M155. RECIPROCAL CHANGES IN WHITE MATTER MICROSTRUCTURE IN 22Q11.2 DELETION AND DUPLICATION SYNDROME

por Seitz, Johanna, Lyons, Monica, Kushan, Leila, Ik Kevin Cho, Kang, Billah, Tashrif, Bouix, Sylvain, Kubicki, Marek, Bearden, Carrie, Pasternak, Ofer
Publicado 2020

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

por Jalal, Rhideeta, Nair, Aarti, Lin, Amy, Eckfeld, Ariel, Kushan, Leila, Zinberg, Jamie, Karlsgodt, Katherine H., Cannon, Tyrone D., Bearden, Carrie E.
Publicado 2021

Opposing white matter microstructure abnormalities in 22q11.2 deletion and duplication carriers

por Seitz-Holland, Johanna, Lyons, Monica, Kushan, Leila, Lin, Amy, Villalon-Reina, Julio E., Cho, Kang Ik Kevin, Zhang, Fan, Billah, Tashrif, Bouix, Sylvain, Kubicki, Marek, Bearden, Carrie E., Pasternak, Ofer
Publicado 2021

Longitudinal trajectories of cortical development in 22q11.2 copy number variants and typically developing controls

por Jalbrzikowski, Maria, Lin, Amy, Vajdi, Ariana, Grigoryan, Vardui, Kushan, Leila, Ching, Christopher R. K., Schleifer, Charles, Hayes, Rebecca A., Chu, Stephanie A., Sugar, Catherine A., Forsyth, Jennifer K., Bearden, Carrie E.
Publicado 2022

Neuroanatomical underpinnings of autism symptomatology in carriers and non-carriers of the 22q11.2 microdeletion

por Gudbrandsen, Maria, Bletsch, Anke, Mann, Caroline, Daly, Eileen, Murphy, Clodagh M., Stoencheva, Vladimira, Blackmore, Charlotte E., Rogdaki, Maria, Kushan, Leila, Bearden, Carrie E., Murphy, Declan G. M., Craig, Michael C., Ecker, Christine
Publicado 2020

Inter-rater reliability of subthreshold psychotic symptoms in individuals with 22q11.2 deletion syndrome

por Moore, Tyler M., Salzer, Deby, Bearden, Carrie E., Calkins, Monica E., Kates, Wendy R., Kushan, Leila, Gallagher, Robert Sean, Frumer, Dafna Sofrin, Weinberger, Ronnie, McDonald-McGinn, Donna M., Gur, Raquel E., Gothelf, Doron
Publicado 2021

Neurobehavioral risk factors influence prevalence and severity of hazardous substance use in youth at genetic and clinical high risk for psychosis

por Amir, Carolyn M., Kapler, Simon, Hoftman, Gil D., Kushan, Leila, Zinberg, Jamie, Cadenhead, Kristin S., Kennedy, Leda, Cornblatt, Barbara A., Keshavan, Matcheri, Mathalon, Daniel H., Perkins, Diana O., Stone, William, Tsuang, Ming T., Walker, Elaine F., Woods, Scott W., Cannon, Tyrone D., Addington, Jean, Bearden, Carrie E.
Publicado 2023

Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia

por 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
Publicado 2020

Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence

por 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, Aurélie, 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
Publicado 2023

Effects of eight neuropsychiatric copy number variants on human brain structure

por Modenato, Claudia, Kumar, Kuldeep, Moreau, Clara, Martin-Brevet, Sandra, Huguet, Guillaume, Schramm, Catherine, Jean-Louis, Martineau, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Douard, Elise, Thébault-Dagher, Fanny, Côté, Valérie, Charlebois, Audrey-Rose, Deguire, Florence, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurèlie, Richetin, Sonia, Melie-Garcia, Lester, Kushan, Leila, Silva, Ana I., van den Bree, Marianne B. M., Linden, David E. J., Owen, Michael J., Hall, Jeremy, Lippé, Sarah, Chakravarty, Mallar, Bzdok, Danilo, Bearden, Carrie E., Draganski, Bogdan, Jacquemont, Sébastien
Publicado 2021

Subcortical brain alterations in carriers of genomic copy number variants

por 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, Richetin, Sonia, 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, Almasy, Laura, Glahn, David C., Bearden, Carrie E., Thompson, Paul M., Jacquemont, Sébastien
Publicado 2023

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

por Sun, Daqiang, Ching, Christopher R. K., Lin, Amy, Forsyth, Jennifer K., Kushan, Leila, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Villalon-Reina, Julio E., Qu, Xiaoping, Jonas, Rachel K., van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, Campbell, Linda E., McCabe, Kathryn L., Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan, Craig, Michael, Vorstman, Jacob, Fiksinski, Ania, Koops, Sanne, Ruparel, Kosha, Roalf, David R., Gur, Raquel E., Schmitt, J. Eric, Simon, Tony J., Goodrich-Hunsaker, Naomi J., Durdle, Courtney A., Bassett, Anne S., Chow, Eva W. C., Butcher, Nancy J., Vila-Rodriguez, Fidel, Doherty, Joanne, Cunningham, Adam, van den Bree, Marianne B.M., Linden, David E. J., Moss, Hayley, Owen, Michael J., Murphy, Kieran C., McDonald-McGinn, Donna M., Emanuel, Beverly, van Erp, Theo G. M., Turner, Jessica A., Thompson, Paul M., Bearden, Carrie E.
Publicado 2018

Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study

por Villalón-Reina, Julio E., Martínez, Kenia, Qu, Xiaoping, Ching, Christopher R. K., Nir, Talia M., Kothapalli, Deydeep, Corbin, Conor, Sun, Daqiang, Lin, Amy, Forsyth, Jennifer K., Kushan, Leila, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Jonas, Rachel K., van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, Campbell, Linda E., McCabe, Kathryn L., Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan, Craig, Michael, Emanuel, Beverly, McDonald-McGinn, Donna M., Vorstman, Jacob A.S., Fiksinski, Ania M., Koops, Sanne, Ruparel, Kosha, Roalf, David, Gur, Raquel E., Eric Schmitt, J., Simon, Tony J., Goodrich-Hunsaker, Naomi J., Durdle, Courtney A., Doherty, Joanne L., Cunningham, Adam C., van den Bree, Marianne, Linden, David E. J., Owen, Michael, Moss, Hayley, Kelly, Sinead, Donohoe, Gary, Murphy, Kieran C., Arango, Celso, Jahanshad, Neda, Thompson, Paul M., Bearden, Carrie E.
Publicado 2019

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs

por Sønderby, Ida E., Ching, Christopher R. K., Thomopoulos, Sophia I., van der Meer, Dennis, Sun, Daqiang, Villalon‐Reina, Julio E., Agartz, Ingrid, Amunts, Katrin, Arango, Celso, Armstrong, Nicola J., Ayesa‐Arriola, Rosa, Bakker, Geor, Bassett, Anne S., Boomsma, Dorret I., Bülow, Robin, Butcher, Nancy J., Calhoun, Vince D., Caspers, Svenja, Chow, Eva W. C., Cichon, Sven, Ciufolini, Simone, Craig, Michael C., Crespo‐Facorro, Benedicto, Cunningham, Adam C., Dale, Anders M., Dazzan, Paola, de Zubicaray, Greig I., Djurovic, Srdjan, Doherty, Joanne L., Donohoe, Gary, Draganski, Bogdan, Durdle, Courtney A., Ehrlich, Stefan, Emanuel, Beverly S., Espeseth, Thomas, Fisher, Simon E., Ge, Tian, Glahn, David C., Grabe, Hans J., Gur, Raquel E., Gutman, Boris A., Haavik, Jan, Håberg, Asta K., Hansen, Laura A., Hashimoto, Ryota, Hibar, Derrek P., Holmes, Avram J., Hottenga, Jouke‐Jan, Hulshoff Pol, Hilleke E., Jalbrzikowski, Maria, Knowles, Emma E. M., Kushan, Leila, Linden, David E. J., Liu, Jingyu, Lundervold, Astri J., Martin‐Brevet, Sandra, Martínez, Kenia, Mather, Karen A., Mathias, Samuel R., McDonald‐McGinn, Donna M., McRae, Allan F., Medland, Sarah E., Moberget, Torgeir, Modenato, Claudia, Monereo Sánchez, Jennifer, Moreau, Clara A., Mühleisen, Thomas W., Paus, Tomas, Pausova, Zdenka, Prieto, Carlos, Ragothaman, Anjanibhargavi, Reinbold, Céline S., Reis Marques, Tiago, Repetto, Gabriela M., Reymond, Alexandre, Roalf, David R., Rodriguez‐Herreros, Borja, Rucker, James J., Sachdev, Perminder S., Schmitt, James E., Schofield, Peter R., Silva, Ana I., Stefansson, Hreinn, Stein, Dan J., Tamnes, Christian K., Tordesillas‐Gutiérrez, Diana, Ulfarsson, Magnus O., Vajdi, Ariana, van 't Ent, Dennis, van den Bree, Marianne B. M., Vassos, Evangelos, Vázquez‐Bourgon, Javier, Vila‐Rodriguez, Fidel, Walters, G. Bragi, Wen, Wei, Westlye, Lars T., Wittfeld, Katharina, Zackai, Elaine H., Stefánsson, Kári, Jacquemont, Sebastien, Thompson, Paul M., Bearden, Carrie E., Andreassen, Ole A.
Publicado 2021

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

por Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Holleman, Aaron M., Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A.S., Bearden, Carrie E., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., Warren, Stephen T., Owen, Michael J., Chopra, Pankaj, Cutler, David J., Duncan, Richard, Kotlar, Alex V., Mulle, Jennifer G., Voss, Anna J., Zwick, Michael E., Diacou, Alexander, Golden, Aaron, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Merico, Daniele, Jin, Andrea, Lilley, Brenna, Salmons, Harold I., Tran, Oanh, Holmans, Peter, Pardinas, Antonio, Walters, James T.R., Demaerel, Wolfram, Boot, Erik, Butcher, Nancy J., Costain, Gregory A., Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese A.M.J, van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koen, Vergaelen, Elfi, Vogels, Annick, Crowley, T. Blaine, McGinn, Daniel E., Moss, Edward M., Sharkus, Robert J., Unolt, Marta, Zackai, Elaine H., Calkins, Monica E., Gallagher, Robert S., Gur, Ruben C., Tang, Sunny X., Fritsch, Rosemarie, Ornstein, Claudia, Repetto, Gabriela M., Breetvelt, Elemi, Duijff, Sasja N., Fiksinski, Ania, Moss, Hayley, Niarchou, Maria, Murphy, Kieran C., Prasad, Sarah E., Daly, Eileen M., Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan G., Buzzanca, Antonio, Di Fabio, Fabio, Digilio, Maria C., Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F., Ousley, Opal Y., Carmel, Miri, Gothelf, Doron, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Kushan, Leila, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stéphan, Sandini, Corrado, Schneider, Maude, Béna, Frédérique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Busa, Tiffany, Philip, Nicole, Campbell, Linda E., McCabe, Kathryn L., Hooper, Stephen R., Schoch, Kelly, Shashi, Vandana, Simon, Tony J., Tassone, Flora, Arango, Celso, Fraguas, David, García-Miñaúr, Sixto, Morey-Canyelles, Jaume, Rosell, Jordi, Suñer, Damià H., Raventos-Simic, Jasna, Epstein, Michael P., Williams, Nigel M., Bassett, Anne S.
Publicado 2020