How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?

por Beaton, Elliott A., Simon, Tony J.
Publicado 2010

Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome

por Stoddard, Joel, Beckett, Laurel, Simon, Tony J.
Publicado 2010

2117: Parenting, anxiety, and adaptive function in children with chromosome 22q11.2 deletion syndrome

por Angkustsiri, Kathleen, Simon, Tony J., Hastings, Paul D.
Publicado 2018

A Cross-Sectional Analysis of the Development of Response Inhibition in Children with Chromosome 22q11.2 Deletion Syndrome

por Shapiro, Heather M., Wong, Ling M., Simon, Tony J.
Publicado 2013

Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment

por DeBoer, Tracy, Wu, Zhongle, Lee, Aaron, Simon, Tony J
Publicado 2007

The development of cognitive control in children with chromosome 22q11.2 deletion syndrome

por Shapiro, Heather M., Tassone, Flora, Choudhary, Nimrah S., Simon, Tony J.
Publicado 2014

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

por Cabaral, Margarita H, Beaton, Elliott A, Stoddard, Joel, Simon, Tony J
Publicado 2012

Temporal dynamics of attentional selection in adult male carriers of the fragile X premutation allele and adult controls

por Wong, Ling M., Tassone, Flora, Rivera, Susan M., Simon, Tony J.
Publicado 2015

Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome

por Simon, Tony J, Wu, Zhongle, Avants, Brian, Zhang, Hui, Gee, James C, Stebbins, Glenn T
Publicado 2008

A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome

por Shapiro, Heather M, Takarae, Yukari, Harvey, Danielle J, Cabaral, Margarita H, Simon, Tony J
Publicado 2012

Mapping the deletion endpoints in individuals with 22q11.2 Deletion Syndrome by droplet digital PCR

por Hwang, Vicki J, Maar, Dianna, Regan, John, Angkustsiri, Kathleen, Simon, Tony J, Tassone, Flora
Publicado 2014

Common and specific impairments in attention functioning in girls with chromosome 22q11.2 deletion, fragile X or Turner syndromes

por Quintero, Andrea I, Beaton, Elliott A, Harvey, Danielle J, Ross, Judith L, Simon, Tony J
Publicado 2014

A cross-sectional analysis of orienting of visuospatial attention in child and adult carriers of the fragile X premutation

por Wong, Ling M, Goodrich-Hunsaker, Naomi J, McLennan, Yingratana A, Tassone, Flora, Rivera, Susan M, Simon, Tony J
Publicado 2014

Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task

por Goodrich-Hunsaker, Naomi J., Wong, Ling M., McLennan, Yingratana, Tassone, Flora, Harvey, Danielle, Rivera, Susan M., Simon, Tony J.
Publicado 2011

Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed

por Wong, Ling M, Goodrich-Hunsaker, Naomi J, McLennan, Yingratana, Tassone, Flora, Harvey, Danielle, Rivera, Susan M, Simon, Tony J
Publicado 2012

Replication of Associations With Psychotic-Like Experiences in Middle Childhood From the Adolescent Brain Cognitive Development (ABCD) Study

por Karcher, Nicole R, Loewy, Rachel L, Savill, Mark, Avenevoli, Shelli, Huber, Rebekah S, Simon, Tony J, Leckliter, Ingrid N, Sher, Kenneth J, Barch, Deanna M
Publicado 2020

Decreased DGCR8 Expression and miRNA Dysregulation in Individuals with 22q11.2 Deletion Syndrome

por Sellier, Chantal, Hwang, Vicki J., Dandekar, Ravi, Durbin-Johnson, Blythe, Charlet-Berguerand, Nicolas, Ander, Bradley P., Sharp, Frank R., Angkustsiri, Kathleen, Simon, Tony J., Tassone, Flora
Publicado 2014

Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome

por McCabe, Kathryn L., Popa, Abbie M., Durdle, Courtney, Amato, Michele, Cabaral, Margarita H., Cruz, Joshua, Wong, Ling M., Harvey, Danielle, Tartaglia, Nicole, Simon, Tony J.
Publicado 2019

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

por Guo, Tingwei, Repetto, Gabriela M., McDonald McGinn, Donna M., Chung, Jonathan H., Nomaru, Hiroko, Campbell, Christopher L., Blonska, Anna, Bassett, Anne S., Chow, Eva W.C., Mlynarski, Elisabeth E., Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E., Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E., Digilio, M. Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E., Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E., Tassone, Flora, Simon, Tony J., van Duin, Esther D.A., van Amelsvoort, Thérèse A., Kates, Wendy R., Zackai, Elaine, Johnston, H. Richard, Cutler, David J., Agopian, A.J., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Emanuel, Beverly S., Morrow, Bernice E.
Publicado 2017

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