תוצאות חיפוש - Guter, Stephen

Lovastatin Treatment of a Patient with a De Novo SYNGAP1 Protein Truncating Variant מאת Cook, Edwin H., Masaki, Jayson T., Guter, Stephen J., Najjar, Fedra

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de Novo Unbalanced Translocation (4p duplication/8p deletion) in a Patient with Autism, OCD, and Overgrowth Syndrome מאת Sagar, Angela, Pinto, Dalila, Najjar, Fedra, Guter, Stephen J., Macmillan, Carol, Cook, Edwin H.

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Variants in Adjacent Oxytocin/Vasopressin Gene Region and Associations with ASD Diagnosis and Other Autism Related Endophenotypes מאת Francis, Sunday M., Kistner-Griffin, Emily, Yan, Zhongyu, Guter, Stephen, Cook, Edwin H., Jacob, Suma

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An ontology for Autism Spectrum Disorder (ASD) to infer ASD phenotypes from Autism Diagnostic Interview–Revised data מאת Mugzach, Omri, Peleg, Mor, Bagley, Steven C., Guter, Stephen J., Cook, Edwin H., Altman, Russ B.

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ASD and Genetic Associations with Receptors for Oxytocin and Vasopressin—AVPR1A, AVPR1B, and OXTR מאת Francis, Sunday M., Kim, Soo-Jeong, Kistner-Griffin, Emily, Guter, Stephen, Cook, Edwin H., Jacob, Suma

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Neurobehavioral Abnormalities in First-Degree Relatives of Individuals With Autism מאת Mosconi, Matthew W., Kay, Margaret, D’Cruz, Anna-Maria, Guter, Stephen, Kapur, Kush, Macmillan, Carol, Stanford, Lisa D., Sweeney, John A.

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Escitalopram pharmacogenetics: CYP2C19 relationships with dosing and clinical outcomes in Autism Spectrum Disorder מאת Bishop, Jeffrey R., Najjar, Fedra, Rubin, Leah H., Guter, Stephen J., Owley, Thomas, Mosconi, Matthew W., Jacob, Suma, Cook, Edwin H.

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()Is there sexual dimorphism of hyperserotonemia in Autism Spectrum Disorder? מאת Shuffrey, Lauren C., Guter, Stephen J., Delaney, Shannon, Jacob, Suma, Anderson, George M., Sutcliffe, James S., Cook, Edwin H., Veenstra-VanderWeele, Jeremy

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A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders מאת Kim, Soo-Jeong, Silva, Raquel M, Flores, Cindi G, Jacob, Suma, Guter, Stephen, Valcante, Gregory, Zaytoun, Annette M, Cook, Edwin H, Badner, Judith A

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Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism מאת Chen, Rui, Davis, Lea K., Guter, Stephen, Wei, Qiang, Jacob, Suma, Potter, Melissa H., Cox, Nancy J., Cook, Edwin H., Sutcliffe, James S., Li, Bingshan

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Vocabulary comprehension in adults with fragile X syndrome (FXS) מאת Hoffmann, Anne, Krause, Sue Ellen, Wuu, Joanne, Leurgans, Sue, Guter, Stephen J., Block, Sandra S., Salt, Jeff, Cook, Edwin, Maino, Dominick M., Berry-Kravis, Elizabeth

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Pharmacogenetic Study of Serotonin Transporter and 5HT2A Genotypes in Autism מאת Najjar, Fedra, Owley, Thomas, Mosconi, Matthew W., Jacob, Suma, Hur, Kwan, Guter, Stephen J., Sweeney, John A., Gibbons, Robert D, Cook, Edwin H., Bishop, Jeffrey R.

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WHOLE BLOOD SEROTONIN AND PLATELET 5-HT(2A) BINDING מאת Aaron, Elizabeth, Veenstra-VanderWeele, Jeremy, Montgomery, Alicia, Ren, Xinguo, Guter, Stephen, Pandey, Ghanshyam N., Cook, Edwin, Anderson, George, Carneiro, Ana MD, Jacob, Suma, Mosconi, Matthew

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Maternal Serotonin Levels Are Associated With Cognitive Ability and Core Symptoms in Autism Spectrum Disorder מאת Montgomery, Alicia K., Shuffrey, Lauren C., Guter, Stephen J., Anderson, George M., Jacob, Suma, Mosconi, Matthew W., Sweeney, John A., Turner, J. Blake, Sutcliffe, James S., Cook, Edwin H., Veenstra-VanderWeele, Jeremy

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A Multi-Site Study of the Clinical Diagnosis of Different Autism Spectrum Disorders מאת Lord, Catherine, Petkova, Eva, Hus, Vanessa, Gan, Weijin, Lu, Feihan, Martin, Donna M., Ousley, Opal, Guy, Lisa, Bernier, Raphael, Gerdts, Jennifer, Algermissen, Molly, Whitaker, Agnes, Sutcliffe, James S., Warren, Zachary, Klin, Ami, Saulnier, Celine, Hanson, Ellen, Hundley, Rachel, Piggot, Judith, Fombonne, Eric, Steiman, Mandy, Miles, Judith, Kanne, Stephen M., Goin-Kochel, Robin P., Peters, Sarika U., Cook, Edwin H., Guter, Stephen, Tjernagel, Jennifer, Green-Snyder, Lee Anne, Bishop, Somer, Esler, Amy, Gotham, Katherine, Luyster, Rhiannon, Miller, Fiona, Olson, Jennifer, Richler, Jennifer, Risi, Susan

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Disruption at the PTCHD1 locus on Xp22.11 in autism spectrum disorder and intellectual disability מאת Noor, Abdul, Whibley, Annabel, Marshall, Christian R., Gianakopoulos, Peter J., Piton, Amelie, Carson, Andrew R., Orlic-Milacic, Marija, Lionel, Anath, Sato, Daisuke, Pinto, Dalila, Drmic, Irene, Noakes, Carolyn, Senman, Lili, Zhang, Xiaoyun, Mo, Rong, Gauthier, Julie, Crosbie, Jennifer, Pagnamenta, Alistair T., Munson, Jeffrey, Estes, Annette M., Fiebig, Andreas, Franke, Andre, Schreiber, Stefan, Stewart, Alexandre F.R., Roberts, Robert, McPherson, Ruth, Guter, Stephen J., Cook, Edwin H., Dawson, Geraldine, Schellenberg, Gerard D., Battaglia, Agatino, Maestrini, Elena, Jeng, Linda, Hutchison, Terry, Rajcan-Separovic, Evica, Chudley, Albert E., Lewis, Suzanne M.E., Liu, Xudong, Holden, Jeanette, Fernandez, Bridget, Zwaigenbaum, Lonnie, Bryson, Susan E., Roberts, Wendy, Szatmari, Peter, Gallagher, Louise, Stratton, Michael R., Gecz, Jozef, Brady, Angela F., Schwartz, Charles E., Schachar, Russell J., Monaco, Anthony P., Rouleau, Guy A., Hui, Chi-chung, Raymond, F. Lucy, Scherer, Stephen W., Vincent, John B.

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Synaptic, transcriptional, and chromatin genes disrupted in autism מאת De Rubeis, Silvia, He, Xin, Goldberg, Arthur P., Poultney, Christopher S., Samocha, Kaitlin, Cicek, A Ercument, Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarjinder, Klei, Lambertus, Kosmicki, Jack, Fu, Shih-Chen, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F., Brownfeld, Jessica M., Cai, Jinlu, Campbell, Nicholas J., Carracedo, Angel, Chahrour, Maria H., Chiocchetti, Andreas G., Coon, Hilary, Crawford, Emily L., Crooks, Lucy, Curran, Sarah R., Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A., Gallagher, Louise, Geller, Evan, Guter, Stephen J., Hill, R. Sean, Ionita-Laza, Iuliana, Gonzalez, Patricia Jimenez, Kilpinen, Helena, Klauck, Sabine M., Kolevzon, Alexander, Lee, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma'ayan, Avi, Marshall, Christian R., McInnes, Alison L., Neale, Benjamin, Owen, Michael J., Ozaki, Norio, Parellada, Mara, Parr, Jeremy R., Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J., Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Wang, Li-San, Weiss, Lauren A., Willsey, A. Jeremy, Yu, Timothy W., Yuen, Ryan K.C., Cook, Edwin H., Freitag, Christine M., Gill, Michael, Hultman, Christina M., Lehner, Thomas, Palotie, Aarno, Schellenberg, Gerard D., Sklar, Pamela, State, Matthew W., Sutcliffe, James S., Walsh, Christopher A., Scherer, Stephen W., Zwick, Michael E., Barrett, Jeffrey C., Cutler, David J., Roeder, Kathryn, Devlin, Bernie, Daly, Mark J., Buxbaum, Joseph D.

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Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders מאת Pinto, Dalila, Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Wang, Zhuozhi, Vorstman, Jacob A.S., Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T., Oliveira, Bárbara, Marshall, Christian R., Magalhaes, Tiago R., Lowe, Jennifer K., Howe, Jennifer L., Griswold, Anthony J., Gilbert, John, Duketis, Eftichia, Dombroski, Beth A., De Jonge, Maretha V., Cuccaro, Michael, Crawford, Emily L., Correia, Catarina T., Conroy, Judith, Conceição, Inês C., Chiocchetti, Andreas G., Casey, Jillian P., Cai, Guiqing, Cabrol, Christelle, Bolshakova, Nadia, Bacchelli, Elena, Anney, Richard, Gallinger, Steven, Cotterchio, Michelle, Casey, Graham, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, Wallace, Simon, van Engeland, Herman, Tryfon, Ana, Thomson, Susanne, Soorya, Latha, 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, Fernandez, Bridget A., Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F., Bölte, Sven, Bernier, Raphael, Baird, Gillian, Bailey, Anthony J., Anagnostou, Evdokia, 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.

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A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder מאת Casey, Jillian P., Magalhaes, Tiago, Conroy, Judith M., Regan, Regina, Shah, Naisha, Anney, Richard, Shields, Denis C., Abrahams, Brett S., Almeida, Joana, Bacchelli, Elena, Bailey, Anthony J., Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Cali, Phil, Correia, Catarina, Corsello, Christina, Coutanche, Marc, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Foley, Suzanne, Fombonne, Eric, Freitag, Christine M., Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Green, Jonathan, Guter, Stephen J., Hakonarson, Hakon, Holt, Richard, Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M., Kolevzon, Alexander, Lamb, Janine A., Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L., Lord, Catherine, Lund, Sabata C., Maestrini, Elena, Mantoulan, Carine, Marshall, Christian R., McConachie, Helen, McDougle, Christopher J., McGrath, Jane, McMahon, William M., Merikangas, Alison, Miller, Judith, Minopoli, Fiorella, Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Nygren, Gudrun, Oliveira, Guiomar, Pagnamenta, Alistair T., Papanikolaou, Katerina, Parr, Jeremy R., Parrini, Barbara, Pickles, Andrew, Pinto, Dalila, Piven, Joseph, Posey, David J., Poustka, Annemarie, Poustka, Fritz, Ragoussis, Jiannis, Roge, Bernadette, Rutter, Michael L., Sequeira, Ana F., Soorya, Latha, Sousa, Inês, Sykes, Nuala, Stoppioni, Vera, Tancredi, Raffaella, Tauber, Maïté, Thompson, Ann P., Thomson, Susanne, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Vorstman, Jacob A. S., Wallace, Simon, Wang, Kai, Wassink, Thomas H., White, Kathy, Wing, Kirsty, Wittemeyer, Kerstin, Yaspan, Brian L., Zwaigenbaum, Lonnie, Betancur, Catalina, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Geschwind, Daniel H., Haines, Jonathan L., Hallmayer, Joachim, Monaco, Anthony P., Nurnberger, John I., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Scherer, Stephen W., Sutcliffe, James S., Szatmari, Peter, Vieland, Veronica J., Wijsman, Ellen M., Green, Andrew, Gill, Michael, Gallagher, Louise, Vicente, Astrid, Ennis, Sean

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements מאת Szatmari, Peter, Paterson, Andrew, Zwaigenbaum, Lonnie, Roberts, Wendy, Brian, Jessica, Liu, Xiao-Qing, Vincent, John, Skaug, Jennifer, Thompson, Ann, Senman, Lili, Feuk, Lars, Qian, Cheng, Bryson, Susan, Jones, Marshall, Marshall, Christian, Scherer, Stephen, Vieland, Veronica, Bartlett, Christopher, Mangin, La Vonne, Goedken, Rhinda, Segre, Alberto, Pericak-Vance, Margaret, Cuccaro, Michael, Gilbert, John, Wright, Harry, Abramson, Ruth, Betancur, Catalina, Bourgeron, Thomas, Gillberg, Christopher, Leboyer, Marion, Buxbaum, Joseph, Davis, Kenneth, Hollander, Eric, Silverman, Jeremy, Hallmayer, Joachim, Lotspeich, Linda, Sutcliffe, James, Haines, Jonathan, Folstein, Susan, Piven, Joseph, Wassink, Thomas, Sheffield, Val, Geschwind, Daniel, Bucan, Maja, Brown, Ted, Cantor, Rita, Constantino, John, Gilliam, Conrad, Herbert, Martha, Lajonchere, Clara, Ledbetter, David, Lese-Martin, Christa, Miller, Janet, Nelson, Stan, Samango-Sprouse, Carol, Spence, Sarah, State, Matthew, Tanzi, Rudolph, Coon, Hilary, Dawson, Geraldine, Devlin, Bernie, Estes, Annette, Flodman, Pamela, Klei, Lambertus, Mcmahon, William, Minshew, Nancy, Munson, Jeff, Korvatska, Elena, Rodier, Patricia, Schellenberg, Gerard, Smith, Moyra, Spence, Anne, Stodgell, Chris, Tepper, Ping Guo, Wijsman, Ellen, Yu, Chang-En, Rogé, Bernadette, Mantoulan, Carine, Wittemeyer, Kerstin, Poustka, Annemarie, Felder, Bärbel, Klauck, Sabine, Schuster, Claudia, Poustka, Fritz, Bölte, Sven, Feineis-Matthews, Sabine, Herbrecht, Evelyn, Schmötzer, Gabi, Tsiantis, John, Papanikolaou, Katerina, Maestrini, Elena, Bacchelli, Elena, Blasi, Francesca, Carone, Simona, Toma, Claudio, Van Engeland, Herman, De Jonge, Maretha, Kemner, Chantal, Koop, Frederieke, Langemeijer, Marjolein, Hijmans, Channa, Staal, Wouter, Baird, Gillian, Bolton, Patrick, Rutter, Michael, Weisblatt, Emma, Green, Jonathan, Aldred, Catherine, Wilkinson, Julie-Anne, Pickles, Andrew, Le Couteur, Ann, Berney, Tom, Mcconachie, Helen, Bailey, Anthony, Francis, Kostas, Honeyman, Gemma, Hutchinson, Aislinn, Parr, Jeremy, Wallace, Simon, Monaco, Anthony, Barnby, Gabrielle, Kobayashi, Kazuhiro, Lamb, Janine, Sousa, Ines, Sykes, Nuala, Cook, Edwin, Guter, Stephen, Leventhal, Bennett, Salt, Jeff, Lord, Catherine, Corsello, Christina, Hus, Vanessa, Weeks, Daniel, Volkmar, Fred, Tauber, Maïté, Fombonne, Eric, Shih, Andy, Meyer, Kacie

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