A functional genetic link between distinct developmental language disorders

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Items 101–200 of 675

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2. Recent advances in Tourette syndrome
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4. Autism spectrum disorders and coexisting disorders in a nationwide Swedish twin study
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5. A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits
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6. Genetics of Speech and Language Disorders
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7. Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
   Elizabeth A. Worthey, Gordana Raca, Jennifer J.S. Laffin, Brandon M. Wilk, Jeremy M. Harris, Kathy J. Jakielski, David Dimmock, Edythe A. Strand, Lawrence D. Shriberg · 2013 · Journal of Neurodevelopmental Disorders
8. Traits contributing to the autistic spectrum
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9. Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment
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10. Structural asymmetries of language-related gray and white matter and their relationship to language function in young children with ASD
    Robert M. Joseph, Zachary P. Fricker, Angela Fenoglio, Kristen A. Lindgren, Tracey A. Knaus, Helen B. Tager-Flusberg · 2013 · Brain Imaging and Behavior
11. Taxometric Analyses of Specific Language Impairment in 6-Year-Old Children
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12. Foxp2 Mutations Impair Auditory-Motor Association Learning
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13. Identification of a 7q33-q35 microdeletion disrupting the CNTNAP2 gene in a Brazilian Stuttering case
    A. Petrin, C. M. Giacheti, L. P. Maximino, D. Abramides, Sthella Zanchetta, N. F. Rossi, A. Richieri-Costa, J. C. Murray · 2010 · American Journal of Medical Genetics. Part A
14. FOXP2 Targets Show Evidence of Positive Selection in European Populations
    Qasim Ayub, Bryndís Yngvadóttir, Yuan Chen, Yali Xue, Min Hu, Sonja C. Vernes, Simon E. Fisher, Chris Tyler‐Smith · 2013 · The American Journal of Human Genetics
15. A Role for Ultrasonic Vocalisation in Social Communication and Divergence of Natural Populations of the House Mouse (Mus musculus domesticus)
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16. Genetically meaningful phenotypic subgroups in autism spectrum disorders
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17. Non-word Repetition Impairment in Autism and Specific Language Impairment: Evidence for Distinct Underlying Cognitive Causes
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18. Language growth and genetics of specific language impairment
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19. TCF4, Schizophrenia, and Pitt-Hopkins Syndrome
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20. Genes Expressed in Specific Areas of the Human Fetal Cerebral Cortex Display Distinct Patterns of Evolution
    Lambert, Nelle, Lambot, Marie-Alexandra, Bilheu, Angéline, Albert, Valérie, Englert, Yvon, Libert, Frédérick, Noel, Jean-Christophe, Sotiriou, Christos, Holloway, Alisha K., Pollard, Katherine S. et al. · 2011 · PLoS ONE
21. Evidence for shared deficits in identifying emotions from faces and from voices in autism spectrum disorders and specific language impairment
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22. Transcriptional Regulation by FOXP1, FOXP2, and FOXP4 Dimerization
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23. Language delay aggregates in toddler siblings of children with autism spectrum disorder
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24. Late Talkers
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25. Toward epigenetic and gene regulation models of specific language impairment: looking for links among growth, genes, and impairments
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26. Literacy Outcomes of Children With Early Childhood Speech Sound Disorders: Impact of Endophenotypes
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27. Mechanisms of developmental regression in autism and the broader phenotype: A neural network modeling approach.
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28. Disentangling the Myriad Genomics of Complex Disorders, Specifically Focusing on Autism, Epilepsy, and Schizophrenia
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29. Klinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin–neurexin hypothesis
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30. Evidence for Distinct Cognitive Profiles in Autism Spectrum Disorders and Specific Language Impairment
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31. The role of Pax6 in brain development and its impact on pathogenesis of autism spectrum disorder
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32. Globularity and language-readiness: generating new predictions by expanding the set of genes of interest
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33. CNTNAP2 is significantly associated with schizophrenia and major depression in the Han Chinese population
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34. Autism genetics – an overview
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35. A Psycholinguistic Framework for Diagnosis and Treatment Planning of Developmental Speech Disorders
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36. Linking neurogenetics and individual differences in language learning: the dopamine hypothesis.
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37. The evolutionary history of genes involved in spoken and written language: beyond FOXP2
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38. DNA methylation signatures of educational attainment
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39. The Role of the FOXP Family of Transcription Factors in ASD
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40. Altered Auditory Processing, Filtering, and Reactivity in theCntnap2Knock-Out Rat Model for Neurodevelopmental Disorders
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41. Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis
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42. Differential language markers of pathology in Autism, Pervasive Developmental Disorder Not Otherwise Specified and Specific Language Impairment
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43. Synaptic Wiring of Corticostriatal Circuits in Basal Ganglia: Insights into the Pathogenesis of Neuropsychiatric Disorders
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44. Speech and Language: Translating the Genome
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45. Chromatin Decondensation by FOXP2 Promotes Human Neuron Maturation and Expression of Neurodevelopmental Disease Genes
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46. Molecular networks of the FOXP2 transcription factor in the brain
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47. Language deficits in schizophrenia and autism as related oscillatory connectomopathies: An evolutionary account
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48. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray
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49. Increased gene expression of FOXP1 in patients with autism spectrum disorders
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50. Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population
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51. Phenotype of FOXP2 haploinsufficiency in a mother and son
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52. Identifying Early‐Risk Markers and Developmental Trajectories for Language Impairment in Neurodevelopmental Disorders
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53. Sonic hedgehogexpressing and responding cells generate neuronal diversity in the medial amygdala
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54. Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment
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55. Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization
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56. No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins
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57. What can mice tell us about Foxp2 function?
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58. Who did Buzz see someone? Grammaticality judgement of wh-questions in typically developing children and children with Grammatical-SLI
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59. Sumoylation of FOXP2 Regulates Motor Function and Vocal Communication Through Purkinje Cell Development
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60. Eight further individuals with intellectual disability and epilepsy carrying bi-allelic <i>CNTNAP2</i> aberrations allow delineation of the mutational and phenotypic spectrum
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61. Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech
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62. Single-Cell Analysis of Foxp1-Driven Mechanisms Essential for Striatal Development
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63. Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population
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67. A Multi-Platform Draft de novo Genome Assembly and Comparative Analysis for the Scarlet Macaw (Ara macao)
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68. Analysis of two language-related genes in autism
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70. Developmental disorders of speech and language
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77. The DISC1 promoter: characterization and regulation by FOXP2
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78. Genetics and the Language Sciences
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80. Haploinsufficiency of CMIP in a Girl With Autism Spectrum Disorder and Developmental Delay due to a De Novo Deletion on Chromosome 16q23.2
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81. Inherited genetic variants in autism-related CNTNAP2 show perturbed trafficking and ATF6 activation
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82. Deficits in volitional oculomotor control align with language status in autism spectrum disorders
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83. Implicit Artificial Syntax Processing: Genes, Preference, and Bounded Recursion
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84. Direct Downregulation of CNTNAP2 by STOX1A is Associated with Alzheimer's Disease
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85. The Autism Candidate Gene Neurobeachin Encodes a Scaffolding Protein Implicated in Membrane Trafficking and Signaling
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86. Imaging genetics of FOXP2 in dyslexia
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87. Bridging the Gap between Genes and Language Deficits in Schizophrenia: An Oscillopathic Approach
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89. A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment
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90. Mutant Mouse Models of Autism Spectrum Disorders
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91. Language‐related <i>Cntnap2</i> gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds
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92. Gene associated with seizures, autism, and hepatomegaly in an Amish girl
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93. Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference
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94. The importance of being human
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96. Subcortical Contributions to Motor Speech: Phylogenetic, Developmental, Clinical
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97. Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders
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98. Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders.
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99. Association of MET with social and communication phenotypes in individuals with autism spectrum disorder
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100. Genome-wide analysis identifies a role for common copy number variants in specific language impairment
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