(2000). Animal models of deficient sensorimotor gating: what we know, what we think we know, and what we hope to know soon.
(2004). Apomorphine-induced prepulse inhibition disruption is associated with a paradoxical enhancement of prepulse stimulus reactivity.
(2007). Atypical behaviors in children with autism and children with a history of language impairment.
(2000). Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome.
(2008). Autism-like behavioral phenotypes in BTBR T+tf/J mice.
(2006). Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP.
(1998). Autistic behavior in young boys with fragile X syndrome.
(2001). Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome.
(2004). Automated apparatus for quantitation of social approach behaviors in mice.
(2002). Behavioral characterization of the Tg2576 transgenic model of Alzheimer’s disease through 19 months.
(2002). Brain anatomy and sensorimotor gating in Asperger’s syndrome.
(2010). Brief Report: Sensorimotor Gating in Idiopathic Autism and Autism Associated with Fragile X Syndrome. J Autism Dev Disord.
CB Lithium ameliorates phenotypic deficits in a mouse model of fragile X syndrome.
(1997). Clomipramine in adults with pervasive developmental disorders: a prospective open-label investigation.
(1998). Comorbid anxiety symptoms in children with pervasive developmental disorders.
Crusio WE (2006) Fmr1 KO mice as a possible model of autistic features.
Crusio WE (2009) Strain-Dependent Changes in Acoustic Startle Response and its Plasticity Across Adolescence in Mice.
(2005). Deficits in trace fear memory and long-term potentiation in a mouse model for fragile X syndrome.
(2010). Distinguishing features of autism in boys with fragile X syndrome.
(2002). Efficacy of sensory and motor interventions for children with autism.
(2005). Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome.
(2002). Epilepsy in autism.
(2008). Evidence for social anxiety and impaired social cognition in a mouse model of fragile X syndrome.
(1994). Fmr1 knockout mice: a model to study fragile X mental retardation.
(2000). Fmr1 knockout mouse has a distinctive strain-specific learning impairment.
(2001). Fragile X mice develop sensory hyperreactivity to auditory stimuli.
(1999). Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function.
(1991). Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
(2009). Increased GABA(B) receptormediated signaling reduces the susceptibility of fragile X knockout mice to audiogenic seizures.
(2002). Knockout mouse model for Fxr2: a model for mental retardation.
(2009). Limbic epileptogenesis in a mouse model of fragile X syndrome.
(2004). Low platelet-poor plasma levels of serotonin in adult autistic patients.
(1998). Measurement of Startle Response, Prepulse Inhibition, and Habituation. Current Protocols in Neuroscience.
(1997). Mildly impaired water maze performance in male Fmr1 knockout mice.
(2007). Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X.
(2007). Mouse behavioral assays relevant to the symptoms of autism.
(2006). Mouse models of autism spectrum disorders: the challenge for behavioral genetics.
(2009). Mouse neurexin1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.
(2010). Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior.
(2008). Nonphysical contact between cagemates alleviates the social isolation syndrome in C57BL/6 male mice.
(2004). Object recognition impairment in Fmr1 knockout mice is reversed by amphetamine: involvement of dopamine in the medial prefrontal cortex.
(2005). On the feasibility to detect and to quantify prepulse-elicited reaction in prepulse inhibition of the acoustic startle reflex in humans.
(2008). On the influence of baseline startle reactivity on the indexation of prepulse inhibition.
(1993). Ontogeny of amicable social behavior in the mouse: gender differences and ongoing isolation outcomes.
(2008). Reduced ultrasonic vocalizations in vasopressin 1b knockout mice.
(2008). Rescue of behavioral phenotype and neuronal protrusion morphology
(1996). Reunion of separated sibling mice: neurobiological and behavioral aspects.
(1997). Risperidone and explosive aggressive autism.
(1998). Risperidone for young children with mood disorders and aggressive behavior.
(2005). Rodent models for autism. a critical review. Drug discovery today: Disease models 2:
(2003). Self-injurious behavior in young boys with fragile X syndrome.
(2004). Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice.
(2004). Sociability and preference for social novelty in five inbred strains: an approach to assess autisticlike behavior in mice.
(2006). Social behavior deficits in the Fmr1 mutant mouse.
(2000). Spatial learning, contextual fear conditioning and conditioned emotional response in Fmr1 knockout mice.
(1982). Spontaneous paroxysmal electroclinical patterns in rat: a model of generalized non-convulsive epilepsy.
(1993). Startle modulation studies in autism.
(2005). Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP.
(2001). Synaptic regulation of protein synthesis and the fragile X protein.
(2001). The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.
(1994). The Dutch-Belgian Fragile X Consortium
(2004). The effects of dizocilpine and phencyclidine on prepulse inhibition of the acoustic startle reflex and on prepulse-elicited reactivity in C57BL6 mice.
(2005). The expression of prepulse inhibition of the acoustic startle reflex as a function of three pulse stimulus intensities, three prepulse stimulus intensities, and three levels of startle responsiveness in C57BL6/J mice.
(2008). The postweaning social isolation in C57BL/6 mice: preferential vulnerability in the male sex.
(2008). The value of incomplete mouse models of Alzheimer’s disease.
(2004). The value of spontaneous alternation behavior (SAB) as a test of retention in pharmacological investigations of memory.
(2006). Time to give up on a single explanation for autism.
(2000). Ultrasonic vocalization by female mice in the presence of a conspecific carrying food cues.
(2008). Unusual repertoire of vocalizations in the BTBR T+tf/J mouse model of autism.
(2008). Wild-type male offspring of fmr-1+/- mothers exhibit characteristics of the fragile X phenotype.