhijn, Jon-Ruben, Wang, Shan, Linda, Katrin, Vitale, Maria R., Zöller, Johanna E. M., van Hugte, Eline J. H., Bak, Jitske, Verboven, Anouk H. A., Selten, Martijn, Negwer, Moritz, Latour, Brooke L., van der Werf, Ilse, Keller, Jason M., Klein Gunnewiek, Teun M., Schoenmaker, Chantal, Oudakker, Astrid, Anania, Alessia, Jansen, Sophie, Lesch, Klaus-Peter, Frega, Monica, van Bokhoven, Hans, Schubert, Dirk, Nadif Kasri, Nael

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Human neuronal networks on micro-electrode arrays are a highly robust tool to study disease-specific genotype-phenotype correlations in vitro von Mossink, Britt, Verboven, Anouk H.A., van Hugte, Eline J.H., Klein Gunnewiek, Teun M., Parodi, Giulia, Linda, Katrin, Schoenmaker, Chantal, Kleefstra, Tjitske, Kozicz, Tamas, van Bokhoven, Hans, Schubert, Dirk, Nadif Kasri, Nael, Frega, Monica

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SCN1A-deficient excitatory neuronal networks display mutation-specific phenotypes von van Hugte, Eline J H, Lewerissa, Elly I, Wu, Ka Man, Scheefhals, Nicky, Parodi, Giulia, van Voorst, Torben W, Puvogel, Sofia, Kogo, Naoki, Keller, Jason M, Frega, Monica, Schubert, Dirk, Schelhaas, Helenius J, Verhoeven, Judith, Majoie, Marian, van Bokhoven, Hans, Nadif Kasri, Nael

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Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment von Bhattacharjee, Rudrarup, Jolly, Lachlan A., Corbett, Mark A., Wee, Ing Chee, Rao, Sushma R., Gardner, Alison E., Ritchie, Tarin, van Hugte, Eline J. H., Ciptasari, Ummi, Piltz, Sandra, Noll, Jacqueline E., Nazri, Nazzmer, van Eyk, Clare L., White, Melissa, Fornarino, Dani, Poulton, Cathryn, Baynam, Gareth, Collins-Praino, Lyndsey E., Snel, Marten F., Nadif Kasri, Nael, Hemsley, Kim M., Thomas, Paul Q., Kumar, Raman, Gecz, Jozef

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NIPT-based screening for Down syndrome and beyond: what do pregnant women think? von van Schendel, Rachèl V., Dondorp, Wybo J., Timmermans, Danielle R. M., van Hugte, Eline J. H., de Boer, Anne, Pajkrt, Eva, Lachmeijer, Augusta M. A., Henneman, Lidewij

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ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal network... von Teunissen, Maria W A, Lewerissa, Elly, van Hugte, Eline J H, Wang, Shan, Ockeloen, Charlotte W, Koolen, David A, Pfundt, Rolph, Marcelis, Carlo L M, Brilstra, Eva, Howe, Jennifer L, Scherer, Stephen W, Le Guillou, Xavier, Bilan, Frédéric, Primiano, Michelle, Roohi, Jasmin, Piton, Amelie, de Saint Martin, Anne, Baer, Sarah, Seiffert, Simone, Platzer, Konrad, Jamra, Rami Abou, Syrbe, Steffen, Doering, Jan H, Lakhani, Shenela, Nangia, Srishti, Gilissen, Christian, Vermeulen, R Jeroen, Rouhl, Rob P W, Brunner, Han G, Willemsen, Marjolein H, Nadif Kasri, Nael

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A human in vitro neuronal model for studying homeostatic plasticity at the network level von Yuan, Xiuming, Puvogel, Sofía, van Rhijn, Jon-Ruben, Ciptasari, Ummi, Esteve-Codina, Anna, Meijer, Mandy, Rouschop, Simon, van Hugte, Eline J.H., Oudakker, Astrid, Schoenmaker, Chantal, Frega, Monica, Schubert, Dirk, Franke, Barbara, Nadif Kasri, Nael

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An in silico and in vitro human neuronal network model reveals cellular mechanisms beyond NaV1.1 underlying Dravet syndrome von Doorn, Nina, van Hugte, Eline J.H., Ciptasari, Ummi, Mordelt, Annika, Meijer, Hil G.E., Schubert, Dirk, Frega, Monica, Nadif Kasri, Nael, van Putten, Michel J.A.M.

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m.3243A > G-Induced Mitochondrial Dysfunction Impairs Human Neuronal Development and Reduces Neuronal Network Activity and Synchronicity von Gunnewiek, Teun M. Klein, Van Hugte, Eline J.H, Frega, Monica, Guardia, Gemma Sole, Foreman, Katharina, Panneman, Daan, Mossink, Britt, Linda, Katrin, Keller, Jason M, Schubert, Dirk, Cassiman, David, Rodenburg, Richard, Folch, Noemi Vidal, Oglesbee, Devin, Perales-Clemente, Ester, Nelson, Timothy J, Morava, Eva, Kasri, Nael Nadif, Kozicz, Tamas

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