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Schizophrenia-Relevant Behavioral Testing in Rodent Models: A Uniquely Human Disorder?

Biological psychiatry (1969), 2006-06, Vol.59 (12), p.1198-1207

2006

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Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments

Proceedings of the National Academy of Sciences - PNAS, 2009-10, Vol.106 (42), p.17998-18003

2009

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Mum's bacteria linked to baby's behaviour

Nature (London), 2017-09, Vol.549 (7673), p.466-467

Powell, Craig M.

2017

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Effects of heterozygous deletion of autism-related gene Cullin-3 in mice

PloS one, 2023-07, Vol.18 (7), p.e0283299-e0283299

2023

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Loss of predominant Shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission

The Journal of neuroscience, 2013-11, Vol.33 (47), p.18448-18468

2013

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Increased Cortical Inhibition in Autism-Linked Neuroligin-3R451C Mice Is Due in Part to Loss of Endocannabinoid Signaling

PloS one, 2015-10, Vol.10 (10), p.e0140638-e0140638

2015

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Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior

The Journal of neuroscience, 2010-02, Vol.30 (6), p.2115-2129

2010

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A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice

Science (American Association for the Advancement of Science), 2007-10, Vol.318 (5847), p.71-76

2007

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"Déjà vu" in an autism gene mouse model modifies social mores

Neuron (Cambridge, Mass.), 2022-05, Vol.110 (9), p.1433-1435

2022

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Pharmacological Inhibition of mTORC1 Suppresses Anatomical, Cellular, and Behavioral Abnormalities in Neural-Specific Pten Knock-Out Mice

The Journal of neuroscience, 2009-02, Vol.29 (6), p.1773-1783

2009

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Autism Screening or Smoke Screen and Mirrors?

JAMA neurology, 2016-04, Vol.73 (4), p.386

Powell, Craig M

2016

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Phelan-McDermid syndrome: a classification system after 30 years of experience

Orphanet journal of rare diseases, 2022-01, Vol.17 (1), p.27-27, Article 27

2022

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Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits

The Journal of neuroscience, 2015-07, Vol.35 (26), p.9648-9665

2015

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Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism

Autism research, 2016-03, Vol.9 (3), p.350-375

2016

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Pitt-Hopkins Syndrome: A Review of Current Literature, Clinical Approach, and 23-Patient Case Series

Journal of Child Neurology, 2018-03, Vol.33 (3), p.233-244

2018

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Kctd13 deletion reduces synaptic transmission via increased RhoA

Nature (London), 2017-11, Vol.551 (7679), p.227-231

2017

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Autism risk gene Cul3 alters neuronal morphology via caspase-3 activity in mouse hippocampal neurons

Frontiers in cellular neuroscience, 2024-05, Vol.18, p.1320784-1320784

2024

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Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium

Human molecular genetics, 2022-02, Vol.31 (4), p.625-637

2022

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Systemic inhibition of mammalian target of rapamycin inhibits fear memory reconsolidation

Neurobiology of learning and memory, 2008-07, Vol.90 (1), p.28-35

2008

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Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity

The Journal of neuroscience, 2017-11, Vol.37 (45), p.10917-10931

2017

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Essential Role of Brain-Derived Neurotrophic Factor in Adult Hippocampal Function

Proceedings of the National Academy of Sciences - PNAS, 2004-07, Vol.101 (29), p.10827-10832

2004

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Aortic Root Dilation and Genotype Associations in Phelan-McDermid Syndrome

American journal of medical genetics. Part A, 2024-09, p.e63872

2024

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Enhanced Polyubiquitination of Shank3 and NMDA Receptor in a Mouse Model of Autism

Cell, 2011-05, Vol.145 (5), p.758-772

2011

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Autism-Related Neuroligin-3 Mutation Alters Social Behavior and Spatial Learning

Autism research, 2014-04, Vol.7 (2), p.264-272

2014

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Schizophrenia-Relevant Behavioral Testing in Rodent Models: A Uniquely Human Disorder?

Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments

Mum's bacteria linked to baby's behaviour

Effects of heterozygous deletion of autism-related gene Cullin-3 in mice

Loss of predominant Shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission

Increased Cortical Inhibition in Autism-Linked Neuroligin-3R451C Mice Is Due in Part to Loss of Endocannabinoid Signaling

Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior

A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice

"Déjà vu" in an autism gene mouse model modifies social mores

Pharmacological Inhibition of mTORC1 Suppresses Anatomical, Cellular, and Behavioral Abnormalities in Neural-Specific Pten Knock-Out Mice

Autism Screening or Smoke Screen and Mirrors?

Phelan-McDermid syndrome: a classification system after 30 years of experience

Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits

Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism

Pitt-Hopkins Syndrome: A Review of Current Literature, Clinical Approach, and 23-Patient Case Series

Kctd13 deletion reduces synaptic transmission via increased RhoA

Autism risk gene Cul3 alters neuronal morphology via caspase-3 activity in mouse hippocampal neurons

Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium

Systemic inhibition of mammalian target of rapamycin inhibits fear memory reconsolidation

Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity

Essential Role of Brain-Derived Neurotrophic Factor in Adult Hippocampal Function

Aortic Root Dilation and Genotype Associations in Phelan-McDermid Syndrome

Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment

Enhanced Polyubiquitination of Shank3 and NMDA Receptor in a Mouse Model of Autism

Autism-Related Neuroligin-3 Mutation Alters Social Behavior and Spatial Learning

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