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Export 23 results:
Author Title Type [ Year(Asc)]
Filters: Keyword is Phenotype  [Clear All Filters]
2015
L. D. Wiggins, Levy, S. E., Daniels, J., Schieve, L., Croen, L. A., DiGuiseppi, C., Blaskey, L., Giarelli, E., Lee, L. - C., Pinto-Martin, J., Reynolds, A., Rice, C., Rosenberg, C. Robinson, Thompson, P., Yeargin-Allsopp, M., Young, L., and Schendel, D., Autism spectrum disorder symptoms among children enrolled in the Study to Explore Early Development (SEED)., J Autism Dev Disord, vol. 45, no. 10, pp. 3183-94, 2015.
D. H. Wolf, Satterthwaite, T. D., Calkins, M. E., Ruparel, K., Elliott, M. A., Hopson, R. D., Jackson, C. T., Prabhakaran, K., Bilker, W. B., Hakonarson, H., Gur, R. C., and Gur, R. E., Functional neuroimaging abnormalities in youth with psychosis spectrum symptoms., JAMA Psychiatry, vol. 72, no. 5, pp. 456-65, 2015.
A. M. Weljie, Meerlo, P., Goel, N., Sengupta, A., Kayser, M. S., Abel, T., Birnbaum, M. J., Dinges, D. F., and Sehgal, A., Oxalic acid and diacylglycerol 36:3 are cross-species markers of sleep debt., Proc Natl Acad Sci U S A, vol. 112, no. 8, pp. 2569-74, 2015.
M. E. Calkins, Merikangas, K. R., Moore, T. M., Burstein, M., Behr, M. A., Satterthwaite, T. D., Ruparel, K., Wolf, D. H., Roalf, D. R., Mentch, F. D., Qiu, H., Chiavacci, R., Connolly, J. J., Sleiman, P. M. A., Gur, R. C., Hakonarson, H., and Gur, R. E., The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative., J Child Psychol Psychiatry, vol. 56, no. 12, pp. 1356-1369, 2015.
2012
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.
I. - T. Judy Wang, Allen, M., Goffin, D., Zhu, X., Fairless, A. H., Brodkin, E. S., Siegel, S. J., Marsh, E. D., Blendy, J. A., and Zhou, Z., Loss of CDKL5 disrupts kinome profile and event-related potentials leading to autistic-like phenotypes in mice., Proc Natl Acad Sci U S A, vol. 109, no. 52, pp. 21516-21, 2012.
M. J. Gandal, Anderson, R. L., Billingslea, E. N., Carlson, G. C., Roberts, T. P. L., and Siegel, S. J., Mice with reduced NMDA receptor expression: more consistent with autism than schizophrenia?, Genes Brain Behav, vol. 11, no. 6, pp. 740-50, 2012.
B. M. Neale, Kou, Y., Liu, L., Ma'ayan, A., Samocha, K. E., Sabo, A., Lin, C. - F., Stevens, C., San Wang, L. -, Makarov, V., Polak, P., Yoon, S., Maguire, J., Crawford, E. L., Campbell, N. G., Geller, E. T., Valladares, O., Schafer, C., Liu, H., Zhao, T., Cai, G., Lihm, J., Dannenfelser, R., Jabado, O., Peralta, Z., Nagaswamy, U., Muzny, D., Reid, J. G., Newsham, I., Wu, Y., Lewis, L., Han, Y., Voight, B. F., Lim, E., Rossin, E., Kirby, A., Flannick, J., Fromer, M., Shakir, K., Fennell, T., Garimella, K., Banks, E., Poplin, R., Gabriel, S., DePristo, M., Wimbish, J. R., Boone, B. E., Levy, S. E., Betancur, C., Sunyaev, S., Boerwinkle, E., Buxbaum, J. D., Cook, E. H., Devlin, B., Gibbs, R. A., Roeder, K., Schellenberg, G. D., Sutcliffe, J. S., and Daly, M. J., Patterns and rates of exonic de novo mutations in autism spectrum disorders., Nature, vol. 485, no. 7397, pp. 242-5, 2012.
X. Gai, Xie, H. M., Perin, J. C., Takahashi, N., Murphy, K., Wenocur, A. S., D'arcy, M., O'Hara, R. J., Goldmuntz, E., Grice, D. E., Shaikh, T. H., Hakonarson, H., Buxbaum, J. D., Elia, J., and White, P. S., Rare structural variation of synapse and neurotransmission genes in autism., Mol Psychiatry, vol. 17, no. 4, pp. 402-11, 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.