Brain enlargement is associated with regression in preschool-age boys with autism spectrum disorders von Nordahl, Christine Wu, Lange, Nicholas, Li, Deana D, Barnett, Lou Ann, Lee, Aaron, Buonocore, Michael H, Simon, Tony J, Rogers, Sally, Ozonoff, Sally, Amaral, David G

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Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome von 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

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Real-time cognitive performance metrics derived from a digital therapeutic for inattention predict ADHD-related clinical outcomes: Replication across three independent trials of AK... von Stamatis, Caitlin A., Heusser, Andrew C., Simon, Tony J., Ala’ilima, Titiimaea, Kollins, Scott H.

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22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia von Karayiorgou, Maria, Simon, Tony J., Gogos, Joseph A.

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The development of cognitive control in children with chromosome 22q11.2 deletion syndrome von Shapiro, Heather M, Tassone, Flora, Choudhary, Nimrah S, Simon, Tony J

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Assessment of the Prodromal Questionnaire–Brief Child Version for Measurement of Self-reported Psychoticlike Experiences in Childhood von Karcher, Nicole R, Barch, Deanna M, Avenevoli, Shelli, Savill, Mark, Huber, Rebekah S, Simon, Tony J, Leckliter, Ingrid N, Sher, Kenneth J, Loewy, Rachel L

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Adult Female Fragile X Premutation Carriers Exhibit Age- and CGG Repeat Length-Related Impairments on an Attentionally Based Enumeration Task von Goodrich-Hunsaker, Naomi J, Wong, Ling M, McLennan, Yingratana, Tassone, Flora, Harvey, Danielle, Rivera, Susan M, Simon, Tony J

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The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety von Scott, Julia A., PhD, Goodrich-Hunsaker, Naomi, PhD, Kalish, Kristopher, MSc, Lee, Aaron, BSc, Hunsaker, Michael R., PhD, Schumann, Cynthia M., PhD, Simon, Tony J., PhD, Carmichael, Owen T., PhD

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

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Eye Movements Reveal Impaired Inhibitory Control in Adult Male Fragile X Premutation Carriers Asymptomatic for FXTAS von Wong, Ling M., Goodrich-Hunsaker, Naomi J., McLennan, Yingratana, Tassone, Flora, Zhang, Melody, Rivera, Susan M., Simon, Tony J.

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Abnormal Trajectories in Cerebellum and Brainstem Volumes in Carriers of the Fragile X Premutation von Wang, Jun Yi, Hessl, David, Hagerman, Randi J, Simon, Tony J, Tassone, Flora, Ferrer, Emilio, Rivera, Susan M

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Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome von Napoli, Eleonora, Tassone, Flora, Wong, Sarah, Angkustsiri, Kathleen, Simon, Tony J., Song, Gyu, Giulivi, Cecilia

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Bullying and psychosis: The impact of chronic traumatic stress on psychosis risk in 22q11.2 deletion syndrome - a uniquely vulnerable population von Mayo, Danessa, Bolden, Khalima A., Simon, Tony J., Niendam, Tara A.

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A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndrome von Shapiro, Heather M, Wong, Ling M, Simon, Tony J

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Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype? von Angkustsiri, Kathleen, Goodlin-Jones, Beth, Deprey, Lesley, Brahmbhatt, Khyati, Harris, Susan, Simon, Tony J.

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Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment von Deboer, Tracy, Wu, Zhongle, Lee, Aaron, Simon, Tony J

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Temporal dynamics of attentional selection in adult male carriers of the fragile X premutation allele and adult controls von Wong, Ling M, Tassone, Flora, Rivera, Susan M, Simon, Tony J

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Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness von 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, van den Bree, Marianne, Crossley, Nicolas A, Repetto, Gabriela M, Thompson, Paul M, Bearden, Carrie E

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Structure-specific statistical mapping of white matter tracts von Yushkevich, Paul A., Zhang, Hui, Simon, Tony J., Gee, James C.

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Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome von Machado, Alexei M.C, Simon, Tony J, Nguyen, Vy, McDonald-McGinn, Donna M, Zackai, Elaine H, Gee, James C

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