Corinne M. Spencer

University of Florida — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

23h-index4.4kcitations39works0.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(14), Autism Spectrum Disorder Research(10), Neuroscience and Neuropharmacology Research(8), Epigenetics and DNA Methylation(4), RNA Research and Splicing(3)

Publications39 total

Anti-CD3 microporous annealed particle hydrogel protects stem cell derived beta cells from autoreactive T cells
2025Open Access
608 Neuroimmune control of adult mammalian scarless skin regeneration
Journal of Investigative Dermatology·2021
1425 Aging suppresses skin-derived circulating SDF1 to promote full-thickness tissue regeneration
Journal of Investigative Dermatology·2018· 7 citedOpen Access
Long‐term consequences of perinatal fatty acid amino hydrolase inhibition
British Journal of Pharmacology·2013· 22 citedOpen Access
Putting Into Perspective the Use of the Fmr1 Knockout Mouse as a Model for Autism Spectrum Disorder
Oxford University Press eBooks·2013· 1 cited
GPR55, a G-Protein Coupled Receptor for Lysophosphatidylinositol, Plays a Role in Motor Coordination
PLoS ONE·2013· 112 citedOpen Access
Kv4.2 knockout mice have hippocampal-dependent learning and memory deficits
Learning & Memory·2012· 54 citedOpen Access
Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits
Human Molecular Genetics·2012· 60 citedOpen Access
Area postrema lesions attenuate LiCl-induced c-Fos expression correlated with conditioned taste aversion learning
Physiology & Behavior·2011· 32 cited
Modifying behavioral phenotypes in <i>Fmr1</i>KO mice: genetic background differences reveal autistic‐like responses
Autism Research·2011· 213 citedOpen Access
Multiple autism-like behaviors in a novel transgenic mouse model
Behavioural Brain Research·2010· 59 citedOpen Access
Altered Ultrasonic Vocalization and Impaired Learning and Memory in Angelman Syndrome Mouse Model with a Large Maternal Deletion from Ube3a to Gabrb3
PLoS ONE·2010· 172 citedOpen Access
A Mouse Model of the Human Fragile X Syndrome I304N Mutation
PLoS Genetics·2009· 138 citedOpen Access
Induced chromosome deletions cause hypersociability and other features of Williams–Beuren syndrome in mice
EMBO Molecular Medicine·2009· 106 citedOpen Access
Reversal of sensorimotor gating abnormalities in Fmr1 knockout mice carrying a human Fmr1 transgene.
Behavioral Neuroscience·2008· 46 cited
Social behavior in Fmr1 knockout mice carrying a human FMR1 transgene.
Behavioral Neuroscience·2008· 90 cited
The Brainstem Area Postrema may Not be Involved in Lithium-induced Activation of the Hypothalamic-pituitary-adrenal Axis
Experimental Neurobiology·2008· 1 cited
Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behavior
Human Molecular Genetics·2006· 58 citedOpen Access
Dynamic Translational and Proteasomal Regulation of Fragile X Mental Retardation Protein Controls mGluR-Dependent Long-Term Depression
Neuron·2006· 461 cited
<i>Tbx1</i> haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome
Proceedings of the National Academy of Sciences·2006· 381 citedOpen Access
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Frequent Co-authors

Richard Paylor(15), Lisa A. Yuva‐Paylor(9), Thomas A. Houpt(7), James Eberwine(6), Kevin Miyashiro(4), David L. Nelson(4), Olga V. Alekseyenko(3), Ekaterina Serysheva(3), Scott A. Mackler(3), Richard H. Finnell(3), Jeong Won Jahng(3), Jeffrey L. Noebels(2), Shannon Hamilton(2), Alexia M. Thomas(2), Chia‐Shan Wu(2), Chris P. Jew(2), Heather B. Bradshaw(2), Ken Mackie(2), Hui‐Chen Lu(2), Deanna Graham(2)