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  1. 1
    Jason W. Bohland, Emma M. Myers, Esther Kim, An Informatics Approach to Integrating Genetic and Neurological Data in Speech and Language Neuroscience, Neuroinformatics, 2014, 12, 1, 39

    CrossRef

  2. 2
    Martine Hoogman, Tulio Guadalupe, Marcel P. Zwiers, Patricia Klarenbeek, Clyde Francks, Simon E. Fisher, Assessing the effects of common variation in the FOXP2 gene on human brain structure, Frontiers in Human Neuroscience, 2014, 8,

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  3. 3
    Michael C. Condro, Stephanie A. White, Distribution of language-related Cntnap2 protein in neural circuits critical for vocal learning, Journal of Comparative Neurology, 2014, 522, 1
  4. 4
    Lauren J. Taylor, Murray T. Maybery, Luke Grayndler, Andrew J. O. Whitehouse, Evidence for Distinct Cognitive Profiles in Autism Spectrum Disorders and Specific Language Impairment, Journal of Autism and Developmental Disorders, 2014, 44, 1, 19

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  5. 5
    Olivia J. Veatch, Julie S. Pendergast, Melissa J. Allen, Roberta M. Leu, Carl Hirschie Johnson, Sarah H. Elsea, Beth A. Malow, Genetic Variation in Melatonin Pathway Enzymes in Children with Autism Spectrum Disorder and Comorbid Sleep Onset Delay, Journal of Autism and Developmental Disorders, 2014,

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  6. 6
    O. J. Veatch, J. Veenstra-VanderWeele, M. Potter, M. A. Pericak-Vance, J. L. Haines, Genetically meaningful phenotypic subgroups in autism spectrum disorders, Genes, Brain and Behavior, 2014, 13, 3
  7. 7
    Rose H. Reader, Laura E. Covill, Ron Nudel, Dianne F. Newbury, Genome-Wide Studies of Specific Language Impairment, Current Behavioral Neuroscience Reports, 2014, 1, 4, 242

    CrossRef

  8. 8
    A. Gialluisi, D. F. Newbury, E. G. Wilcutt, R. K. Olson, J. C. DeFries, W. M. Brandler, B. F. Pennington, S. D. Smith, T. S. Scerri, N. H. Simpson, M. Luciano, D. M. Evans, T. C. Bates, J. F. Stein, J. B. Talcott, A. P. Monaco, S. Paracchini, C. Francks, S. E. Fisher, Genome-wide screening for DNA variants associated with reading and language traits, Genes, Brain and Behavior, 2014, 13, 7
  9. 9
    Dianne Newbury, Anthony Monaco, Silvia Paracchini, Reading and Language Disorders: The Importance of Both Quantity and Quality, Genes, 2014, 5, 2, 285

    CrossRef

  10. 10
    A G Chiocchetti, M Kopp, R Waltes, D Haslinger, E Duketis, T A Jarczok, F Poustka, A Voran, U Graab, J Meyer, S M Klauck, S Fulda, C M Freitag, Variants of the CNTNAP2 5′ promoter as risk factors for autism spectrum disorders: a genetic and functional approach, Molecular Psychiatry, 2014,

    CrossRef

  11. 11
    Catherine A French, Simon E Fisher, What can mice tell us about Foxp2 function?, Current Opinion in Neurobiology, 2014, 28, 72

    CrossRef

  12. 12
    Eberhard Schneider, Nady El Hajj, Steven Richter, Justin Roche-Santiago, Indrajit Nanda, Werner Schempp, Peter Riederer, Bianca Navarro, Ronald E Bontrop, Ivanela Kondova, Claus Jürgen Scholz, Thomas Haaf, Widespread differences in cortex DNA methylation of the “language gene”CNTNAP2between humans and chimpanzees, Epigenetics, 2014, 9, 4, 533

    CrossRef

  13. 13
    Lauren J. Taylor, Murray T. Maybery, Andrew J.O. Whitehouse, Communication in Autism, 2014,

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  14. 14
    M. Luciano, D. M. Evans, N. K. Hansell, S. E. Medland, G. W. Montgomery, N. G. Martin, M. J. Wright, T. C. Bates, A genome-wide association study for reading and language abilities in two population cohorts, Genes, Brain and Behavior, 2013, 12, 6
  15. 15
    D. V. M. Bishop, Cerebral Asymmetry and Language Development: Cause, Correlate, or Consequence?, Science, 2013, 340, 6138, 1230531

    CrossRef

  16. 16
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  17. 17
    H. Huang, T. Jeon, G. Sedmak, M. Pletikos, L. Vasung, X. Xu, P. Yarowsky, L. J. Richards, I. Kostovic, N. Sestan, S. Mori, Coupling Diffusion Imaging with Histological and Gene Expression Analysis to Examine the Dynamics of Cortical Areas across the Fetal Period of Human Brain Development, Cerebral Cortex, 2013, 23, 11, 2620

    CrossRef

  18. 18
    Sarah A Graham, Simon E Fisher, Decoding the genetics of speech and language, Current Opinion in Neurobiology, 2013, 23, 1, 43

    CrossRef

  19. 19
    Ron Nudel, Dianne F Newbury, FOXP2, Wiley Interdisciplinary Reviews: Cognitive Science, 2013, 4, 5
  20. 20
    Qasim Ayub, Bryndis Yngvadottir, Yuan Chen, Yali Xue, Min Hu, Sonja C. Vernes, Simon E. Fisher, Chris Tyler-Smith, FOXP2 Targets Show Evidence of Positive Selection in European Populations, The American Journal of Human Genetics, 2013, 92, 5, 696

    CrossRef

  21. 21
    Adam Szalontai, Katalin Csiszar, Genetic insights into the functional elements of language, Human Genetics, 2013, 132, 9, 959

    CrossRef

  22. 22
    John D. Eicher, Jeffrey R. Gruen, Imaging-genetics in dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments, Molecular Genetics and Metabolism, 2013, 110, 3, 201

    CrossRef

  23. 23
    Mabel L. Rice, Language growth and genetics of specific language impairment*, International Journal of Speech-Language Pathology, 2013, 15, 3, 223

    CrossRef

  24. 24
    Víctor Acosta Rodríguez, Sergio Hernández Expósito, Lenguaje y funciones ejecutivas en alumnado con Trastorno Específico del Lenguaje, Revista de Logopedia, Foniatría y Audiología, 2013, 33, 4, 155

    CrossRef

  25. 25
    Steven Klein, Pantea Sharifi-Hannauer, Julian A. Martinez-Agosto, Macrocephaly as a Clinical Indicator of Genetic Subtypes in Autism, Autism Research, 2013, 6, 1
  26. 26
    Amaia Carrion-Castillo, Barbara Franke, Simon E. Fisher, Molecular Genetics of Dyslexia: An Overview, Dyslexia, 2013, 19, 4
  27. 27
    Tom Valeo, NEWS FROM THE SOCIETY OF NEUROSCIENCE ANNUAL MEETING, Neurology Today, 2013, 13, 1, 13

    CrossRef

  28. 28
    David Williams, Heather Payne, Chloë Marshall, Non-word Repetition Impairment in Autism and Specific Language Impairment: Evidence for Distinct Underlying Cognitive Causes, Journal of Autism and Developmental Disorders, 2013, 43, 2, 404

    CrossRef

  29. 29
    Angela Morgan, Speech-language pathology insights into genetics and neuroscience: Beyond surface behaviour*, International Journal of Speech-Language Pathology, 2013, 15, 3, 245

    CrossRef

  30. 30
    Elizabeth A Worthey, Gordana Raca, Jennifer J Laffin, Brandon M Wilk, Jeremy M Harris, Kathy J Jakielski, David P Dimmock, Edythe A Strand, Lawrence D Shriberg, Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech, Journal of Neurodevelopmental Disorders, 2013, 5, 1, 29

    CrossRef

  31. 31
    Sunil Q. Mehta, Daniel H. Geschwind, Emery and Rimoin's Principles and Practice of Medical Genetics, 2013,

    CrossRef

  32. 32
    A. J. O. Whitehouse, D. V. M. Bishop, Q. W. Ang, C. E. Pennell, S. E. Fisher, CNTNAP2 variants affect early language development in the general population, Genes, Brain and Behavior, 2012, 11, 4
  33. 33
    Amel Al-Murrani, Fern Ashton, Salim Aftimos, Alice M. George, Donald R. Love, Amino-Terminal Microdeletion within the CNTNAP2 Gene Associated with Variable Expressivity of Speech Delay, Case Reports in Genetics, 2012, 2012, 1

    CrossRef

  34. 34
    Ning Li, Christopher W. Bartlett, Defining the genetic architecture of human developmental language impairment, Life Sciences, 2012, 90, 13-14, 469

    CrossRef

  35. 35
    Suzanne Coghlan, Jamie Horder, Becky Inkster, M. Andreina Mendez, Declan G. Murphy, David J. Nutt, GABA system dysfunction in autism and related disorders: From synapse to symptoms, Neuroscience & Biobehavioral Reviews, 2012, 36, 9, 2044

    CrossRef

  36. 36
    Christopher W. Bartlett, Judy F. Flax, Zena Fermano, Abby Hare, Liping Hou, Stephen A. Petrill, Steven Buyske, Linda M. Brzustowicz, Gene × Gene Interaction in Shared Etiology of Autism and Specific Language Impairment, Biological Psychiatry, 2012, 72, 8, 692

    CrossRef

  37. 37
    G. Falivelli, A. De Jaco, F. L. Favaloro, H. Kim, J. Wilson, N. Dubi, M. H. Ellisman, B. S. Abrahams, P. Taylor, D. Comoletti, Inherited genetic variants in autism-related CNTNAP2 show perturbed trafficking and ATF6 activation, Human Molecular Genetics, 2012, 21, 21, 4761

    CrossRef

  38. 38
    Patrick C.M. Wong, Kara Morgan-Short, Marc Ettlinger, Jing Zheng, Linking neurogenetics and individual differences in language learning: The dopamine hypothesis, Cortex, 2012, 48, 9, 1091

    CrossRef

  39. 39
    Mabel L Rice, Toward epigenetic and gene regulation models of specific language impairment: looking for links among growth, genes, and impairments, Journal of Neurodevelopmental Disorders, 2012, 4, 1, 27

    CrossRef

  40. 40
    Olga Peñagarikano, Daniel H. Geschwind, What does CNTNAP2 reveal about autism spectrum disorder?, Trends in Molecular Medicine, 2012, 18, 3, 156

    CrossRef

  41. 41
    Jayne Moyle, Stephanie F. Stokes, Thomas Klee, Early Language Delay and Specific Language Impairment, Developmental Disabilities Research Reviews, 2011, 17, 2
  42. 42
    Daniel H. Geschwind, Genetics of autism spectrum disorders, Trends in Cognitive Sciences, 2011, 15, 9, 409

    CrossRef

  43. 43
    Katalin Csiszar, Adam Szalontai, Genetics of Language Disorders, eLS,