Copy-number variations associated with neuropsychiatric conditions von Scherer, Stephen W, Cook Jr, Edwin H

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Between a ROC and a hard place: decision making and making decisions about using the SCQ von Corsello, Christina, Hus, Vanessa, Pickles, Andrew, Risi, Susan, Cook Jr, Edwin H., Leventhal, Bennett L., Lord, Catherine

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Autism as a paradigmatic complex genetic disorder von Veenstra-Vanderweele, Jeremy, Christian, Susan L, Cook, Jr, Edwin H

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Self-injury in autism spectrum disorder: An effect of serotonin transporter gene promoter variants von Kolevzon, Alexander, Lim, Teresa, Schmeidler, James, Martello, Toni, Cook Jr., Edwin H, Silverman, Jeremy M

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A framework for the interpretation of de novo mutation in human disease von Samocha, Kaitlin E, Robinson, Elise B, Sanders, Stephan J, Stevens, Christine, Sabo, Aniko, McGrath, Lauren M, Kosmicki, Jack A, Rehnström, Karola, Mallick, Swapan, Kirby, Andrew, Wall, Dennis P, MacArthur, Daniel G, Gabriel, Stacey B, DePristo, Mark, Purcell, Shaun M, Palotie, Aarno, Boerwinkle, Eric, Buxbaum, Joseph D, Cook, Edwin H, Gibbs, Richard A, Schellenberg, Gerard D, Sutcliffe, James S, Devlin, Bernie, Roeder, Kathryn, Neale, Benjamin M, Daly, Mark J

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Combining Information From Multiple Sources in the Diagnosis of Autism Spectrum Disorders von RISI, SUSAN, LORD, CATHERINE, GOTHAM, KATHERINE, CORSELLO, CHRISTINA, CHRYSLER, CHRISTINA, SZATMARI, PETER, COOK, EDWIN H., LEVENTHAL, BENNETT L., PICKLES, ANDREW

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Dopamine transporter genotype and stimulant side effect factors in youth diagnosed with attention-deficit/hyperactivity disorder von Gruber, Reut, Joober, Ridha, Grizenko, Natalie, Leventhal, Bennett L, Cook, Jr, Edwin H, Stein, Mark A

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An association study of the brain-derived neurotrophic factor Val66Met polymorphism and amphetamine response von Flanagin, Brody A., Cook Jr, Edwin H., de Wit, Harriet

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Environmental and state-level regulatory factors affect the incidence of autism and intellectual disability von Rzhetsky, Andrey, Bagley, Steven C, Wang, Kanix, Lyttle, Christopher S, Cook, Jr, Edwin H, Altman, Russ B, Gibbons, Robert D

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common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism von Celestino-Soper, Patrícia B. S, Violante, Sara, Crawford, Emily L, Luo, Rui, Lionel, Anath C, Delaby, Elsa, Cai, Guiqing, Sadikovic, Bekim, Lee, Kwanghyuk, Lo, Charlene, Gao, Kun, Person, Richard E, Moss, Timothy J, German, Jennifer R, Huang, Ni, Shinawi, Marwan, Treadwell-Deering, Diane, Szatmari, Peter, Roberts, Wendy, Fernandez, Bridget, Schroer, Richard J, Stevenson, Roger E, Buxbaum, Joseph D, Betancur, Catalina, Scherer, Stephen W, Sanders, Stephan J, Geschwind, Daniel H, Sutcliffe, James S, Hurles, Matthew E, Wanders, Ronald J. A, Shaw, Chad A, Leal, Suzanne M, Cook, Edwin H. Jr, Goin-Kochel, Robin P, Vaz, Frédéric M, Beaudet, Arthur L

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A functional common polymorphism in a Sp1 recognition site of the epidermal growth factor receptor gene promoter von WANQING LIU, INNOCENTI, Federico, WU, Michael H, DESAI, Apurva A, DOLAN, M. Eileen, COOK, Edwin H, RATAIN, Mark J

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Training of child and adolescent psychiatry fellows in autism and intellectual disability von Marrus, Natasha, Veenstra-VanderWeele, Jeremy, Hellings, Jessica A, Stigler, Kimberly A, Szymanski, Ludwik, King, Bryan H, Carlisle, L Lee, Cook, Edwin H, Pruett, John R

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Dopamine transporter genotype and stimulant dose-response in youth with attention-deficit/hyperactivity disorder von Stein, Mark A, Waldman, Irwin, Newcorn, Jeffrey, Bishop, Jeffrey, Kittles, Rick, Cook, Jr, Edwin H

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Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2 von Chaste, Pauline, Sanders, Stephan J., Mohan, Kommu N., Klei, Lambertus, Song, Youeun, Murtha, Michael T., Hus, Vanessa, Lowe, Jennifer K., Willsey, A. Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W., Fombonne, Eric, Geschwind, Daniel, Grice, Dorothy E., Ledbetter, David H., Lord, Catherine, Mane, Shrikant M., Martin, Donna M., Morrow, Eric M., Walsh, Christopher A., Sutcliffe, James S., State, Matthew W., Martin, Christa Lese, Devlin, Bernie, Beaudet, Arthur L., Cook Jr, Edwin H., Kim, Soo-Jeong

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The Screening and Diagnosis of Autistic Spectrum Disorders von Filipek, Pauline A, Accardo, Pasquale J, Baranek, Grace T, Cook, Edwin H., Jr, Dawson, Geraldine, Gordon, Barry, Gravel, Judith S, Johnson, Chris P, Kallen, Ronald J, Levy, Susan E, Minshew, Nancy J, Prizant, Barry M, Rapin, Isabelle, Rogers, Sally J, Stone, Wendy L, Teplin, Stuart, Tuchman, Roberto F, Volkmar, Fred R

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Interethnic Difference in the Allelic Distribution of Human Epidermal Growth Factor Receptor Intron 1 Polymorphism von WANQING LIU, INNOCENTI, Federico, PEIXIAN CHEN, DAS, Soma, COOK, Edwin H, RATAIN, Mark J

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Evidence for a Susceptibility Locus on Chromosome 10p15 in Early-Onset Obsessive-Compulsive Disorder von Hanna, Gregory L, Veenstra-VanderWeele, Jeremy, Cox, Nancy J, Van Etten, Michelle, Fischer, Daniel J, Himle, Joseph A, Bivens, Nancy Chiu, Wu, Xiaolin, Roe, Cheryl A, Hennessy, Kathleen A, Dickel, Diane E, Leventhal, Bennett L, Cook, Edwin H

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An Open-Label Trial of Escitalopram in Pervasive Developmental Disorders von OWLEY, THOMAS, WALTON, LAURA, SALT, JEFF, GUTER, STEPHEN J., WINNEGA, MARREA, LEVENTHAL, BENNETT L., COOK, EDWIN H.

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Heritability and linkage analysis of sensitivity to cisplatin-induced cytotoxicity von DOLAN, M. Eileen, NEWBOLD, Karla G, NAGASUBRAMANIAN, Ramamoorthy, XIAOLIN WU, RATAIN, Mark J, COOK, Edwin H, BADNER, Judith A

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Parent-of-origin effects of the serotonin transporter gene associated with autism von Kistner-Griffin, Emily, Brune, Camille W., Davis, Lea K., Sutcliffe, James S., Cox, Nancy J., Cook Jr, Edwin H.

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