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Universal Screening for Autism in Toddlers

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D. S. Mandell and Barry, C. L., Care for Autism and Other Disabilities - A Future in Jeopardy., N Engl J Med, vol. 376, no. 10, p. e15, 2017.
M. Luo, Fan, J., Wenger, T. L., Harr, M. H., Racobaldo, M., Mulchandani, S., Dubbs, H., Zackai, E. H., Spinner, N. B., and Conlin, L. K., CMIP haploinsufficiency in two patients with autism spectrum disorder and co-occurring gastrointestinal issues., Am J Med Genet A, vol. 173, no. 8, pp. 2101-2107, 2017.
H. J. Nuske, Hedley, D., Woollacott, A., Thomson, P., Macari, S., and Dissanayake, C., Developmental delays in emotion regulation strategies in preschoolers with autism., Autism Res, vol. 10, no. 11, pp. 1808-1822, 2017.
L. D. Wiggins, Tian, L. H., Levy, S. E., Rice, C., Lee, L. - C., Schieve, L., Pandey, J., Daniels, J., Blaskey, L., Hepburn, S., Landa, R., Edmondson-Pretzel, R., and Thompson, W., Homogeneous Subgroups of Young Children with Autism Improve Phenotypic Characterization in the Study to Explore Early Development., J Autism Dev Disord, vol. 47, no. 11, pp. 3634-3645, 2017.
A. F. Dimian, Botteron, K. N., Dager, S. R., Elison, J. T., Estes, A. M., Pruett, J. R., Schultz, R. T., Zwaigenbaum, L., Piven, J., and Wolff, J. J., Potential Risk Factors for the Development of Self-Injurious Behavior among Infants at Risk for Autism Spectrum Disorder., J Autism Dev Disord, vol. 47, no. 5, pp. 1403-1415, 2017.
D. D'Angelo, Lebon, S., Chen, Q., Martin-Brevet, S., Snyder, L. A. Green, Hippolyte, L., Hanson, E., Maillard, A. M., W Faucett, A., Macé, A., Pain, A., Bernier, R., Chawner, S. J. R. A., David, A., Andrieux, J., Aylward, E., Baujat, G., Caldeira, I., Conus, P., Ferrari, C., Forzano, F., Gérard, M., Goin-Kochel, R. P., Grant, E., Hunter, J. V., Isidor, B., Jacquette, A., Jønch, A. E., Keren, B., Lacombe, D., Le Caignec, C., Martin, C. Lese, Männik, K., Metspalu, A., Mignot, C., Mukherjee, P., Owen, M. J., Passeggeri, M., Rooryck-Thambo, C., Rosenfeld, J. A., Spence, S. J., Steinman, K. J., Tjernagel, J., Van Haelst, M., Shen, Y., Draganski, B., Sherr, E. H., Ledbetter, D. H., van den Bree, M. B. M., Beckmann, J. S., Spiro, J. E., Reymond, A., Jacquemont, S., and Chung, W. K., Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities., JAMA Psychiatry, vol. 73, no. 1, pp. 20-30, 2016.
T. D. Satterthwaite, Connolly, J. J., Ruparel, K., Calkins, M. E., Jackson, C., Elliott, M. A., Roalf, D. R., Hopson, R., Prabhakaran, K., Behr, M., Qiu, H., Mentch, F. D., Chiavacci, R., Sleiman, P. M. A., Gur, R. C., Hakonarson, H., and Gur, R. E., The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth., Neuroimage, vol. 124, no. Pt B, pp. 1115-1119, 2016.
J. I. Berman, Chudnovskaya, D., Blaskey, L., Kuschner, E., Mukherjee, P., Buckner, R., Nagarajan, S., Chung, W. K., Sherr, E. H., and Roberts, T. P. L., Relationship between M100 Auditory Evoked Response and Auditory Radiation Microstructure in 16p11.2 Deletion and Duplication Carriers., AJNR Am J Neuroradiol, vol. 37, no. 6, pp. 1178-84, 2016.
F. Zufferey, Sherr, E. H., Beckmann, N. D., Hanson, E., Maillard, A. M., Hippolyte, L., Macé, A., Ferrari, C., Kutalik, Z., Andrieux, J., Aylward, E., Barker, M., Bernier, R., Bouquillon, S., Conus, P., Delobel, B., W Faucett, A., Goin-Kochel, R. P., Grant, E., Harewood, L., Hunter, J. V., Lebon, S., Ledbetter, D. H., Martin, C. Lese, Männik, K., Martinet, D., Mukherjee, P., Ramocki, M. B., Spence, S. J., Steinman, K. J., Tjernagel, J., Spiro, J. E., Reymond, A., Beckmann, J. S., Chung, W. K., and Jacquemont, S., A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders., J Med Genet, vol. 49, no. 10, pp. 660-8, 2012.
N. Kharod Sell, Giarelli, E., Blum, N., Hanlon, A. L., and Levy, S. E., A comparison of autism spectrum disorder DSM-IV criteria and associated features among African American and white children in Philadelphia County., Disabil Health J, vol. 5, no. 1, pp. 9-17, 2012.
J. A. Saunders, Gandal, M. J., Roberts, T. P., and Siegel, S. J., NMDA antagonist MK801 recreates auditory electrophysiology disruption present in autism and other neurodevelopmental disorders., Behav Brain Res, vol. 234, no. 2, pp. 233-7, 2012.
J. T. Glessner, Connolly, J. J. M., and Hakonarson, H., Rare genomic deletions and duplications and their role in neurodevelopmental disorders., Curr Top Behav Neurosci, vol. 12, pp. 345-60, 2012.
M. Zimmer and Desch, L., Sensory integration therapies for children with developmental and behavioral disorders., Pediatrics, vol. 129, no. 6, pp. 1186-9, 2012.
D. E. Schendel, DiGuiseppi, C., Croen, L. A., M Fallin, D., Reed, P. L., Schieve, L. A., Wiggins, L. D., Daniels, J., Grether, J., Levy, S. E., Miller, L., Newschaffer, C., Pinto-Martin, J., Robinson, C., Windham, G. C., Alexander, A., Aylsworth, A. S., Bernal, P., Bonner, J. D., Blaskey, L., Bradley, C., Collins, J., Ferretti, C. J., Farzadegan, H., Giarelli, E., Harvey, M., Hepburn, S., Herr, M., Kaparich, K., Landa, R., Lee, L. - C., Levenseller, B., Meyerer, S., Rahbar, M. H., Ratchford, A., Reynolds, A., Rosenberg, S., Rusyniak, J., Shapira, S. K., Smith, K., Souders, M., Thompson, P. Aaron, Young, L., and Yeargin-Allsopp, M., The Study to Explore Early Development (SEED): a multisite epidemiologic study of autism by the Centers for Autism and Developmental Disabilities Research and Epidemiology (CADDRE) network., J Autism Dev Disord, vol. 42, no. 10, pp. 2121-40, 2012.