Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome by Huang, Alden Y., Yu, Dongmei, Davis, Lea K., Sul, Jae Hoon, Tsetsos, Fotis, Ramensky, Vasily, Zelaya, Ivette, Ramos, Eliana Marisa, Osiecki, Lisa, Chen, Jason A., McGrath, Lauren M., Illmann, Cornelia, Sandor, Paul, Barr, Cathy L., Grados, Marco, Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, King, Robert A., Dion, Yves, Rouleau, Guy, Budman, Cathy L., Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Müller-Vahl, Kirsten R., Stuhrmann, Manfred, Aschauer, Harald, Stamenkovic, Mara, Schloegelhofer, Monika, Konstantinidis, Anastasios, Lyon, Gholson J., McMahon, William M., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Batterson, James R., Rizzo, Renata, Cath, Danielle C., Wolanczyk, Tomasz, Berlin, Cheston, Malaty, Irene A., Okun, Michael S., Woods, Douglas W., Rees, Elliott, Pato, Carlos N., Pato, Michele T., Knowles, James A., Posthuma, Danielle, Pauls, David L., Cox, Nancy J., Neale, Benjamin M., Freimer, Nelson B., Paschou, Peristera, Mathews, Carol A., Scharf, Jeremiah M., Coppola, Giovanni, Bruun, Ruth D., Chouinard, Sylvain, Darrow, Sabrina, Greenberg, Erica, Hirschtritt, Matthew E., Kurlan, Roger, Leckman, James F., Robertson, Mary M., Smit, Jan

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De Novo Coding Variants Are Strongly Associated with Tourette Disorder by 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.

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Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses by Keen-Kim, Dianne, Mathews, Carol A., Reus, Victor I., Lowe, Thomas L., Herrera, Luis Diego, Budman, Cathy L., Gross-Tsur, Varda, Pulver, Ann E., Bruun, Ruth D., Erenberg, Gerald, Naarden, Allan, Sabatti, Chiara, Freimer, Nelson B.

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Association Between Maternal Smoking and Increased Symptom Severity in Tourette's Syndrome by Mathews, Carol A., Bimson, Brianne, Lowe, Thomas L., Herrera, Luis Diego, Budman, Cathy L., Erenberg, Gerald, Naarden, Allen, Bruun, Ruth D., Freimer, Nelson B., Reus, Victor I.

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Tic Symptom Profiles in Subjects with Tourette Syndrome from two Genetically Isolated Populations by Mathews, Carol A, Jang, Kerry L, Herrera, Luis Diego, Lowe, Thomas L, Budman, Cathy L, Erenberg, Gerald, Naarden, Allan, Bruun, Ruth D, Schork, Nicholas J, Freimer, Nelson B, Reus, Victor I

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Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies by Yu, Dongmei, Sul, Jae Hoon, Tsetsos, Fotis, Nawaz, Muhammad S, Huang, Alden Y, Zelaya, Ivette, Illmann, Cornelia, Osiecki, Lisa, Darrow, Sabrina M, Hirschtritt, Matthew E, Greenberg, Erica, Muller-Vahl, Kirsten R, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Sandor, Paul, Barr, Cathy L, Grados, Marco, Singer, Harvey S, Nöthen, Markus M, Hebebrand, Johannes, Hinney, Anke, King, Robert A, Fernandez, Thomas V, Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L, Rizzo, Renata, Lyon, Gholson J, McMahon, William M, Batterson, James R, Cath, Danielle C, 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, Dietrich, Andrea, Hoekstra, Pieter J, Kuperman, Samuel, Zinner, Samuel H, Luðvigsson, Pétur, Sæmundsen, Evald, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Wagner, Michael, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N, Pato, Michele T, Knowles, James A, Roffman, Joshua L, Smoller, Jordan W, Buckner, Randy L, Willsey, A. Jeremy, Tischfield, Jay A, Heiman, Gary A, Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Cox, Nancy J, Pauls, David L, Freimer, Nelson B, Neale, Benjamin M, Davis, Lea K, Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A, Scharf, Jeremiah M

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De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis by 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.

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Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette Syndrome and Obsessive-Compulsive Disorder by Yu, Dongmei, Mathews, Carol A., Scharf, Jeremiah M., Neale, Benjamin M., Davis, Lea K., Gamazon, Eric R., Derks, Eske M., Evans, Patrick, Edlund, Christopher K., Crane, Jacquelyn, Fagerness, Jesen A., Osiecki, Lisa, Gallagher, Patience, Gerber, Gloria, Haddad, Stephen, Illmann, Cornelia, McGrath, Lauren M., Mayerfeld, Catherine, Arepalli, Sampath, Barlassina, Cristina, Barr, Cathy L., Bellodi, Laura, Benarroch, Fortu, Berrió, Gabriel Bedoya, Bienvenu, O. Joseph, Black, Donald, Bloch, Michael H., Brentani, Helena, Bruun, Ruth D., Budman, Cathy L., Camarena, Beatriz, Campbell, Desmond D., Cappi, Carolina, Cardona Silgado, Julio C., Cavallini, Maria C., Chavira, Denise A., Chouinard, Sylvain, Cook, Edwin H., Cookson, M. R., Coric, Vladimir, Cullen, Bernadette, Cusi, Daniele, Delorme, Richard, Denys, Damiaan, Dion, Yves, Eapen, Valsama, Egberts, Karin, Falkai, Peter, Fernandez, Thomas, Fournier, Eduardo, Garrido, Helena, Geller, Daniel, Gilbert, Donald, Girard, Simon L., Grabe, Hans J., Grados, Marco A., Greenberg, Benjamin D., Gross-Tsur, Varda, Grünblatt, Edna, Hardy, John, Heiman, Gary A., Hemmings, Sian M.J., Herrera, Luis D., Hezel, Dianne M., Hoekstra, Pieter J., Jankovic, Joseph, Kennedy, James L., King, Robert A., Konkashbaev, Anuar I., Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F., Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, 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., Ochoa, William Cornejo, Ophoff, Roel A., Pakstis, Andrew J., Pato, Michele T., Pato, Carlos N., Piacentini, John, Pittenger, Christopher, Pollak, Yehuda, Rauch, Scott L.

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Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture: e1003864 by Davis, Lea K, Yu, Dongmei, Keenan, Clare L, Gamazon, Eric R, Konkashbaev, Anuar I, Derks, Eske M, Yang, Jian, Lee, S Hong, Barr, Cathy L, Bellodi, Laura, Benarroch, tu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J, Bloch, Michael H, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Cappi, Carolina, Silgado, Julio CCardona, Cath, Danielle C, Cavallini, Maria C, Chouinard, Sylvain, Conti, David V, Cook, Edwin H, Coric, Vladimir, Cullen, Bernadette A, Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K, Egberts, Karin, Falkai, Peter, Fernandez, Thomas V, Geller, Daniel, Girard, Simon L, Grados, Marco A, Haddad, Stephen, Heiman, Gary A, Hemmings, Sian MJ, Hounie, Ana G, Jankovic, Joseph, Jenike, Michael A, Kennedy, James L, King, Robert A, Kremeyer, Barbara, Kurlan, Roger, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Macciardi, Fabio, McCracken, James T, McGrath, Lauren M, Restrepo, Sandra CMesa, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Ochoa, William Cornejo, Ophoff, Roel A, Osiecki, Lisa, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Rauch, Scott L, Renner, Tobias J, Reus, Victor I, Richter, Margaret A, Riddle, Mark A, Robertson, Mary M, Rosàrio, Maria C, Rosenberg, David, Rouleau, Guy A, Ruhrmann, Stephan, Ruiz-Linares, Andres, Sampaio, Aline S, Samuels, Jack, Sheppard, Brooke, Smit, Jan H, Tischfield, Jay A, Duarte, Ana VValencia, Vallada, Homero, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Wang, Ying, Westenberg, Herman GM, Shugart, Yin Yao, Miguel, Euripedes C, McMahon, William, Nicolini, Humberto, Posthuma, Danielle, Hanna, Gregory L, Arnold, Paul D, Nestadt, Gerald, Freimer, Nelson B, Wray, Naomi R, Stewart, S Evelyn, Knowles, James A, Cox, Nancy J, Scharf, Jeremiah M

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Tic symptom profiles in subjects with tourette syndrome from two genetically isolated populations: Progress and challenges in OCD research by MATHEWS, Carol A, JANG, Kerry L, REUS, Victor I, DIEGO HERRERA, Luis, LOWE, Thomas L, BUDMAN, Cathy L, ERENBERG, Gerald, NAARDEN, Allan, BRUUN, Ruth D, SCHORK, Nicholas J, FREIMER, Nelson B

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Tourette's syndrome: summary of data on 34 patients by Shapiro, A K, Shapiro, E, Wayne, H L, Clarkin, J, Bruun, R D

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Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree by Halvorsen, Matthew, Szatkiewicz, Jin, Mudgal, Poorva, Yu, Dongmei, Nordsletten, Ashley E., Mataix-Cols, David, Mathews, Carol A., Scharf, Jeremiah M., Mattheisen, Manuel, Robertson, Mary M., McQuillin, Andrew, Crowley, James J.

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Outcomes of influenza A(H1N1)pdm09 virus infection: results from two international cohort studies by Lynfield, Ruth, Davey, Richard, Dwyer, Dominic E, Losso, Marcelo H, Wentworth, Deborah, Cozzi-Lepri, Alessandro, Herman-Lamin, Kathy, Cholewinska, Grazyna, David, Daniel, Kuetter, Stefan, Ternesgen, Zelalem, Uyeki, Timothy M, Lane, H Clifford, Lundgren, Jens, Neaton, James D

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Coprophenomena in Tourette syndrome by FREEMAN, ROGER D, ZINNER, SAMUEL H, MÜLLER‐VAHL, KIRSTEN R, FAST, DIANE K, BURD, LARRY J, KANO, YUKIKO, ROTHENBERGER, ARIBERT, ROESSNER, VEIT, KERBESHIAN, JACOB, STERN, JEREMY S

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Tic disorders and ADHD: answers from a world-wide clinical dataset on Tourette syndrome by Freeman, Roger D

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Developmental psychopathology of children and adolescents with Tourette syndrome--impact of ADHD by Roessner, Veit, Becker, Andreas, Banaschewski, Tobias, Freeman, Roger D, Rothenberger, Aribert

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