| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Simon Fisher | Q7518750 |
| Constance Scharff | Q22036075 | ||
| P2860 | cites work | Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. | Q21092748 |
| Accelerated FoxP2 evolution in echolocating bats | Q21144431 | ||
| Ultrasonic songs of male mice | Q21146080 | ||
| Molecular evolution of FOXP2, a gene involved in speech and language | Q22122513 | ||
| MRI analysis of an inherited speech and language disorder: structural brain abnormalities | Q24292386 | ||
| Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene | Q24305575 | ||
| Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders | Q24305646 | ||
| Foxp2 inhibits Nkx2.1-mediated transcription of SP-C via interactions with the Nkx2.1 homeodomain | Q24309256 | ||
| A functional genetic link between distinct developmental language disorders | Q24312638 | ||
| Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene | Q24530590 | ||
| Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits | Q24530823 | ||
| The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder | Q24538769 | ||
| FOXP2 is not a major susceptibility gene for autism or specific language impairment | Q24563830 | ||
| Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits | Q24594611 | ||
| Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions | Q24603791 | ||
| A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism | Q24643479 | ||
| Neural basis of an inherited speech and language disorder. | Q24643907 | ||
| Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain | Q24648621 | ||
| High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders | Q24648773 | ||
| FoxP2 regulation during undirected singing in adult songbirds | Q24658427 | ||
| Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language | Q24658435 | ||
| Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia | Q24672211 | ||
| The derived FOXP2 variant of modern humans was shared with Neandertals | Q28137489 | ||
| A forkhead-domain gene is mutated in a severe speech and language disorder | Q28190379 | ||
| Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia | Q28211302 | ||
| Short-term synaptic plasticity | Q28217342 | ||
| Localisation of a gene implicated in a severe speech and language disorder | Q28261550 | ||
| Foxp2 and Foxp1 cooperatively regulate lung and esophagus development | Q28508512 | ||
| The level of sonic hedgehog signaling regulates the complexity of cerebellar foliation | Q28508934 | ||
| Generation of mice with a conditional Foxp2 null allele | Q28586785 | ||
| Close correspondence between quantitative- and molecular-genetic divergence times for Neandertals and modern humans | Q28755152 | ||
| Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells | Q28755340 | ||
| Domain-specific regulation of foxP2 CNS expression by lef1 | Q28756604 | ||
| Birdsong decreases protein levels of FoxP2, a molecule required for human speech | Q28756693 | ||
| Many forkheads in the road to regulation. Symposium on forkhead transcription factor networks in development, signalling and disease | Q28757415 | ||
| A comparative study of the behavioral deficits following lesions of various parts of the zebra finch song system: implications for vocal learning | Q29547789 | ||
| An ultra-sparse code underlies the generation of neural sequences in a songbird | Q29547819 | ||
| For whom the bird sings: context-dependent gene expression | Q29547834 | ||
| Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2 | Q29616085 | ||
| FoxP2 expression in avian vocal learners and non-learners | Q29618488 | ||
| Singing-related activity of identified HVC neurons in the zebra finch | Q29618781 | ||
| Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction | Q29618801 | ||
| Precise auditory-vocal mirroring in neurons for learned vocal communication | Q29618824 | ||
| Auditory processing of vocal sounds in birds | Q30011022 | ||
| An evolutionary perspective on FoxP2: strictly for the birds? | Q30011031 | ||
| FoxP2 in song-learning birds and vocal-learning mammals | Q30011055 | ||
| Prevalence of specific language impairment in kindergarten children. | Q30371988 | ||
| Conservation and diversity of Foxp2 expression in muroid rodents: functional implications | Q30484346 | ||
| Expression profiling of intermingled long-range projection neurons harvested by laser capture microdissection | Q33245612 | ||
| Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. | Q33957708 | ||
| Deciphering the genetic basis of speech and language disorders | Q34170013 | ||
| On the nature and evolution of the neural bases of human language | Q34185578 | ||
| Auditory responses in avian vocal motor neurons: a motor theory for song perception in birds | Q34198830 | ||
| Genetic and environmental risks for specific language impairment in children | Q34228034 | ||
| Language fMRI abnormalities associated with FOXP2 gene mutation | Q34269471 | ||
| Ultrasonic vocalisation emitted by infant rodents: a tool for assessment of neurobehavioural development. | Q34420605 | ||
| Genetic influences on language impairment and phonological short-term memory. | Q34454474 | ||
| Voltage-gated ion channels in the axon initial segment of human cortical pyramidal cells and their relationship with chandelier cells | Q34479857 | ||
| Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2. | Q34540341 | ||
| Functional genetic analysis of mutations implicated in a human speech and language disorder | Q34567203 | ||
| Behavioral dopamine signals | Q34614382 | ||
| Expression of FOXP2 in the developing monkey forebrain: comparison with the expression of the genes FOXP1, PBX3, and MEIS2. | Q34776605 | ||
| Infant rodent ultrasounds -- a gate to the understanding of sound communication | Q36021621 | ||
| Genome-wide analyses of human perisylvian cerebral cortical patterning. | Q36140593 | ||
| The eloquent ape: genes, brains and the evolution of language | Q36348747 | ||
| Genes, cognition and dyslexia: learning to read the genome | Q36468500 | ||
| Tangled webs: tracing the connections between genes and cognition | Q36501821 | ||
| Molecular windows into speech and language disorders | Q36843734 | ||
| A major susceptibility locus for specific language impairment is located on 13q21. | Q37362284 | ||
| Behavior. A biolinguistic agenda | Q38385651 | ||
| Novel quantitative phenotypes of exercise training in mouse models. | Q39738960 | ||
| Multiple transcription start sites for FOXP2 with varying cellular specificities | Q40006477 | ||
| Evidence for "direct" and "indirect" pathways through the song system basal ganglia | Q42474461 | ||
| The timing of selection at the human FOXP2 gene | Q43244655 | ||
| Postsynaptic endocannabinoid release is critical to long-term depression in the striatum | Q43971441 | ||
| Molecular cloning and developmental expression of foxP2 in zebrafish | Q46607659 | ||
| FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder | Q47742684 | ||
| Expression of FoxP2 during zebrafish development and in the adult brain | Q48096977 | ||
| Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. | Q48340477 | ||
| The role of protein synthesis in striatal long-term depression. | Q48368959 | ||
| Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review. | Q51906415 | ||
| Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. | Q52026281 | ||
| Genetic basis of specific language impairment: evidence from a twin study. | Q52211359 | ||
| Basal ganglia and cerebellar loops: motor and cognitive circuits | Q73553166 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 166-77 | |
| P577 | publication date | 2009-04-01 | |
| P1433 | published in | Trends in Genetics | Q2451468 |
| P1476 | title | FOXP2 as a molecular window into speech and language | |
| P478 | volume | 25 |
| Q30529890 | 12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech |
| Q46295534 | 3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination |
| Q51664960 | A Bayesian phylogenetic approach to estimating the stability of linguistic features and the genetic biasing of tone. |
| Q28730604 | A Bird's Eye View of Human Language Evolution |
| Q36062997 | A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus |
| Q38849781 | A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker |
| Q42154263 | A Distributed Recurrent Network Contributes to Temporally Precise Vocalizations |
| Q28597125 | A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice |
| Q88913028 | A Phosphomimetic Study Implicates Ser557 in Regulation of FOXP2 DNA Binding |
| Q91081180 | A TBR1-K228E Mutation Induces Tbr1 Upregulation, Altered Cortical Distribution of Interneurons, Increased Inhibitory Synaptic Transmission, and Autistic-Like Behavioral Deficits in Mice |
| Q34810936 | A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits |
| Q54337492 | A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus. |
| Q36695687 | A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment |
| Q99571371 | A de novo frameshift pathogenic variant in TBR1 identified in autism without intellectual disability |
| Q48702112 | A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate cortices. |
| Q24596655 | A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3. |
| Q42678844 | A recent evolutionary change affects a regulatory element in the human FOXP2 gene |
| Q49789088 | A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development. |
| Q28661088 | ASD-relevant Animal Models of the Foxp Family of Transcription Factors |
| Q26698262 | Action and language mechanisms in the brain: data, models and neuroinformatics |
| Q89597899 | Altered Hippocampal Epigenetic Regulation Underlying Reduced Cognitive Development in Response to Early Life Environmental Insults |
| Q60334405 | An Evolutionary Anthropological Perspective on Modern Human Origins |
| Q28714759 | An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning |
| Q30661644 | An informatics approach to integrating genetic and neurological data in speech and language neuroscience. |
| Q28564993 | Androgen modulation of Foxp1 and Foxp2 in the developing rat brain: impact on sex specific vocalization |
| Q28606827 | Animal Models of Speech and Vocal Communication Deficits Associated With Psychiatric Disorders |
| Q37872654 | Animal models of human genetic diseases: do they need to be faithful to be useful? |
| Q36194890 | Annual Research Review: Development of the cerebral cortex: implications for neurodevelopmental disorders |
| Q28651108 | Approaching motor and language deficits in autism from below: a biolinguistic perspective |
| Q37880120 | Are languages really independent from genes? If not, what would a genetic bias affecting language diversity look like? |
| Q41561119 | Assessing the effects of common variation in the FOXP2 gene on human brain structure |
| Q46182579 | Association between FOXP2 gene and speech sound disorder in Chinese population |
| Q104478258 | Autism Spectrum Disorder and Childhood Apraxia of Speech: Early Language-Related Hallmarks across Structural MRI Study |
| Q41903470 | Bards, poets, and cliques: frequency-dependent selection and the evolution of language genes |
| Q30379075 | Beyond Words: How Humans Communicate Through Sound. |
| Q37706948 | Birdsong and the brain: the syntax of memory |
| Q60334981 | Brain Plasticity and Human Evolution |
| Q30010598 | Brain mechanisms of acoustic communication in humans and nonhuman primates: an evolutionary perspective |
| Q47225738 | Brain, know thy transcriptome, know thyself |
| Q30412243 | Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour |
| Q28714875 | CNTNAP2 and language processing in healthy individuals as measured with ERPs |
| Q35087702 | CNTNAP2 variants affect early language development in the general population |
| Q38047676 | Cancer genetics and genomics of human FOX family genes |
| Q48416757 | Cell type-specific expression of FoxP2 in the ferret and mouse retina. |
| Q39334486 | Cerebellar and Striatal Pathologies in Mouse Models of Autism Spectrum Disorder |
| Q46317206 | Charting the protomap of the human telencephalon |
| Q26748761 | Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders |
| Q28743405 | Colloquium paper: gene-culture coevolution in the age of genomics |
| Q35985503 | Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development |
| Q88692028 | Comparing Postnatal Development of Gonadal Hormones and Associated Social Behaviors in Rats, Mice, and Humans |
| Q22064518 | Computational morphometry for detecting changes in brain structure due to development, aging, learning, disease and evolution |
| Q42457662 | Conserved role of Drosophila melanogaster FoxP in motor coordination and courtship song |
| Q38289489 | Control of Neuronal Development by T-Box Genes in the Brain |
| Q28740290 | Convergent differential regulation of parvalbumin in the brains of vocal learners |
| Q28585356 | Convergent evidence for the molecular basis of musical traits |
| Q34292894 | Convergent repression of Foxp2 3'UTR by miR-9 and miR-132 in embryonic mouse neocortex: implications for radial migration of neurons. |
| Q28647966 | Core and Shell Song Systems Unique to the Parrot Brain |
| Q100509488 | Creativity and ADHD: A review of behavioral studies, the effect of psychostimulants and neural underpinnings |
| Q21134854 | Dating the origin of language using phonemic diversity |
| Q42271297 | De novo PacBio long-read and phased avian genome assemblies correct and add to reference genes generated with intermediate and short reads. |
| Q34419403 | De novo TBR1 mutations in sporadic autism disrupt protein functions |
| Q24303420 | De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment |
| Q33702797 | Decoding human gene expression signatures in the brain |
| Q38066309 | Decoding the genetics of speech and language |
| Q28711712 | Defects in ultrasonic vocalization of cadherin-6 knockout mice |
| Q38434613 | Deficits in narrative abilities in child British Sign Language users with specific language impairment. |
| Q27025429 | Defining the biological bases of individual differences in musicality |
| Q103787739 | Developmental Language Disorder: Wake and Sleep Epileptiform Discharges and Co-morbid Neurodevelopmental Disorders |
| Q90380736 | Differential and Overlapping Pattern of Foxp1 and Foxp2 Expression in the Striatum of Adult Mouse Brain |
| Q39064897 | Differential coexpression of FoxP1, FoxP2, and FoxP4 in the Zebra Finch (Taeniopygia guttata) song system |
| Q64083818 | Differential effects of Foxp2 disruption in distinct motor circuits |
| Q28660849 | Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability |
| Q41774236 | Discovery and assessment of conserved Pax6 target genes and enhancers |
| Q28654557 | Dissection and downstream analysis of zebra finch embryos at early stages of development |
| Q33517120 | Domain requirements and sequence specificity of DNA binding for the forkhead transcription factor FOXP3 |
| Q55411733 | Downregulation of FOXP2 promotes breast cancer migration and invasion through TGFβ/SMAD signaling pathway. |
| Q27322342 | Drosophila FoxP mutants are deficient in operant self-learning |
| Q24604488 | Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder |
| Q57898640 | Duetting as a Collective Behavior |
| Q27318552 | Dynamic expression of cadherins regulates vocal development in a songbird |
| Q33929361 | Dysregulated nitric oxide signaling as a candidate mechanism of fragile X syndrome and other neuropsychiatric disorders |
| Q38077738 | Early language delay and specific language impairment. |
| Q30821531 | Early neuroimaging markers of FOXP2 intragenic deletion |
| Q28690660 | Ecological Validity and the Study of Procedural and Episodic Memory Function in Songbirds |
| Q30457923 | Encoding, memory, and transcoding deficits in Childhood Apraxia of Speech |
| Q30010940 | Endophenotypes of FOXP2: dysfunction within the human articulatory network |
| Q30398496 | Enhanced procedural learning of speech sound categories in a genetic variant of FOXP2. |
| Q24597258 | Evo-devo, deep homology and FoxP2: implications for the evolution of speech and language |
| Q92984180 | Evolution of Speech: Anatomy and Control |
| Q39044606 | Evolution of bird genomes-a transposon's-eye view. |
| Q34122142 | Evolution of hominin cranial ontogeny |
| Q39587338 | Evolution of language: Lessons from the genome |
| Q34322221 | Evolution, brain, and the nature of language |
| Q34346486 | Evolution. Culture, genes, and the human revolution |
| Q26779657 | Executive functioning in preschoolers with specific language impairment |
| Q91471903 | Extending research on language foundations and evolution: Reply to comments on "Rethinking foundations of language from a multidisciplinary perspective" |
| Q57733903 | FOXP1mutations cause intellectual disability and a recognizable phenotype |
| Q30010939 | FOXP2 and the role of cortico-basal ganglia circuits in speech and language evolution |
| Q92695628 | FOXP2 contributes to the cognitive impairment in chronic patients with schizophrenia |
| Q38871216 | FOXP2 gene deletion and infant feeding difficulties: a case report |
| Q36817343 | FOXP2 targets show evidence of positive selection in European populations |
| Q46248347 | FOXP2 variation in great ape populations offers insight into the evolution of communication skills |
| Q46923878 | Female song is widespread and ancestral in songbirds |
| Q39281641 | First knockdown gene expression in bat (Hipposideros armiger) brain mediated by lentivirus |
| Q28743752 | Food for song: expression of c-Fos and ZENK in the zebra finch song nuclei during food aversion learning |
| Q27322723 | FoxP1 orchestration of ASD-relevant signaling pathways in the striatum |
| Q44619420 | FoxP2 and olfaction: divergence of FoxP2 expression in olfactory tubercle between different feeding habit bats |
| Q39156045 | FoxP2 in songbirds. |
| Q37059389 | FoxP2 is a parvocellular-specific transcription factor in the visual thalamus of monkeys and ferrets. |
| Q48716307 | FoxP2 is significantly associated with schizophrenia and major depression in the Chinese Han population. |
| Q48306713 | Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization. |
| Q47402230 | Foxp1 regulation of neonatal vocalizations via cortical development. |
| Q48636628 | Foxp2 Regulates Identities and Projection Patterns of Thalamic Nuclei During Development. |
| Q28569031 | Foxp2 mediates sex differences in ultrasonic vocalization by rat pups and directs order of maternal retrieval. |
| Q28731446 | Foxp2 mutations impair auditory-motor association learning |
| Q64083825 | Foxp2 regulates anatomical features that may be relevant for vocal behaviors and bipedal locomotion |
| Q21144946 | Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain |
| Q57831417 | Functional Genomic Dissection of Speech and Language Disorders |
| Q64070075 | Functional characterization of two enhancers located downstream FOXP2 |
| Q35221518 | Functional dissection of the neural substrates for sexual behaviors in Drosophila melanogaster |
| Q57831402 | Genetic Pathways Implicated in Speech and Language |
| Q24609855 | Genetic advances in the study of speech and language disorders |
| Q34349576 | Genetic insights into the functional elements of language |
| Q97075023 | Genetic pathways involved in human speech disorders |
| Q43165977 | Genetic susceptibility to stuttering |
| Q36135992 | Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach. |
| Q34248551 | Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. |
| Q48851799 | Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals. |
| Q62673933 | Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients |
| Q57831364 | Genetics and the Language Sciences |
| Q90568720 | Genetics of language and its implications on language interventions |
| Q28566355 | Genoarchitecture of the extended amygdala in zebra finch, and expression of FoxP2 in cell corridors of different genetic profile |
| Q102218135 | Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band |
| Q21199585 | Genome-wide matching of genes to cellular roles using guilt-by-association models derived from single sample analysis |
| Q34195610 | Genome-wide screening for DNA variants associated with reading and language traits |
| Q89747485 | Genomic influences on self-reported childhood maltreatment |
| Q64920088 | Genomics studies on musical aptitude, music perception, and practice |
| Q28651479 | Globularity and language-readiness: generating new predictions by expanding the set of genes of interest |
| Q34091765 | Heritability of the specific cognitive ability of face perception |
| Q106384980 | How Do Living Systems Create Meaning? |
| Q55554471 | How hierarchical is language use? |
| Q64083808 | Human Genetics: The Evolving Story of FOXP2 |
| Q28744614 | Human brain evolution: harnessing the genomics (r)evolution to link genes, cognition, and behavior |
| Q33740129 | Human face recognition ability is specific and highly heritable |
| Q42480395 | Humanized Foxp2 specifically affects cortico-basal ganglia circuits |
| Q21261330 | Identification of differentially expressed microRNAs in human male breast cancer |
| Q37500060 | Identifying essential cell types and circuits in autism spectrum disorders. |
| Q35679721 | Imaging genetics of FOXP2 in dyslexia |
| Q90492178 | Inhibition of Upf2-Dependent Nonsense-Mediated Decay Leads to Behavioral and Neurophysiological Abnormalities by Activating the Immune Response |
| Q36678939 | Insights into the Neural and Genetic Basis of Vocal Communication |
| Q38322139 | Insights into the genetic foundations of human communication |
| Q38012939 | Interaction between lexical and grammatical language systems in the brain |
| Q47294781 | Introduction: integrating genetic and cultural evolutionary approaches to language |
| Q64266259 | Inverse Control of Turning Behavior by Dopamine D1 Receptor Signaling in Columnar and Ring Neurons of the Central Complex in Drosophila |
| Q42548894 | Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer |
| Q27320217 | Investigating the effects of copy number variants on reading and language performance |
| Q30010959 | Knockdown of FoxP2 alters spine density in Area X of the zebra finch. |
| Q27330219 | Knockout of Foxp2 disrupts vocal development in mice |
| Q28676984 | LOC689986, a unique gene showing specific expression in restricted areas of the rodent neocortex |
| Q39926815 | Language Evolution: Constraints and Opportunities From Modern Genetics. |
| Q37415157 | Language Impairment Resulting from a de novo Deletion of 7q32.1q33. |
| Q28741951 | Language development after cochlear implantation: an epigenetic model |
| Q58227196 | Language impairment resulting from a de novo deletion of 7q32.1-q33: a case report |
| Q33811010 | Language production and working memory in classic galactosemia from a cognitive neuroscience perspective: future research directions |
| Q40082812 | Lentiviral-Mediated Transgenesis in Songbirds |
| Q30441297 | Linking neurogenetics and individual differences in language learning: the dopamine hypothesis. |
| Q27301287 | Localized brain activation related to the strength of auditory learning in a parrot |
| Q47572790 | Loss of Intercalated Cells (ITCs) in the Mouse Amygdala of Tshz1 Mutants Correlates with Fear, Depression, and Social Interaction Phenotypes |
| Q38927953 | MSC-regulated microRNAs converge on the transcription factor FOXP2 and promote breast cancer metastasis |
| Q47214707 | Mapping the distribution of language related genes FoxP1, FoxP2 and CntnaP2 in the brains of vocal learning bat species. |
| Q48290041 | Maternal vitamin D deficiency alters fetal brain development in the BALB/c mouse. |
| Q47661198 | Mice lacking cyclin-dependent kinase-like 5 manifest autistic and ADHD-like behaviors |
| Q28652714 | Mice lacking the cerebral cortex develop normal song: insights into the foundations of vocal learning |
| Q41152831 | Modification of spectral features by nonhuman primates |
| Q46599097 | Modified sound-evoked brainstem potentials in Foxp2 mutant mice |
| Q90348642 | Molecular and cellular evolution of corticogenesis in amniotes |
| Q38153350 | Molecular genetics of dyslexia: an overview |
| Q34341154 | Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex |
| Q34483411 | Monogenic and chromosomal causes of isolated speech and language impairment |
| Q82822297 | Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment |
| Q28660771 | Mouse vocal communication system: are ultrasounds learned or innate? |
| Q42935075 | Multiple microRNAs regulate human FOXP2 gene expression by targeting sequences in its 3' untranslated region |
| Q37914343 | Neural bases of childhood speech disorders: lateralization and plasticity for speech functions during development |
| Q109040740 | Neuroanatomy of the grey seal brain: bringing pinnipeds into the neurobiological study of vocal learning |
| Q59789743 | Neuroemergentism: Levels and constraints |
| Q38055949 | Neurogenetics of birdsong |
| Q108899153 | Neurogenomic insights into the behavioral and vocal development of the zebra finch |
| Q27001068 | Neurogenomics of speech and language disorders: the road ahead |
| Q38836044 | Neuroimaging genetic analyses of novel candidate genes associated with reading and language |
| Q33601252 | Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment |
| Q28650527 | Nitric oxide signaling in the development and evolution of language and cognitive circuits |
| Q28680670 | On the antiquity of language: the reinterpretation of Neandertal linguistic capacities and its consequences |
| Q57514204 | Operant Behavior in Model Systems |
| Q47782527 | Pandora's growing box: Inferring the evolution and development of hominin brains from endocasts |
| Q52618605 | Phenotype of FOXP2 haploinsufficiency in a mother and son. |
| Q26866162 | Pontine mechanisms of respiratory control |
| Q30436913 | Pre-clinical models of neurodevelopmental disorders: focus on the cerebellum |
| Q44529557 | Preliminary evidence of an interaction between the FOXP2 gene and childhood emotional abuse predicting likelihood of auditory verbal hallucinations in schizophrenia |
| Q30361483 | Primate vocal production and the riddle of language evolution |
| Q58227226 | Problematic aspects of the genetic analysis of the specific disorders of the language: FOXP2 as paradigm |
| Q28661205 | Rapid diversification of FoxP2 in teleosts through gene duplication in the teleost-specific whole genome duplication event |
| Q33891684 | Reading and language disorders: the importance of both quantity and quality. |
| Q28748712 | Recent advances in the genetics of language impairment |
| Q99552843 | Reduced Language Lateralization in Autism and the Broader Autism Phenotype as Assessed with Robust Individual-Subjects Analyses |
| Q57167282 | Regulatory genes and pathways disrupted in autism spectrum disorders |
| Q36413225 | Reinforcement learning in young adults with developmental language impairment |
| Q88514630 | Rethinking foundations of language from a multidisciplinary perspective |
| Q41967067 | SUMOylation of FOXP1 regulates transcriptional repression via CtBP1 to drive dendritic morphogenesis |
| Q36849255 | Salivary FOXP2 expression and oral feeding success in premature infants |
| Q50946863 | Segregating polymorphisms of FOXP2 are associated with measures of inner speech, speech fluency and strength of handedness in a healthy population. |
| Q28658802 | Sex hormone influence on human infants' sound characteristics: melody in spontaneous crying |
| Q108898749 | Sex-Specific Social Behavior and Amygdala Proteomic Deficits in Foxp2+/− Mutant Mice |
| Q37657514 | Sexual differentiation of the brain in man and animals: of relevance to Klinefelter syndrome? |
| Q55287009 | Sociability and synapse subtype-specific defects in mice lacking SRPX2, a language-associated gene. |
| Q33942392 | Sonic hedgehog expressing and responding cells generate neuronal diversity in the medial amygdala. |
| Q33604217 | Space and Language in Williams syndrome: Insights from typical development |
| Q64937673 | Species-Specific Changes in a Primate Transcription Factor Network Provide Insights into the Molecular Evolution of the Primate Prefrontal Cortex. |
| Q38646330 | Speech and Language: Translating the Genome |
| Q50783864 | Speech-language pathologists' knowledge of genetics: perceived confidence, attitudes, knowledge acquisition and practice-based variables. |
| Q37851634 | Spontaneous decisions and operant conditioning in fruit flies |
| Q38676952 | Subcortical Contributions to Motor Speech: Phylogenetic, Developmental, Clinical |
| Q92089986 | Synaptic Wiring of Corticostriatal Circuits in Basal Ganglia: Insights into the Pathogenesis of Neuropsychiatric Disorders |
| Q33268995 | Talking Heads |
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