Translational animal models of autism and neurodevelopmental disorders
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[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.