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IAN Research Report #13 - February 2010: From First Concern to Diagnosis and Beyond - References

  1. Attwood, T. (1998). Asperger's syndrome: A guide for parents and professionals. London and Philadelphia: Jessica Kingsley Publishers.
  2. Klin, A., McPartland, J., & Volkmar, F. (2005). Asperger syndrome. In F. R. Volkmar, R. Paul, A. Klin, & D. Cohen (Eds.), Handbook of autism and pervasive developmental disorders (3rd ed., pp. 88-125). Hoboken, NJ: John Wiley & Sons.
  3. Kluth, P. (2003). You're going to love this kid: Teaching students with autism in the inclusive classroom. Baltimore: Paul Brooks Publishing.
  4. Laurent, A. C., & Rubin, E. (2004). Challenges in emotional regulation in Asperger syndrome and high-functioning autism. Topics in Language Disorders, 24(4), 286-297.
  5. American Psychiatric Association. (2000). Diagnostic and statistical manual of mental disorders (4th ed., text revision). Washington, DC: American Psychiatric Association.
  6. Hatton, D. D., Sideris, J., Skinner, M., Mankowski, J., Bailey, D. B., Jr., Roberts, J., et al. (2006). Autistic behavior in children with fragile X syndrome: Prevalence, stability, and the impact of FMRP. American Journal of Medical Genetics. Part A, 140A(17), 1804-1813. View Abstract
  7. Smalley, S. L. (1998). Autism and tuberous sclerosis. Journal of Autism and Developmental Disorders, 28(5), 407-414. View Abstract
  8. Volkmar, F. R., Wiesner, L. A., & Westphal, A. (2006). Healthcare issues for children on the autism spectrum. Current Opinion in Psychiatry, 19(4), 361-366. View Abstract
  9. Zafeiriou, D. I., Ververi, A., & Vargiami, E. (2007). Childhood autism and associated comorbidities. Brain & Development, 29(5), 257-272. View Abstract
  10. Zhao, X., Leotta, A., Kustanovich, V., Lajonchere, C., Geschwind, D. H., Law, K., et al. (2007). A unified genetic theory for sporadic and inherited autism. Proceedings of the National Academy of Sciences of the United States of America, 104(31), 12831-12836. View Abstract
  11. Wang, K., Zhang, H., Ma, D., Bucan, M., Glessner, J. T., Abrahams, B. S., et al. (2009). Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature, 459(7246), 528-533. View Abstract
  12. Glessner, J. T., Wang, K., Cai, G., Korvatska, O., Kim, C. E., Wood, S., et al. (2009). Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature, 459(7246), 569-573. View Abstract
  13. Morrow, E. M., Yoo, S. Y., Flavell, S. W., Kim, T. K., Lin, Y., Hill, R. S., et al. (2008). Identifying autism loci and genes by tracing recent shared ancestry. Science, 321(5886), 218-223. View Abstract
  14. Weiss, L., A., Shen, Y., Korn, J. M., Arking, D. E., Miller, D. T., Fossdal, R., et al. (2008). Association between microdeletion and microduplication at 16p11.2 and autism. The New England Journal of Medicine, 358(7):667-675. View Abstract
  15. American Psychiatric Association. (2009a). DSM-V: The future manual. Retrieved February 22, 2010.
  16. American Psychiatric Association. (2009b). Report of the DSM-V Neurodevelopmental Disorders Work Group. Retrieved February 22, 2010.

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