Richard Paylor

Baylor College of Medicine — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

70h-index21.8kcitations143works0.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(38), Neuroscience and Neuropharmacology Research(31), Memory and Neural Mechanisms(28), Receptor Mechanisms and Signaling(24), Autism Spectrum Disorder Research(22)

Publications143 total

155. Contactin-Associated Protein-Like 2 Deficiency in Juvenile Rats Recapitulates the Broad Phenotypic Spectrum in CNTNAP2-Related Disorders
Biological Psychiatry·2017
Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome
Human Molecular Genetics·2016· 66 citedOpen Access
Selective Disruption of Metabotropic Glutamate Receptor 5-Homer Interactions Mimics Phenotypes of Fragile X Syndrome in Mice
Journal of Neuroscience·2016· 54 citedOpen Access
Applying the ARRIVE Guidelines to an In Vivo Database
PLoS Biology·2015· 94 citedOpen Access
Fmr1 and Nlgn3 knockout rats: Novel tools for investigating autism spectrum disorders.
Behavioral Neuroscience·2014· 148 cited
Deficits in Adult Neurogenesis, Contextual Fear Conditioning, and Spatial Learning in a<i>Gfap</i>Mutant Mouse Model of Alexander Disease
Journal of Neuroscience·2013· 47 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
Animal Models in Psychiatric Disorders of Childhood Onset
Oxford University Press eBooks·2013
Reversal of Disease-Related Pathologies in the Fragile X Mouse Model by Selective Activation of GABA<sub>B</sub>Receptors with Arbaclofen
Science Translational Medicine·2012· 241 citedOpen Access
Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits
Human Molecular Genetics·2012· 60 citedOpen Access
Genetic background modulates behavioral impairments in R6/2 mice and suggests a role for dominant genetic modifiers in Huntington’s disease pathogenesis
Mammalian Genome·2012· 11 citedOpen Access
Neuronal aggregates are associated with phenotypic onset in the R6/2 Huntington's disease transgenic mouse
Behavioural Brain Research·2012· 14 cited
Onset and Progression of Behavioral and Molecular Phenotypes in a Novel Congenic R6/2 Line Exhibiting Intergenerational CAG Repeat Stability
PLoS ONE·2011· 20 citedOpen Access
Genetic reduction of muscarinic M4 receptor modulates analgesic response and acoustic startle response in a mouse model of fragile X syndrome (FXS)
Behavioural Brain Research·2011· 57 citedOpen Access
Mouse Genetic Models of Neurodevelopmental Disorders: Challenges and Applications
Neurotoxicology and Teratology·2011
Group I metabotropic glutamate receptor antagonists alter select behaviors in a mouse model for fragile X syndrome
Psychopharmacology·2011· 101 cited
Genetic reduction of group 1 metabotropic glutamate receptors alters select behaviors in a mouse model for fragile X syndrome
Behavioural Brain Research·2011· 73 citedOpen Access
Modulation of behavioral phenotypes by a muscarinic M1 antagonist in a mouse model of fragile X syndrome
Psychopharmacology·2011· 60 cited
Modifying behavioral phenotypes in <i>Fmr1</i>KO mice: genetic background differences reveal autistic‐like responses
Autism Research·2011· 213 citedOpen Access
The modulation of fragile X behaviors by the muscarinic M4 antagonist, tropicamide.
Behavioral Neuroscience·2011· 32 citedOpen Access
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Frequent Co-authors

Lisa A. Yuva‐Paylor(11), Corinne M. Spencer(9), Jeanne M. Wehner(8), J. David Sweatt(6), Jacqueline N. Crawley(5), Anthony Wynshaw‐Boris(4), Kellie L. McIlwain(4), Huda Y. Zoghbi(4), Susumu Tonegawa(3), Barbara Antalffy(3), Alexia M. Thomas(3), Edwin J. Weeber(3), Joel C. Selcher(3), Ekaterina Serysheva(3), Arthur L. Beaudet(3), Jerry W. Rudy(3), Shinji Hirotsune(2), Allan C. Collins(2), Alcino J. Silva(2), Jeffrey L. Noebels(2)