Wallace, Arianne Stevens

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population

Hanson, E., Bernier, R., Porche, K., Jackson, F. I., Goin-Kochel, R. P., Snyder, L. G., Snow, A. V., Wallace, A. S., Campe, K. L., Zhang, Y., et al. (2015) · Biological Psychiatry

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

Cited by 277

Quantifying the effects of 16p11.2 copy number variants on brain structure: a multisite genetic-first study

Martin-Brevet, S., Rodríguez-Herreros, B., Nielsen, J. A., Moreau, C., Modenato, C., Maillard, A. M., Pain, A., Richetin, S., Jønch, A. E., Qureshi, A. Y., et al. (2018) · Biological Psychiatry

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 75

Autism spectrum disorder, developmental and psychiatric features in 16p11.2 duplication

on behalf of the Simons VIP consortium, Green Snyder, L., D’Angelo, D., Chen, Q., Bernier, R., Goin-Kochel, R. P., Wallace, A. S., Gerdts, J., Kanne, S., Berry, L., et al. (2016) · Journal of Autism and Developmental Disorders

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

Cited by 61

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

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