Sudden Death in a Child With Ocular Lesions von Martin, Bree E, Vargas, Sara O, Hindman, Holly B, Rothstein, Anna, Folberg, Robert, Goldstein, Richard D

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Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome von Schneider, Maude, Debbané, Martin, Bassett, Anne S., Chow, Eva W.C., Fung, Wai Lun Alan, van den Bree, Marianne B.M., Owen, Michael, Murphy, Kieran C., Niarchou, Maria, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, McDonald-McGinn, Donna M., Gur, Raquel E., Zackai, Elaine H., Vorstman, Jacob, Duijff, Sasja N., Klaassen, Petra W.J., Swillen, Ann, Gothelf, Doron, Green, Tamar, Weizman, Abraham, Van Amelsvoort, Therese, Evers, Laurens, Boot, Erik, Shashi, Vandana, Hooper, Stephen R., Bearden, Carrie E., Jalbrzikowski, Maria, Armando, Marco, Vicari, Stefano, Murphy, Declan G., Ousley, Opal, Campbell, Linda E., Simon, Tony J., Eliez, Stephan

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Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology von Jacquemont, Sébastien, Huguet, Guillaume, Klein, Marieke, Chawner, Samuel J.R.A, Donald, Kirsten A, van den Bree, Marianne B.M, Sebat, Jonathan, Ledbetter, David H, Constantino, John N, Earl, Rachel K, McDonald-McGinn, Donna M, van Amelsvoort, Therese, Swillen, Ann, O’Donnell-Luria, Anne H, Glahn, David C, Almasy, Laura, Eichler, Evan E, Scherer, Stephen W, Robinson, Elise, Bassett, Anne S, Martin, Christa Lese, Finucane, Brenda, Vorstman, Jacob A.S, Bearden, Carrie E, Gur, Raquel E

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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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Modeling SHH-driven medulloblastoma with patient iPS cell-derived neural stem cells von Susanto, Evelyn, Navarro, Ana Marin, Zhou, Leilei, Sundström, Anders, van Bree, Niek, Stantic, Marina, Moslem, Mohsen, Tailor, Jignesh, Rietdijk, Jonne, Zubillaga, Veronica, Hübner, Jens-Martin, Weishaupt, Holger, Wolfsberger, Johanna, Alafuzoff, Irina, Nordgren, Ann, Magnaldo, Thierry, Siesjö, Peter, Johnsen, John Inge, Kool, Marcel, Tammimies, Kristiina, Darabi, Anna, Swartling, Fredrik J., Falk, Anna, Wilhelm, Margareta

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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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Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants von Kumar, Kuldeep, Modenato, Claudia, Moreau, Clara, Ching, Christopher R K, Harvey, Annabelle, Martin-Brevet, Sandra, Huguet, Guillaume, Jean-Louis, Martineau, Douard, Elise, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Maillard, Anne M, Rodriguez-Herreros, Borja, Pain, Aurélie, Kushan, Leila, Isaev, Dmitry, Alpert, Kathryn, Ragothaman, Anjani, Turner, Jessica A, Wang, Lei, Ho, Tiffany C, Schmaal, Lianne, Silva, Ana I, van den Bree, Marianne B M, Linden, David E J, Owen, Michael J, Hall, Jeremy, Lippé, Sarah, Dumas, Guillaume, Draganski, Bogdan, Gutman, Boris A, Sønderby, Ida E, Andreassen, Ole A, Schultz, Laura M, Almasy, Laura, Glahn, David C, Bearden, Carrie E, Thompson, Paul M, Jacquemont, Sébastien

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Young adults' adoption and use of mental health apps: efficient, effective, but no replacement for in-person care von Holtz, Bree E., Kanthawala, Shaheen, Martin, Kaley, Nelson, Victoria, Parrott, Scott

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Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions von 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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Adverse drug events caused by three high‐risk drug–drug interactions in patients admitted to intensive care units: A multicentre retrospective observational study von Klopotowska, Joanna E., Leopold, Jan‐Hendrik, Bakker, Tinka, Yasrebi‐de Kom, Izak, Engelaer, Frouke M., Jonge, Evert, Haspels‐Hogervorst, Esther K., Bergh, Walter M., Renes, Maurits H., Jong, Bas T., Kieft, Hans, Wieringa, Andre, Hendriks, Stefaan, Lau, Cedric, Bree, Sjoerd H. W., Lammers, Hendrick J. W., Wierenga, Peter C., Bosman, Rob J., Jong, Vincent M., Slijkhuis, Mirjam, Franssen, Eric J. F., Vermeijden, Wytze J., Masselink, Joost, Purmer, Ilse M., Bosma, Liesbeth E., Hoeksema, Martin, Wesselink, Elsbeth, Lange, Dylan W., Keizer, Nicolette F., Dongelmans, Dave A., Abu‐Hanna, Ameen

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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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Immunogenicity of a 5‐dose pneumococcal vaccination schedule following allogeneic hematopoietic stem cell transplantation von Garcia Garrido, Hannah M., Haggenburg, Sabine, Schoordijk, Marieke C. E., Meijer, Ellen, Tanck, Michael W. T., Hazenberg, Mette D., Rutten, Caroline E., Bree, Godelieve J., Nur, Erfan, Meek, Bob, Grobusch, Martin P., Goorhuis, Abraham

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Therapeutic options for CTLA-4 insufficiency von Egg, David, Rump, Ina Caroline, Mitsuiki, Noriko, Rojas-Restrepo, Jessica, Maccari, Maria-Elena, Schwab, Charlotte, Gabrysch, Annemarie, Warnatz, Klaus, Goldacker, Sigune, Patiño, Virginia, Wolff, Daniel, Okada, Satoshi, Hayakawa, Seiichi, Shikama, Yoshiaki, Kanda, Kenji, Imai, Kohsuke, Sotomatsu, Manabu, Kuwashima, Makoto, Kamiya, Takahiro, Morio, Tomohiro, Matsumoto, Kazuaki, Mori, Takeshi, Yoshimoto, Yuri, Dybedal, Ingunn, Kanariou, Maria, Kucuk, Zeynep Yesim, Chapdelaine, Hugo, Petruzelkova, Lenka, Lorenz, Hanns-Martin, Sullivan, Kathleen E., Heimall, Jennifer, Moutschen, Michel, Litzman, Jiri, Recher, Mike, Albert, Michael H., Hauck, Fabian, Seneviratne, Suranjith, Pachlopnik Schmid, Jana, Kolios, Antonios, Unglik, Gary, Klemann, Christian, Snapper, Scott, Giulino-Roth, Lisa, Svaton, Michael, Platt, Craig D., Hambleton, Sophie, Neth, Olaf, Gosse, Geraldine, Reinsch, Steffen, Holzinger, Dirk, Kim, Yae-Jean, Bakhtiar, Shahrzad, Atschekzei, Faranaz, Schmidt, Reinhold, Sogkas, Georgios, Chandrakasan, Shanmuganathan, Rae, William, Derfalvi, Beata, Marquart, Hanne Vibeke, Ozen, Ahmet, Kiykim, Ayca, Karakoc-Aydiner, Elif, Králíčková, Pavlína, de Bree, Godelieve, Kiritsi, Dimitra, Seidel, Markus G., Kobbe, Robin, Dantzer, Jennifer, Alsina, Laia, Armangue, Thais, Lougaris, Vassilios, Agyeman, Philipp, Nyström, Sofia, Buchbinder, David, Arkwright, Peter D., Grimbacher, Bodo

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Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence von Kopal, Jakub, Kumar, Kuldeep, Saltoun, Karin, Modenato, Claudia, Moreau, Clara A., Martin-Brevet, Sandra, Huguet, Guillaume, Jean-Louis, Martineau, Martin, Charles-Olivier, Saci, Zohra, Younis, Nadine, Tamer, Petra, Douard, Elise, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurèlie, Richetin, Sonia, 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., Jacquemont, Sébastien, Bzdok, Danilo

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Mutations in DEPDC5 cause familial focal epilepsy with variable foci von Dibbens, Leanne M, de Vries, Boukje, Donatello, Simona, Heron, Sarah E, Hodgson, Bree L, Chintawar, Satyan, Crompton, Douglas E, Hughes, James N, Bellows, Susannah T, Klein, Karl Martin, Callenbach, Petra M C, Corbett, Mark A, Gardner, Alison E, Kivity, Sara, Iona, Xenia, Regan, Brigid M, Weller, Claudia M, Crimmins, Denis, O'Brien, Terence J, Guerrero-López, Rosa, Mulley, John C, Dubeau, Francois, Licchetta, Laura, Bisulli, Francesca, Cossette, Patrick, Thomas, Paul Q, Gecz, Jozef, Serratosa, Jose, Brouwer, Oebele F, Andermann, Frederick, Andermann, Eva, van den Maagdenberg, Arn M J M, Pandolfo, Massimo, Berkovic, Samuel F, Scheffer, Ingrid E

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Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition von van der Meer, Dennis, Sønderby, Ida E, Kaufmann, Tobias, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Blackburn, Nicholas B, Boomsma, Dorret I, Brodaty, Henry, Brouwer, Rachel M, Cahn, Wiepke, Calhoun, Vince D, Caspers, Svenja, Cavalleri, Gianpiero L, Ching, Christopher R. K, Corvin, Aiden, Crespo-Facorro, Benedicto, Dalvie, Shareefa, Dazzan, Paola, de Geus, Eco J. C, de Zubicaray, Greig I, de Zwarte, Sonja M. C, Delanty, Norman, Desrivieres, Sylvane, Di Forti, Marta, Doherty, Joanne L, Donohoe, Gary, Eising, Else, Espeseth, Thomas, Fisher, Simon E, Fladby, Tormod, Frei, Oleksandr, Frouin, Vincent, Fukunaga, Masaki, Gareau, Thomas, Glahn, David C, Grabe, Hans J, Gústafsson, Ómar, Haavik, Jan, Haberg, Asta K, Hashimoto, Ryota, Hehir-Kwa, Jayne Y, Hibar, Derrek P, Hillegers, Manon H. J, Hoffmann, Per, Holleran, Laurena, Hulshoff Pol, Hilleke E, Ikeda, Masashi, Jacquemont, Sébastien, Jahanshad, Neda, Jockwitz, Christiane, Johansson, Stefan, Jönsson, Erik G, Kikuchi, Masataka, Knowles, Emma E. M, Liu, Jingyu, Lundervold, Arvid, Lundervold, Astri J, Martin, Nicholas G, McMahon, Katie L, McRae, Allan F, Medland, Sarah E, Moberget, Torgeir, Morris, Derek W, Murray, Robin M, Nyberg, Lars, Olde Loohuis, Loes M, Ophoff, Roel A, Owen, Michael J, Paus, Tomas, Pausova, Zdenka, Peralta, Juan M, Prieto, Carlos, Quinlan, Erin Burke, Reinbold, Céline S, Reis Marques, Tiago, Rucker, James J. H, Sando, Sigrid B, Schofield, Peter R, Shumskaya, Elena, Silva, Ana I, Steen, Vidar M, Stein, Dan J, Strike, Lachlan T, Thalamuthu, Anbupalam, Tordesillas-Gutiérrez, Diana, Uhlmann, Anne, Úlfarsson, Magnús Ö, van ’t Ent, Dennis, Wen, Wei, Wittfeld, Katharina, Wright, Margaret J, Zayats, Tetyana, Dale, Anders M, Djurovic, Srdjan, Westlye, Lars T, Stefánsson, Hreinn, Stefánsson, Kári, Thompson, Paul M, Andreassen, Ole A

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Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities von D’Angelo, Debra, Lebon, Sébastien, Chen, Qixuan, Martin-Brevet, Sandra, Snyder, LeeAnne Green, Hippolyte, Loyse, Hanson, Ellen, Maillard, Anne M, Faucett, W. Andrew, Macé, Aurélien, Pain, Aurélie, Bernier, Raphael, Chawner, Samuel J. R. A, David, Albert, Andrieux, Joris, Aylward, Elizabeth, Baujat, Genevieve, Caldeira, Ines, Conus, Philippe, Ferrari, Carrina, Forzano, Francesca, Gérard, Marion, Goin-Kochel, Robin P, Grant, Ellen, Hunter, Jill V, Isidor, Bertrand, Jacquette, Aurélia, Jønch, Aia E, Keren, Boris, Lacombe, Didier, Le Caignec, Cédric, Martin, Christa Lese, Männik, Katrin, Metspalu, Andres, Mignot, Cyril, Mukherjee, Pratik, Owen, Michael J, Passeggeri, Marzia, Rooryck-Thambo, Caroline, Rosenfeld, Jill A, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Van Haelst, Mieke, Shen, Yiping, Draganski, Bogdan, Sherr, Elliott H, Ledbetter, David H, van den Bree, Marianne B. M, Beckmann, Jacques S, Spiro, John E, Reymond, Alexandre, Jacquemont, Sébastien, Chung, Wendy K

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Thyrotrophin and thyroxine support immune homeostasis in humans von Jaeger, Martin, Sloot, Yvette J.E, Horst, Rob Ter, Chu, Xiaojing, Koenen, Hans J.P.M., Koeken, Valerie A.C.M., Moorlag, Simone J.C.F.M., Bree, Charlotte J., Mourits, Vera P., Lemmers, Heidi, Dijkstra, Helga, Medici, Marco, Herwaarden, Antonius E., Joosten, Irma, Joosten, Leo A.B., Li, Yang, Smit, Johannes W.A., Netea, Mihai G., Netea‐Maier, Romana T.

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Afucosylated IgG characterizes enveloped viral responses and correlates with COVID-19 severity von Larsen, Mads Delbo, de Graaf, Erik L., Sonneveld, Myrthe E., Plomp, H. Rosina, Nouta, Jan, Hoepel, Willianne, Chen, Hung-Jen, Linty, Federica, Visser, Remco, Brinkhaus, Maximilian, Sustic, Tonci, de Taeye, Steven W., Bentlage, Arthur E. H., Toivonen, Suvi, Koeleman, Carolien A. M., Sainio, Susanna, Kootstra, Neeltje A., Brouwer, Philip J. M., Geyer, Chiara Elisabeth, Derksen, Ninotska I. L., Wolbink, Gertjan, de Winther, Menno, Sanders, Rogier W., van Gils, Marit J., de Bruin, Sanne, Vlaar, Alexander P. J., Rispens, Theo, den Dunnen, Jeroen, Zaaijer, Hans L., Wuhrer, Manfred, van dDer Schoot, C. Ellen, Vidarsson, Gestur

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P20-04: Complements on Enniatin B metabolism for interspecies QIVIVE and risk assessment in human von Henri, J., Dubreil, E., Fessard, V., Martin, S., Bree, F., Le Hegarat, L.

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