The Autism Palette: Combinations of Impairments Explain the Heterogeneity in ASD

por Fóthi, Ábel, Soorya, Latha, Lőrincz, András
Publicado 2020

Examining a stepped-care telehealth program for parents of young children with autism: a proof-of-concept trial

por Wainer, Allison L., Arnold, Zachary E., Leonczyk, Caroline, Valluripalli Soorya, Latha
Publicado 2021

Community-based care for autistic youth: community providers’ reported use of treatment practices in the United States

por Drahota, Amy, Sridhar, Aksheya, Moskowitz, Lauren J., Kerns, Connor M., Soorya, Latha, Wainer, Allison, Cohn, Elizabeth, Lerner, Matthew D.
Publicado 2023

Examining indicators of psychosocial risk and resilience in parents of autistic children

por Dimachkie Nunnally, Amanda, Factor, Reina S., Sturm, Alexandra, Valluripalli Soorya, Latha, Wainer, Allison, Taylor, Sandra, Ponzini, Matthew, Abbeduto, Leonard, Gulsrud, Amanda C.
Publicado 2023

Autonomic and brain responses associated with empathy deficits in autism spectrum disorder

por Gu, Xiaosi, Eilam‐Stock, Tehila, Zhou, Thomas, Anagnostou, Evdokia, Kolevzon, Alexander, Soorya, Latha, Hof, Patrick R., Friston, Karl J., Fan, Jin
Publicado 2015

Impaired Structural Connectivity of Socio-Emotional Circuits in Autism Spectrum Disorders: A Diffusion Tensor Imaging Study

por Ameis, Stephanie H., Fan, Jin, Rockel, Conrad, Voineskos, Aristotle N., Lobaugh, Nancy J., Soorya, Latha, Wang, A. Ting, Hollander, Eric, Anagnostou, Evdokia
Publicado 2011

Neural selectivity for communicative auditory signals in Phelan-McDermid syndrome

por Wang, A. Ting, Lim, Teresa, Jamison, Jesslyn, Bush, Lauren, Soorya, Latha V., Tavassoli, Teresa, Siper, Paige M., Buxbaum, Joseph D., Kolevzon, Alexander
Publicado 2016

Erratum to: Neural selectivity for communicative auditory signals in Phelan-McDermid syndrome

por Wang, A. Ting, Lim, Teresa, Jamison, Jesslyn, Bush, Lauren, Soorya, Latha V., Tavassoli, Teresa, Siper, Paige M., Buxbaum, Joseph D., Kolevzon, Alexander
Publicado 2016

Intranasal oxytocin versus placebo in the treatment of adults with autism spectrum disorders: a randomized controlled trial

por Anagnostou, Evdokia, Soorya, Latha, Chaplin, William, Bartz, Jennifer, Halpern, Danielle, Wasserman, Stacey, Wang, A Ting, Pepa, Lauren, Tanel, Nadia, Kushki, Azadeh, Hollander, Eric
Publicado 2012

A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome

por Kolevzon, Alexander, Bush, Lauren, Wang, A Ting, Halpern, Danielle, Frank, Yitzchak, Grodberg, David, Rapaport, Robert, Tavassoli, Teresa, Chaplin, William, Soorya, Latha, Buxbaum, Joseph D
Publicado 2014

Erratum: A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome

por Kolevzon, Alexander, Bush, Lauren, Wang, A Ting, Halpern, Danielle, Frank, Yitzchak, Grodberg, David, Rapaport, Robert, Tavassoli, Teresa, Chaplin, William, Soorya, Latha, Buxbaum, Joseph D
Publicado 2015

Functional deficits of the attentional networks in autism

por Fan, Jin, Bernardi, Silvia, Dam, Nicholas T, Anagnostou, Evdokia, Gu, Xiaosi, Martin, Laura, Park, Yunsoo, Liu, Xun, Kolevzon, Alexander, Soorya, Latha, Grodberg, David, Hollander, Eric, Hof, Patrick R
Publicado 2012

Usual care for youth with autism spectrum disorder: Community-based providers’ reported familiarity with treatment practices

por Lerner, Matthew D., Brown, Cynthia E., Sridhar, Aksheya, Tschida, Jessica E., Felsman, Peter, Libsack, Erin J., Kerns, Connor M., Moskowitz, Lauren J., Soorya, Latha, Wainer, Allison, Cohn, Elizabeth, Drahota, Amy
Publicado 2022

Parent-reported measure of repetitive behavior in Phelan-McDermid syndrome

por Srivastava, Siddharth, Condy, Emma, Carmody, Erin, Filip-Dhima, Rajna, Kapur, Kush, Bernstein, Jonathan A., Berry-Kravis, Elizabeth, Powell, Craig M., Soorya, Latha, Thurm, Audrey, Buxbaum, Joseph D., Sahin, Mustafa, Kolevzon, Alexander
Publicado 2021

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a nov...

por Cai, Guiqing, Edelmann, Lisa, Goldsmith, Juliet E, Cohen, Ninette, Nakamine, Alisa, Reichert, Jennifer G, Hoffman, Ellen J, Zurawiecki, Danielle M, Silverman, Jeremy M, Hollander, Eric, Soorya, Latha, Anagnostou, Evdokia, Betancur, Catalina, Buxbaum, Joseph D
Publicado 2008

Large 22q13.3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome

por Breen, Michael S., Fan, Xuanjia, Levy, Tess, Pollak, Rebecca M., Collins, Brett, Osman, Aya, Tocheva, Anna S., Sahin, Mustafa, Berry-Kravis, Elizabeth, Soorya, Latha, Thurm, Audrey, Powell, Craig M., Bernstein, Jonathan A., Kolevzon, Alexander, Buxbaum, Joseph D.
Publicado 2022

Atypical Functional Connectivity During Unfamiliar Music Listening in Children With Autism

por Freitas, Carina, Hunt, Benjamin A. E., Wong, Simeon M., Ristic, Leanne, Fragiadakis, Susan, Chow, Stephanie, Iaboni, Alana, Brian, Jessica, Soorya, Latha, Chen, Joyce L., Schachar, Russell, Dunkley, Benjamin T., Taylor, Margot J., Lerch, Jason P., Anagnostou, Evdokia
Publicado 2022

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency

por Soorya, Latha, Kolevzon, Alexander, Zweifach, Jessica, Lim, Teresa, Dobry, Yuriy, Schwartz, Lily, Frank, Yitzchak, Wang, A Ting, Cai, Guiqing, Parkhomenko, Elena, Halpern, Danielle, Grodberg, David, Angarita, Benjamin, Willner, Judith P, Yang, Amy, Canitano, Roberto, Chaplin, William, Betancur, Catalina, Buxbaum, Joseph D
Publicado 2013

Shifted phase of EEG cross-frequency coupling in individuals with Phelan-McDermid syndrome

por Mariscal, Michael. G., Berry-Kravis, Elizabeth, Buxbaum, Joseph D., Ethridge, Lauren E., Filip-Dhima, Rajna, Foss-Feig, Jennifer H., Kolevzon, Alexander, Modi, Meera. E., Mosconi, Matthew W., Nelson, Charles A., Powell, Craig M., Siper, Paige M., Soorya, Latha, Thaliath, Andrew, Thurm, Audrey, Zhang, Bo, Sahin, Mustafa, Levin, April R.
Publicado 2021

Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium

por Levy, Tess, Foss-Feig, Jennifer H, Betancur, Catalina, Siper, Paige M, Trelles-Thorne, Maria del Pilar, Halpern, Danielle, Frank, Yitzchak, Lozano, Reymundo, Layton, Christina, Britvan, Bari, Bernstein, Jonathan A, Buxbaum, Joseph D, Berry-Kravis, Elizabeth, Powell, Craig M, Srivastava, Siddharth, Sahin, Mustafa, Soorya, Latha, Thurm, Audrey, Kolevzon, Alexander
Publicado 2021