P822: Navigating genetic risk: Mapping variant's probability of occurring de novo and inferring their effect sizes on neurodevelopmental symptoms
England, Jade, Huguet, Guillaume, Jizi, Khadijé, Poulain, Cécile, Douard, Élise, Saci, Zohra, Maftei, Catalina, Lemyre, Emmanuelle, Jacquemont, Sébastien
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability
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
Published in Molecular psychiatry (01.06.2021)
Published in Molecular psychiatry (01.06.2021)
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Author Correction: Using rare genetic mutations to revisit structural brain asymmetry
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
Published in Nature communications (10.04.2024)
Published in Nature communications (10.04.2024)
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Journal Article
Using rare genetic mutations to revisit structural brain asymmetry
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
Published in Nature communications (26.03.2024)
Published in Nature communications (26.03.2024)
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F61. PARTIAL DUPLICATION AND DELETION OF NEURODEVELOPMENTAL GENES AND THEIR CLINICAL INTERPRETATION
England, Jade, Huguet, Guillaume, Jizi, Khadijé, Poulain, Cécile, Douard, Elise, Saci, Zohra, Jacquemont, Sébastien
Published in European neuropsychopharmacology (01.10.2023)
Published in European neuropsychopharmacology (01.10.2023)
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Genotype–phenotype correlation at codon 1740 of SETD2
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
Published in American journal of medical genetics. Part A (01.09.2020)
Published in American journal of medical genetics. Part A (01.09.2020)
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Epigenotype-genotype-phenotype correlations in SETD1A and SETD2 chromatin disorders
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
Published in Human molecular genetics (03.11.2023)
Published in Human molecular genetics (03.11.2023)
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Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications
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.
Published in Molecular psychiatry (24.07.2024)
Published in Molecular psychiatry (24.07.2024)
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Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions
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
Published in Brain (London, England : 1878) (19.04.2023)
Published in Brain (London, England : 1878) (19.04.2023)
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Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry
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
Published in Biological psychiatry (1969) (01.01.2023)
Published in Biological psychiatry (1969) (01.01.2023)
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Further delineation of the rare GDACCF (global developmental delay, absent or hypoplastic corpus callosum, dysmorphic facies syndrome): genotype and phenotype of 22 patients with ZNF148 mutations
Szakszon, Katalin, Lourenco, Charles Marques, Callewaert, Bert Louis, Geneviève, David, Rouxel, Flavien, Morin, Denis, Denommé-Pichon, Anne-Sophie, Vitobello, Antonio, Patterson, Wesley G, Louie, Raymond, Pinto E Vairo, Filippo, Klee, Eric, Kaiwar, Charu, Gavrilova, Ralitza H, Agre, Katherine E, Jacquemont, Sebastien, Khadijé, Jizi, Giltay, Jacques, van Gassen, Koen, Merő, Gabriella, Gerkes, Erica, Van Bon, Bregje W, Rinne, Tuula, Pfundt, Rolph, Brunner, Han G, Caluseriu, Oana, Grasshoff, Ute, Kehrer, Martin, Haack, Tobias B, Khelifa, Melik Malek, Bergmann, Anke Katharina, Cueto-González, Anna Maria, Martorell, Ariadna Campos, Ramachandrappa, Shwetha, Sawyer, Lindsey B, Fasel, Pascale, Braun, Dominique, Isis, Atallah, Superti-Furga, Andrea, McNiven, Vanda, Chitayat, David, Ahmed, Syed Anas, Brennenstuhl, Heiko, Schwaibolf, Eva Mc, Battisti, Gladys, Parmentier, Benoit, Stevens, Servi J C
Published in Journal of medical genetics (01.02.2024)
Published in Journal of medical genetics (01.02.2024)
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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
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
Published in Imaging neuroscience (Cambridge, Mass.) (26.07.2024)
Published in Imaging neuroscience (Cambridge, Mass.) (26.07.2024)
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Journal Article
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications
Gur, Ruben, Bearden, Carrie, Jacquemont, Sébastien, Jizi, Khadije, Amelsvoort van, Therese, van den Bree, Marianne, Vorstman, Jacob, Sebat, Jonathan, Ruparel, Kosha, Gallagher, Robert, Swillen, Ann, McClellan, Emily, White, Lauren, Crowley, Terrence, Giunta, Victoria, Kushan, Leila, O'Hora, Kathleen, Verbesselt, Jente, Vandensande, Ans, Vingerhoets, Claudia, van Haelst, Mieke, Hall, Jessica, Harwood, Janet, Chawner, Samuel, Patel, Nishi, Palad, Katrina, Hong, Oanh, Guevara, James, Martin, Charles-Olivier, Bélanger, Anne-Marie, Scherer, Stephen, Bassett, Anne, McDonald-McGinn, Donna, Gur, Raquel
Published in Research square (29.12.2023)
Published in Research square (29.12.2023)
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Journal Article
Using rare genetic mutations to revisit structural brain asymmetry
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
Published in bioRxiv : the preprint server for biology (18.04.2023)
Published in bioRxiv : the preprint server for biology (18.04.2023)
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Journal Article
Genome wide analysis of gene dosage in 24,092 individuals shows that 10,000 genes modulate cognitive ability
Huguet, Guillaume, Schramm, Catherine, Douard, Elise, Tamer Petra, Main, Antoine, Monin, Pauline, England, Jade, Jizi, Khadije, Renne, Thomas, Poirier, Myriam, Nowak, Sabrina, Charles-Olivier, Martin, Younis, Nadine, Knoth, Inga Sophia, Martineau Jean-Louis, 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, Celia Mt Greenwood, Jacquemont, Sébastien
Published in bioRxiv (05.10.2020)
Published in bioRxiv (05.10.2020)
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