Works matching AU Halpern, Danielle

Results: 23

Measuring Sensory Reactivity in Autism Spectrum Disorder: Application and Simplification of a Clinician-Administered Sensory Observation Scale.

Published in:

Journal of Autism & Developmental Disorders, 2016, v. 46, n. 1, p. 287, doi. 10.1007/s10803-015-2578-3

By:

Tavassoli, Teresa;
Bellesheim, Katherine;
Siper, Paige;
Wang, A.;
Halpern, Danielle;
Gorenstein, Michelle;
Grodberg, David;
Kolevzon, Alexander;
Buxbaum, Joseph

Publication type:

Article

The Autism Mental Status Exam: Sensitivity and Specificity Using DSM-5 Criteria for Autism Spectrum Disorder in Verbally Fluent Adults.

Published in:

Journal of Autism & Developmental Disorders, 2014, v. 44, n. 3, p. 609, doi. 10.1007/s10803-013-1917-5

By:

Grodberg, David;
Weinger, Paige;
Halpern, Danielle;
Parides, Michael;
Kolevzon, Alexander;
Buxbaum, Joseph

Publication type:

Article

Reduced engagement of visual attention in children with autism spectrum disorder.

Published in:

Autism: The International Journal of Research & Practice, 2021, v. 25, n. 7, p. 2064, doi. 10.1177/13623613211010072

By:

McLaughlin, Christopher S;
Grosman, Hannah E;
Guillory, Sylvia B;
Isenstein, Emily L;
Wilkinson, Emma;
Trelles, Maria del Pilar;
Halpern, Danielle B;
Siper, Paige M;
Kolevzon, Alexander;
Buxbaum, Joseph D;
Wang, A Ting;
Foss-Feig, Jennifer H

Publication type:

Article

Investigating social orienting in children with Phelan-McDermid syndrome and 'idiopathic' autism.

Published in:

Journal of Neurodevelopmental Disorders, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s11689-024-09564-7

By:

San José Cáceres, Antonia;
Wilkinson, Emma;
Cooke, Jennifer;
Baskett, Victoria;
Blackmore, Charlotte;
Crawley, Daisy Victoria;
Durkin, Allison;
Halpern, Danielle;
Núñez, María;
Siper, Page;
Murphy, Declan G.;
Foss-Feig, Jennifer;
Kolevzon, Alexander;
Loth, Eva

Publication type:

Article

Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s11689-024-09541-0

By:

Levy, Tess;
Gluckman, Jacob;
Siper, Paige M.;
Halpern, Danielle;
Zweifach, Jessica;
Filip-Dhima, Rajna;
Holder Jr., J. Lloyd;
Trelles, M. Pilar;
Johnson, Kristina;
Bernstein, Jonathan A.;
Berry-Kravis, Elizabeth;
Powell, Craig M.;
Soorya, Latha Valluripalli;
Thurm, Audrey;
Buxbaum, Joseph D.;
Sahin, Mustafa;
Kolevzon, Alexander;
Srivastava, Siddharth

Publication type:

Article

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

Published in:

Journal of Neurodevelopmental Disorders, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s11689-021-09400-2

By:

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.

Publication type:

Article

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

Published in:

Human Molecular Genetics, 2022, v. 31, n. 15, p. 2582, doi. 10.1093/hmg/ddac018

By:

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

Publication type:

Article

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

Published in:

Human Molecular Genetics, 2022, v. 31, n. 4, p. 625, doi. 10.1093/hmg/ddab280

By:

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;
Consortium, the Developmental Synaptopathies

Publication type:

Article

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

Published in:

Genes, 2021, v. 12, n. 3, p. 351, doi. 10.3390/genes12030351

By:

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;
Gonda, Xenia

Publication type:

Article

Asperger's Syndrome and High-Functioning Autism.

Published in:

Pediatric Annals, 2009, v. 38, n. 1, p. 30, doi. 10.3928/00904481-20090101-01

By:

Carpenter, Laura Arnstein;
Soorya, Latha;
Halpern, Danielle

Publication type:

Article

Psychosocial Interventions for Motor Coordination, Executive Functions, and Socialization Deficits in ADHD and ASD.

Published in:

Primary Psychiatry, 2009, v. 16, n. 1, p. 48

By:

Soorya, Latha V.;
Halpern, Danielle

Publication type:

Article

Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by <italic>SHANK3</italic> point mutations.

Published in:

Molecular Autism, 2018, v. 9, n. 1, p. N.PAG, doi. 10.1186/s13229-018-0205-9

By:

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

Publication type:

Article

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

Published in:

Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-54

By:

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

Publication type:

Article

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

Published in:

Molecular Autism, 2013, v. 4, n. 1, p. 1, doi. 10.1186/2040-2392-4-18

By:

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

Publication type:

Article

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

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 16, doi. 10.1186/2040-2392-3-16

By:

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

Publication type:

Article

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

Published in:

Human Genetics, 2023, v. 142, n. 9, p. 1385, doi. 10.1007/s00439-023-02578-6

By:

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

Publication type:

Article

A Family Peer Advocate Model to Address Disparities in Access to Care for Minority Autistic Children with Co-Occurring Attention-Deficit/Hyperactivity Disorder.

Published in:

Journal of Developmental & Physical Disabilities, 2025, v. 37, n. 2, p. 217, doi. 10.1007/s10882-024-10001-9

By:

Trelles, Pilar;
Mahjani, Behrang;
Wilkinson, Emma;
Buonagura, Nicholas;
Donnelly, Lauren;
Foss Feig, Jennifer;
Halpern, Danielle;
McKay, Mary;
Siper, Paige;
Buxbaum, Joseph D;
Kolevzon, Alexander

Publication type:

Article

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

Published in:

Frontiers in Neuroscience, 2022, p. 1, doi. 10.3389/fnins.2022.815933

By:

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.

Publication type:

Article

Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms.

Published in:

Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00469-z

By:

Trelles, M. Pilar;
Levy, Tess;
Lerman, Bonnie;
Siper, Paige;
Lozano, Reymundo;
Halpern, Danielle;
Walker, Hannah;
Zweifach, Jessica;
Frank, Yitzchak;
Foss-Feig, Jennifer;
Kolevzon, Alexander;
Buxbaum, Joseph

Publication type:

Article

Prospective and detailed behavioral phenotyping in DDX3X syndrome.

Published in:

Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00431-z

By:

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.

Publication type:

Article

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

Published in:

Autism Research: Official Journal of the International Society for Autism Research, 2022, v. 15, n. 6, p. 988, doi. 10.1002/aur.2704

By:

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.

Publication type:

Article

Social cognitive skills groups increase medial prefrontal cortex activity in children with autism spectrum disorder.

Published in:

Autism Research: Official Journal of the International Society for Autism Research, 2021, v. 14, n. 12, p. 2495, doi. 10.1002/aur.2603

By:

Ibrahim, Karim;
Soorya, Latha V.;
Halpern, Danielle B.;
Gorenstein, Michelle;
Siper, Paige M.;
Wang, A. Ting

Publication type:

Article

De novo SCN2A splice site mutation in a boy with Autism spectrum disorder.

Published in:

BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-35

By:

Tavassoli, Teresa;
Kolevzon, Alexander;
Wang, A. Ting;
Curchack-Lichtin, Jocelyn;
Halpern, Danielle;
Schwartz, Lily;
Soffes, Sarah;
Bush, Lauren;
Grodberg, David;
Guiqing Cai;
Buxbaum, Joseph D.

Publication type:

Article