Caitlin Vose

Two unrelated children with overlapping 6q25.3 deletions, motor speech disorders, and language delays

Beate Peter, Hope Sparks Lancaster, Caitlin Vose et al. · American Journal of Medical Genetics Part A · 2017 · 60 citations

Sequential processing deficit as a shared persisting biomarker in dyslexia and childhood apraxia of speech

Beate Peter, Hope Sparks Lancaster, Caitlin Vose et al. · Clinical Linguistics & Phonetics · 2017 · 39 citations

Neuropsychology, Acquired Apraxia Of Speech, Psycholinguistics +18

Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects

Beate Peter, Valentin Dinu, Li Liu et al. · Behavior Genetics · 2019 · 26 citations

Neurodevelopmental Disorders, Syndromic Autism, Exome Sequencing +9

Toward a paradigm shift from deficit-based to proactive speech and language treatment: Randomized pilot trial of the Babble Boot Camp in infants with classic galactosemia

Beate Peter, Nancy L. Potter, Jennifer Davis et al. · F1000Research · 2020 · 17 citations · Full text

Toward a paradigm shift from deficit-based to proactive speech and language treatment: Randomized pilot trial of the Babble Boot Camp in infants with classic galactosemia

Beate Peter, Nancy L. Potter, Jennifer Davis et al. · F1000Research · 2019 · 14 citations · Full text

Language Development, Babble Boot Camp, Atypical Language Development +25