Treffer 1 - 20 von 42 für Suche 'Gholson, James J.', Suchdauer: 1,75s Treffer weiter einschränken
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    De Novo Coding Variants Are Strongly Associated with Tourette Disorder von Willsey, A. Jeremy, Yu, Dongmei, King, Robert A., Dietrich, Andrea, Xing, Jinchuan, Richer, Petra, Smith, Louw, Dong, Shan, Samocha, Kaitlin E., Bohnenpoll, Julia, Bromberg, Yana, Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., Deng, Li, Dong, Shan, Elzerman, Lonneke, Fernandez, Thomas V., Fründt, Odette, Garcia-Delgar, Blanca, Gedvilaite, Erika, Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heiman, Gary A., Heyman, Isobel, Hoekstra, Pieter J., Hong, Hyun Ju, Ibanez-Gomez, Laura, Kim, Young Key, Kim, Young-Shin, King, Robert A., Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Lamerz, Andreas, Ludolph, Andrea G., Lühr da Silva, Claudia, Madruga-Garrido, Marcos, Mir, Pablo, Münchau, Alexander, Murphy, Tara L., Nasello, Cara, Openneer, Thaïra J.C., Plessen, Kerstin J., Richer, Petra, Roessner, Veit, Sanders, Stephan, Smith, Louw, Song, Dong-Ho, State, Matthew W., Stolte, Anne Marie, Sun, Nawei, Tischfield, Jay A., Tübing, Jennifer, Visscher, Frank, Walker, Michael F., Wanderer, Sina, Wang, Shuoguo, Willsey, A. Jeremy, Woods, Martin, Xing, Jinchuan, Zhang, Yeting, Zhou, Anbo, Zinner, Samuel H., Batterson, James R., Berlin, Cheston, Bruun, Ruth D., Budman, Cathy L., Cath, Danielle C., Chouinard, Sylvain, Coppola, Giovanni, Cox, Nancy J., Darrow, Sabrina, Davis, Lea K., Freimer, Nelson B., Grados, Marco A., Hirschtritt, Matthew E., Illmann, Cornelia, Kurlan, Roger, Lyon, Gholson J., Malaty, Irene A., Mathews, Carol A., Neale, Benjamin M., Okun, Michael S., Osiecki, Lisa, Posthuma, Danielle, Ramensky, Vasily, Robertson, Mary M., Rouleau, Guy A., Sandor, Paul, Singer, Harvey S., Yu, Dongmei, Neale, Benjamin M., Coppola, Giovanni, Mathews, Carol A., Tischfield, Jay A., Scharf, Jeremiah M., State, Matthew W., Heiman, Gary A.

    Veröffentlicht in Neuron (Cambridge, Mass.)

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    Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome von Jain, Pritesh, Yang, Zhiyu, Yu, Dongmei, Tumer, Zeynep, Hartmann, Andreas, Müller-Vahl, Kirsten R., Boomsma, Dorret I., Wolanczyk, Tomasz, Nemoda, Zsofia, Padmanabhuni, Shanmukha S., Grice, Dorothy, Glennon, Jeffrey, Stefansson, Hreinn, Stamatoyannopoulos, John A., Benaroya-Milshtein, Noa, Cardona, Francesco, Heyman, Isobel, Mir, Pablo, Munchau, Alexander, Plessen, Kerstin J., Roessner, Veit, Martino, Davide, Barr, Cathy L., Batterson, James R., Budman, Cathy L., Coppola, Giovanni, Darrow, Sabrina, Freimer, Nelson B., Grados, Marco A., Greenberg, Erica, Huang, Alden Y., Illmann, Cornelia, Kurlan, Roger, Leckman, James F., Malaty, Irene A., McMahon, William M., Neale, Benjamin M., Osiecki, Lisa, Rouleau, Guy A., Sul, Jae Hoon, Androutsos, Christos, Basha, Entela, Farkas, Luca, Janik, Piotr, Kapisyzi, Mira, Karagiannidis, Iordanis, Koumoula, Anastasia, Nagy, Peter, Puchala, Joanna, Szymanska, Urszula, Apter, Alan, Bodmer, Benjamin, Bognar, Emese, Buse, Judith, Fremer, Carolin, Garcia-Delgar, Blanca, Hagen, Annelieke, Hagstrøm, Julie, Madruga-Garrido, Marcos, Silvestri, Paola Rosaria, Skov, Liselotte, Steinberg, Tamar, Turner, Victoria L., Alexander, John, Aranyi, Tamas, Fan, Siyan, Forde, Natalie J., Gerasch, Sarah, Kanaan, Ahmad S., Möller, Harald E., Poelmans, Geert, Pouwels, Petra J.W., Rizzo, Francesca, Veltman, Dick J., van der Werf, Ysbrand D., Widomska, Joanna, Zilhäo, Nuno R., Brown, Lawrence W., Cheon, Keun-Ah, Fernandez, Thomas V., Kim, Eun-Joo, Kim, Young Key, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Maras, Athanasios, Murphy, Tara L., Shin, Eun-Young, Song, Dong-Ho, State, Matthew W., Visscher, Frank, Heiman, Gary A., Willsey, A. Jeremy, Dietrich, Andrea, Davis, Lea K., Crowley, James J., Scharf, Jeremiah M., Georgitsi, Marianthi, Hoekstra, Pieter J., Paschou, Peristera

    Veröffentlicht in Biological psychiatry (1969)

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    Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies von Cheng, Hanyin, Dharmadhikari, Avinash V., Varland, Sylvia, Ma, Ning, Domingo, Deepti, Kleyner, Robert, Rope, Alan F., Yoon, Margaret, Stray-Pedersen, Asbjørg, Posey, Jennifer E., Crews, Sarah R., Eldomery, Mohammad K., Akdemir, Zeynep Coban, Lewis, Andrea M., Sutton, Vernon R., Rosenfeld, Jill A., Conboy, Erin, Agre, Katherine, Xia, Fan, Walkiewicz, Magdalena, Longoni, Mauro, High, Frances A., van Slegtenhorst, Marjon A., Mancini, Grazia M.S., Finnila, Candice R., van Haeringen, Arie, den Hollander, Nicolette, Ruivenkamp, Claudia, Naidu, Sakkubai, Mahida, Sonal, Palmer, Elizabeth E., Murray, Lucinda, Lim, Derek, Jayakar, Parul, Parker, Michael J., Giusto, Stefania, Stracuzzi, Emanuela, Romano, Corrado, Beighley, Jennifer S., Bernier, Raphael A., Küry, Sébastien, Nizon, Mathilde, Corbett, Mark A., Shaw, Marie, Gardner, Alison, Barnett, Christopher, Armstrong, Ruth, Kassahn, Karin S., Van Dijck, Anke, Vandeweyer, Geert, Kleefstra, Tjitske, Schieving, Jolanda, Jongmans, Marjolijn J., de Vries, Bert B.A., Pfundt, Rolph, Kerr, Bronwyn, Rojas, Samantha K., Boycott, Kym M., Person, Richard, Willaert, Rebecca, Eichler, Evan E., Kooy, R. Frank, Yang, Yaping, Wu, Joseph C., Lupski, James R., Arnesen, Thomas, Cooper, Gregory M., Chung, Wendy K., Gecz, Jozef, Stessman, Holly A.F., Meng, Linyan, Lyon, Gholson J.


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    DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders von Lessel, Ivana, Baresic, Anja, Chinn, Ivan K, May, Jonathan, Goenka, Anu, Chandler, Kate E, Posey, Jennifer E, Afenjar, Alexandra, Averdunk, Luisa, Bedeschi, Maria Francesca, Besnard, Thomas, Brager, Rae, Brick, Lauren, Brugger, Melanie, Brunet, Theresa, Byrne, Susan, Calle-Martín, Oscar de la, Capra, Valeria, Cardenas, Paul, Chappé, Céline, Chong, Hey J, Cogne, Benjamin, Conboy, Erin, Cope, Heidi, Courtin, Thomas, Deb, Wallid, Dilena, Robertino, Dubourg, Christèle, Elgizouli, Magdeldin, Fernandes, Erica, Fitzgerald, Kristi K, Gangi, Silvana, George-Abraham, Jaya K, Gucsavas-Calikoglu, Muge, Haack, Tobias B, Hadonou, Medard, Hanker, Britta, Hüning, Irina, Iascone, Maria, Isidor, Bertrand, Järvelä, Irma, Jin, Jay J, Jorge, Alexander A L, Josifova, Dragana, Kalinauskiene, Ruta, Kamsteeg, Erik-Jan, Keren, Boris, Kessler, Elena, Kölbel, Heike, Kozenko, Mariya, Kubisch, Christian, Kuechler, Alma, Leal, Suzanne M, Leppälä, Juha, Luu, Sharon M, Lyon, Gholson J, Madan-Khetarpal, Suneeta, Mancardi, Margherita, Marchi, Elaine, Mehta, Lakshmi, Menendez, Beatriz, Morel, Chantal F, Harasink, Sue Moyer, Nevay, Dayna-Lynn, Nigro, Vincenzo, Odent, Sylvie, Oegema, Renske, Pappas, John, Pastore, Matthew T, Perilla-Young, Yezmin, Platzer, Konrad, Powell-Hamilton, Nina, Rabin, Rachel, Rekab, Aisha, Rezende, Raissa C, Robert, Leema, Romano, Ferruccio, Scala, Marcello, Poths, Karin, Schrauwen, Isabelle, Sebastian, Jessica, Short, John, Sidlow, Richard, Sullivan, Jennifer, Szakszon, Katalin, Tan, Queenie K G, Wagner, Matias, Wieczorek, Dagmar, Yuan, Bo, Maeding, Nicole, Strunk, Dirk, Begtrup, Amber, Banka, Siddharth, Lupski, James R, Tolosa, Eva, Lessel, Davor


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    Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders von Strom, Nora I., Halvorsen, Matthew W., Grove, Jakob, Ásbjörnsdóttir, Bergrún, Thorarensen, Ólafur, de Schipper, Elles, Bäckmann, Julia, Tian, Chao, Sul, Jae Hoon, Tsetsos, Fotis, Zelaya, Ivette, Osiecki, Lisa, Darrow, Sabrina M., Hirschtritt, Matthew E., Greenberg, Erica, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Barr, Cathy L., Grados, Marco, Hinney, Anke, King, Robert A., Fernandez, Thomas V., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L., Lyon, Gholson J., McMahon, William M., Batterson, James R., Malaty, Irene A., Okun, Michael S., Berlin, Cheston, Woods, Douglas W., Lee, Paul C., Jankovic, Joseph, Robertson, Mary M., Gilbert, Donald L., Brown, Lawrence W., Coffey, Barbara J., Hoekstra, Pieter J., Zinner, Samuel H., Luðvigsson, Pétur, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N., Knowles, James A., Buckner, Randy L., Willsey, Jeremy A., Tischfield, Jay A., Heiman, Gary A., Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Pauls, David L., Freimer, Nelson B., Davis, Lea K., Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A., Scharf, Jeremiah M., Agee, Michelle, Auton, Adam, Elson, Sarah L., Furlotte, Nicholas A., Hicks, Barry, Jewett, Ethan M., Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K., McIntyre, Matthew H., McManus, Kimberly F., Mountain, Joanna L., Pitts, Steven J., Poznik, G. David, Sathirapongsasuti, J. Fah, Shelton, Janie F., Shringarpure, Suyash, Tung, Joyce Y., Wang, Xin, Als, Thomas Damm, Meier, Sandra M., Bybjerg-Grauholm, Jonas, Hougaard, David M., Werge, Thomas, Børglum, Anders D., Hinds, David A., Rück, Christian, Mataix-Cols, David, Mattheisen, Manuel

    Veröffentlicht in BIOLOGICAL PSYCHIATRY

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    De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis von Wang, Sheng, Mandell, Jeffrey D., Kumar, Yogesh, Sun, Nawei, Nasello, Cara, Dong, Shan, Duhn, Clif, Zhao, Xin, Yang, Zhiyu, Padmanabhuni, Shanmukha S., Yu, Dongmei, King, Robert A., Dietrich, Andrea, Dahl, Niklas, Huang, Alden Y., Neale, Benjamin M., Mathews, Carol A., Abdulkadir, Mohamed, Arbelaez, Juan, Bodmer, Benjamin, Coffey, Barbara J., Deng, Li, Dietrich, Andrea, Duhn, Clif, Fernandez, Thomas V., Fremer, Carolin, Gilbert, Donald L., Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heiman, Gary A., Hong, Hyun Ju, Huyser, Chaim, Kim, Eun-Joo, Kim, Young Key, Kim, Young-Shin, King, Robert A., Kuperman, Samuel, Mandell, Jeffrey D., Maras, Athanasios, Müller-Vahl, Kirsten, Münchau, Alexander, Nasello, Cara, Plessen, Kerstin J., Poisner, Hannah, Roessner, Veit, Sanders, Stephan J., Song, Jungeun, State, Matthew W., Tischfield, Jay A., Wanderer, Sina, Wang, Sheng, Willsey, A Jeremy, Xing, Jinchuan, Zhang, Yeting, Zhao, Xin, Zinner, Samuel H., Androutsos, Christos, Barta, Csaba, Farkas, Luca, Janik, Piotr, Karagiannidis, Iordanis, Koumoula, Anastasia, Nagy, Peter, Rizzo, Renata, Szymanska, Urszula, Tarnok, Zsanett, Tsironi, Vaia, Zekanowski, Cezary, Batterson, James R., Berlin, Cheston, Bruun, Ruth D., Budman, Cathy L., Chouinard, Sylvain, Coppola, Giovanni, Darrow, Sabrina, Dion, Yves, Freimer, Nelson B., Grados, Marco A., Hirschtritt, Matthew E., Kurlan, Roger, Lyon, Gholson J., Malaty, Irene A., MacMahon, William M., Neale, Benjamin M., Pauls, David L., Ramensky, Vasily, Robertson, Mary M., Scharf, Jeremiah M., Singer, Harvey S., Smit, Jan, Sul, Jae-Hoon, Yu, Dongmei, Fernandez, Thomas V., De Rubeis, Silvia, Xing, Jinchuan, Tischfield, Jay A., Paschou, Peristera, Willsey, A. Jeremy, State, Matthew W.

    Veröffentlicht in Cell reports (Cambridge)

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