Damon Page

Affiliations: 
Scripps Research Institute, La Jolla, La Jolla, CA, United States 
Area:
social brain, development
Google:
"Damon Page"
Mean distance: 13.5 (cluster 6)
 
SNBCP

Children

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Yao Chen research assistant MRC-LMB
Emma Andraka research assistant 2021-2021 Scripps Research Institute Florida
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Publications

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Carbonell AU, Freire-Cobo C, Deyneko IV, et al. (2023) Comparing synaptic proteomes across five mouse models for autism reveals converging molecular similarities including deficits in oxidative phosphorylation and Rho GTPase signaling. Frontiers in Aging Neuroscience. 15: 1152562
Clipperton-Allen AE, Swick H, Botero V, et al. (2022) haploinsufficiency causes desynchronized growth of brain areas involved in sensory processing. Iscience. 25: 103796
Joseph NF, Zucca A, Wingfield JL, et al. (2021) Molecular motor KIF3B in the prelimbic cortex constrains the consolidation of contextual fear memory. Molecular Brain. 14: 162
Clipperton-Allen AE, Zhang A, Cohen OS, et al. (2021) Environmental Enrichment Rescues Social Behavioral Deficits and Synaptic Abnormalities in Haploinsufficient Mice. Genes. 12
Swarnkar S, Avchalumov Y, Espadas I, et al. (2021) Molecular motor protein KIF5C mediates structural plasticity and long-term memory by constraining local translation. Cell Reports. 36: 109369
Levy JA, LaFlamme CW, Tsaprailis G, et al. (2021) Dyrk1a Mutations Cause Undergrowth of Cortical Pyramidal Neurons via Dysregulated Growth Factor Signaling. Biological Psychiatry
Huang WC, Zucca A, Levy J, et al. (2020) Social Behavior Is Modulated by Valence-Encoding mPFC-Amygdala Sub-circuitry. Cell Reports. 32: 107899
Xu ZX, Kim GH, Tan JW, et al. (2020) Elevated protein synthesis in microglia causes autism-like synaptic and behavioral aberrations. Nature Communications. 11: 1797
Clipperton-Allen AE, Page DT. (2019) Connecting Genotype with Behavioral Phenotype in Mouse Models of Autism Associated with Mutations. Cold Spring Harbor Perspectives in Medicine
Clipperton-Allen AE, Cohen OS, Aceti M, et al. (2019) Pten haploinsufficiency disrupts scaling across brain areas during development in mice. Translational Psychiatry. 9: 329
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