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    Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people von Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L, Wang, Carol A, Truong, Dongnhu T, Allegrini, Andrea G, Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G, Gerritse, Margot L, Molz, Barbara, Alagöz, Gökberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R, Andlauer, Till F M, Bates, Timothy C, Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Børglum, Anders D, Bourgeron, Thomas, Brandeis, Daniel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S, de Jong, Peter F, DeFries, John C, Démonet, Jean-François, Demontis, Ditte, Feng, Yu, Gordon, Scott D, Guger, Sharon L, Hayiou-Thomas, Marianna E, Hernández-Cabrera, Juan A, Hottenga, Jouke-Jan, Hulme, Charles, Kere, Juha, Kerr, Elizabeth N, Koomar, Tanner, Landerl, Karin, Leonard, Gabriel T, Lovett, Maureen W, Lyytinen, Heikki, Martin, Nicholas G, Martinelli, Angela, Maurer, Urs, Michaelson, Jacob J, Moll, Kristina, Monaco, Anthony P, Morgan, Angela T, Nöthen, Markus M, Pausova, Zdenka, Pennell, Craig E, Pennington, Bruce F, Price, Kaitlyn M, Rajagopal, Veera M, Ramus, Franck, Richer, Louis, Simpson, Nuala H, Smith, Shelley D, Snowling, Margaret J, Stein, John, Strug, Lisa J, Talcott, Joel B, Tiemeier, Henning, van der Schroeff, Marc P, Verhoef, Ellen, Watkins, Kate E, Wilkinson, Margaret, Wright, Margaret J, Barr, Cathy L, Boomsma, Dorret I, Carreiras, Manuel, Franken, Marie-Christine J, Gruen, Jeffrey R, Luciano, Michelle, Müller-Myhsok, Bertram, Newbury, Dianne F, Olson, Richard K, Paracchini, Silvia, Paus, Tomáš, Plomin, Robert, Reilly, Sheena, Schulte-Körne, Gerd, Tomblin, J Bruce, van Bergen, Elsje, Whitehouse, Andrew J O, Willcutt, Erik G, St Pourcain, Beate, Francks, Clyde, Fisher, Simon E


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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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    Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy von Banks, Emily, Francis, Vincent, Lin, Sheng-Jia, Kharfallah, Fares, Fonov, Vladimir, Lévesque, Maxime, Han, Chanshuai, Kulasekaran, Gopinath, Tuznik, Marius, Bayati, Armin, Al-Khater, Reem, Alkuraya, Fowzan S., Argyriou, Loukas, Babaei, Meisam, Bahlo, Melanie, Bakhshoodeh, Behnoosh, Barr, Eileen, Bartik, Lauren, Bassiony, Mahmoud, Bertrand, Miriam, Braun, Dominique, Buchert, Rebecca, Budetta, Mauro, Cadieux-Dion, Maxime, Calame, Daniel G., Cope, Heidi, Cushing, Donna, Efthymiou, Stephanie, Elmaksoud, Marwa Abd, El Said, Huda G., Froukh, Tawfiq, Gill, Harinder K., Gleeson, Joseph G., Gogoll, Laura, Goh, Elaine S.-Y., Gowda, Vykuntaraju K., Haack, Tobias B., Hashem, Mais O., Hauser, Stefan, Hoffman, Trevor L., Hogue, Jacob S., Hosokawa, Akimoto, Houlden, Henry, Huang, Kevin, Huynh, Stephanie, Karimiani, Ehsan G., Kaulfuß, Silke, Korenke, G. Christoph, Kritzer, Amy, Lee, Hane, Lupski, James R., Marco, Elysa J., McWalter, Kirsty, Minassian, Arakel, Minassian, Berge A., Murphy, David, Neira-Fresneda, Juanita, Northrup, Hope, Nyaga, Denis M., Oehl-Jaschkowitz, Barbara, Osmond, Matthew, Person, Richard, Pehlivan, Davut, Petree, Cassidy, Sadleir, Lynette G., Saunders, Carol, Schoels, Ludger, Shashi, Vandana, Spillmann, Rebecca C., Srinivasan, Varunvenkat M., Torbati, Paria N., Tos, Tulay, Zaki, Maha S., Zhou, Dihong, Zweier, Christiane, Trempe, Jean-François, Durcan, Thomas M., Gan-Or, Ziv, Avoli, Massimo, Alves, Cesar, Varshney, Gaurav K., Maroofian, Reza, Rudko, David A., McPherson, Peter S.

    Veröffentlicht in Nature communications

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    Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD von Yu, Dongmei, Davis, Lea K., Gamazon, Eric R., Derks, Eske M., Evans, Patrick, Crane, Jacquelyn, Osiecki, Lisa, Gerber, Gloria, Haddad, Stephen, McGrath, Lauren M., Mayerfeld, Catherine, Arepalli, Sampath, Barlassina, Cristina, Barr, Cathy L., Black, Donald W., Bloch, Michael H., Brentani, Helena, Camarena, Beatriz, Campbell, Desmond D., Cavallini, Maria C., Chavira, Denise A., Cook, Edwin H., Cookson, M.R., Cullen, Bernadette, Denys, Damiaan, Dion, Yves, Eapen, Valsama, Egberts, Karin, Fernandez, Thomas, Fournier, Eduardo, Garrido, Helena, Geller, Daniel, Girard, Simon L., Grabe, Hans J., Greenberg, Benjamin D., Heiman, Gary A., Hemmings, Sian M.J., Herrera, Luis D., Hezel, Dianne M., Jankovic, Joseph, Kremeyer, Barbara, Lanzagorta, Nuria, Lowe, Thomas L., Lupoli, Sara, Macciardi, Fabio, Maier, Wolfgang, Manunta, Paolo, Marconi, Maurizio, McCracken, James T., Mesa Restrepo, Sandra C., Moessner, Rainald, Moorjani, Priya, Morgan, Jubel, Muller, Heike, Murphy, Dennis L., Naarden, Allan L., Nurmi, Erika, Ochoa, William Cornejo, Pato, Carlos N., Piacentini, John, Pittenger, Christopher, Rauch, Scott L., Renner, Tobias, Reus, Victor I., Riddle, Mark A., Romero, Roxana, Rosenberg, David, Ruhrmann, Stephan, Sabatti, Chiara, Salvi, Erika, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S., Stein, Dan J., Strengman, Eric, Tischfield, Jay A., Turiel, Maurizio, Vallada, Homero, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Wang, Ying, Weale, Mike, Weiss, Robert, Wendland, Jens R., Westenberg, Herman G.M., Shugart, Yin Yao, Hounie, Ana G., Wagner, Michael, Ruiz-Linares, Andres, Cath, Danielle C., Posthuma, Danielle, Heutink, Peter, Hanna, Gregory L., Conti, David V., Arnold, Paul D., Freimer, Nelson B., Stewart, S. Evelyn, Knowles, James A., Pauls, David L.


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