Functional genetic analysis of mutations implicated in a human speech and language disorder

Cited by (167)

Items 101–167 of 167

  1. A Proposed Neurological Interpretation of Language Evolution
    Alfredo Ardila · 2015 · Behavioural Neurology
  2. Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population
    Wen‐Wang Rao, Xiangdong Du, Yingyang Zhang, Qiong Yu, Li Hui, Yaqin Yu, Changgui Kou, Guangzhong Yin, Xiaomin Zhu, Lijuan Man et al. · 2017 · Journal of Neural Transmission
  3. Zebrafish foxP2 Zinc Finger Nuclease Mutant Has Normal Axon Pathfinding
    Lingyan Xing, Kazuyuki Hoshijima, David Jonah Grunwald, Esther Fujimoto, Tyler S. Quist, Jacob Sneddon, Chi-Bin Chien, Tamara J. Stevenson, Joshua L. Bonkowsky · 2012 · PLoS ONE
  4. Segregating polymorphisms of FOXP2 are associated with measures of inner speech, speech fluency and strength of handedness in a healthy population
    Bernard J. Crespi, Silven Read, Peter L. Hurd · 2017 · Brain and Language
  5. An Etiological Foxp2 Mutation Impairs Neuronal Gain in Layer VI Cortico-Thalamic Cells through Increased GABAB/GIRK Signaling
    Mélanie Druart, Matthias Groszer, Corentin Le Magueresse · 2020 · Journal of Neuroscience
  6. Molecular Windows into Speech and Language Disorders
    Simon E. Fisher · 2007 · Folia Phoniatrica et Logopaedica
  7. Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders
    Lin Han, Meilin Chen, Yazhe Wang, Huidan Wu, Yingting Quan, Ting Bai, Kuokuo Li, Guiqin Duan, Yan Gao, Zhengmao Hu et al. · 2019 · Molecular Genetics & Genomic Medicine
  8. PolyQ length-based molecular encoding of vocalization frequency in FOXP2
    Serena Vaglietti, Veronica Villeri, Marco Dell’Oca, Chiara Marchetti, Federico Cesano, Francesca Rizzo, Dave Miller, Louis LaPierre, Ilaria Pelassa, Francisco J. Monje et al. · 2023 · iScience
  9. Genetic bases of language control in bilinguals: Evidence from an EEG study
    Dongxue Liu, Zehui Xing, Junjun Huang, John Wayne Schwieter, Huanhuan Liu · 2023 · Human Brain Mapping
  10. First Knockdown Gene Expression in Bat (Hipposideros armiger) Brain Mediated by Lentivirus
    Qi Chen, Tengteng Zhu, Gareth Jones, Junpeng Zhang, Yi Sun · 2012 · Molecular Biotechnology
  11. A Molecular Genetic Perspective on Speech and Language
    Simon E. Fisher · 2015 · Elsevier eBooks
  12. Forkhead Box P Family Members at the Crossroad Between Tolerance and Immunity: A Balancing Act
    Veerle Fleskens, Ruben van Boxtel · 2013 · International Reviews of Immunology
  13. The FKH domain in FOXP3 mRNA frequently contains mutations in hepatocellular carcinoma that influence the subcellular localization and functions of FOXP3
    Jianwei Ren, Yi Liu, Shanshan Wang, Yu Wang, Wende Li, Siyu Chen, Dexuan Cui, Shengli Yang, Mingyue Li, Bo Feng et al. · 2020 · Journal of Biological Chemistry
  14. FOXP2 promotes the nuclear translocation of POT1, but FOXP2(R553H), mutation related to speech-language disorder, partially prevents it
    Yuko Tanabe, Eriko Fujita, Takashi Momoi · 2011 · Biochemical and Biophysical Research Communications
  15. ASD-relevant Animal Models of the Foxp Family of Transcription Factors
    J. Michael Bowers · 2012 · Autism - Open Access
  16. Origins of magic: review of genetic and epigenetic effects
    Sreeram V. Ramagopalan, Marian Knight, George C. Ebers · 2007 · BMJ
  17. No association between FOXP2 rs10447760 and schizophrenia in a replication study of the Chinese Han population
    Jiajun Yin, Ningren Jia, Yansong Liu, Chunhui Jin, Fuquan Zhang, Shui Yu, Jun Wang, Jianmin Yuan · 2018 · Psychiatric Genetics
  18. Temporal expression and mitochondrial localization of a Foxp2 isoform lacking the forkhead domain in developing Purkinje cells
    Yuko Tanabe, Yuji Fujiwara, Ayumi Matsuzaki, Eriko Fujita, Tadashi Kasahara, Shigeki Yuasa, Takashi Momoi · 2011 · Journal of Neurochemistry
  19. No association between common genetic variation in FOXP2 and language impairment in schizophrenia
    Nina S. McCarthy, Melanie L. Clark, Assen V Jablensky, Johanna Claire Badcock · 2018 · Psychiatry Research
  20. Origins of the language: Correlation between brain evolution and language development
    Alfredo Ardila · 2009 · Cambridge University Press eBooks
  21. Aspectos problemáticos del análisis genético de los trastornos específicos del lenguaje: FOXP2 como paradigma
    Antonio Benítez‐Burraco · 2011 · Neurología
  22. FOXP2 and language alterations in psychiatric pathology
    Xóchitl Helga Castro-Martínez, María Dolores Moltó, Mirna Edith Morales-Marín, Julio C. Flóres-Lázaro, Javier González-Fernández, Nora Gutiérrez-Nájera, Daniel Eduardo Alvarez-Amado, José Humberto Nicolini Sánchez · 2019 · Salud Mental
  23. Problematic aspects of the genetic analysis of the specific disorders of the language: FOXP2 as paradigm
    Antonio Benítez‐Burraco · 2012 · Neurología (English Edition)
  24. Non-verbal victims in the adversarial criminal process: communication, competency, and credibility
    Jonathan Doak, Lauran Doak · 2017 · Northern Ireland Legal Quarterly
  25. FoxP in bees: A comparative study on the developmental and adult expression pattern in three bee species considering isoforms and circuitry
    Adriana Schatton, Ezequiel Mendoza, Kathrin Grube, Constance Scharff · 2018 · The Journal of Comparative Neurology
  26. Biolinguistics: A Scientometric Analysis of Research on (Children’s) Molecular Genetics of Speech and Language (Disorders)
    Ahmed Mohammed Saleh Alduais, Shrouq Almaghlouth, Hind Abdulaziz Alfadda, Fawaz Ali Ahmed Qasem · 2022 · Children
  27. Classically intoxicated: correlations between quantity of alcohol consumed and alcohol related problems in a classical Greek text
    Christopher C. H. Cook, Helen Tarbet, David Ball · 2007 · BMJ
  28. ON THE INFERENCE 'NEANDERTHALS HAD FOXP2 = THEY HAD COMPLEX LANGUAGE'
    Antonio Benítez‐Burraco, Víctor Manuel Longa Martínez · 2012 · The Evolution of Language
  29. Involvement of the Urokinase Receptor and Its Endogenous Ligands in the Development of the Brain and the Formation of Cognitive Functions
    Ekaterina V. Semina, Kseniya A. Rubina, Victoria V. Stepanova, Tkachuk Va · 2017 · Neuroscience and Behavioral Physiology
  30. Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the FOXP2 Gene
    Orsolya Nagy, Judit Kárteszi, Beatrix Elmont, Anikó Újfalusi · 2021 · Frontiers in Pediatrics
  31. Why the Caged Mouse Sings: Studies of the Mouse Ultrasonic Song System and Vocal Behavior
    Gustavo Arriaga · 2013 · Springer eBooks
  32. Genetic Pathways Implicated in Speech and Language
    Sonja C. Vernes, Simon E. Fisher · 2013 · Springer eBooks
  33. Dosis génica y lenguaje: a propósito de la región cromosómica 7q11.23
    Antonio Benítez‐Burraco · 2009 · Revista de Logopedia Foniatría y Audiología
  34. Genomic Investigations of Spoken and Written Language Abilities: A Guide to Advances in Approaches, Technologies, and Discovery
    Simon E. Fisher · 2025 · Journal of Speech Language and Hearing Research
  35. DNA facilitates heterodimerization between human transcription factors FoxP1 and FoxP2 by increasing their conformational flexibility
    Ricardo Coñuecar, Isabel Asela, Maira Rivera, Pablo Galaz‐Davison, Jorge González-Higueras, George L. Hamilton, Felipe Engelberger, César A. Ramírez‐Sarmiento, Jorge Babul, Hugo Sanabria et al. · 2023 · iScience
  36. Insights into the pathogenicity of missense variants in the forkhead domain of FOX proteins underlying Mendelian disorders
    Luis Bermúdez-Guzmán, Reiner A. Veitia · 2021 · Human Genetics
  37. Developing Embodied Multisensory Dialogue Agents
    Michał B. Paradowski · 2011 · arXiv (Cornell University)
  38. Exploring ASR-Based WAV2VEC2 for Automated Speech Disorder Assessment: Insights and Analysis
    Tuan Anh Nguyen, Corinne Fredouille, Alain Ghio, Mathieu Balaguer, Virginie Woisard · 2024 · IEEE Spoken Language Technology Workshop (SLT)
  39. CHIRP-Seq: FOXP2 transcriptional targets in zebra finch brain include numerous speech and language-related genes
    Gregory L. Gedman, Todd Haswell Kimball, Lee L. Atkinson, Daniella Factor, Gabriela Vojtova, Madza Farias-Virgens, Timothy F. Wright, Stephanie A. White · 2025 · BMC Neuroscience
  40. Intronic miRNA miR-3666 Modulates its Host Gene FOXP2 Functions in Neurodevelopment and May Contribute to Pathogenesis of Neurological Disorders Schizophrenia and Autism
    Abul Bashar Mir Md. Khademul Islam · 2017 · Journal of Applied Biotechnology & Bioengineering
  41. Functional Genomic Dissection of Speech and Language Disorders
    Sonja C. Vernes, Simon E. Fisher · 2010 · Advances in neurobiology
  42. Decoding the biology of language and its implications in language acquisition
    D. R. Rahul, R. Joseph Ponniah · 2019 · Journal of Biosciences
  43. The Genetics of Language
    Paolo Devanna, Dan Dediu, Sonja C. Vernes · 2018 · Oxford University Press eBooks
  44. Origins of Language
    Alfredo Ardila · 2017 · Perspectives in cultural-historical research
  45. Myths of the Baltic Sea eutrophication
    Oleg Savchuk · 2018 · Journal of Aquaculture & Marine Biology
  46. Language and Genes
    J. Bruce Tomblin, K L Mueller · 2013 · Wiley eBooks
  47. The Embodied Language: Why Language Should Not Be Conceived of in Abstraction from the Brain and Body, and the Consequences for Robotics
    Michał B. Paradowski · 2011 · SSRN Electronic Journal
  48. Differential Gene Expression in the Developing Lateral Geniculate Nucleus and Medial Geniculate Nucleus Reveals Novel Roles for Zic4 and Foxp2 in Visual and
    Gabriel Kreiman, Marissa Cathleen Blank, Kathleen J. Millen · 2009 · DSpace@MIT (Massachusetts Institute of Technology)
  49. The strange malady of Alessandro’s uncle
    Neil A. Holtzman · 2007 · BMJ
  50. FOXP 2: A gene for language and speech
    Hakim Arif · 1970 · Dhaka University Journal of Linguistics
  51. Biología y Lenguaje: pasado, presente y futuro de una relación obligada
    Antonio Benítez‐Burraco · 2011 · University of Valladolid Documentary Repository (University of Valladolid)
  52. Early speech motor and language skills in childhood apraxia of speech: evidence for a core deficit in speech motor control?
    Chantelle Highman · 2010 · eSpace (Curtin University)
  53. The Embodied Language. Why language should not be conceived of in abstraction from the brain and body, why there is more to it than sensorimotor and semantic resonance, and the consequences for robotics
    Michał B. Paradowski · 2011 · arXiv (Cornell University)
  54. EL PAPEL DEL ADN FÓSIL EN PALEOANTROPOLOGÍA: FOXP2, NEANDERTALES Y LENGUAJE 1 The role of fossil DNA in Paleoanthropology: FOXP2, Neanderthals, and language
    Antonio Benítez‐Burraco, Víctor Manuel Longa Martínez · 2011
  55. Molecular Mechanisms Regulating Mammalian Forebrain Development
    David Chun Cheong Tsui · 2014 · TSpace (University of Toronto)
  56. Genetic studies on speech and language disorders
    Changsoo Paul Kang · 2015 · Journal of Biomedical Research
  57. The role of FoxP2 in striatal circuitry
    Jon-Ruben van Rhijn · 2019 · MPG.PuRe (Max Planck Society)
  58. مظاهر اضطرابات النطق واللغة لدى أطفال فرط الحرکة وتشتت الانتباه من وجهة نظر أولياء أمورهم في ضوء بعض المتغيرات بمدينة جدة
    نوره بنت عبد الله بن علي الغامدي, محمد بن مبارك الشهراني · 2021 · المجلة العربية لعلوم الإعاقة والموهبة
  59. Grand Celebration: 10th Anniversary of the Human Genome Project
    Pabulo Henrique Rampelotto, John Burn, Lupski, James, Nelson, Karen · 2016 · MDPI eBooks
  60. Testdiagnostik
    Elisabeth Höwler · 2020 · Springer eBooks
  61. Testdiagnostik
    Elisabeth Höwler · 2016 · Springer eBooks
  62. FOXP4 Variants Are Associated With Plateau Iris and Angle Closure Glaucoma
    William Presley, Su Qing Wang, Bin Guan et al. · 2025 · Investigative Ophthalmology & Visual Science
  63. Challenges in Applying DNA-Binding Protein Predictors to Biological Research
    Graydon Cowgill, Steven Anthony Strazza, Savannah Wilson · 2025 · International Journal of Molecular Sciences
  64. Identification and characterization of disease-related copy number variations (CNVs) by high-dense SNP oligonucleotide microarrays
    Núria Rivera‐Bruguès · 2012 · Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)
  65. Altérations de la connectivité corticale au cours de périodes critiques du développement
    Mélanie Druart · 2020 · theses.fr (ABES)
  66. Fonction et régulation des gènes Dlx5/6 dans les neurones GABAergiques corticaux : Implications pour le comportement et pour le mécanisme d'action des antidépresseurs
    Rym Aouci · 2024 · theses.fr (ABES)
  67. Molecular and cell type-specific determinants of inferior colliculus development and auditory function
    Miranda J. Jankovic, Yuan-Tai Huang, Andrew J. Holley, Sophia Kirkland, Ashwinikumar Kulkarni, Hitomi Sakano, Jay R. Gibson, Geneviève Konopka · 2026 · bioRxiv (Cold Spring Harbor Laboratory)