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Universal Screening for Autism in Toddlers

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Author Title [ Type(Desc)] Year
Filters: Author is McDonald-McGinn, Donna M  [Clear All Filters]
Journal Article
W. P. Kennedy, Mudd, P. A., Maguire, M. A., Souders, M. C., McDonald-McGinn, D. M., Marcus, C. L., Zackai, E. H., Solot, C. B., Mason, T. B. Alexande, Jackson, O. A., and Elden, L. M., “22q11.2 Deletion syndrome and obstructive sleep apnea.”, Int J Pediatr Otorhinolaryngol, vol. 78, no. 8, pp. 1360-4, 2014.
T. L. Wenger, Miller, J. S., DePolo, L. M., de Marchena, A. B., Clements, C. C., Emanuel, B. S., Zackai, E. H., McDonald-McGinn, D. M., and Schultz, R. T., “22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening.”, Mol Autism, vol. 7, p. 27, 2016.
E. J Schmitt, Vandekar, S., Yi, J., Calkins, M. E., Ruparel, K., Roalf, D. R., Whinna, D., Souders, M. C., Satterwaite, T. D., Prabhakaran, K., McDonald-McGinn, D. M., Zackai, E. H., Gur, R. C., Emanuel, B. S., and Gur, R. E., “Aberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome.”, Biol Psychiatry, vol. 78, no. 2, pp. 135-43, 2015.
T. L. Wenger, Bhoj, E. J., Wetmore, R. F., Mennuti, M. T., Bartlett, S. P., Mollen, T. J., McDonald-McGinn, D. M., and Zackai, E. H., “Beare-Stevenson syndrome: two new patients, including a novel finding of tracheal cartilaginous sleeve.”, Am J Med Genet A, vol. 167A, no. 4, pp. 852-7, 2015.
J. J. Yi, Tang, S. X., McDonald-McGinn, D. M., Calkins, M. E., Whinna, D. A., Souders, M. C., Zackai, E. H., Goldmuntz, E., Gaynor, J. W., Gur, R. C., Emanuel, B. S., and Gur, R. E., “Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome.”, Am J Med Genet B Neuropsychiatr Genet, vol. 165B, no. 2, pp. 137-47, 2014.
C. C. Clements, Wenger, T. L., Zoltowski, A. R., Bertollo, J. R., Miller, J. S., de Marchena, A. B., Mitteer, L. M., Carey, J. C., Yerys, B. E., Zackai, E. H., Emanuel, B. S., McDonald-McGinn, D. M., and Schultz, R. T., “Critical region within 22q11.2 linked to higher rate of autism spectrum disorder.”, Mol Autism, vol. 8, p. 58, 2017.
E. J Schmitt, Yi, J., Calkins, M. E., Ruparel, K., Roalf, D. R., Cassidy, A., Souders, M. C., Satterthwaite, T. D., McDonald-McGinn, D. M., Zackai, E. H., Gur, R. C., Emanuel, B. S., and Gur, R. E., “Disrupted anatomic networks in the 22q11.2 deletion syndrome.”, Neuroimage Clin, vol. 12, pp. 420-8, 2016.
J. J. Yi, Calkins, M. E., Tang, S. X., Kohler, C. G., McDonald-McGinn, D. M., Zackai, E. H., Savitt, A. P., Bilker, W. B., Whinna, D. A., Souders, M. C., Emanuel, B. S., Gur, R. C., and Gur, R. E., “Impact of psychiatric comorbidity and cognitive deficit on function in 22q11.2 deletion syndrome.”, J Clin Psychiatry, vol. 76, no. 10, pp. e1262-70, 2015.
T. L. Wenger, Kao, C., McDonald-McGinn, D. M., Zackai, E. H., Bailey, A., Schultz, R. T., Morrow, B. E., Emanuel, B. S., and Hakonarson, H., “The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder.”, Sci Rep, vol. 6, p. 19372, 2016.
S. X. Tang, Yi, J. J., Moore, T. M., Calkins, M. E., Kohler, C. G., Whinna, D. A., Souders, M. C., Zackai, E. H., McDonald-McGinn, D. M., Emanuel, B. S., Bilker, W. B., Gur, R. C., and Gur, R. E., “Subthreshold psychotic symptoms in 22q11.2 deletion syndrome.”, J Am Acad Child Adolesc Psychiatry, vol. 53, no. 9, pp. 991-1000.e2, 2014.
D. R. Roalf, J Schmitt, E., Vandekar, S. N., Satterthwaite, T. D., Shinohara, R. T., Ruparel, K., Elliott, M. A., Prabhakaran, K., McDonald-McGinn, D. M., Zackai, E. H., Gur, R. C., Emanuel, B. S., and Gur, R. E., “White matter microstructural deficits in 22q11.2 deletion syndrome.”, Psychiatry Res Neuroimaging, vol. 268, pp. 35-44, 2017.