Hudac, Caitlin M.

Neural signatures of autism

Kaiser, M. D., Hudac, C. M., Shultz, S., Lee, S. M., Cheung, C., Berken, A. M., Deen, B., Pitskel, N. B., Sugrue, D. R., Voos, A. C., et al. (2010) · Proceedings of the National Academy of Sciences

Autism Spectrum Disorder ResearchAction Observation and Synchronization

Cited by 352

Brain mechanisms underlying the impact of attachment-related stress on social cognition

Nolte, T., Bolling, D. Z., Hudac, C. M., Fonagy, P., Mayes, L., & Pelphrey, K. A. (2013) · Frontiers in Human Neuroscience

Action Observation and SynchronizationFace Recognition and Perception

Cited by 176

Early enhanced processing and delayed habituation to deviance sounds in autism spectrum disorder

Hudac, C. M., DesChamps, T. D., Arnett, A. B., Cairney, B. E., Ma, R., Webb, S. J., & Bernier, R. A. (2018) · Brain and Cognition

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 81

Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers

Hudac, C. M., Bove, J., Barber, S., Duyzend, M., Wallace, A., Martin, C. L., Ledbetter, D. H., Hanson, E., Goin‐Kochel, R. P., Green‐Snyder, L., et al. (2020) · Autism Research

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

Cited by 31

Auditory perception is associated with implicit language learning and receptive language ability in autism spectrum disorder

Arnett, A. B., Hudac, C. M., DesChamps, T. D., Cairney, B. E., Gerdts, J., Wallace, A. S., Bernier, R. A., & Webb, S. J. (2018) · Brain and Language

Autism Spectrum Disorder ResearchLanguage Development and Disorders

Cited by 26

Interactive Effects of Prenatal Antidepressant Exposure and Likely Gene Disrupting Mutations on the Severity of Autism Spectrum Disorder

Ackerman, S., Schoenbrun, S., Hudac, C., & Bernier, R. (2017) · Journal of Autism and Developmental Disorders

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 12

Longitudinal report of child with de novo 16p11.2 triplication

Wallace, A. S., Hudac, C. M., Steinman, K. J., Peterson, J. L., DesChamps, T. D., Duyzend, M. H., Nuttle, X., Eichler, E. E., & Bernier, R. A. (2018) · Clinical Case Reports

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 9