Intellectual and Developmental Disabilities (IDDs): Scientific Articles

Featured Articles

The following featured articles include those from NICHD researchers or NICHD-supported researchers.

  • Bish, L. T., Yarchoan, M., Sleeper, M. M., Gazzara, J. A., Morine, K. J., Acosta, P., et al. (2011). Chronic losartan administration reduces mortality and preserves cardiac but not skeletal muscle function in dystrophic mice. PLOS ONE, 6, e20856. PMID: 21731628
  • Dawson, G., Rogers, S., Munson, J., Smith, M., Winter, J., Greenson J., et al. (2010). Randomized, controlled trial of an intervention for toddlers with autism: The Early Start Denver Model. Pediatrics, 125, e17-e23. PMID: 19948568
  • Delahanty, R. J., Kang, J. Q., Brune, C. W., Kistner, E. O., Courchesne, E., Cox, N. J., et al. (2011). Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism. Molecular Psychiatry, 16, 86-96. PMID: 19935738
  • Goldman, S. E., Urbano, R. C., & Hodapp, R. M. (2011). Determining the amount, timing and causes of mortality among infants with Down syndrome. Journal of Intellectual Disability Research, 55, 85-94. PMID: 21108677
  • Goldstein, J. A., Kelly, S. M., LoPresti, P. P., Heydemann, A., Earley, J. U., Ferguson, E. L., et al. (2010). SMAD signaling drives heart and muscle dysfunction in a Drosophila model of muscular dystrophy. Human Molecular Genetics, 20, 894-904. PMID: 21138941
  • Gross, C., Nakamoto, M., Yao, X., Chan, C. B., Yim, S.Y., Ye, K., et al. (2010). Excess phosphoinositide 3-kinase subunit synthesis and activity as a novel therapeutic target in fragile X syndrome. Journal of Neuroscience, 30, 10624-10638. PMID: 20702695
  • Jenkins, E. C., Ye, L., Gu, H., Ni, S. A., Velinov, M., Pang, D., et al. (2010). Shorter telomeres may indicate dementia status in older individuals with Down syndrome. Neurobiology of Aging, 31, 765-771. PMID: 18635289
  • Muddashetty, R. S., Nalavadi, V. C., Gross, C., Yao, X., Xing, L., Laur, O., et al. (2011). Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation, and mGluR signaling. Molecular Cell, 42, 673-688. PMID: 21658607
  • Peters, S. U., Kaufmann, W. E., Bacino, C. A., Anderson, A. W., Adapa, P., Chu, Z., et al. (2011). Alterations in white matter pathways in Angelman syndrome. Developmental Medicine and Child Neurology, 53, 361-367. PMID: 21121904
  • Pierce, K., Conant, D., Hazin, R., Stoner, R., & Desmond, J. (2011). Preference for geometric patterns early in life as a risk factor for autism. Archives of General Psychiatry, 68, 101-109. PMID: 20819977
  • Pinto, D., Pagnamenta, A. T., Klei, L., Anney, R., Merico, D., Regan, R., et al. (2010). Functional impact of global rare copy number variation in autism spectrum disorders. Nature, 466, 368-372. PMID: 20531469
  • Symons, F. J., Harper, V., Shinde, S. K., Clary, J., & Bodfish, J. W. (2010). Evaluating a sham-controlled sensory-testing protocol for nonverbal adults with neurodevelopmental disorders: Self-injury and gender effects. Journal of Pain. 11, 773-781. PMID: 20418171

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