ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017
Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity.
Erratum issuedOpen access · bronzeAbstract read
In one paragraph
Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 48 papers.
0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
48 citing papers in PubMed, 80 citations in OpenAlex.
- Examining Genetic Variants Associated with FOXP1 Syndrome through Molecular Dynamics of Its DNA-Binding Domain and Self-Organizing Maps.Journal of chemical information and modeling · 2026Article
- Single-cell spatiotemporal transcriptomic and chromatin accessibility profiling in developing postnatal human and macaque prefrontal cortex.Nature neuroscience · 2026Article
- The dynamic nature of genetic risk for schizophrenia within genes regulated by FOXP1 during neurodevelopment.Human molecular genetics · 2026Article
- Cortex-Restricted Deletion of Foxp1 Impairs Visual Responses by Disrupting Geniculocortical Connections in a Mouse Model of Autism.Investigative ophthalmology & visual science · 2026Article
- Transdiagnostic and Disorder-Level Genome-Wide Association Studies Enhance Precision of Substance Use and Psychiatric Genetic Risk Profiles in African and European Ancestries.Biological psychiatry · 2026Article
- Examining the Potential Link Between Forkhead Box P1 and Severity and Social Impairment in Children with Autism Spectrum Disorder.Journal of clinical medicine · 2025Article
- Adolescent methamphetamine exposure drives neuroinflammation and aberrant neurogenesis linked to anxiety and cognitive impairments in adult mice.Translational psychiatry · 2025Article
- Evolutionary History of Bilaterian FoxP Genes: Complex Ancestral Functions and Evolutionary Changes Spanning 2R-WGD in the Vertebrate Lineage.Molecular biology and evolution · 2025Article
- Cell-type-specific roles of FOXP1 in the excitatory neuronal lineage during early neocortical murine development.Cell reports · 2025Article
- Multimodal single-cell analyses reveal molecular markers of neuronal senescence in human drug-resistant epilepsy.The Journal of clinical investigation · 2025Article
- Prenatal Valproic Acid Exposure Impairs Offspring Cognition Through Disturbing Interneuron Development.CNS neuroscience & therapeutics · 2025Article
- Analysis of downstream targets of PAX6 and LHX2, fundamental regulators of the developing mammalian neocortex.Journal of biosciences · 2025Article
- Compensation between FOXP transcription factors maintains proper striatal function.Cell reports · 2024Article
- Combining Transdiagnostic and Disorder-Level GWAS Enhances Precision of Psychiatric Genetic Risk Profiles in a Multi-Ancestry Sample.medRxiv : the preprint server for health sciences · 2024Article
- FOXP1 regulates the development of excitatory synaptic inputs onto striatal neurons and induces phenotypic reversal with reinstatement.Science advances · 2024Article
- CircRNA-associated ceRNA regulatory networks as emerging mechanisms governing the development and biophysiopathology of epilepsy.CNS neuroscience & therapeutics · 2024Review
- Autism risk geneFrontiers in cellular neuroscience · 2024Article
- Possible roles of deep cortical neurons and oligodendrocytes in the neural basis of human sociality.Anatomical science international · 2024Review
- Identification of a NovelGenes · 2023Article
- Cortex-restricted deletion of Foxp1 impairs barrel formation and induces aberrant tactile responses in a mouse model of autism.Molecular autism · 2023Article
Corrections and comments
- Erratum issued
Authors and funding
13 authors at 6 institutions in 3 countries.
Daniel J AraujoDepartment of Neuroscience.
Kazuya ToriumiDepartment of Neuroscience.ORCID 0000-0002-8593-3269
Christine O EscamillaDepartment of Neurology, and.ORCID 0000-0002-4273-6361
Ashwinikumar KulkarniDepartment of Neuroscience.
Ashley G AndersonDepartment of Neuroscience.
Matthew HarperDepartment of Neuroscience.ORCID 0000-0002-0748-5392
Noriyoshi UsuiDepartment of Neuroscience.ORCID 0000-0001-8079-8013
Jacob EllegoodMouse Imaging Centre, The Hospital for Sick Children, Toronto, Ontario M5T 3H7, Canada.ORCID 0000-0003-1504-3321
Jason P LerchMouse Imaging Centre, The Hospital for Sick Children, Toronto, Ontario M5T 3H7, Canada.
Shari G BirnbaumDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas 75390.ORCID 0000-0001-9311-0310
Haley O TuckerUniversity of Texas at Austin, Section of Molecular Genetics and Microbiology, Austin, Texas 78712.ORCID 0000-0001-7735-2862
Craig M PowellDepartment of Neuroscience.ORCID 0000-0001-5451-2165
Genevieve KonopkaDepartment of Neuroscience, genevieve.konopka@utsouthwestern.edu.ORCID 0000-0002-3363-7302
The University of Texas Southwestern Medical Center · USHospital for Sick Children · CASouthwestern Medical Center · USThe University of Texas at Austin · USTokyo Metropolitan Matsuzawa Hospital · JPUniversity of Toronto · CA
Funding
NOVEL GENETIC MODELS OF AUTISMR01HD069560 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI POWELL, CRAIG M · 2011 to 2020
$4.8MBasic Science Training Program in the Neurobiology of Mental IllnessT32MH076690 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI TAMMINGA, CAROL A · 2007 to 2017
$2.3MThe role of Foxp1-regulated signaling pathways in brain development and behaviorR01MH102603 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI KONOPKA, GENEVIEVE · 2015 to 2019
$2.2MFunctional dissection of mammalian vocal communicationR01DC014702 · NIDCD · UT SOUTHWESTERN MEDICAL CENTER · PI KONOPKA, GENEVIEVE · 2016 to 2020
$1.7MStriatal synaptic Abnormalities in Models of AutismR01MH093697 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI POWELL, CRAIG M · 2012 to 2015
$1.6MNICHD NIH HHS R01 HD069560NIDCD NIH HHS R01 DC014702NIMH NIH HHS R01 MH093697NIMH NIH HHS R01 MH102603NIMH NIH HHS T32 MH076690
Abstract
Genetic perturbations of the transcription factor
Indexed as
AnimalsAutism Spectrum DisorderBehavior, AnimalCA1 Region, HippocampalFemaleForkhead Transcription FactorsGene ExpressionLearning DisabilitiesMaleMemory DisordersMiceMice, Inbred C57BLMice, KnockoutNeocortexNeuronal PlasticityPyramidal CellsForkhead Transcription FactorsFoxp1 protein, mouseRepressor Proteinsautismgene expressionhippocampusspatial learningsynaptic plasticity
Identifiers
What OpenQuestion holds
Textmetadata
Read underepoch 390
Registered trials
None linked
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.