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Number of items: 10.

Doherty, Joanne L., Cunningham, Adam C., Chawner, Samuel J. R. A., Moss, Hayley M., Dima, Diana C. ORCID: https://orcid.org/0000-0002-9612-5574, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 and Singh, Krish D. ORCID: https://orcid.org/0000-0002-3094-2475 2023. Atypical cortical networks in children at high-genetic risk of psychiatric and eurodevelopmental disorders. Neuropsychopharmacology 10.1038/s41386-023-01628-x
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Cleynen, Isabelle, International q.DS Brain and Behavior Consortium, 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 ORCID: https://orcid.org/0000-0002-4426-3254, Emanuel, Beverley S., Vermeesch, Joris R., Warren, Stephen T., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, 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 ORCID: https://orcid.org/0000-0003-0870-9412, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Demaeral, Wolfman, 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, Koren, Vergaelen, Elfi, Vogels, Annick, Crowley, 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 ORCID: https://orcid.org/0000-0002-8855-7393, Murphy, Kieran C., Prasad, Sarah E., Daly, Eileen M., Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan C., Buzzanca, Antonio, Fabio, Fabio Di, 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, Stephan, Sandini, Corrado, Schneider, Maude, Bena, Frederique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Busa, Tiffany, McCabe, Kathryn L., Philip, Nicole, Campbell, Linda E., Shashi, Vandana, Hooper, Stephen R., Schoch, Kelly, Simon, Tony J., Tassone, Flora, Arango, Celso, Fraguas, David, Garcia-Miñaur, Sixto, Morey-Canyelles, Jaume, Rosell, Jordi, Suner, Damia H., Raventos-Simic, Jasna, Epstein, Michael, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931 and Bassett, Anne S. 2021. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry , pp. 4496-4510. 10.1038/s41380-020-0654-3
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Forsyth, Jennifer K., Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher R. K., Villalon-Reina, Julio E., Thompson, Paul M., Bearden, Carrie E., Cunningham, Adam, Doherty, Joanne L., Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292, Moss, Hayley, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2021. Prioritizing genetic contributors to cortical alterations in 22q11.2 deletion syndrome using imaging transcriptomics. Cerebral Cortex 31 (7) , pp. 3285-3298. 10.1093/cercor/bhab008
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Villalon-Reina, Julio, Martinez, Kenia, Qu, Xiaoping, Ching, Christopher, Nir, Talia, Kothapalli, Deydeep, Corbin, Conor, Dagiang, Sun, Lin, Amy, Forsyth, Jennifer, Kushan, Lelia, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Jonas, Rachel, van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy, Antshel, Kevin, Fremont, Wanda, Campbell, Linda, McCable, Kathryn, Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh, Murphy, Declan, Craig, Michael, Emanual, Beverly, McDonna-McGinn, Donna, Vorstman, Jacob, Fiksinski, Ania, Koops, Sanne, Ruparel, Kosha, Roalf, David, Raquel, Gur, Eric, Schmitt, Simon, Tony, Goodrich-Hunsaker, Naomi, Durdle, Courtney, Doherty, Joanne, Cunningham, Adam, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Moss, Hayley, Kelly, Sinead, Donohoe, Gary, Murphy, Kieran, Arango, Celso, Jahanshad, Neda, Thompson, Paul and Bearden, Carrie 2020. Altered white matter microstructure in 22q11.2 deletion syndrome: a multi-site diffusion tensor imaging study. Molecular Psychiatry 25 , pp. 2818-2831. 10.1038/s41380-019-0450-0
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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. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C., McDonald-McGinn, Donna M., Emanuel, Beverly, van Erp, Theo G. M., Turner, Jessica A., Thompson, Paul M. and Bearden, Carrie E. 2020. Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Molecular Psychiatry 25 , pp. 1822-1834. 10.1038/s41380-018-0078-5
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Ching, Christopher R.K., Gutman, Boris A., Sun, Daqiang, Villalon Reina, Julio, Ragothaman, Anjanibhargavi, Isaev, Dmitry, Zavaliangos-Petropulu, Artemis, Lin, Amy, Jonas, Rachel K., Kushan, Leila, Pacheco-Hansen, Laura, Vajdi, Ariana, Forsyth, Jennifer K., Jalbrzikowski, Maria, Bakker, Geor, van Amelsvoort, Therese, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Campbell, Linda E., McCabe, Kathryn L., Craig, Michael C., Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan G., Murphy, Kieran C., Fiksinski, Ania, Koops, Sanne, Vorstman, Jacob, Crowley, T. Blaine, Emanuel, Beverly S., Gur, Raquel E., McDonald-McGinn, Donna M., Roalf, David R., Ruparel, Kosha, Schmitt, J. Eric, Zackai, Elaine H., Durdle, Courtney A., Goodrich-Hunsaker, Naomi J., Simon, Tony J., Bassett, Anne S., Butcher, Nancy J., Chow, Eva W.C., Vila-Rodriguez, Fidel, Cunningham, Adam, Doherty, Joanne, Linden, David E., Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Crossley, Nicolas A., Repetto, Gabriela M., Thompson, Paul M. and Bearden, Carrie E. 2020. Mapping subcortical brain alterations in 22q11.2 deletion syndrome: effects of seletion size and convergence with idiopathic neuropsychiatric illness. American Journal of Psychiatry 177 (7) , pp. 589-600. 10.1176/appi.ajp.2019.19060583

Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A.S., Gothelf, Doron, Zackai, Elaine, Agopian, A.J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E., Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P., Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D.A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong and Zwick, Michael 2020. Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects. American Journal of Human Genetics 106 (1) , pp. 26-40. 10.1016/j.ajhg.2019.11.010
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Brieva, Jorge, Lepore, Natasha, Romero, Eduardo, Cunningham, Adam C., Goodrich-Hunsaker, Naomi J., Simon, Tony J., Schmitt, Eric, Gur, Raquel E., Roalf, David, Ruparel, Kosha, McDonald-McGinn, Donna, Emanuel, Beverly, Craig, Michael, Murphy, Declan, Murphy, Clodaph, Gudbrandsen, Maria, Daly, Eileen, Kates, Wendy R., Bakker, Geor, van Amelsvoort, Therese, Jonas, Rachel, Hansen, Laura, Lin, Amy, Nir, Talia, Sun, Daqiang V., Kothapalli, Deydeep, Ching, Christopher R., Thompson, Paul M., Bearden, Carrie E., Jahanshad, Neda, Moss, Hayley, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Linden, David E., Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Doherty, Joanne, Durdle, Courtney A., McCabe, Kathryn L., Campbell, Linda E., Fremont, Wanda, Antshel, Kevin M., Jalbrzikowski, Maria, Vajdi, Ariana V., Kushan, Leila V., Forsyth, Jennifer K. and Villalón-Reina, Julio 2018. Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome. Presented at: 14th International Symposium on Medical Information Processing and Analysis,, Mazatlán, Mexico, 24-26 October 2018. Published in: Romero, Eduardo, Lepore, Natasha and Brieva, Jorge eds. 14th International Symposium on Medical Information Processing and Analysis. Proceedings of SPIE , vol.10975 Bellingham, Washington: SPIE, p. 51. 10.1117/12.2513788

Chawner, Samuel J.R.A., Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Doherty, Joanne L., Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2018. The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome. Journal of Psychiatric Research 109 , pp. 10-17. 10.1016/j.jpsychires.2018.11.002
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Chawner, Samuel, Doherty, Joanne L., Moss, Hayley, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254 2017. Childhood cognitive development in 22q11.2 deletion syndrome: case–control study. British Journal of Psychiatry 211 (4) , pp. 223-230. 10.1192/bjp.bp.116.195651
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This list was generated on Tue Sep 26 05:32:30 2023 BST.


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