Research Library

New CAR Research Sheds Light on

 

Universal Screening for Autism in Toddlers

Export 21 results:
[ Author(Asc)] Title Type Year
Filters: First Letter Of Last Name is A  [Clear All Filters]
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
A
G. Azad and Mandell, D. S., Concerns of parents and teachers of children with autism in elementary school., Autism, vol. 20, no. 4, pp. 435-41, 2016.
G. F. Azad, Marcus, S. C., Sheridan, S. M., and Mandell, D. S., Partners in School: An Innovative Parent-Teacher Consultation Model for Children with Autism Spectrum Disorder., J Educ Psychol Consult, vol. 28, no. 4, pp. 460-486, 2018.
G. F. Azad, Locke, J., Kasari, C., and Mandell, D. S., Race, disability, and grade: Social relationships in children with autism spectrum disorders., Autism, vol. 21, no. 1, pp. 92-99, 2017.
G. F. Azad, Kim, M., Marcus, S. C., Sheridan, S. M., and Mandell, D. S., PARENT-TEACHER COMMUNICATION ABOUT CHILDREN WITH AUTISM SPECTRUM DISORDER: AN EXAMINATION OF COLLABORATIVE PROBLEM-SOLVING, Psychology in the Schools, vol. 53, pp. 1071–1084, 2016.
G. F. Azad, Marcus, S. C., Sheridan, S. M., and Mandell, D. S., Partners in School: An Innovative Parent-Teacher Consultation Model for Children with Autism Spectrum Disorder, Journal of Educational and Psychological Consultation, pp. 1–27, 2018.
G. Azad, Reisinger, E., Xie, M., and Mandell, D. S., Parent and Teacher Concordance on the Social Responsiveness Scale for Children with Autism., School Ment Health, vol. 8, no. 3, pp. 368-376, 2016.
G. F. Azad, Locke, J., Downey, M. Mary, Xie, M., and Mandell, D. S., One-to-One Assistant Engagement in Autism Support Classrooms., Teach Educ Spec Educ, vol. 38, no. 4, pp. 337-346, 2015.
S. P. Awate, Win, L., Yushkevich, P., Schultz, R. T., and Gee, J. C., 3D cerebral cortical morphometry in autism: increased folding in children and adolescents in frontal, parietal, and temporal lobes., Med Image Comput Comput Assist Interv, vol. 11, no. Pt 1, pp. 559-67, 2008.
Prevalence of autism spectrum disorders--Autism and Developmental Disabilities Monitoring Network, 14 sites, United States, 2008., MMWR Surveill Summ, vol. 61, no. 3, pp. 1-19, 2012.
Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006., MMWR Surveill Summ, vol. 58, no. 10, pp. 1-20, 2009.
M. Assaf, Hyatt, C. J., Wong, C. G., Johnson, M. R., Schultz, R. T., Hendler, T., and Pearlson, G. D., Mentalizing and motivation neural function during social interactions in autism spectrum disorders., Neuroimage Clin, vol. 3, pp. 321-31, 2013.
M. Assaf, Jagannathan, K., Calhoun, V. D., Miller, L., Stevens, M. C., Sahl, R., O'Boyle, J. G., Schultz, R. T., and Pearlson, G. D., Abnormal functional connectivity of default mode sub-networks in autism spectrum disorder patients., Neuroimage, vol. 53, no. 1, pp. 247-56, 2010.
L. Gutermuth Anthony, Kenworthy, L., Yerys, B. E., Jankowski, K. F., James, J. D., Harms, M. B., Martin, A., and Wallace, G. L., Interests in high-functioning autism are more intense, interfering, and idiosyncratic than those in neurotypical development., Dev Psychopathol, vol. 25, no. 3, pp. 643-52, 2013.
L. Antezana, Mosner, M. G., Troiani, V., and Yerys, B. E., Social-Emotional Inhibition of Return in Children with Autism Spectrum Disorder Versus Typical Development., J Autism Dev Disord, vol. 46, no. 4, pp. 1236-46, 2016.
R. Anney, Klei, L., Pinto, D., Almeida, J., Bacchelli, E., Baird, G., Bolshakova, N., Bölte, S., Bolton, P. F., Bourgeron, T., Brennan, S., Brian, J., Casey, J., Conroy, J., Correia, C., Corsello, C., Crawford, E. L., de Jonge, M., Delorme, R., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Fombonne, E., Gilbert, J., Gillberg, C., Glessner, J. T., Green, A., Green, J., Guter, S. J., Heron, E. A., Holt, R., Howe, J. L., Hughes, G., Hus, V., Igliozzi, R., Jacob, S., Kenny, G. P., Kim, C., Kolevzon, A., Kustanovich, V., Lajonchere, C. M., Lamb, J. A., Law-Smith, M., Leboyer, M., Le Couteur, A., Leventhal, B. L., Liu, X. - Q., Lombard, F., Lord, C., Lotspeich, L., Lund, S. C., Magalhaes, T. R., Mantoulan, C., McDougle, C. J., Melhem, N. M., Merikangas, A., Minshew, N. J., Mirza, G. K., Munson, J., Noakes, C., Nygren, G., Papanikolaou, K., Pagnamenta, A. T., Parrini, B., Paton, T., Pickles, A., Posey, D. J., Poustka, F., Ragoussis, J., Regan, R., Roberts, W., Roeder, K., Rogé, B., Rutter, M. L., Schlitt, S., Shah, N., Sheffield, V. C., Soorya, L., Sousa, I., Stoppioni, V., Sykes, N., Tancredi, R., Thompson, A. P., Thomson, S., Tryfon, A., Tsiantis, J., van Engeland, H., Vincent, J. B., Volkmar, F., Vorstman, J. A. S., Wallace, S., Wing, K., Wittemeyer, K., Wood, S., Zurawiecki, D., Zwaigenbaum, L., Bailey, A. J., Battaglia, A., Cantor, R. M., Coon, H., Cuccaro, M. L., Dawson, G., Ennis, S., Freitag, C. M., Geschwind, D. H., Haines, J. L., Klauck, S. M., McMahon, W. M., Maestrini, E., Miller, J., Monaco, A. P., Nelson, S. F., Nurnberger, J. I., Oliveira, G., Parr, J. R., Pericak-Vance, M. A., Piven, J., Schellenberg, G. D., Scherer, S. W., Vicente, A. M., Wassink, T. H., Wijsman, E. M., Betancur, C., Buxbaum, J. D., Cook, E. H., Gallagher, L., Gill, M., Hallmayer, J., Paterson, A. D., Sutcliffe, J. S., Szatmari, P., Vieland, V. J., Hakonarson, H., and Devlin, B., Individual common variants exert weak effects on the risk for autism spectrum disorders., Hum Mol Genet, vol. 21, no. 21, pp. 4781-92, 2012.
R. Anney, Klei, L., Pinto, D., Regan, R., Conroy, J., Magalhaes, T. R., Correia, C., Abrahams, B. S., Sykes, N., Pagnamenta, A. T., Almeida, J., Bacchelli, E., Bailey, A. J., Baird, G., Battaglia, A., Berney, T., Bolshakova, N., Bölte, S., Bolton, P. F., Bourgeron, T., Brennan, S., Brian, J., Carson, A. R., Casallo, G., Casey, J., Chu, S. H., Cochrane, L., Corsello, C., Crawford, E. L., Crossett, A., Dawson, G., de Jonge, M., Delorme, R., Drmic, I., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Fombonne, E., Freitag, C. M., Gilbert, J., Gillberg, C., Glessner, J. T., Goldberg, J., Green, J., Guter, S. J., Hakonarson, H., Heron, E. A., Hill, M., Holt, R., Howe, J. L., Hughes, G., Hus, V., Igliozzi, R., Kim, C., Klauck, S. M., Kolevzon, A., Korvatska, O., Kustanovich, V., Lajonchere, C. M., Lamb, J. A., Laskawiec, M., Leboyer, M., Le Couteur, A., Leventhal, B. L., Lionel, A. C., Liu, X. - Q., Lord, C., Lotspeich, L., Lund, S. C., Maestrini, E., Mahoney, W., Mantoulan, C., Marshall, C. R., McConachie, H., McDougle, C. J., McGrath, J., McMahon, W. M., Melhem, N. M., Merikangas, A., Migita, O., Minshew, N. J., Mirza, G. K., Munson, J., Nelson, S. F., Noakes, C., Noor, A., Nygren, G., Oliveira, G., Papanikolaou, K., Parr, J. R., Parrini, B., Paton, T., Pickles, A., Piven, J., Posey, D. J., Poustka, A., Poustka, F., Prasad, A., Ragoussis, J., Renshaw, K., Rickaby, J., Roberts, W., Roeder, K., Rogé, B., Rutter, M. L., Bierut, L. J., Rice, J. P., Salt, J., Sansom, K., Sato, D., Segurado, R., Senman, L., Shah, N., Sheffield, V. C., Soorya, L., Sousa, I., Stoppioni, V., Strawbridge, C., Tancredi, R., Tansey, K., Thiruvahindrapduram, B., Thompson, A. P., Thomson, S., Tryfon, A., Tsiantis, J., van Engeland, H., Vincent, J. B., Volkmar, F., Wallace, S., Wang, K., Wang, Z., Wassink, T. H., Wing, K., Wittemeyer, K., Wood, S., Yaspan, B. L., Zurawiecki, D., Zwaigenbaum, L., Betancur, C., Buxbaum, J. D., Cantor, R. M., Cook, E. H., Coon, H., Cuccaro, M. L., Gallagher, L., Geschwind, D. H., Gill, M., Haines, J. L., Miller, J., Monaco, A. P., Nurnberger, J. I., Paterson, A. D., Pericak-Vance, M. A., Schellenberg, G. D., Scherer, S. W., Sutcliffe, J. S., Szatmari, P., Vicente, A. M., Vieland, V. J., Wijsman, E. M., Devlin, B., Ennis, S., and Hallmayer, J., A genome-wide scan for common alleles affecting risk for autism., Hum Mol Genet, vol. 19, no. 20, pp. 4072-82, 2010.
R. J. L. Anney, Kenny, E. M., O'Dushlaine, C., Yaspan, B. L., Parkhomenka, E., Buxbaum, J. D., Sutcliffe, J., Gill, M., Gallagher, L., Buxbaum, J. D., Sutcliffe, J., Gill, M., and Gallagher, L., Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders., Eur J Hum Genet, vol. 19, no. 10, pp. 1082-9, 2011.
C. Anderson, J Law, K., Daniels, A., Rice, C., Mandell, D. S., Hagopian, L., and Law, P. A., Occurrence and family impact of elopement in children with autism spectrum disorders., Pediatrics, vol. 130, no. 5, pp. 870-7, 2012.
A. F. Alexander-Bloch, Shou, H., Liu, S., Satterthwaite, T. D., Glahn, D. C., Shinohara, R. T., Vandekar, S. N., and Raznahan, A., On testing for spatial correspondence between maps of human brain structure and function., Neuroimage, vol. 178, pp. 540-551, 2018.
T. Abel, Havekes, R., Saletin, J. M., and Walker, M. P., Sleep, plasticity and memory from molecules to whole-brain networks., Curr Biol, vol. 23, no. 17, pp. R774-88, 2013.
T. Abel and Klann, E., Molecular and cellular cognition: Neurobiology of Learning and Memory Special Issue 2013., Neurobiol Learn Mem, vol. 105, pp. 1-2, 2013.