| scholarly article | Q13442814 |
| P50 | author | Robert Malenka | Q16731868 |
| Brad A. Grueter | Q42822736 | ||
| Gül Dölen | Q57513534 | ||
| Georgia Panagiotakos | Q91171869 | ||
| Ricardo E Dolmetsch | Q92200942 | ||
| Thomas Portmann | Q120647496 | ||
| Jason Lerch | Q33276631 | ||
| P2093 | author name string | Mu Yang | |
| Michael A Miller | |||
| Mehrdad Shamloo | |||
| Jacob Ellegood | |||
| Rong Mao | |||
| Jacqueline N Crawley | |||
| Mark Henkelman | |||
| Katherine Clifford | |||
| Carleton Goold | |||
| Darren Loureiro | |||
| David Kalikhman | |||
| Elaine Fisher | |||
| Nay L Saw | |||
| Patrick L Bader | |||
| Pavitra Rengarajan | |||
| Zhou Zhengqui | |||
| P2860 | cites work | Advances in autism genetics: on the threshold of a new neurobiology | Q22251023 |
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| The prevalence of autism | Q28198161 | ||
| Thresholding of statistical maps in functional neuroimaging using the false discovery rate | Q28208414 | ||
| Prevalence of autism-spectrum conditions: UK school-based population study | Q28246681 | ||
| Association between microdeletion and microduplication at 16p11.2 and autism | Q28264205 | ||
| Npas4: a neuronal transcription factor with a key role in social and cognitive functions relevant to developmental disorders | Q28389182 | ||
| Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism | Q35345720 | ||
| Thy1-hAPP(Lond/Swe+) mouse model of Alzheimer's disease displays broad behavioral deficits in sensorimotor, cognitive and social function | Q35937214 | ||
| KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant | Q36004324 | ||
| D1 receptor modulation of action potential firing in a subpopulation of layer 5 pyramidal neurons in the prefrontal cortex | Q36193930 | ||
| Towards the classification of subpopulations of layer V pyramidal projection neurons | Q36423401 | ||
| Gain control by layer six in cortical circuits of vision | Q36797150 | ||
| Simple behavioral assessment of mouse olfaction | Q37365567 | ||
| A Cre/loxP-deleter transgenic line in mouse strain 129S1/SvImJ. | Q40744891 | ||
| Origin and molecular specification of striatal interneurons. | Q41753651 | ||
| Distinct roles for direct and indirect pathway striatal neurons in reinforcement. | Q41894840 | ||
| Origin and molecular specification of globus pallidus neurons | Q42467736 | ||
| Endocannabinoid-mediated rescue of striatal LTD and motor deficits in Parkinson's disease models | Q42508054 | ||
| The asparaginyl endopeptidase legumain after experimental stroke | Q42575403 | ||
| Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder | Q44735745 | ||
| Dopamine increases the gain of the input-output response of rat prefrontal pyramidal neurons | Q46653916 | ||
| Quantitative morphology of the corpus callosum in attention deficit hyperactivity disorder | Q48127289 | ||
| Mouse behavioral mutants have neuroimaging abnormalities | Q48201375 | ||
| Survey of 21 inbred mouse strains in two laboratories reveals that BTBR T/+ tf/tf has severely reduced hippocampal commissure and absent corpus callosum | Q48337652 | ||
| Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. | Q50341332 | ||
| Laminar and areal expression of unc5d and its role in cortical cell survival. | Q53276944 | ||
| Semaphorin 3E-Plexin-D1 signaling controls pathway-specific synapse formation in the striatum | Q28506348 | ||
| Neuronal subtype-specific genes that control corticospinal motor neuron development in vivo | Q28507231 | ||
| SOX5 controls the sequential generation of distinct corticofugal neuron subtypes | Q28508706 | ||
| The cortical subventricular zone-specific molecule Svet1 is part of the nuclear RNA coded by the putative netrin receptor gene Unc5d and is expressed in multipolar migrating cells | Q28509542 | ||
| Sociability and motor functions in Shank1 mutant mice | Q28592494 | ||
| Ctip2 controls the differentiation of medium spiny neurons and the establishment of the cellular architecture of the striatum | Q28593246 | ||
| Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size | Q29544005 | ||
| Autism spectrum disorders: developmental disconnection syndromes | Q29616818 | ||
| A gene expression atlas of the central nervous system based on bacterial artificial chromosomes | Q29617753 | ||
| Automated three-chambered social approach task for mice | Q30381493 | ||
| Comprehensive behavioral phenotyping of Ts65Dn mouse model of Down syndrome: activation of β1-adrenergic receptor by xamoterol as a potential cognitive enhancer | Q30459302 | ||
| Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice | Q30461096 | ||
| Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice | Q30465549 | ||
| Mouse model of Timothy syndrome recapitulates triad of autistic traits. | Q30474075 | ||
| Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice | Q30488800 | ||
| Postsynaptic TRPV1 triggers cell type–specific long-term depression in the nucleus accumbens | Q30500199 | ||
| Response of neural reward regions to food cues in autism spectrum disorders | Q30524779 | ||
| Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome | Q30529349 | ||
| Neuroanatomical analysis of the BTBR mouse model of autism using magnetic resonance imaging and diffusion tensor imaging | Q30537523 | ||
| Autism spectrum disorder susceptibility gene TAOK2 affects basal dendrite formation in the neocortex | Q33594808 | ||
| Social reward requires coordinated activity of nucleus accumbens oxytocin and serotonin | Q33881046 | ||
| Gene expression profiling in single cells from the pancreatic islets of Langerhans reveals lognormal distribution of mRNA levels | Q34056088 | ||
| Mammalian genes are transcribed with widely different bursting kinetics | Q34171559 | ||
| MicroRNA-mediated conversion of human fibroblasts to neurons. | Q34200249 | ||
| Satb2 regulates callosal projection neuron identity in the developing cerebral cortex | Q34746949 | ||
| Update on models of basal ganglia function and dysfunction | Q34764284 | ||
| The Fezf2-Ctip2 genetic pathway regulates the fate choice of subcortical projection neurons in the developing cerebral cortex | Q34804095 | ||
| Developmental trajectories of the corpus callosum in attention-deficit/hyperactivity disorder. | Q34810058 | ||
| Novel subtype-specific genes identify distinct subpopulations of callosal projection neurons | Q35005831 | ||
| Is social attachment an addictive disorder? | Q35211181 | ||
| P433 | issue | 4 | |
| P921 | main subject | basal ganglia | Q464210 |
| P304 | page(s) | 1077-1092 | |
| P577 | publication date | 2014-05-01 | |
| P1433 | published in | Cell Reports | Q5058165 |
| P1476 | title | Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome | |
| P478 | volume | 7 |
| Q30362781 | 16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions. |
| Q30390740 | 16p11.2 Deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasks |
| Q50308097 | 16p11.2 Locus modulates response to satiety before the onset of obesity. |
| Q47248416 | 16p11.2 deletion syndrome mice perseverate with active coping response to acute stress - rescue by blocking 5-HT2A receptors. |
| Q59064242 | 5-HT release in nucleus accumbens rescues social deficits in mouse autism model |
| Q55420895 | A Guide to Single-Cell Transcriptomics in Adult Rodent Brain: The Medium Spiny Neuron Transcriptome Revisited. |
| Q97884878 | A role for TGFβ signalling in medium spiny neuron differentiation of human pluripotent stem cells |
| Q99207743 | A standardized social preference protocol for measuring social deficits in mouse models of autism |
| Q92200945 | Aberrant calcium channel splicing drives defects in cortical differentiation in Timothy syndrome |
| Q50301356 | Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling. |
| Q64119941 | Altered sleep architecture, rapid eye movement (REM) sleep, and neural oscillation in a mouse model of human chromosome 16p11.2 microdeletion |
| Q47355327 | Altered synaptic transmission and maturation of hippocampal CA1 neurons in a mouse model of human chr16p11.2 microdeletion |
| Q61814671 | An interaction-based model for neuropsychiatric features of copy-number variants |
| Q52590731 | Analysis of neuroanatomical differences in mice with genetically modified serotonin transporters assessed by structural magnetic resonance imaging. |
| Q36030004 | Animal Models Are Valid to Uncover Disease Mechanisms |
| Q26768231 | Autism Spectrum Disorders and Drug Addiction: Common Pathways, Common Molecules, Distinct Disorders? |
| Q39353531 | Autism spectrum disorder: neuropathology and animal models |
| Q89326890 | Autism-specific maternal autoantibodies produce behavioral abnormalities in an endogenous antigen-driven mouse model of autism |
| Q38575839 | Autism: Oxytocin, serotonin, and social reward |
| Q88758867 | Autistic traits in epilepsy models: Why, when and how? |
| Q27025227 | Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism |
| Q53443934 | Behavioral and neuroanatomical approaches in models of neurodevelopmental disorders: opportunities for translation. |
| Q26781645 | Characterizing autism spectrum disorders by key biochemical pathways |
| Q64948646 | Chemogenetic Activation of Prefrontal Cortex Rescues Synaptic and Behavioral Deficits in a Mouse Model of 16p11.2 Deletion Syndrome. |
| Q35589414 | Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity |
| Q28547298 | Comprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder |
| Q42059359 | Contribution of mGluR5 to pathophysiology in a mouse model of human chromosome 16p11.2 microdeletion |
| Q40066573 | Dopaminergic dysfunction in neurodevelopmental disorders: recent advances and synergistic technologies to aid basic research |
| Q97681262 | Drug-responsive autism phenotypes in the 16p11.2 deletion mouse model: a central role for gene-environment interactions |
| Q38478012 | Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders |
| Q90781271 | Gene network analysis reveals a role for striatal glutamatergic receptors in dysregulated risk-assessment behavior of autism mouse models |
| Q91850695 | Home-cage hypoactivity in mouse genetic models of autism spectrum disorder |
| Q47807134 | Hyperactivity and male-specific sleep deficits in the 16p11.2 deletion mouse model of autism. |
| Q38792691 | Imaging sex/gender and autism in the brain: Etiological implications. |
| Q55122086 | Linking spatial gene expression patterns to sex-specific brain structural changes on a mouse model of 16p11.2 hemideletion. |
| Q37683516 | MAPK3 at the Autism-Linked Human 16p11.2 Locus Influences Precise Synaptic Target Selection at Drosophila Larval Neuromuscular Junctions |
| Q59635221 | Magnetoencephalography as a Tool in Psychiatric Research: Current Status and Perspective |
| Q51740141 | Major vault protein, a candidate gene in 16p11.2 microdeletion syndrome, is required for the homeostatic regulation of visual cortical plasticity. |
| Q41303129 | Male and Female Mice Lacking Neuroligin-3 Modify the Behavior of Their Wild-Type Littermates. |
| Q47241090 | Male-specific deficits in natural reward learning in a mouse model of neurodevelopmental disorders |
| Q26770859 | Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements |
| Q48289037 | Neuroanatomical Phenotypes Are Consistent With Autism-Like Behavioral Phenotypes in the 15q11-13 Duplication Mouse Model |
| Q36825003 | Neurobiology of rodent self-grooming and its value for translational neuroscience |
| Q28071696 | Neuronal mechanisms and circuits underlying repetitive behaviors in mouse models of autism spectrum disorder |
| Q46165200 | Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndrome. |
| Q90196750 | Neuropilin 2 Signaling Mediates Corticostriatal Transmission, Spine Maintenance, and Goal-Directed Learning in Mice |
| Q50209842 | OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome |
| Q34067282 | Opposing brain differences in 16p11.2 deletion and duplication carriers |
| Q38442124 | Oxytocin: parallel processing in the social brain? |
| Q89206465 | Pharmacological Inhibition of ERK Signaling Rescues Pathophysiology and Behavioral Phenotype Associated with 16p11.2 Chromosomal Deletion in Mice |
| Q46193943 | R-Baclofen Reverses Cognitive Deficits and Improves Social Interactions in Two Lines of 16p11.2 Deletion Mice |
| Q27309937 | Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes |
| Q53426251 | Recurrent reciprocal copy number variants: Roles and rules in neurodevelopmental disorders. |
| Q33805524 | Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism |
| Q90628333 | Resolving the Synaptic versus Developmental Dichotomy of Autism Risk Genes |
| Q37142800 | Reversal of dendritic phenotypes in 16p11.2 microduplication mouse model neurons by pharmacological targeting of a network hub. |
| Q30354621 | Sensory processing in autism spectrum disorders and Fragile X syndrome-From the clinic to animal models. |
| Q41760096 | Separate effects of sex hormones and sex chromosomes on brain structure and function revealed by high-resolution magnetic resonance imaging and spatial navigation assessment of the Four Core Genotype mouse model |
| Q42164701 | Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases |
| Q26768226 | Striatal Circuits as a Common Node for Autism Pathophysiology |
| Q92089986 | Synaptic Wiring of Corticostriatal Circuits in Basal Ganglia: Insights into the Pathogenesis of Neuropsychiatric Disorders |
| Q45986630 | TAOK2 Kinase Mediates PSD95 Stability and Dendritic Spine Maturation through Septin7 Phosphorylation. |
| Q28511185 | TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons |
| Q47675041 | The 16p11.2 deletion mouse model of autism exhibits altered cortical progenitor proliferation and brain cytoarchitecture linked to the ERK MAPK pathway. |
| Q47948174 | The 16p11.2 homologs fam57ba and doc2a generate certain brain and body phenotypes |
| Q35059423 | The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity |
| Q38863882 | The Role of mGlu Receptors in Hippocampal Plasticity Deficits in Neurological and Psychiatric Disorders: Implications for Allosteric Modulators as Novel Therapeutic Strategies |
| Q57165601 | The neural circuitry of restricted repetitive behavior: Magnetic resonance imaging in neurodevelopmental disorders and animal models |
| Q38992286 | The road to precision psychiatry: translating genetics into disease mechanisms. |
| Q38367189 | The utility of rodent models of autism spectrum disorders |
| Q28394524 | Translational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics |
| Q97531129 | Vascular contributions to 16p11.2 deletion autism syndrome modeled in mice |
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