Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model von Haslinger, Denise, Waltes, Regina, Yousaf, Afsheen, Lindlar, Silvia, Schneider, Ines, Lim, Chai K, Tsai, Meng-Miao, Garvalov, Boyan K, Acker-Palmer, Amparo, Krezdorn, Nicolas, Rotter, Björn, Acker, Till, Guillemin, Gilles J, Fulda, Simone, Freitag, Christine M, Chiocchetti, Andreas G

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Drug-Resistant Juvenile Myoclonic Epilepsy: Misdiagnosis of Progressive Myoclonus Epilepsy von Martin, Sarah, Strzelczyk, Adam, Lindlar, Silvia, Krause, Kristina, Reif, Philipp S., Menzler, Katja, Chiocchetti, Andreas G., Rosenow, Felix, Knake, Susanne, Klein, Karl Martin

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The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing von Brauchitsch, Sophie, Haslinger, Denise, Lindlar, Silvia, Thiele, Holger, Bernsen, Natalie, Zahnert, Felix, Reif, Philipp S., Balcik, Yunus, Au, Ping Yee Billie, Josephson, Colin B., Altmüller, Janine, Strzelczyk, Adam, Knake, Susanne, Rosenow, Felix, Chiocchetti, Andreas, Klein, Karl Martin

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The STAR collaborative nonsuicidal self-injury study: methods and sample description of the face-to-face sample von Spohrs, Jennifer, Michelsen, Anna, Abler, Birgit, Chioccheti, Andreas G, Ebner Priemer, Ulrich W, Fegert, Jörg M, Höper, Saskia, In-Albon, Tina, Kaess, Michael, Koelch, Michael, Koenig, Elisa, Koenig, Julian, Kraus, Laura, Nickel, Sandra, Santangelo, Philip, Schmahl, Christian, Sicorello, Maurizio, van der Venne, Patrice, Plener, Paul L

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Training approaches for the dissemination of clinical guidelines for NSSI: a quasi-experimental trial von Koenig, Elisa, Hoffmann, Ulrike, Fegert, Jörg M, Keller, Ferdinand, Sicorello, Maurizio, Spohrs, Jennifer, Kraus, Laura, Nickel, Sandra, Schmahl, Christian, Abler, Birgit, In-Albon, Tina, Koenig, Julian, Ougrin, Dennis, Kaess, Michael, Plener, Paul L

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SPECIFIC ASD PHENOTYPES ARE MODULATED BY DISTINCT GENETIC VARIANTS CONVERGING AT NETWORK LEVEL von Chiocchetti, Andreas G., Waltes, Regina, Haslinger, Denise, Lindlar, Silvia, Klauck, Sabine, Duketis, Eftichia, Sachse, Michael, Voran, Anette, Biscaldi, Monica, Schulte-Rüther, Martin, Kupferschmid, Stephan, Cichon, Sven, Nöthen, Markus, Ackermann, Jörg, Koch, Ina, Freitag, Christine M.

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M14 - SPECIFIC ASD PHENOTYPES ARE MODULATED BY DISTINCT GENETIC VARIANTS CONVERGING AT NETWORK LEVEL von Chiocchetti, Andreas G., Waltes, Regina, Haslinger, Denise, Lindlar, Silvia, Klauck, Sabine, Duketis, Eftichia, Sachse, Michael, Voran, Anette, Biscaldi, Monica, Schulte-Rüther, Martin, Kupferschmid, Stephan, Cichon, Sven, Nöthen, Markus, Ackermann, Jörg, Koch, Ina, Freitag, Christine M.

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Additional file 3:Â Supplementary table S3. of Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model von Haslinger, Denise, Waltes, Regina, Afsheen Yousaf, Lindlar, Silvia, Schneider, Ines, Lim, Chai, Meng-Miao Tsai, Garvalov, Boyan, Acker-Palmer, Amparo, Krezdorn, Nicolas, BjĂśrn Rotter, Acker, Till, Guillemin, Gilles, Fulda, Simone, Freitag, Christine, Chiocchetti, Andreas

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Additional file 2:Â Supplementary table S2. of Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model von Haslinger, Denise, Waltes, Regina, Afsheen Yousaf, Lindlar, Silvia, Schneider, Ines, Lim, Chai, Meng-Miao Tsai, Garvalov, Boyan, Acker-Palmer, Amparo, Krezdorn, Nicolas, BjĂśrn Rotter, Acker, Till, Guillemin, Gilles, Fulda, Simone, Freitag, Christine, Chiocchetti, Andreas

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