Translational animal models of autism and neurodevelopmental disorders

Autism is a neurodevelopmental disorder whose diagnosis is based on three behavioral criteria: unusual reciprocal social interactions, deficits in communication, and stereotyped repetitive behaviors with restricted interests. A large number of de novo single gene mutations and chromosomal deletions are associated with autism spectrum disorders. Based on the strong genetic evidence, mice with targeted mutations in homologous genes have been generated as translational research tools. Mouse models of autism have revealed behavioral and biological outcomes of mutations in risk genes. The field is now poised to employ the most robust phenotypes in the most replicable mouse models for preclinical screening of novel therapeutics.

[1]  D. Geschwind,et al.  Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits , 2011, Cell.

[2]  R. Paylor,et al.  Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety , 2009, Psychopharmacology.

[3]  T. Holy,et al.  Ultrasonic Songs of Male Mice , 2005, PLoS biology.

[4]  M. Sahin,et al.  Clinical Presentation and Diagnosis of Tuberous Sclerosis Complex in Infancy , 2008, Journal of child neurology.

[5]  M. Mishkin,et al.  Long-term effects of neonatal medial temporal ablations on socioemotional behavior in monkeys (Macaca mulatta). , 2010, Behavioral neuroscience.

[6]  L. Lee,et al.  Changes in autism spectrum disorder prevalence in 4 areas of the United States. , 2010, Disability and health journal.

[7]  Kenny Q. Ye,et al.  Strong Association of De Novo Copy Number Mutations with Autism , 2007, Science.

[8]  R. D'Hooge,et al.  Restoring the phenotype of fragile X syndrome: insight from the mouse model. , 2001, Current molecular medicine.

[9]  Thomas C. Südhof,et al.  Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function , 2011, Proceedings of the National Academy of Sciences.

[10]  S. Moshé,et al.  Convulsing toward the pathophysiology of autism , 2009, Brain and Development.

[11]  Y. Takai,et al.  SAPAPs. A family of PSD-95/SAP90-associated proteins localized at postsynaptic density. , 1997, The Journal of biological chemistry.

[12]  Robert P. Carson,et al.  Neuronal and glia abnormalities in Tsc1-deficient forebrain and partial rescue by rapamycin , 2012, Neurobiology of Disease.

[13]  K. Mirnics,et al.  Maternal Immune Activation Alters Fetal Brain Development through Interleukin-6 , 2007, The Journal of Neuroscience.

[14]  Alcino J. Silva,et al.  Reversal of learning deficits in a Tsc2+/− mouse model of tuberous sclerosis , 2008, Nature Medicine.

[15]  Jacqueline N. Crawley,et al.  Unusual Repertoire of Vocalizations in the BTBR T+tf/J Mouse Model of Autism , 2008, PloS one.

[16]  Edward S. Brodkin,et al.  BALB/c mice: Low sociability and other phenotypes that may be relevant to autism , 2007, Behavioural Brain Research.

[17]  T. Insel,et al.  Infant Vocalization, Adult Aggression, and Fear Behavior of an Oxytocin Null Mutant Mouse , 2000, Hormones and Behavior.

[18]  Zachary Warren,et al.  A multisite study of the clinical diagnosis of different autism spectrum disorders. , 2012, Archives of general psychiatry.

[19]  G. Lynch,et al.  Brain-Derived Neurotrophic Factor Rescues Synaptic Plasticity in a Mouse Model of Fragile X Syndrome , 2007, The Journal of Neuroscience.

[20]  L. Kanner Child psychiatry; mental deficiency. , 1946, The American journal of psychiatry.

[21]  Ben A. Oostra,et al.  Absence of expression of the FMR-1 gene in fragile X syndrome , 1991, Cell.

[22]  M. Sahin,et al.  Translational research: Rett syndrome and tuberous sclerosis complex , 2011, Current opinion in pediatrics.

[23]  J. N. Crawley,et al.  Unusual repertoire of vocalizations in adult BTBR T+tf/J mice during three types of social encounters , 2011, Genes, brain, and behavior.

[24]  Jacqueline N. Crawley,et al.  Autism-Relevant Social Abnormalities and Cognitive Deficits in Engrailed-2 Knockout Mice , 2012, PloS one.

[25]  J. Rabe-Jabłońska,et al.  [Affective disorders in the fourth edition of the classification of mental disorders prepared by the American Psychiatric Association -- diagnostic and statistical manual of mental disorders]. , 1993, Psychiatria polska.

[26]  C. Lord,et al.  Behavioural phenotyping assays for mouse models of autism , 2010, Nature Reviews Neuroscience.

[27]  Johannes Schwarz,et al.  A Humanized Version of Foxp2 Affects Cortico-Basal Ganglia Circuits in Mice , 2009, Cell.

[28]  W. M. Fox Reflex-ontogeny and behavioural development of the mouse. , 1965, Animal behaviour.

[29]  H. Faras,et al.  Autism spectrum disorders , 2010, Annals of Saudi medicine.

[30]  Maria Luisa Scattoni,et al.  Ultrasonic vocalizations: A tool for behavioural phenotyping of mouse models of neurodevelopmental disorders , 2009, Neuroscience & Biobehavioral Reviews.

[31]  W. Spooren,et al.  The effect of the mGlu5 receptor antagonist MPEP in rodent tests of anxiety and cognition: a comparison , 2005, Psychopharmacology.

[32]  H. Asperger,et al.  Die „Autistischen Psychopathen” im Kindesalter , 1944, Archiv für Psychiatrie und Nervenkrankheiten.

[33]  Jacqueline N. Crawley,et al.  Mouse behavioral tasks relevant to autism: Phenotypes of 10 inbred strains , 2007, Behavioural Brain Research.

[34]  J. Hutsler,et al.  Increased dendritic spine densities on cortical projection neurons in autism spectrum disorders , 2010, Brain Research.

[35]  J. Darnell,et al.  Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome , 2001, Cell.

[36]  Russell S. Kirby,et al.  Socioeconomic Inequality in the Prevalence of Autism Spectrum Disorder: Evidence from a U.S. Cross-Sectional Study , 2010, PloS one.

[37]  Todd H. Ahern,et al.  Evaluation of two automated metrics for analyzing partner preference tests , 2009, Journal of Neuroscience Methods.

[38]  J. Crawley,et al.  Simple Behavioral Assessment of Mouse Olfaction , 2009, Current protocols in neuroscience.

[39]  Valerie J. Bolivar,et al.  Expression of social behaviors of C57BL/6J versus BTBR inbred mouse strains in the visible burrow system , 2010, Behavioural Brain Research.

[40]  J. Crawley,et al.  Postnatal lesion evidence against a primary role for the corpus callosum in mouse sociability , 2009, The European journal of neuroscience.

[41]  Geraldine Dawson,et al.  Behavioral interventions in children and adolescents with autism spectrum disorder: a review of recent findings , 2011, Current opinion in pediatrics.

[42]  Joseph D. Buxbaum,et al.  Multiple rare variants in the etiology of autism spectrum disorders , 2009, Dialogues in clinical neuroscience.

[43]  Shiaoching Gong,et al.  Minimal aberrant behavioral phenotypes of neuroligin‐3 R451C knockin mice , 2008, Autism research : official journal of the International Society for Autism Research.

[44]  Jacqueline N. Crawley,et al.  Social approach behaviors in oxytocin knockout mice: Comparison of two independent lines tested in different laboratory environments , 2007, Neuropeptides.

[45]  Mark J. Harris,et al.  Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication , 2010, Molecular autism.

[46]  Kathryn Roeder,et al.  Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism , 2011, Neuron.

[47]  M. Greenberg,et al.  Brain-Derived Neurotrophic Factor Expression and Respiratory Function Improve after Ampakine Treatment in a Mouse Model of Rett Syndrome , 2007, The Journal of Neuroscience.

[48]  Wei Zhang,et al.  Pharmacological Inhibition of mTORC1 Suppresses Anatomical, Cellular, and Behavioral Abnormalities in Neural-Specific Pten Knock-Out Mice , 2009, The Journal of Neuroscience.

[49]  Larry J. Young,et al.  The prairie vole: an emerging model organism for understanding the social brain , 2010, Trends in Neurosciences.

[50]  Jens Frahm,et al.  Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism , 2008, Proceedings of the National Academy of Sciences.

[51]  K. Brennand,et al.  EMBRYONIC STEM CELLS / INDUCED PLURIPOTENT STEM CELLS Concise Review : The Promise of Human Induced Pluripotent Stem Cell-Based Studies of Schizophrenia , 2011 .

[52]  宁北芳,et al.  疟原虫var基因转换速率变化导致抗原变异[英]/Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A , 2005 .

[53]  Thomas Bourgeron,et al.  Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism , 2003, Nature Genetics.

[54]  F. Goodwin,et al.  Preliminary report of a simple animal behavior model for the anxiolytic effects of benzodiazepines , 1980, Pharmacology Biochemistry and Behavior.

[55]  D. Amaral,et al.  Emergence of Stereotypies in Juvenile Monkeys (macaca Mulatta) with Neonatal Amygdala or Hippocampus Lesions , 2022 .

[56]  J. Silverman,et al.  Automated Three‐Chambered Social Approach Task for Mice , 2011, Current protocols in neuroscience.

[57]  P. Curatolo,et al.  Long-term neurological outcome in children with early-onset epilepsy associated with tuberous sclerosis , 2011, Epilepsy & Behavior.

[58]  D. Amaral,et al.  The Development of Social Behavior Following Neonatal Amygdala Lesions in Rhesus Monkeys , 2004, Journal of Cognitive Neuroscience.

[59]  Boris Yamrom,et al.  Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders , 2011, Neuron.

[60]  T. Miyakawa,et al.  Comprehensive Behavioral Phenotyping of Ryanodine Receptor type 3 (RyR3) Knockout Mice: Decreased Social Contact Duration in Two Social Interaction Tests , 2009, Front. Behav. Neurosci..

[61]  G. Lynch,et al.  The likelihood of cognitive enhancement , 2011, Pharmacology Biochemistry and Behavior.

[62]  D. Lawrence,et al.  Aberrant Immune Responses in a Mouse with Behavioral Disorders , 2011, PloS one.

[63]  J. Sebat,et al.  Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. , 2008, American journal of human genetics.

[64]  T. Südhof,et al.  Increased anxiety‐like behavior in mice lacking the inhibitory synapse cell adhesion molecule neuroligin 2 , 2009, Genes, brain, and behavior.

[65]  R. Nonneman,et al.  Social approach and repetitive behavior in eleven inbred mouse strains , 2008, Behavioural Brain Research.

[66]  C. Rice Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006. , 2009, Morbidity and mortality weekly report. Surveillance summaries.

[67]  J. Crawley Mouse Behavioral Assays Relevant to the Symptoms of Autism * , 2007, Brain pathology.

[68]  Jacqueline N. Crawley,et al.  Social deficits in BTBR T + tf/J mice are unchanged by cross-fostering with C57BL/6J mothers , 2007, International Journal of Developmental Neuroscience.

[69]  Michael E. Ragozzino,et al.  Differences in BTBR T+ tf/J and C57BL/6J mice on probabilistic reversal learning and stereotyped behaviors , 2012, Behavioural Brain Research.

[70]  J. Crawley Exploratory behavior models of anxiety in mice , 1985, Neuroscience & Biobehavioral Reviews.

[71]  N. Harada,et al.  Sexual Partner Preference Requires a Functional Aromatase (Cyp19) Gene in Male Mice , 2002, Hormones and Behavior.

[72]  W. Young,et al.  Vasopressin 1a receptor knockout mice have a subtle olfactory deficit but normal aggression , 2007, Genes, brain, and behavior.

[73]  J. Lauterborn,et al.  Fragile X syndrome and targeted treatment trials. , 2012, Results and problems in cell differentiation.

[74]  Hewlet G McFarlane,et al.  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 , 2007, Frontiers in behavioral neuroscience.

[75]  Heather C Whalley,et al.  Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals , 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[76]  S. Rogers,et al.  Annotation: what do we know about sensory dysfunction in autism? A critical review of the empirical evidence. , 2005, Journal of child psychology and psychiatry, and allied disciplines.

[77]  Joseph T. Glessner,et al.  A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder , 2011, Human Genetics.

[78]  Edwin H. Cook,et al.  Copy-number variations associated with neuropsychiatric conditions , 2008, Nature.

[79]  D. Blanchard,et al.  A new test paradigm for social recognition evidenced by urinary scent marking behavior in C57BL/6J mice , 2008, Behavioural Brain Research.

[80]  K. Miczek,et al.  Aggressive behavioral phenotypes in mice , 2001, Behavioural Brain Research.

[81]  Mark F. Bear,et al.  Correction of Fragile X Syndrome in Mice , 2007, Neuron.

[82]  Takeshi Sakurai,et al.  The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders , 2009, Trends in Neurosciences.

[83]  Y. Jan,et al.  Altered ultrasonic vocalizations in a tuberous sclerosis mouse model of autism , 2010, Proceedings of the National Academy of Sciences.

[84]  G. Baird,et al.  Commentary: Effects of diagnostic thresholds and research vs service and administrative diagnosis on autism prevalence. , 2009, International journal of epidemiology.

[85]  G. Laviola,et al.  Scoring of Social Interactions and Play in Mice During Adolescence , 2005, Current protocols in toxicology.

[86]  J. Piven,et al.  Autism Spectrum Disorders in Older Adults: Toward Defining a Research Agenda , 2011, Journal of the American Geriatrics Society.

[87]  I. Lucki,et al.  The spectrum of behaviors influenced by serotonin , 1998, Biological Psychiatry.

[88]  Larry J Young,et al.  Profound Impairment in Social Recognition and Reduction in Anxiety-Like Behavior in Vasopressin V1a Receptor Knockout Mice , 2004, Neuropsychopharmacology.

[89]  H. McFarlane,et al.  Autism‐like behavioral phenotypes in BTBR T+tf/J mice , 2008, Genes, brain, and behavior.

[90]  J. Crawley,et al.  Social deficits, stereotypy and early emergence of repetitive behavior in the C58/J inbred mouse strain , 2010, Behavioural Brain Research.

[91]  T. Südhof,et al.  Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior , 2010, The Journal of Neuroscience.

[92]  Carlos S. Moreno,et al.  Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes , 2011, PLoS genetics.

[93]  Mark F. Bear,et al.  Mutations causing syndromic autism define an axis of synaptic pathophysiology , 2011, Nature.

[94]  Jacqueline N. Crawley,et al.  Negative Allosteric Modulation of the mGluR5 Receptor Reduces Repetitive Behaviors and Rescues Social Deficits in Mouse Models of Autism , 2012, Science Translational Medicine.

[95]  T. Südhof Neuroligins and neurexins link synaptic function to cognitive disease , 2008, Nature.

[96]  Thomas Bourgeron,et al.  A synaptic trek to autism , 2009, Current Opinion in Neurobiology.

[97]  V. Bolivar,et al.  Oxytocin receptor knockout mice display deficits in the expression of autism-related behaviors , 2012, Hormones and Behavior.

[98]  Steven J. Siegel,et al.  mGluR5-Antagonist Mediated Reversal of Elevated Stereotyped, Repetitive Behaviors in the VPA Model of Autism , 2011, PloS one.

[99]  M. Sur,et al.  Haploinsufficiency for Pten and Serotonin transporter cooperatively influences brain size and social behavior , 2009, Proceedings of the National Academy of Sciences.

[100]  Huilin Li,et al.  The Postsynaptic Density Proteins Homer and Shank Form a Polymeric Network Structure , 2009, Cell.

[101]  T. Lanthorn,et al.  Male and female Fmr1 knockout mice on C57 albino background exhibit spatial learning and memory impairments , 2010, Genes, brain, and behavior.

[102]  J. Crawley,et al.  Absence of preference for social novelty and increased grooming in integrin β3 knockout mice: Initial studies and future directions , 2011, Autism research : official journal of the International Society for Autism Research.

[103]  M. Wöhr,et al.  Reduced scent marking and ultrasonic vocalizations in the BTBR T+tf/J mouse model of autism , 2011, Genes, brain, and behavior.

[104]  Mark F. Bear,et al.  Altered synaptic plasticity in a mouse model of fragile X mental retardation , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[105]  Michael P. Stryker,et al.  Reversing Neurodevelopmental Disorders in Adults , 2008, Neuron.

[106]  B. Manning,et al.  A complex interplay between Akt, TSC2 and the two mTOR complexes. , 2009, Biochemical Society transactions.

[107]  T. Rubino,et al.  Pharmacologic Rescue of Impaired Cognitive Flexibility, Social Deficits, Increased Aggression, and Seizure Susceptibility in Oxytocin Receptor Null Mice: A Neurobehavioral Model of Autism , 2011, Biological Psychiatry.

[108]  Jacqueline N. Crawley,et al.  Sociability and motor functions in Shank1 mutant mice , 2011, Brain Research.

[109]  R. Landa,et al.  Diagnosis of autism spectrum disorders in the first 3 years of life , 2008, Nature Clinical Practice Neurology.

[110]  Valerie J. Bolivar,et al.  Assessing autism-like behavior in mice: Variations in social interactions among inbred strains , 2007, Behavioural Brain Research.

[111]  David G. Amaral,et al.  Stereotypies and hyperactivity in rhesus monkeys exposed to IgG from mothers of children with autism , 2008, Brain, Behavior, and Immunity.

[112]  G. Feng,et al.  Shank3 mutant mice display autistic-like behaviours and striatal dysfunction , 2011, Nature.

[113]  P. LoRusso,et al.  Targeting phosphatidylinositol 3 kinase (PI3K)-Akt beyond rapalogs , 2011, Targeted Oncology.

[114]  S. Tonegawa,et al.  Inhibition of p21-activated kinase rescues symptoms of fragile X syndrome in mice , 2007, Proceedings of the National Academy of Sciences.

[115]  Garet P. Lahvis,et al.  Affiliative Behavior, Ultrasonic Communication and Social Reward Are Influenced by Genetic Variation in Adolescent Mice , 2007, PloS one.

[116]  D. Wesson,et al.  Enhanced urinary odor discrimination in female aromatase knockout (ArKO) mice , 2006, Hormones and Behavior.

[117]  Alcino J. Silva,et al.  Adult reversal of cognitive phenotypes in neurodevelopmental disorders , 2009, Journal of Neurodevelopmental Disorders.

[118]  Luigi Boccuto,et al.  Association between deletion size and important phenotypes expands the genomic region of interest in Phelan–McDermid syndrome (22q13 deletion syndrome) , 2011, Journal of Medical Genetics.

[119]  T. Insel,et al.  Oxytocin and Social Bonding a , 1992, Annals of the New York Academy of Sciences.

[120]  R. Hagerman,et al.  Fragile X: Leading the way for targeted treatments in autism , 2010, Neurotherapeutics.

[121]  J. Crawley,et al.  Social transmission of food preference in mice: methodology and application to galanin-overexpressing transgenic mice. , 2003, Behavioral neuroscience.

[122]  M. State,et al.  The genetics of autism: key issues, recent findings, and clinical implications. , 2010, The Psychiatric clinics of North America.

[123]  J. Buxbaum,et al.  Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[124]  M. Sheng,et al.  The Shank family of scaffold proteins. , 2000, Journal of cell science.

[125]  Timothy M. DeLorey,et al.  Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: A potential model of autism spectrum disorder , 2008, Behavioural Brain Research.

[126]  P. Penzes,et al.  Dendritic spine pathology in neuropsychiatric disorders , 2011, Nature Neuroscience.

[127]  D C Blanchard,et al.  Motor and cognitive stereotypies in the BTBR T+tf/J mouse model of autism , 2011, Genes, brain, and behavior.

[128]  A. Beaudet,et al.  Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3. , 2011, Human molecular genetics.

[129]  Jack W. Tsao,et al.  What's wrong with my mouse: Behavioral phenotyping of transgenic and knockout mice, J. Crawley. Wiley-Interscience, Hoboken, NJ (2007), 523 pages, $99.95 , 2008 .

[130]  Matthew P. Anderson,et al.  Increased Gene Dosage of Ube3a Results in Autism Traits and Decreased Glutamate Synaptic Transmission in Mice , 2011, Science Translational Medicine.

[131]  G. Martins,et al.  Loss of Embryonic MET Signaling Alters Profiles of Hippocampal Interneurons , 2006, Developmental Neuroscience.

[132]  J. Frahm,et al.  Neuroligin‐3‐deficient mice: model of a monogenic heritable form of autism with an olfactory deficit , 2009, Genes, brain, and behavior.

[133]  Jill L Silverman,et al.  Repetitive Self-Grooming Behavior in the BTBR Mouse Model of Autism is Blocked by the mGluR5 Antagonist MPEP , 2010, Neuropsychopharmacology.

[134]  Ami Klin,et al.  Autism and autism spectrum disorders: diagnostic issues for the coming decade. , 2009, Journal of child psychology and psychiatry, and allied disciplines.

[135]  M. Hofer,et al.  Ultrasonic vocalization, laryngeal braking, and thermogenesis in rat pups: a reappraisal. , 1993, Behavioral neuroscience.

[136]  Wim E. Crusio,et al.  Social behavior deficits in the Fmr1 mutant mouse , 2006, Behavioural Brain Research.

[137]  M. Chiappalone,et al.  Importance of Shank3 Protein in Regulating Metabotropic Glutamate Receptor 5 (mGluR5) Expression and Signaling at Synapses , 2011, The Journal of Biological Chemistry.

[138]  S. Bryson,et al.  Clinical Assessment and Management of Toddlers With Suspected Autism Spectrum Disorder: Insights From Studies of High-Risk Infants , 2009, Pediatrics.

[139]  H. Zoghbi,et al.  Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome. , 2005, Human molecular genetics.

[140]  C. McDougle,et al.  Pharmacologic Treatment of Behavioral Symptoms Associated With Autism and Other Pervasive Developmental Disorders , 2010, Current treatment options in neurology.

[141]  W. Young,et al.  Normal maternal behavior, but increased pup mortality, in conditional oxytocin receptor knockout females. , 2010, Behavioral neuroscience.

[142]  H. Zoghbi Rett syndrome: what do we know for sure? , 2009, Nature Neuroscience.

[143]  E. C. Grant,et al.  A comparison of the social postures of some common laboratory rodents. , 1963 .

[144]  X. Cui,et al.  Targeted integration in rat and mouse embryos with zinc-finger nucleases , 2011, Nature Biotechnology.

[145]  Mark F Bear,et al.  Toward fulfilling the promise of molecular medicine in fragile X syndrome. , 2011, Annual review of medicine.

[146]  Mariko Y Momoi,et al.  Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells , 2008, Proceedings of the National Academy of Sciences.

[147]  P. Hagerman,et al.  Fragile X and autism: Intertwined at the molecular level leading to targeted treatments , 2010, Molecular autism.

[148]  J. Crawley,et al.  Olfactory cues are sufficient to elicit social approach behaviors but not social transmission of food preference in C57BL/6J mice , 2008, Behavioural Brain Research.

[149]  S. Horvath,et al.  Transcriptomic Analysis of Autistic Brain Reveals Convergent Molecular Pathology , 2011, Nature.

[150]  G. Lynch,et al.  Physiological Activation of Synaptic Rac>PAK (p-21 Activated Kinase) Signaling Is Defective in a Mouse Model of Fragile X Syndrome , 2010, The Journal of Neuroscience.

[151]  J. Piven,et al.  Automated apparatus for quantitation of social approach behaviors in mice , 2004, Genes, brain, and behavior.

[152]  J. Yeomans,et al.  Ultrasonic Vocalizations Induced by Sex and Amphetamine in M2, M4, M5 Muscarinic and D2 Dopamine Receptor Knockout Mice , 2008, PloS one.

[153]  D. Mav,et al.  Low-level neonatal thimerosal exposure: further evaluation of altered neurotoxic potential in SJL mice. , 2008, Toxicological sciences : an official journal of the Society of Toxicology.

[154]  E. Fombonne Epidemiology of Pervasive Developmental Disorders , 2009, Pediatric Research.

[155]  Kiyoshi Inoue,et al.  Abnormal Behavior in a Chromosome- Engineered Mouse Model for Human 15q11-13 Duplication Seen in Autism , 2009, Cell.

[156]  J. Sutcliffe,et al.  Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox , 1991, Cell.

[157]  J. Crawley Designing mouse behavioral tasks relevant to autistic-like behaviors. , 2004, Mental Retardation and Developmental Disabilities Research Reviews.