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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Parental broader autism subphenotypes in ASD affected families: relationship to gender, child's symptoms, SSRI treatment, and platelet serotonin
Levin-Decanini, T, Maltman, N, Francis, S M, Guter, S, Anderson, G M, Cook, E, Jacob, S
Published in Autism research (01.12.2013)
Published in Autism research (01.12.2013)
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Transmission disequilibrium mapping at the serotonin transporter gene 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 Jr, E H
Published in Molecular psychiatry (01.03.2002)
Published in Molecular psychiatry (01.03.2002)
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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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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
Satterstrom, F. Kyle, Breen, Michael S., Grove, Jakob, Klei, Lambertus, Xu, Xinyi, Norman, Utku, Brand, Harrison, Schwartz, Grace, Barbosa, Mafalda, Bybjerg-Grauholm, Jonas, Carracedo, Angel, Chiocchetti, Andreas G., Chung, Brian H.Y., Coon, Hilary, Cuccaro, Michael L., Dalla Bernardina, Bernardo, Domenici, Enrico, Dong, Shan, Freitag, Christine M., González-Peñas, Javier, Guter, Stephen, He, Xin, Herman, Gail E., Hertz-Picciotto, Irva, Hougaard, David M., Ionita-Laza, Iuliana, Jacob, Suma, Jamison, Jesslyn, Jugessur, Astanand, Kolevzon, Alexander, Kushima, Itaru, Lee, So Lun, Lehtimäki, Terho, Lim, Elaine T., Lipkin, W. Ian, Lopergolo, Diego, Lopes, Fátima, Ludena, Yunin, Maciel, Patricia, Meiri, Gal, Menashe, Idan, Miller, Judith, Montenegro, Eduarda M.S., Muglia, Pierandrea, Nordentoft, Merete, Ozaki, Norio, Palotie, Aarno, Parellada, Mara, Passos-Bueno, Maria Rita, Persico, Antonio M., Pessah, Isaac, Puura, Kaija, Renieri, Alessandra, Riberi, Evelise, Robinson, Elise B., Samocha, Kaitlin E., Sandin, Sven, Santangelo, Susan L., Schellenberg, Gerry, Scherer, Stephen W., Schmitt, Lauren, Silva, Isabela M.W., Singh, Tarjinder, Siper, Paige M., Soares, Gabriela, Susser, Ezra, Szatmari, Peter, Tang, Lara, Tassone, Flora, Teufel, Karoline, Trelles, Maria del Pilar, Werge, Thomas, Werling, Donna M., Wigdor, Emilie M., Yu, Mullin H.C., Zachi, Elaine, Agerbo, Esben, Als, Thomas Damm, Bækvad-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Maller, Julian, Mattheisen, Manuel, Moran, Jennifer, Pallesen, Jonatan, Poulsen, Jesper Buchhave, Ripke, Stephan, Gallagher, Louise, Gill, Michael, Zwick, Michael E., State, Matthew W., Daly, Mark J., Buxbaum, Joseph D.
Published in Cell (06.02.2020)
Published in Cell (06.02.2020)
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Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Pinto, Dalila, Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Vorstman, Jacob A.S., Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T., Oliveira, Bárbara, Magalhaes, Tiago R., Lowe, Jennifer K., Howe, Jennifer L., Gilbert, John, Duketis, Eftichia, Dombroski, Beth A., Cuccaro, Michael, Crawford, Emily L., Correia, Catarina T., Conroy, Judith, Conceição, Inês C., Chiocchetti, Andreas G., Casey, Jillian P., Cai, Guiqing, Cabrol, Christelle, Bacchelli, Elena, Gallinger, Steven, Cotterchio, Michelle, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, van Engeland, Herman, Tryfon, Ana, Thomson, Susanne, Rogé, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, McInnes, L. Alison, McGrew, Susan G., Lord, Catherine, Leboyer, Marion, Le Couteur, Ann S., Kolevzon, Alexander, Jiménez González, Patricia, Jacob, Suma, Holt, Richard, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F., Bernier, Raphael, Baird, Gillian, Bailey, Anthony J., Almeida, Joana, Wijsman, Ellen M., Vieland, Veronica J., Vicente, Astrid M., Schellenberg, Gerard D., Pericak-Vance, Margaret, Paterson, Andrew D., Parr, Jeremy R., Oliveira, Guiomar, Nurnberger, John I., Monaco, Anthony P., Maestrini, Elena, Klauck, Sabine M., Hakonarson, Hakon, Haines, Jonathan L., Geschwind, Daniel H., Freitag, Christine M., Folstein, Susan E., Ennis, Sean, Coon, Hilary, Battaglia, Agatino, Szatmari, Peter, Sutcliffe, James S., Hallmayer, Joachim, Gill, Michael, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Gallagher, Louise, Betancur, Catalina, Scherer, Stephen W.
Published in American journal of human genetics (01.05.2014)
Published in American journal of human genetics (01.05.2014)
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Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability
Tan, Natalie B, Pagnamenta, Alistair T, Ferla, Matteo P, Gadian, Jonathan, Chung, Brian HY, Chan, Marcus CY, Fung, Jasmine LF, Cook, Edwin, Guter, Stephen, Boschann, Felix, Heinen, Andre, Schallner, Jens, Mignot, Cyril, Keren, Boris, Whalen, Sandra, Sarret, Catherine, Mittag, Dana, Demmer, Laurie, Stapleton, Rachel, Saida, Ken, Matsumoto, Naomichi, Miyake, Noriko, Sheffer, Ruth, Mor-Shaked, Hagar, Barnett, Christopher P, Byrne, Alicia B, Scott, Hamish S, Kraus, Alison, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Iorio, Raffaele, Di Dato, Fabiola, Pais, Lynn S, Yeung, Alison, Tan, Tiong Y, Taylor, Jenny C, Christodoulou, John, White, Susan M
Published in Journal of medical genetics (01.05.2022)
Published in Journal of medical genetics (01.05.2022)
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A Genomewide Screen for Autism: Strong Evidence for Linkage to Chromosomes 2q, 7q, and 16p
Published in American journal of human genetics
(01.09.2001)
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An Open-Label Trial of Escitalopram in Pervasive Developmental Disorders
Owley, Thomas, Walton, Laura, Salt, Jeff, Guter, Stephen J., Jr, Winnega, Marrea, Leventhal, Bennett L, Cook, Edwin H., Jr
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.04.2005)
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.04.2005)
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