Autism as a disorder of neural information processing: directions for research and targets for therapy
BELMONTE, M. K, COOK, E. H, PERRY, E. K, JIANG, Y. H, DELOREY, T. M, TIERNEY, E, ANDERSON, G. M, RUBENSTEIN, J. L. R, GREENOUGH, W. T, BECKEL-MITCHENER, A, COURCHESNE, E, BOULANGER, L. M, POWELL, S. B, LEVITT, P. R
Published in Molecular psychiatry (01.07.2004)
Published in Molecular psychiatry (01.07.2004)
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De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder
HAMILTON, P. J, CAMPBELL, N. G, MCHAOURAB, H. S, MATTHIES, H. J. G, SUTCLIFFE, J. S, GALLI, A, SHARMA, S, ERREGER, K, HERBORG HANSEN, F, SAUNDERS, C, BELOVICH, A. N, SAHAI, M. A, COOK, E. H, GETHER, U
Published in Molecular psychiatry (01.12.2013)
Published in Molecular psychiatry (01.12.2013)
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Association between a GABRB3 polymorphism and autism
BUXBAUM, J. D, SILVERMAN, J. M, SMITH, C. J, GREENBERG, D. A, KILIFARSKI, M, REICHERT, J, COOK, E. H, FANG, Y, SONG, C-Y, VITALE, R
Published in Molecular psychiatry (01.01.2002)
Published in Molecular psychiatry (01.01.2002)
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Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients
Yan, J, Oliveira, G, Coutinho, A, Yang, C, Feng, J, Katz, C, Sram, J, Bockholt, A, Jones, I R, Craddock, N, Cook, Jr, E H, Vicente, A, Sommer, S S
Published in Molecular psychiatry (01.04.2005)
Published in Molecular psychiatry (01.04.2005)
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5HT2A receptor blockade in dorsomedial striatum reduces repetitive behaviors in BTBR mice
Amodeo, D. A., Rivera, E., Cook, E. H., Sweeney, J. A., Ragozzino, M. E.
Published in Genes, brain and behavior (01.03.2017)
Published in Genes, brain and behavior (01.03.2017)
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Transmission disequilibrium testing of arginine vasopressin receptor 1a (AVPR1A) polymorphisms in autism
KIM, S.-J, YOUNG, L. J, GONEN, D, VEENSTRA-VANDERWEELE, J, COURCHESNE, R, COURCHESNE, E, LORD, C, LEVENTHAL, B. L, COOK, E. H, INSEL, T. R
Published in Molecular psychiatry (01.01.2002)
Published in Molecular psychiatry (01.01.2002)
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Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism
DELAHANTY, R. J, KANG, J. Q, BRUNE, C. W, KISTNER, E. O, COURCHESNE, E, COX, N. J, COOK, E. H, MACDONALD, R. L, SUTCLIFFE, J. S
Published in Molecular psychiatry (01.01.2011)
Published in Molecular psychiatry (01.01.2011)
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Journal Article
Autism and the serotonin transporter: the long and short of it
DEVLIN, B, COOK, E. H, RODIER, P. M, STODGELL, C, SCHELLENBERG, G. D, COON, H, DAWSON, G, GRIGORENKO, E. L, MCMAHON, W, MINSHEW, N, PAULS, D, SMITH, M, SPENCE, M. A
Published in Molecular psychiatry (01.12.2005)
Published in Molecular psychiatry (01.12.2005)
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Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society
Filipek, P A, Accardo, P J, Ashwal, S, Baranek, G T, Cook, Jr, E H, Dawson, G, Gordon, B, Gravel, J S, Johnson, C P, Kallen, R J, Levy, S E, Minshew, N J, Ozonoff, S, Prizant, B M, Rapin, I, Rogers, S J, Stone, W L, Teplin, S W, Tuchman, R F, Volkmar, F R
Published in Neurology (22.08.2000)
Published in Neurology (22.08.2000)
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Journal Article
Evidence of linkage between the serotonin transporter and autistic disorder
Cook, Jr, E H, Courchesne, R, Lord, C, Cox, N J, Yan, S, Lincoln, A, Haas, R, Courchesne, E, Leventhal, B L
Published in Molecular psychiatry (01.05.1997)
Published in Molecular psychiatry (01.05.1997)
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Journal Article
A MEMS diamond hemispherical resonator
Bernstein, J J, Bancu, M G, Cook, E H, Chaparala, M V, Teynor, W A, Weinberg, M S
Published in Journal of micromechanics and microengineering (01.12.2013)
Published in Journal of micromechanics and microengineering (01.12.2013)
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Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder
KIM, S.-J, COX, N, COURCHESNE, R, LORD, C, CORSELLO, C, AKSHOOMOFF, N, GUTER, S, LEVENTHAL, B. L, COURCHESNE, E, COOK, E. H
Published in Molecular psychiatry (01.01.2002)
Published in Molecular psychiatry (01.01.2002)
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Journal Article
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
COOK, E. H, LINDGREN, V, LEVENTHAL, B. L, COURCHESNE, R, LINCOLN, A, SHULMAN, C, LORD, C, COURCHESNES, E
Published in American journal of human genetics (01.04.1997)
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Published in American journal of human genetics (01.04.1997)
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Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior
Wakschlag, L S, Kistner, E O, Pine, D S, Biesecker, G, Pickett, K E, Skol, A D, Dukic, V, Blair, R J R, Leventhal, B L, Cox, N J, Burns, J L, Kasza, K E, Wright, R J, Cook, Jr, E H
Published in Molecular psychiatry (01.09.2010)
Published in Molecular psychiatry (01.09.2010)
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Journal Article
Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis
Davis, L.K., Maltman, N., Mosconi, M.W., Macmillan, C., Schmitt, L., Moore, K., Francis, S.M., Jacob, S., Sweeney, J.A., Cook, E.H.
Published in American journal of medical genetics. Part A (01.07.2012)
Published in American journal of medical genetics. Part A (01.07.2012)
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The Autism Diagnostic Observation Schedule-Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism
Lord, Catherine, Risi, Susan, Lambrecht, Linda, Cook, Edwin H., Jr, Leventhal, Bennett L, DiLavore, Pamela C, Pickles, Andrew, Rutter, Michael
Published in Journal of autism and developmental disorders (01.06.2000)
Published in Journal of autism and developmental disorders (01.06.2000)
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Journal Article
Linkage-Disequilibrium Mapping of Autistic Disorder, with 15q11-13 Markers
Cook, Edwin H., Courchesne, Rachel Y., Cox, Nancy J., Lord, Catherine, Gonen, David, Guter, Stephen J., Lincoln, Alan, Nix, Kristi, Haas, Richard, Leventhal, Bennett L., Courchesne, Eric
Published in American journal of human genetics (01.05.1998)
Published in American journal of human genetics (01.05.1998)
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Journal Article
Association of attention-deficit disorder and the dopamine transporter gene
COOK, E. H, STEIN, M. A, KRASOWSKI, M. D, COX, N. J, OLKON, D. M, KIEFFER, J. E, LEVENTHAL, B. L
Published in American journal of human genetics (01.04.1995)
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Published in American journal of human genetics (01.04.1995)
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