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Whitney Guthrie

Researcher at Children's Hospital of Philadelphia

Publications -  35
Citations -  2023

Whitney Guthrie is an academic researcher from Children's Hospital of Philadelphia. The author has contributed to research in topics: Autism & Autism spectrum disorder. The author has an hindex of 15, co-authored 27 publications receiving 1441 citations. Previous affiliations of Whitney Guthrie include University of Pennsylvania & Center for Autism and Related Disorders.

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Parent-Implemented Social Intervention for Toddlers With Autism: An RCT

TL;DR: The efficacy of a parent-implemented intervention using little professional time has potential for community viability, which is particularly important in light of the lack of main effects on child outcomes of most other parent-injury interventions.
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Early diagnosis of autism spectrum disorder: stability and change in clinical diagnosis and symptom presentation

TL;DR: Stability was documented for children diagnosed at 19 months on average, although a minority of children initially showed unclear diagnostic presentations, and findings highlight utility of the ADOS-T in making early diagnoses and predicting follow-up diagnoses.
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The Autism Diagnostic Observation Schedule, Toddler Module: Standardized Severity Scores

TL;DR: Toddler Module CSS increases comparability of ADOS-2 scores across modules and allows studies of symptom trajectories to extend to earlier ages and reduces associations between total and domain CSS and participant characteristics.
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Convergent Validity of the Mullen Scales of Early Learning and the Differential Ability Scales in Children With Autism Spectrum Disorders

TL;DR: Convergent validity of the MSEL and the Differential Ability Scales was examined in children with autism spectrum disorder and 19 children with nonspectrum diagnoses, showing good convergent validity with respect to nonverbal IQ, verbal IQ, and NVIQ-VIQ profiles.
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Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement

TL;DR: A series of recommendations are outlined that document the consensus of a group of international experts on clinical diagnostic criteria, both for classic and non-classic Cornelia de Lange syndrome phenotypes, molecular investigations, long-term management and care planning.