Using developmental regression to reorganize the clinical importance of autistic atypicalities von Gagnon, David, Zeribi, Abderrahim, Douard, Élise, Courchesne, Valérie, Huguet, Guillaume, Jacquemont, Sébastien, Loum, Mor Absa, Mottron, Laurent

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Bayonet-shaped language development in autism with regression: a retrospective study von Gagnon, David, Zeribi, Abderrahim, Douard, Élise, Courchesne, Valérie, Rodríguez-Herreros, Borja, Huguet, Guillaume, Jacquemont, Sébastien, Loum, Mor Absa, Mottron, Laurent

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P822: Navigating genetic risk: Mapping variant's probability of occurring de novo and inferring their effect sizes on neurodevelopmental symptoms von England, Jade, Huguet, Guillaume, Jizi, Khadijé, Poulain, Cécile, Douard, Élise, Saci, Zohra, Maftei, Catalina, Lemyre, Emmanuelle, Jacquemont, Sébastien

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Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry von Moreau, Clara A., Harvey, Annabelle, Kumar, Kuldeep, Huguet, Guillaume, Urchs, Sebastian G.W., Douard, Elise A., Schultz, Laura M., Sharmarke, Hanad, Jizi, Khadije, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Rolland, Thomas, Martineau, Jean-Louis, Orban, Pierre, Silva, Ana Isabel, Hall, Jeremy, van den Bree, Marianne B.M., Owen, Michael J., Linden, David E.J., Labbe, Aurelie, Lippé, Sarah, Bearden, Carrie E., Almasy, Laura, Glahn, David C., Thompson, Paul M., Bourgeron, Thomas, Bellec, Pierre, Jacquemont, Sebastien

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A framework for the investigation of rare genetic disorders in neuropsychiatry von Sanders, Stephan J., Sahin, Mustafa, Hostyk, Joseph, Thurm, Audrey, Jacquemont, Sebastien, Avillach, Paul, Douard, Elise, Martin, Christa L., Modi, Meera E., Moreno-De-Luca, Andres, Raznahan, Armin, Anticevic, Alan, Dolmetsch, Ricardo, Feng, Guoping, Geschwind, Daniel H., Glahn, David C., Goldstein, David B., Ledbetter, David H., Mulle, Jennifer G., Pasca, Sergiu P., Samaco, Rodney, Sebat, Jonathan, Pariser, Anne, Lehner, Thomas, Gur, Raquel E., Bearden, Carrie E.

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Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples von Huguet, Guillaume, Schramm, Catherine, Douard, Elise, Jiang, Lai, Labbe, Aurélie, Tihy, Frédérique, Mathonnet, Géraldine, Nizard, Sonia, Lemyre, Emmanuelle, Mathieu, Alexandre, Poline, Jean-Baptiste, Loth, Eva, Toro, Roberto, Schumann, Gunter, Conrod, Patricia, Pausova, Zdenka, Greenwood, Celia, Paus, Tomas, Bourgeron, Thomas, Jacquemont, Sébastien

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Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia von Moreau, Clara A., Urchs, Sebastian G. W., Kuldeep, Kumar, Orban, Pierre, Schramm, Catherine, Dumas, Guillaume, Labbe, Aurélie, Huguet, Guillaume, Douard, Elise, Quirion, Pierre-Olivier, Lin, Amy, Kushan, Leila, Grot, Stephanie, Luck, David, Mendrek, Adrianna, Potvin, Stephane, Stip, Emmanuel, Bourgeron, Thomas, Evans, Alan C., Bearden, Carrie E., Bellec, Pierre, Jacquemont, Sebastien

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Using rare genetic mutations to revisit structural brain asymmetry von Kopal, Jakub, Kumar, Kuldeep, Shafighi, Kimia, Saltoun, Karin, Modenato, Claudia, Moreau, Clara A., Huguet, Guillaume, Jean-Louis, Martineau, Martin, Charles-Olivier, Saci, Zohra, Younis, Nadine, Douard, Elise, Jizi, Khadije, Beauchamp-Chatel, Alexis, Kushan, Leila, Silva, Ana I., van den Bree, Marianne B. M., Linden, David E. J., Owen, Michael J., Hall, Jeremy, Lippé, Sarah, Draganski, Bogdan, Sønderby, Ida E., Andreassen, Ole A., Glahn, David C., Thompson, Paul M., Bearden, Carrie E., Zatorre, Robert, Jacquemont, Sébastien, Bzdok, Danilo

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Author Correction: Using rare genetic mutations to revisit structural brain asymmetry von Kopal, Jakub, Kumar, Kuldeep, Shafighi, Kimia, Saltoun, Karin, Modenato, Claudia, Moreau, Clara A., Huguet, Guillaume, Jean-Louis, Martineau, Martin, Charles-Olivier, Saci, Zohra, Younis, Nadine, Douard, Elise, Jizi, Khadije, Beauchamp-Chatel, Alexis, Kushan, Leila, Silva, Ana I., van den Bree, Marianne B. M., Linden, David E. J., Owen, Michael J., Hall, Jeremy, Lippé, Sarah, Draganski, Bogdan, Sønderby, Ida E., Andreassen, Ole A., Glahn, David C., Thompson, Paul M., Bearden, Carrie E., Zatorre, Robert, Jacquemont, Sébastien, Bzdok, Danilo

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Clinical correlates of diagnostic certainty in children and youths with Autistic Disorder von Rødgaard, Eya-Mist, Rodríguez-Herreros, Borja, Zeribi, Abderrahim, Jensen, Kristian, Courchesne, Valérie, Douard, Elise, Gagnon, David, Huguet, Guillaume, Jacquemont, Sebastien, Mottron, Laurent

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Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances von Tesfaye, Rackeb, Huguet, Guillaume, Schmilovich, Zoe, Renne, Thomas, Loum, Mor Absa, Douard, Elise, Saci, Zohra, Jean-Louis, Martineau, Martineau, Jean Luc, Whelan, Rob, Desrivieres, Sylvane, Heinz, Andreas, Schumann, Gunter, Hayward, Caroline, Elsabbagh, Mayada, Jacquemont, Sebastien

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Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability von Schmilovich, Zoe, Bourque, Vincent-Raphaël, Douard, Elise, Huguet, Guillaume, Poulain, Cécile, Ross, Jay P, Alipour, Paria, Castonguay, Charles-Étienne, Younis, Nadine, Jean-Louis, Martineau, Saci, Zohra, Pausova, Zdenka, Paus, Tomas, Schuman, Gunter, Porteous, David, Davies, Gail, Redmond, Paul, Harris, Sarah E, Deary, Ian J, Whalley, Heather, Hayward, Caroline, Dion, Patrick A, Jacquemont, Sébastien, Rouleau, Guy A

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Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age von Brownstein, Catherine A., Douard, Elise, Haynes, Robin L., Koh, Hyun Yong, Haghighi, Alireza, Keywan, Christine, Martin, Bree, Alexandrescu, Sanda, Haas, Elisabeth A., Vargas, Sara O., Wojcik, Monica H., Jacquemont, Sébastien, Poduri, Annapurna H., Goldstein, Richard D., Holm, Ingrid A.

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Brief Report: Virtual Reality to Raise Awareness About Autism von Koniou, Ioulia, Douard, Elise, Lanovaz, Marc J

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The Family Game to support parents with intellectual disability in managing challenging behaviours: A replication von Tremblay, Joany, Douard, Elise, Lanovaz, Marc J.

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F61. PARTIAL DUPLICATION AND DELETION OF NEURODEVELOPMENTAL GENES AND THEIR CLINICAL INTERPRETATION von England, Jade, Huguet, Guillaume, Jizi, Khadijé, Poulain, Cécile, Douard, Elise, Saci, Zohra, Jacquemont, Sébastien

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Assessing the Effects of Rare Copy Number Variants on Psychiatric Symptoms and Cognitive Ability in 1M Individuals von Glahn, David, Knowles, Emma, Douard, Elise, Mollon, Josephine, Huguet, Guillaume, Schultz, Laura, Almasy, Laura, Jacquemont, Sébastien

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P397. Genomic Deletions and Duplications Show Mirror Effects on Cognitive Ability According to Spatial Patterns of Gene Expression in the Human Brain von Kumar, Kuldeep, Kazem, Sayeh, Huguet, Guillaume, Douard, Elise, Saci, Zohra, Almasy, Laura, Glahn, David, Dumas, Guillaume, Jacquemont, Sébastien

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ASSESSING THE EFFECTS OF RARE COPY NUMBER VARIANTS ON PSYCHIATRIC SYMPTOMS AND COGNITIVE ABILITY IN ∼1M INDIVIDUALS von Glahn, David, Knowles, Emma, Douard, Elise, Mollon, Josephine, Huguet, Guillaume, Schultz, Laura, Almasy, Laura, Jacquemont, Sébastien

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THE EFFECT SIZE OF GENES ON COGNITIVE ABILITIES IS LINKED TO THEIR EXPRESSION ALONG THE MAJOR HIERARCHICAL GRADIENT IN THE HUMAN BRAIN von Jacquemont, Sébastien, Huguet, Guillaume, Douard, Elise, Saci, Zohra, Dumas, Guillaume, Almasy, Laura, Glahn, David

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