Yang, Mu
University of California Davis Medical Center · University of California, Davis
16 papers on CoChatORCID 0000-0003-0091-0365
Most cited papers
- Verified
Behavioural phenotyping assays for mouse models of autism
Silverman, J. L., Yang, M., Lord, C., & Crawley, J. N. (2010) · Nature Reviews Neuroscience
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 1,462
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Autism‐like behavioral phenotypes in BTBR T+tf/J mice
McFarlane, H. G., Kusek, G. K., Yang, M., Phoenix, J. L., Bolivar, V. J., & Crawley, J. N. (2008) · Genes, Brain and Behavior
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 812
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Automated Three‐Chambered Social Approach Task for Mice
Yang, M., Silverman, J. L., & Crawley, J. N. (2011) · Current Protocols in Neuroscience
Autism Spectrum Disorder ResearchNeuroendocrine regulation and behavior
Cited by 598
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Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
Bozdagi, O., Sakurai, T., Papapetrou, D., Wang, X., Dickstein, D. L., Takahashi, N., Kajiwara, Y., Yang, M., Katz, A. M., Scattoni, M. L., et al. (2010) · Molecular Autism
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 584
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Reduced Excitatory Neurotransmission and Mild Autism-Relevant Phenotypes in Adolescent Shank3 Null Mutant Mice
Yang, M., Bozdagi, O., Scattoni, M. L., Wöhr, M., Roullet, F. I., Katz, A. M., Abrams, D. N., Kalikhman, D., Simon, H., Woldeyohannes, L., et al. (2012) · The Journal of Neuroscience
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 369
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Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome
Portmann, T., Yang, M., Mao, R., Panagiotakos, G., Ellegood, J., Dolen, G., Bader, P. L., Grueter, B. A., Goold, C., Fisher, E., et al. (2014) · Cell Reports
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 245
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Low stress reactivity and neuroendocrine factors in the BTBR T+tf/J mouse model of autism
Silverman, J. L., Yang, M., Turner, S. M., Katz, A. M., Bell, D. B., Koenig, J. I., & Crawley, J. N. (2010) · Neuroscience
Autism Spectrum Disorder ResearchStress Responses and Cortisol
Cited by 146
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Social deficits in BTBR T + tf/J mice are unchanged by cross‐fostering with C57BL/6J mothers
Yang, M., Zhodzishsky, V., & Crawley, J. N. (2007) · International Journal of Developmental Neuroscience
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 132
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Social approach behaviors are similar on conventional versus reverse lighting cycles, and in replications across cohorts, in BTBR T+ tf/J, C57BL/6J, and vasopressin receptor 1B mutant mice
Yang, M. (2007) · Frontiers in Behavioral Neuroscience
Neuroendocrine regulation and behaviorNeurotransmitter Receptor Influence on Behavior
Cited by 124
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Postnatal lesion evidence against a primary role for the corpus callosum in mouse sociability
Yang, M., Clarke, A. M., & Crawley, J. N. (2009) · European Journal of Neuroscience
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 117
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Low sociability in BTBR T+tf/J mice is independent of partner strain
Yang, M., Abrams, D. N., Zhang, J. Y., Weber, M. D., Katz, A. M., Clarke, A. M., Silverman, J. L., & Crawley, J. N. (2012) · Physiology & Behavior
Autism Spectrum Disorder ResearchNeuroendocrine regulation and behavior
Cited by 112
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Social peers rescue autism‐relevant sociability deficits in adolescent mice
Yang, M., Perry, K., Weber, M. D., Katz, A. M., & Crawley, J. N. (2011) · Autism Research
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 106
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16p11.2 deletion syndrome mice display sensory and ultrasonic vocalization deficits during social interactions
Yang, M., Mahrt, E. J., Lewis, F., Foley, G., Portmann, T., Dolmetsch, R. E., Portfors, C. V., & Crawley, J. N. (2015) · Autism Research
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 96
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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
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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
- Verified
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
Cited by 28
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