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12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech

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Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

Gialluisi, A., Andlauer, T. F. M., Mirza‐Schreiber, N., Moll, K., Becker, J., Hoffmann, P., Ludwig, K. U., Czamara, D., Pourcain, B. S., Brandler, W. M., et al. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0402-0 · Cited by 111

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals

Whalley, H. C., O’Connell, G., Sussmann, J. E., Peel, A., Stanfield, A. C., Hayiou‐Thomas, M. E., Johnstone, E. C., Lawrie, S. M., McIntosh, A. M., & Hall, J. (2011) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.31241 · Cited by 108

Altered Structural Brain Connectivity in Healthy Carriers of the Autism Risk Gene, CNTNAP2

Dennis, E. L., Jahanshad, N., Rudie, J. D., Brown, J. A., Johnson, K., McMahon, K. L., de Zubicaray, G. I., Montgomery, G. W., Martin, N. G., Wright, M. J., et al. (2011) · Brain Connectivity · doi:10.1089/brain.2011.0064 · Cited by 105

The genetic basis of thought disorder and language and communication disturbances in schizophrenia

Levy, D. L., Coleman, M. J., Sung, H., Ji, F., Matthysse, S., Mendell, N. R., & Titone, D. A. (2009) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2009.08.003 · Cited by 101

Recent advances in the genetics of language impairment

Newbury, D. F., Fisher, S. E., & Monaco, A. P. (2010) · Genome Medicine · doi:10.1186/gm127 · Cited by 146

Genetics, Medicine, and the Plain People

Strauss, K. A., & Puffenberger, E. G. (2009) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082908-150040 · Cited by 100

Comprehension of reflexive and personal pronouns in children with autism: A syntactic or pragmatic deficit?

Perovic, A., Modyanova, N., & Wexler, K. N. (2012) · Applied Psycholinguistics · doi:10.1017/s0142716412000033 · Cited by 98

Knockdown of FoxP2 alters spine density in Area X of the zebra finch

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Grammar Is Differentially Impaired in Subgroups of Autism Spectrum Disorders: Evidence from an Investigation of Tense Marking and Morphosyntax

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Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment

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GL.03 Molecular windows into speech and language disorders

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Unravelling neurogenetic networks implicated in developmental language disorders

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Functional Genomic Dissection of Speech and Language Disorders

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A Molecular Genetic Perspective on Speech and Language

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