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Author Title Type [ Year(Asc)]
Filters: Author is Wenger, Tara L  [Clear All Filters]
2021
T. L. Wenger, Perkins, J., Parish-Morris, J., Hing, A. V., Chen, M. L., Cielo, C. M., Li, D., Bhoj, E. J., Hakonarson, H., Zackai, E., McDonald-McGinn, D. M., Taylor, J. A., Jackson, O., Sie, K., Bly, R., Dahl, J., and Evans, K. N., “Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequence.”, Am J Med Genet A, vol. 185, no. 12, pp. 3694-3700, 2021.
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.
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.
2016
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.
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.
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.