Crawley, Jacqueline N.

16p11.2 deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasks

Yang, M., Lewis, F. C., Sarvi, M. S., Foley, G. M., & Crawley, J. N. (2015) · Learning & Memory

Genomic variations and chromosomal abnormalitiesMemory and Neural Mechanisms

Cited by 70

Quantitative trait loci for interhemispheric commissure development and social behaviors in the BTBR T+ tf/J mouse model of autism

Jones-Davis, D. M., Yang, M., Rider, E., Osbun, N. C., da Gente, G. J., Li, J., Katz, A. M., Weber, M. D., Sen, S., Crawley, J., et al. (2013) · PLoS ONE

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 61

In tribute to Bob Blanchard: Divergent behavioral phenotypes of 16p11.2 deletion mice reared in same-genotype versus mixed-genotype cages

Yang, M., Lewis, F., Foley, G., & Crawley, J. N. (2015) · Physiology & Behavior

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

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Normal Performance of Fmr1 Mice on a Touchscreen Delayed Nonmatching to Position Working Memory Task

Leach, P. T., Hayes, J., Pride, M., Silverman, J. L., & Crawley, J. N. (2016) · eneuro

Genetics and Neurodevelopmental DisordersWilliams Syndrome Research

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