Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability by Huguet, Guillaume, Schramm, Catherine, Douard, Elise, Tamer, Petra, Main, Antoine, Monin, Pauline, England, Jade, Jizi, Khadije, Renne, Thomas, Poirier, Myriam, Nowak, Sabrina, Martin, Charles-Olivier, Younis, Nadine, Knoth, Inga Sophia, Jean-Louis, Martineau, Saci, Zohra, Auger, Maude, Tihy, Frédérique, Mathonnet, Géraldine, Maftei, Catalina, Léveillé, France, Porteous, David, Davies, Gail, Redmond, Paul, Harris, Sarah E., Hill, W. David, Lemyre, Emmanuelle, Schumann, Gunter, Bourgeron, Thomas, Pausova, Zdenka, Paus, Tomas, Karama, Sherif, Lippe, Sarah, Deary, Ian J., Almasy, Laura, Labbe, Aurélie, Glahn, David, Greenwood, Celia M. T., Jacquemont, Sébastien

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

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Epigenotype-genotype-phenotype correlations in SETD1A and SETD2 chromatin disorders by Lee, Sunwoo, Menzies, Lara, Hay, Eleanor, Ochoa, Eguzkine, Docquier, France, Rodger, Fay, Deshpande, Charu, Foulds, Nicola C, Jacquemont, Sébastien, Jizi, Khadije, Kiep, Henriette, Kraus, Alison, Löhner, Katharina, Morrison, Patrick J, Popp, Bernt, Richardson, Ruth, Haeringen, Arie, Martin, Ezequiel, Toribio, Ana, Li, Fudong, Jones, Wendy D, Sansbury, Francis H, Maher, Eamonn R

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Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications by Gur, Ruben C, Bearden, Carrie E, Jacquemont, Sebastien, Swillen, Ann, van Amelsvoort, Therese, van den Bree, Marianne, Vorstman, Jacob, Sebat, Jonathan, Ruparel, Kosha, Gallagher, Robert Sean, McClellan, Emily, White, Lauren, Crowley, Terrence Blaine, Giunta, Victoria, Kushan, Leila, O'Hora, Kathleen, Verbesselt, Jente, Vandensande, Ans, Vingerhoets, Claudia, van Haelst, Mieke, Hall, Jessica, Harwood, Janet, Chawner, Samuel J R A, Patel, Nishi, Palad, Katrina, Hong, Oanh, Guevara, James, Martin, Charles Olivier, Jizi, Khadije, Bélanger, Anne-Marie, Scherer, Stephen W, Bassett, Anne S, McDonald-McGinn, Donna M, Gur, Raquel E

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Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions by Moreau, Clara A, Kumar, Kuldeep, Harvey, Annabelle, Huguet, Guillaume, Urchs, Sebastian G W, Schultz, Laura M, Sharmarke, Hanad, Jizi, Khadije, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Martineau, Jean-Louis, Orban, Pierre, Silva, Ana Isabel, Hall, Jeremy, van den Bree, Marianne B M, Owen, Michael J, Linden, David E J, Lippé, Sarah, Bearden, Carrie E, Almasy, Laura, Glahn, David C, Thompson, Paul M, Bourgeron, Thomas, Bellec, Pierre, Jacquemont, Sebastien

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Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry by 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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Challenges in multi-task learning for fMRI-based diagnosis: Benefits for psychiatric conditions and CNVs would likely require thousands of patients by Harvey, Annabelle, Moreau, Clara A., Kumar, Kuldeep, Huguet, Guillaume, Urchs, Sebastian G.W., Sharmarke, Hanad, Jizi, Khadije, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Martineau, Jean-Louis, Orban, Pierre, Silva, Ana Isabel, Hall, Jeremy, van den Bree, Marianne B.M., Owen, Michael J., Linden, David E.J., Lippé, Sarah, Bearden, Carrie E., Dumas, Guillaume, Jacquemont, Sébastien, Bellec, Pierre

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

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Genotype–phenotype correlation at codon 1740 of SETD2 by Rabin, Rachel, Radmanesh, Alireza, Glass, Ian A., Dobyns, William B., Aldinger, Kimberly A., Shieh, Joseph T., Romoser, Shelby, Bombei, Hannah, Dowsett, Leah, Trapane, Pamela, Bernat, John A., Baker, Janice, Mendelsohn, Nancy J., Popp, Bernt, Siekmeyer, Manuela, Sorge, Ina, Sansbury, Francis Hugh, Watts, Patrick, Foulds, Nicola C., Burton, Jennifer, Hoganson, George, Hurst, Jane A., Menzies, Lara, Osio, Deborah, Kerecuk, Larissa, Cobben, Jan M., Jizi, Khadijé, Jacquemont, Sebastien, Bélanger, Stacey A., Löhner, Katharina, Veenstra‐Knol, Hermine E., Lemmink, Henny H., Keller‐Ramey, Jennifer, Wentzensen, Ingrid M., Punj, Sumit, McWalter, Kirsty, Lenberg, Jerica, Ellsworth, Katarzyna A., Radtke, Kelly, Akbarian, Schahram, Pappas, John

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