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Unusual repertoire of vocalizations in the BTBR T+tf/J mouse model of autism

PloS one, 2008-08, Vol.3 (8), p.e3067-e3067

2008

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Behavioral Abnormalities and Circuit Defects in the Basal Ganglia of a Mouse Model of 16p11.2 Deletion Syndrome

Cell reports (Cambridge), 2014-05, Vol.7 (4), p.1077-1092

2014

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Communication impairments in mice lacking Shank1: reduced levels of ultrasonic vocalizations and scent marking behavior

PloS one, 2011-06, Vol.6 (6), p.e20631-e20631

2011

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Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice

PloS one, 2012-07, Vol.7 (7), p.e40914-e40914

2012

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Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior

Proceedings of the National Academy of Sciences - PNAS, 2012-04, Vol.109 (14), p.5469-5474

2012

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Twenty years of discoveries emerging from mouse models of autism

Neuroscience and biobehavioral reviews, 2023-03, Vol.146, p.105053-105053, Article 105053

Crawley, Jacqueline N.

2023

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Behavioral Phenotyping Strategies for Mutant Mice

Neuron (Cambridge, Mass.), 2008-03, Vol.57 (6), p.809-818

Crawley, Jacqueline N.

2008

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Mouse Behavioral Assays Relevant to the Symptoms of Autism

Brain pathology (Zurich, Switzerland), 2007-10, Vol.17 (4), p.448-459

Crawley, Jacqueline N.

2007

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Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

Molecular autism, 2010-12, Vol.1 (1), p.15-15, Article 15

2010

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Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism

Molecular autism, 2017-06, Vol.8 (1), p.26-26, Article 26

2017

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Translational animal models of autism and neurodevelopmental disorders

Dialogues in clinical neuroscience, 2012-09, Vol.14 (3), p.293-305

Crawley, Jacqueline N.

2012

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Male mice emit distinct ultrasonic vocalizations when the female leaves the social interaction arena

Frontiers in behavioral neuroscience, 2013-11, Vol.7, p.159-159

2013

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SynDIG4/Prrt1 Is Required for Excitatory Synapse Development and Plasticity Underlying Cognitive Function

Cell reports (Cambridge), 2018-02, Vol.22 (9), p.2246-2253

2018

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Preclinical research in Rett syndrome: setting the foundation for translational success

Disease models & mechanisms, 2012-11, Vol.5 (6), p.733-745

2012

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Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism

Neurotherapeutics, 2015-07, Vol.12 (3), p.521-533

2015

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Behavioural phenotyping assays for mouse models of autism

Nature reviews. Neuroscience, 2010-07, Vol.11 (7), p.490-502

2010

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Behavioral Evaluation of Angelman Syndrome Mice at Older Ages

Neuroscience, 2020-10, Vol.445, p.163-171

2020

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Hippocampal Transcriptomic and Proteomic Alterations in the BTBR Mouse Model of Autism Spectrum Disorder

Frontiers in physiology, 2015-11, Vol.6, p.324-324

2015

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Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice

Nature (London), 2012-08, Vol.488 (7413), p.647-651

2012

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Simple behavioral assessment of mouse olfaction

Current protocols in neuroscience, 2009-07, Vol.Chapter 8, p.Unit 8.24

2009

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Autism and Cancer Share Risk Genes, Pathways, and Drug Targets

Trends in genetics, 2016-03, Vol.32 (3), p.139-146

2016

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Automated three-chambered social approach task for mice

Current protocols in neuroscience, 2011-07, Vol.Chapter 8, p.Unit 8.26

2011

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Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome

Nature reviews. Drug discovery, 2018-04, Vol.17 (4), p.280

2018

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Repetitive Self-Grooming Behavior in the BTBR Mouse Model of Autism is Blocked by the mGluR5 Antagonist MPEP

Neuropsychopharmacology (New York, N.Y.), 2010-03, Vol.35 (4), p.976-989

2010

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Progressive behavioral deficits in DJ-1 -deficient mice are associated with normal nigrostriatal function

Neurobiology of disease, 2008-03, Vol.29 (3), p.505-514

2008

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Unusual repertoire of vocalizations in the BTBR T+tf/J mouse model of autism

Behavioral Abnormalities and Circuit Defects in the Basal Ganglia of a Mouse Model of 16p11.2 Deletion Syndrome

Communication impairments in mice lacking Shank1: reduced levels of ultrasonic vocalizations and scent marking behavior

Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice

Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior

Twenty years of discoveries emerging from mouse models of autism

Behavioral Phenotyping Strategies for Mutant Mice

Mouse Behavioral Assays Relevant to the Symptoms of Autism

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism

Translational animal models of autism and neurodevelopmental disorders

Male mice emit distinct ultrasonic vocalizations when the female leaves the social interaction arena

SynDIG4/Prrt1 Is Required for Excitatory Synapse Development and Plasticity Underlying Cognitive Function

Preclinical research in Rett syndrome: setting the foundation for translational success

Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism

Behavioural phenotyping assays for mouse models of autism

Behavioral Evaluation of Angelman Syndrome Mice at Older Ages

Hippocampal Transcriptomic and Proteomic Alterations in the BTBR Mouse Model of Autism Spectrum Disorder

Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice

Simple behavioral assessment of mouse olfaction

Autism and Cancer Share Risk Genes, Pathways, and Drug Targets

Automated three-chambered social approach task for mice

Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome

Repetitive Self-Grooming Behavior in the BTBR Mouse Model of Autism is Blocked by the mGluR5 Antagonist MPEP

Progressive behavioral deficits in DJ-1 -deficient mice are associated with normal nigrostriatal function

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