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Genetics and SLI reference list

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This document provides references for research on the genetics of specific language impairment (SLI). It lists reviews and other papers that have studied the role of genes in SLI, including the identification of specific genes like FOXP2 that have been linked to developmental speech and language deficits. Genome-wide scans have also identified two novel loci involved in SLI. The heritability of SLI depends on the diagnostic criteria used. Overall, the references examine the genetic factors and molecular mechanisms underlying SLI and efforts to unravel the relationship between SLI, dyslexia, and autism.

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1 Genetics and Specific Language Impairment References Reviews Bishop, D. V. M. (2002). The role of genes in the etiology of specific language impairment. Journal of Communication Disorders, 35, 311-328. Bishop, D. V. M. (2006). What causes specific language impairment in children? Current Directions in Psychological Science, 15, 217-221. Bishop, D. V. M. (2008). Specific language impairment, dyslexia, and autism: Using genetics to unravel their relationship. In C. F. Norbury & J. B. Tomblin & D. V. M. Bishop (Eds.), Understanding developmental language disorders: from theory to practice (pp. 67-78). Hove: Psychology Press. Fisher, S. E. (2005). Dissection of molecular mechanisms underlying speech and language disorders. Applied Psycholinguistics, 26, 111-128. Fisher, S. E. (2006). Tangled webs: tracing the connections between genes and cognition. Cognition, 10, 270-297. Kang, C., & Drayna, D. (2011). Genetics of speech and language disorders. Annual Review of Genomics and Human Genetics, 12, 145-164. Li, N., & Bartlett, C. W. (2012). Defining the genetic architecture of human developmental language impairment. Life Sciences, 90(13-14), 469-475. Newbury, D. F., & Monaco, A. P. (2008). The application of molecular genetics to the study of language impairments. In C. F. Norbury & J. B. Tomblin & D. V. M. Bishop (Eds.), Understanding Developmental Language Disorders. Hove: Psychology Press. Rutter, M. (2006). Genes and Behavior: Nature-Nurture Interplay Explained. Oxford: Blackwell.
2 Other papers Bishop, D. V. M., & Hayiou-Thomas, M. E. (2008). Heritability of specific language impairment depends on diagnostic criteria. Genes, Brain and Behavior, 7, 365-372. Macdermot, K. D., Bonora, E., Sykes, N., Coupe, A. M., Lai, C. S., Vernes, S. C., Vargha-Khadem, F., McKenzie, F., Smith, R. L., Monaco, A. P., & Fisher, S. E. (2005). Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. American Journal of Human Genetics, 76, 1074-1080. Newbury, D. F., Bonora, E., Lamb, J. A., Fisher, S. E., Lai, C. S. L., Baird, G., Jannoun, L., Slonims, V., Stott, C. M., Merricks, M. J., Bolton, P. F., Bailey, A. J., Monaco, A. P., & International Molecular Genetic Study of Autism Consortium. (2002). FOXP2 is not a major susceptibility gene for autism or specific language impairment. American Journal of Human Genetics, 70, 1318-1327. Sing, C. F., & Reilly, S. L. (1993). Genetics of common diseases that aggregate, but do not segregate in families. In C. F. Sing & C. L. Hanis (Eds.), Genetics of cellular, individual, family and population variability (pp. 140-161). New York: Oxford University Press. SLI Consortium. (2002). A genome-wide scan identifies two novel loci involved in specific language impairment (SLI). American Journal of Human Genetics, 70, 384-398. SLI Consortium. (2004). Highly significant linkage to SLI1 locus in an expanded sample of individuals affected by Specific Language Impairment (SLI). American Journal of Human Genetics, 94, 1225-1238. Vernes, S. C., Newbury, D. F., Abrahams, B. S., Winchester, L., Nicod, J., Groszer, M., Alarcón, M., Oliver, P. L., Davies, K. E., Geschwind, D. H., Monaco, A. P., & Fisher, S. E. (2008). A functional genetic link between distinct developmental language disorders. New England Journal of Medicine, 359.

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Genetics and SLI reference list

  • 1. 1 Genetics and Specific Language Impairment References Reviews Bishop, D. V. M. (2002). The role of genes in the etiology of specific language impairment. Journal of Communication Disorders, 35, 311-328. Bishop, D. V. M. (2006). What causes specific language impairment in children? Current Directions in Psychological Science, 15, 217-221. Bishop, D. V. M. (2008). Specific language impairment, dyslexia, and autism: Using genetics to unravel their relationship. In C. F. Norbury & J. B. Tomblin & D. V. M. Bishop (Eds.), Understanding developmental language disorders: from theory to practice (pp. 67-78). Hove: Psychology Press. Fisher, S. E. (2005). Dissection of molecular mechanisms underlying speech and language disorders. Applied Psycholinguistics, 26, 111-128. Fisher, S. E. (2006). Tangled webs: tracing the connections between genes and cognition. Cognition, 10, 270-297. Kang, C., & Drayna, D. (2011). Genetics of speech and language disorders. Annual Review of Genomics and Human Genetics, 12, 145-164. Li, N., & Bartlett, C. W. (2012). Defining the genetic architecture of human developmental language impairment. Life Sciences, 90(13-14), 469-475. Newbury, D. F., & Monaco, A. P. (2008). The application of molecular genetics to the study of language impairments. In C. F. Norbury & J. B. Tomblin & D. V. M. Bishop (Eds.), Understanding Developmental Language Disorders. Hove: Psychology Press. Rutter, M. (2006). Genes and Behavior: Nature-Nurture Interplay Explained. Oxford: Blackwell.
  • 2. 2 Other papers Bishop, D. V. M., & Hayiou-Thomas, M. E. (2008). Heritability of specific language impairment depends on diagnostic criteria. Genes, Brain and Behavior, 7, 365-372. Macdermot, K. D., Bonora, E., Sykes, N., Coupe, A. M., Lai, C. S., Vernes, S. C., Vargha-Khadem, F., McKenzie, F., Smith, R. L., Monaco, A. P., & Fisher, S. E. (2005). Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. American Journal of Human Genetics, 76, 1074-1080. Newbury, D. F., Bonora, E., Lamb, J. A., Fisher, S. E., Lai, C. S. L., Baird, G., Jannoun, L., Slonims, V., Stott, C. M., Merricks, M. J., Bolton, P. F., Bailey, A. J., Monaco, A. P., & International Molecular Genetic Study of Autism Consortium. (2002). FOXP2 is not a major susceptibility gene for autism or specific language impairment. American Journal of Human Genetics, 70, 1318-1327. Sing, C. F., & Reilly, S. L. (1993). Genetics of common diseases that aggregate, but do not segregate in families. In C. F. Sing & C. L. Hanis (Eds.), Genetics of cellular, individual, family and population variability (pp. 140-161). New York: Oxford University Press. SLI Consortium. (2002). A genome-wide scan identifies two novel loci involved in specific language impairment (SLI). American Journal of Human Genetics, 70, 384-398. SLI Consortium. (2004). Highly significant linkage to SLI1 locus in an expanded sample of individuals affected by Specific Language Impairment (SLI). American Journal of Human Genetics, 94, 1225-1238. Vernes, S. C., Newbury, D. F., Abrahams, B. S., Winchester, L., Nicod, J., Groszer, M., Alarcón, M., Oliver, P. L., Davies, K. E., Geschwind, D. H., Monaco, A. P., & Fisher, S. E. (2008). A functional genetic link between distinct developmental language disorders. New England Journal of Medicine, 359.