Adam P. Vogel

This study conducts a GWAS meta-analysis of stuttering, identifying genetic links with speech disorders and highlighting shared genetic architecture across different ascertainment methods.

This study uses multimodal non-invasive assessments to characterize structural and functional alterations in ADSS1 myopathy, identifying biomarkers for disease monitoring.

This study characterizes 29 individuals with FOXP2 variants, showing high prevalence of speech disorders and language impairments, with relatively specific phenotypes compared to other monogenic conditions.

This study evaluates cerebellar function scores in relation to axonal loss in multiple sclerosis using diffusion MRI and clinical assessments.