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2016
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.
D. R. Roalf, Quarmley, M., Elliott, M. A., Satterthwaite, T. D., Vandekar, S. N., Ruparel, K., Gennatas, E. D., Calkins, M. E., Moore, T. M., Hopson, R., Prabhakaran, K., Jackson, C. T., Verma, R., Hakonarson, H., Gur, R. C., and Gur, R. E., The impact of quality assurance assessment on diffusion tensor imaging outcomes in a large-scale population-based cohort., Neuroimage, vol. 125, pp. 903-919, 2016.
R. G. Port, J Edgar, C., Ku, M., Bloy, L., Murray, R., Blaskey, L., Levy, S. E., and Roberts, T. P. L., Maturation of auditory neural processes in autism spectrum disorder - A longitudinal MEG study., Neuroimage Clin, vol. 11, pp. 566-577, 2016.
M. Yaari, Yitzhak, N., Harel, A., Friedlander, E., Bar-Oz, B., Eventov-Friedman, S., Mankuta, D., Gamliel, I., and Yirmiya, N., Stability of early risk assessment for autism spectrum disorder in preterm infants., Autism, vol. 20, no. 7, pp. 856-67, 2016.
T. D. Satterthwaite, Wolf, D. H., Calkins, M. E., Vandekar, S. N., Erus, G., Ruparel, K., Roalf, D. R., Linn, K. A., Elliott, M. A., Moore, T. M., Hakonarson, H., Shinohara, R. T., Davatzikos, C., Gur, R. C., and Gur, R. E., Structural Brain Abnormalities in Youth With Psychosis Spectrum Symptoms., JAMA Psychiatry, vol. 73, no. 5, pp. 515-24, 2016.
2015
E. A. Hartung, Laney, N., Kim, J. Young, Ruebner, R. L., Detre, J. A., Liu, H. - S., Davatzikos, C., Erus, G., Doshi, J. J., Schultz, R. T., Herrington, J. D., Jawad, A. F., Moodalbail, D. G., Gur, R. C., Port, A. M., Radcliffe, J., Hooper, S. R., and Furth, S. L., Design and methods of the NiCK study: neurocognitive assessment and magnetic resonance imaging analysis of children and young adults with chronic kidney disease., BMC Nephrol, vol. 16, p. 66, 2015.
D. R. Roalf, Vandekar, S. N., Almasy, L., Ruparel, K., Satterthwaite, T. D., Elliott, M. A., Podell, J., Gallagher, S., Jackson, C. T., Prasad, K., Wood, J., Pogue-Geile, M. F., Nimgaonkar, V. L., Gur, R. C., and Gur, R. E., Heritability of subcortical and limbic brain volume and shape in multiplex-multigenerational families with schizophrenia., Biol Psychiatry, vol. 77, no. 2, pp. 137-46, 2015.
G. Erus, Battapady, H., Satterthwaite, T. D., Hakonarson, H., Gur, R. E., Davatzikos, C., and Gur, R. C., Imaging patterns of brain development and their relationship to cognition., Cereb Cortex, vol. 25, no. 6, pp. 1676-84, 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
D. S. Mandell, Xie, M., Morales, K. H., Lawer, L., McCarthy, M., and Marcus, S. C., The interplay of outpatient services and psychiatric hospitalization among Medicaid-enrolled children with autism spectrum disorders., Arch Pediatr Adolesc Med, vol. 166, no. 1, pp. 68-73, 2012.
J. P. Casey, Magalhaes, T., Conroy, J. M., Regan, R., Shah, N., Anney, R., Shields, D. C., Abrahams, B. S., Almeida, J., Bacchelli, E., Bailey, A. J., Baird, G., Battaglia, A., Berney, T., Bolshakova, N., Bolton, P. F., Bourgeron, T., Brennan, S., Cali, P., Correia, C., Corsello, C., Coutanche, M., Dawson, G., de Jonge, M., Delorme, R., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Foley, S., Fombonne, E., Freitag, C. M., Gilbert, J., Gillberg, C., Glessner, J. T., Green, J., Guter, S. J., Hakonarson, H., Holt, R., Hughes, G., Hus, V., Igliozzi, R., Kim, C., Klauck, S. M., Kolevzon, A., Lamb, J. A., Leboyer, M., Le Couteur, A., Leventhal, B. L., Lord, C., Lund, S. C., Maestrini, E., Mantoulan, C., Marshall, C. R., McConachie, H., McDougle, C. J., McGrath, J., McMahon, W. M., Merikangas, A., Miller, J., Minopoli, F., Mirza, G. K., Munson, J., Nelson, S. F., Nygren, G., Oliveira, G., Pagnamenta, A. T., Papanikolaou, K., Parr, J. R., Parrini, B., Pickles, A., Pinto, D., Piven, J., Posey, D. J., Poustka, A., Poustka, F., Ragoussis, J., Rogé, B., Rutter, M. L., Sequeira, A. F., Soorya, L., Sousa, I., Sykes, N., Stoppioni, V., Tancredi, R., Tauber, M., Thompson, A. P., Thomson, S., Tsiantis, J., van Engeland, H., Vincent, J. B., Volkmar, F., Vorstman, J. A. S., Wallace, S., Wang, K., Wassink, T. H., White, K., Wing, K., Wittemeyer, K., Yaspan, B. L., Zwaigenbaum, L., Betancur, C., Buxbaum, J. D., Cantor, R. M., Cook, E. H., Coon, H., Cuccaro, M. L., Geschwind, D. H., Haines, J. L., Hallmayer, J., Monaco, A. P., Nurnberger, J. I., Pericak-Vance, M. A., Schellenberg, G. D., Scherer, S. W., Sutcliffe, J. S., Szatmari, P., Vieland, V. J., Wijsman, E. M., Green, A., Gill, M., Gallagher, L., Vicente, A., and Ennis, S., A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder., Hum Genet, vol. 131, no. 4, pp. 565-79, 2012.
2009
J. T. Glessner, Wang, K., Cai, G., Korvatska, O., Kim, C. E., Wood, S., Zhang, H., Estes, A., Brune, C. W., Bradfield, J. P., Imielinski, M., Frackelton, E. C., Reichert, J., Crawford, E. L., Munson, J., Sleiman, P. M. A., Chiavacci, R., Annaiah, K., Thomas, K., Hou, C., Glaberson, W., Flory, J., Otieno, F., Garris, M., Soorya, L., Klei, L., Piven, J., Meyer, K. J., Anagnostou, E., Sakurai, T., Game, R. M., Rudd, D. S., Zurawiecki, D., McDougle, C. J., Davis, L. K., Miller, J., Posey, D. J., Michaels, S., Kolevzon, A., Silverman, J. M., Bernier, R., Levy, S. E., Schultz, R. T., Dawson, G., Owley, T., McMahon, W. M., Wassink, T. H., Sweeney, J. A., Nurnberger, J. I., Coon, H., Sutcliffe, J. S., Minshew, N. J., Grant, S. F. A., Bućan, M., Cook, E. H., Buxbaum, J. D., Devlin, B., Schellenberg, G. D., and Hakonarson, H., Autism genome-wide copy number variation reveals ubiquitin and neuronal genes., Nature, vol. 459, no. 7246, pp. 569-73, 2009.
K. Wang, Zhang, H., Ma, D., Bućan, M., Glessner, J. T., Abrahams, B. S., Salyakina, D., Imielinski, M., Bradfield, J. P., Sleiman, P. M. A., Kim, C. E., Hou, C., Frackelton, E., Chiavacci, R., Takahashi, N., Sakurai, T., Rappaport, E., Lajonchere, C. M., Munson, J., Estes, A., Korvatska, O., Piven, J., Sonnenblick, L. I., Retuerto, A. I. Alvarez, Herman, E. I., Dong, H., Hutman, T., Sigman, M., Ozonoff, S., Klin, A., Owley, T., Sweeney, J. A., Brune, C. W., Cantor, R. M., Bernier, R., Gilbert, J. R., Cuccaro, M. L., McMahon, W. M., Miller, J., State, M. W., Wassink, T. H., Coon, H., Levy, S. E., Schultz, R. T., Nurnberger, J. I., Haines, J. L., Sutcliffe, J. S., Cook, E. H., Minshew, N. J., Buxbaum, J. D., Dawson, G., Grant, S. F. A., Geschwind, D. H., Pericak-Vance, M. A., Schellenberg, G. D., and Hakonarson, H., Common genetic variants on 5p14.1 associate with autism spectrum disorders., Nature, vol. 459, no. 7246, pp. 528-33, 2009.
M. Bućan, Abrahams, B. S., Wang, K., Glessner, J. T., Herman, E. I., Sonnenblick, L. I., Retuerto, A. I. Alvarez, Imielinski, M., Hadley, D., Bradfield, J. P., Kim, C., Gidaya, N. B., Lindquist, I., Hutman, T., Sigman, M., Kustanovich, V., Lajonchere, C. M., Singleton, A., Kim, J., Wassink, T. H., McMahon, W. M., Owley, T., Sweeney, J. A., Coon, H., Nurnberger, J. I., Li, M., Cantor, R. M., Minshew, N. J., Sutcliffe, J. S., Cook, E. H., Dawson, G., Buxbaum, J. D., Grant, S. F. A., Schellenberg, G. D., Geschwind, D. H., and Hakonarson, H., Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes., PLoS Genet, vol. 5, no. 6, p. e1000536, 2009.
M. C. Souders, Mason, T. B. A., Valladares, O., Bućan, M., Levy, S. E., Mandell, D. S., Weaver, T. E., and Pinto-Martin, J., Sleep behaviors and sleep quality in children with autism spectrum disorders., Sleep, vol. 32, no. 12, pp. 1566-78, 2009.
D. M. Rubin, Feudtner, C., Localio, R., and Mandell, D. S., State variation in psychotropic medication use by foster care children with autism spectrum disorder., Pediatrics, vol. 124, no. 2, pp. e305-12, 2009.