Neuropsychological Assessment in Autism Spectrum Disorder

por Braconnier, Megan L., Siper, Paige M.
Publicado 2021

Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiency

por Levy, Tess, Pichardo, Thariana, Silver, Hailey, Lerman, Bonnie, Zweifach, Jessica, Halpern, Danielle, Siper, Paige M., Kolevzon, Alexander, Buxbaum, Joseph D.
Publicado 2023

CHAMP1 disorder is associated with a complex neurobehavioral phenotype including autism, ADHD, repetitive behaviors and sensory symptoms

por Levy, Tess, Lerman, Bonnie, Halpern, Danielle, Frank, Yitzchak, Layton, Christina, Zweifach, Jessica, Siper, Paige M, Buxbaum, Joseph D, Kolevzon, Alexander
Publicado 2022

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

Sensory Reactivity Phenotype in Phelan–McDermid Syndrome Is Distinct from Idiopathic ASD

por Tavassoli, Teresa, Layton, Christina, Levy, Tess, Rowe, Mikaela, George-Jones, Julia, Zweifach, Jessica, Lurie, Stacey, Buxbaum, Joseph D., Kolevzon, Alexander, Siper, Paige M.
Publicado 2021

FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring

por Lozano, Reymundo, Gbekie, Catherine, Siper, Paige M., Srivastava, Shubhika, Saland, Jeffrey M., Sethuram, Swathi, Tang, Lara, Drapeau, Elodie, Frank, Yitzchak, Buxbaum, Joseph D., Kolevzon, Alexander
Publicado 2021

Rapid and Objective Assessment of Neural Function in Autism Spectrum Disorder Using Transient Visual Evoked Potentials

por Siper, Paige M., Zemon, Vance, Gordon, James, George-Jones, Julia, Lurie, Stacey, Zweifach, Jessica, Tavassoli, Teresa, Wang, A. Ting, Jamison, Jesslyn, Buxbaum, Joseph D., Kolevzon, Alexander
Publicado 2016

Brief Report: Assessment of a Caregiver-Implemented Intervention for Improving Social Communication Skills in Toddlers and Young Children with Autism

por Rouhandeh, Audrey A., Honsberger, Christine, Shanok, Nathaniel A., Lozott, Erin Brooker, Levy, Tess, Kolevzon, Alexander, Buxbaum, Joseph D., Sotelo, Marlene, Foss-Feig, Jennifer, Siper, Paige M.
Publicado 2022

Neural Markers of Auditory Response and Habituation in Phelan-McDermid Syndrome

por Isenstein, Emily L., Grosman, Hannah E., Guillory, Sylvia B., Zhang, Yian, Barkley, Sarah, McLaughlin, Christopher S., Levy, Tess, Halpern, Danielle, Siper, Paige M., Buxbaum, Joseph D., Kolevzon, Alexander, Foss-Feig, Jennifer H.
Publicado 2022

Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations

por De Rubeis, Silvia, Siper, Paige M., Durkin, Allison, Weissman, Jordana, Muratet, François, Halpern, Danielle, Trelles, Maria del Pilar, Frank, Yitzchak, Lozano, Reymundo, Wang, A. Ting, Holder, J. Lloyd, Betancur, Catalina, Buxbaum, Joseph D., Kolevzon, Alexander
Publicado 2018

Assessing the utility of electronic measures as a proxy for cognitive ability

por Levy, Tess, Britvan, Bari, Grosman, Hannah, Giserman‐Kiss, Ivy, Meyering, Kristin, Weissman, Jordana, Halpern, Danielle, Zweifach, Jessica, Trelles, M. Pilar, Foss‐Feig, Jennifer H., Kolevzon, Alexander, Sanders, Stephan J., Robinson, Elise B., Buxbaum, Joseph D., Bishop, Somer, Siper, Paige M.
Publicado 2022

Prospective investigation of FOXP1 syndrome

por Siper, Paige M., De Rubeis, Silvia, Trelles, Maria del Pilar, Durkin, Allison, Di Marino, Daniele, Muratet, François, Frank, Yitzchak, Lozano, Reymundo, Eichler, Evan E., Kelly, Morgan, Beighley, Jennifer, Gerdts, Jennifer, Wallace, Arianne S., Mefford, Heather C., Bernier, Raphael A., Kolevzon, Alexander, Buxbaum, Joseph D.
Publicado 2017

Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis

por Siper, Paige M., Layton, Christina, Levy, Tess, Lurie, Stacey, Benrey, Nurit, Zweifach, Jessica, Rowe, Mikaela, Tang, Lara, Guillory, Sylvia, Halpern, Danielle, Giserman-Kiss, Ivy, Del Pilar Trelles, Maria, Foss-Feig, Jennifer H., De Rubeis, Silvia, Tavassoli, Teresa, Buxbaum, Joseph D., Kolevzon, Alexander
Publicado 2021

Social visual attentional engagement and memory in Phelan-McDermid syndrome and autism spectrum disorder: a pilot eye tracking study

por Guillory, Sylvia B., Baskett, Victoria Z., Grosman, Hannah E., McLaughlin, Christopher S., Isenstein, Emily L., Wilkinson, Emma, Weissman, Jordana, Britvan, Bari, Trelles, M. Pilar, Halpern, Danielle B., Buxbaum, Joseph D., Siper, Paige M., Wang, A. Ting, Kolevzon, Alexander, Foss-Feig, Jennifer H.
Publicado 2021

An open-label study evaluating the safety, behavioral, and electrophysiological outcomes of low-dose ketamine in children with ADNP syndrome

por Kolevzon, Alexander, Levy, Tess, Barkley, Sarah, Bedrosian-Sermone, Sandra, Davis, Matthew, Foss-Feig, Jennifer, Halpern, Danielle, Keller, Katherine, Kostic, Ana, Layton, Christina, Lee, Rebecca, Lerman, Bonnie, Might, Matthew, Sandin, Sven, Siper, Paige M., Sloofman, Laura G., Walker, Hannah, Zweifach, Jessica, Buxbaum, Joseph D.
Publicado 2022

Prospective and detailed behavioral phenotyping in DDX3X syndrome

por Tang, Lara, Levy, Tess, Guillory, Sylvia, Halpern, Danielle, Zweifach, Jessica, Giserman-Kiss, Ivy, Foss-Feig, Jennifer H., Frank, Yitzchak, Lozano, Reymundo, Belani, Puneet, Layton, Christina, Lerman, Bonnie, Frowner, Emanuel, Breen, Michael S., De Rubeis, Silvia, Kostic, Ana, Kolevzon, Alexander, Buxbaum, Joseph D., Siper, Paige M., Grice, Dorothy E.
Publicado 2021

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