Software Testing Automation of VR-Based Systems With Haptic Interfaces von Corrêa, Cléber G, Delamaro, Márcio E, Chaim, Marcos L, Nunes, Fátima L S

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Contextualizing spectrum-based fault localization von de Souza, Higor A., Mutti, Danilo, Chaim, Marcos L., Kon, Fabio

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EasyAffecta: A framework to develop serious games for virtual rehabilitation with affective adaptation von Aranha, Renan V., Chaim, Marcos L., Monteiro, Carlos B. M., Silva, Talita D., Guerreiro, Francisca A. A. C., Silva, Willian S., Nunes, Fátima L. S.

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A debugging strategy based on the requirements of testing von Chaim, Marcos L., Maldonado, José C., Jino, Mario

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Spectrum-based Software Fault Localization: A Survey of Techniques, Advances, and Challenges von de Souza, Higor A, Chaim, Marcos L, Kon, Fabio

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Spectrum-based Software Fault Localization: A Survey of Techniques, Advances, and Challenges von de Souza, Higor A, Chaim, Marcos L, Kon, Fabio

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A generic policy-free framework for fault-tolerant systems: Experiments on WSNs von Beder, D. M., Ueyama, J., Chaim, M. L.

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Twenty-Five Years of Research in Structural and Mutation Testing von Delamaro, M. E., Chaim, M. L., Vincenzi, A. M. R., Jino, M., Maldonado, J. C.

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Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility von Zhao, Jian, Wu, Hui, Khosravi, Melanie, Cui, Huijuan, Qian, Xiaoxia, Kelly, Jennifer A, Kaufman, Kenneth M, Langefeld, Carl D, Williams, Adrienne H, Comeau, Mary E, Ziegler, Julie T, Marion, Miranda C, Adler, Adam, Glenn, Stuart B, Alarcón-Riquelme, Marta E, Pons-Estel, Bernardo A, Harley, John B, Bae, Sang-Cheol, Bang, So-Young, Cho, Soo-Kyung, Jacob, Chaim O, Vyse, Timothy J, Niewold, Timothy B, Gaffney, Patrick M, Moser, Kathy L, Kimberly, Robert P, Edberg, Jeffrey C, Brown, Elizabeth E, Alarcon, Graciela S, Petri, Michelle A, Ramsey-Goldman, Rosalind, Vilá, Luis M, Reveille, John D, James, Judith A, Gilkeson, Gary S, Kamen, Diane L, Freedman, Barry I, Anaya, Juan-Manuel, Merrill, Joan T, Criswell, Lindsey A, Scofield, R Hal, Stevens, Anne M, Guthridge, Joel M, Chang, Deh-Ming, Song, Yeong Wook, Park, Ji Ah, Lee, Eun Young, Boackle, Susan A, Grossman, Jennifer M, Hahn, Bevra H, Goodship, Timothy H J, Cantor, Rita M, Yu, Chack-Yung, Shen, Nan, Tsao, Betty P

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Whole-exome sequencing identifies genes associated with Tourette’s disorder in multiplex families von Cao, Xiaolong, Zhang, Yeting, Abdulkadir, Mohamed, Deng, Li, Fernandez, Thomas V., Garcia-Delgar, Blanca, Hagstrøm, Julie, Hoekstra, Pieter J., King, Robert A., Koesterich, Justin, Kuperman, Samuel, Morer, Astrid, Nasello, Cara, Plessen, Kerstin J., Thackray, Joshua K., Zhou, Lisheng, Dietrich, Andrea, Tischfield, Jay A., Heiman, Gary A., Xing, Jinchuan

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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.

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PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes von Namjou, Bahram, Kim-Howard, Xana, Sun, Celi, Adler, Adam, Chung, Sharon A, Kaufman, Kenneth M, Kelly, Jennifer A, Glenn, Stuart B, Guthridge, Joel M, Scofield, Robert H, Kimberly, Robert P, Brown, Elizabeth E, Alarcón, Graciela S, Edberg, Jeffrey C, Kim, Jae-Hoon, Choi, Jiyoung, Ramsey-Goldman, Rosalind, Petri, Michelle A, Reveille, John D, Vilá, Luis M, Boackle, Susan A, Freedman, Barry I, Tsao, Betty P, Langefeld, Carl D, Vyse, Timothy J, Jacob, Chaim O, Pons-Estel, Bernardo, Niewold, Timothy B, Moser Sivils, Kathy L, Merrill, Joan T, Anaya, Juan-Manuel, Gilkeson, Gary S, Gaffney, Patrick M, Bae, Sang-Cheol, Alarcón-Riquelme, Marta E, Harley, John B, Criswell, Lindsey A, James, Judith A, Nath, Swapan K

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MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus von Deng, Yun, Zhao, Jian, Sakurai, Daisuke, Kaufman, Kenneth M, Edberg, Jeffrey C, Kimberly, Robert P, Kamen, Diane L, Gilkeson, Gary S, Jacob, Chaim O, Scofield, R Hal, Langefeld, Carl D, Kelly, Jennifer A, Ramsey-Goldman, Rosalind, Petri, Michelle A, Reveille, John D, Vilá, Luis M, Alarcón, Graciela S, Vyse, Timothy J, Pons-Estel, Bernardo A, Freedman, Barry I, Gaffney, Patrick M, Sivils, Kathy Moser, James, Judith A, Gregersen, Peter K, Anaya, Juan-Manuel, Niewold, Timothy B, Merrill, Joan T, Criswell, Lindsey A, Stevens, Anne M, Boackle, Susan A, Cantor, Rita M, Chen, Weiling, Grossman, Jeniffer M, Hahn, Bevra H, Harley, John B, Alarcόn-Riquelme, Marta E, Brown, Elizabeth E, Tsao, Betty P

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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

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Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome von Jain, Pritesh, Miller-Fleming, Tyne, Topaloudi, Apostolia, Yu, Dongmei, Drineas, Petros, Georgitsi, Marianthi, Yang, Zhiyu, Rizzo, Renata, Müller-Vahl, Kirsten R., Tumer, Zeynep, Mol Debes, Nanette, Hartmann, Andreas, Depienne, Christel, Worbe, Yulia, Mir, Pablo, Cath, Danielle C., Boomsma, Dorret I., Roessner, Veit, Wolanczyk, Tomasz, Janik, Piotr, Szejko, Natalia, Zekanowski, Cezary, Barta, Csaba, Nemoda, Zsofia, Tarnok, Zsanett, Buxbaum, Joseph D., Grice, Dorothy, Glennon, Jeffrey, Stefansson, Hreinn, Hengerer, Bastian, Benaroya-Milshtein, Noa, Cardona, Francesco, Hedderly, Tammy, Heyman, Isobel, Huyser, Chaim, Morer, Astrid, Mueller, Norbert, Munchau, Alexander, Plessen, Kerstin J., Porcelli, Cesare, Walitza, Susanne, Schrag, Anette, Martino, Davide, Dietrich, Andrea, Mathews, Carol A., Scharf, Jeremiah M., Hoekstra, Pieter J., Davis, Lea K., Paschou, Peristera

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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.

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Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD von Wang, Sheng, Wang, Belinda, Drury, Vanessa, Drake, Sam, Sun, Nawei, Alkhairo, Hasan, Arbelaez, Juan, Duhn, Clif, Bal, Vanessa H., Langley, Kate, Martin, Joanna, Hoekstra, Pieter J., Dietrich, Andrea, Xing, Jinchuan, Heiman, Gary A., Tischfield, Jay A., Fernandez, Thomas V., Owen, Michael J., O’Donovan, Michael C., Thapar, Anita, State, Matthew W., Willsey, A. Jeremy

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Vitamin D levels in children and adolescents with chronic tic disorders: a multicentre study von Bond, Molly, Moll, Natalie, Rosello, Alicia, Bond, Rod, Schnell, Jaana, Burger, Bianka, Hoekstra, Pieter J., Dietrich, Andrea, Schrag, Anette, Kocovska, Eva, Martino, Davide, Mueller, Norbert, Schwarz, Markus, Meier, Ute-Christiane

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Tic disorders in children and adolescents: does the clinical presentation differ in males and females? A report by the EMTICS group von Garcia-Delgar, Blanca, Servera, Mateu, Coffey, Barbara J., Lázaro, Luisa, Openneer, Thaïra, Benaroya-Milshtein, Noa, Steinberg, Tami, Hoekstra, Pieter J., Dietrich, Andrea, Morer, Astrid

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Investigation of gene–environment interactions in relation to tic severity von Abdulkadir, Mohamed, Yu, Dongmei, Osiecki, Lisa, King, Robert A., Fernandez, Thomas V., Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., Garcia-Delgar, Blanca, Gilbert, Donald L., Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heyman, Isobel, Hong, Hyun Ju, Huyser, Chaim, Ibanez-Gomez, Laura, Kim, Young Key, Kim, Young-Shin, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Leventhal, Bennett, Madruga-Garrido, Marcos, Maras, Athanasios, Mir, Pablo, Morer, Astrid, Münchau, Alexander, Plessen, Kerstin J., Roessner, Veit, Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, Visscher, Frank, Zinner, Samuel H., Mathews, Carol A., Scharf, Jeremiah M., Tischfield, Jay A., Heiman, Gary A., Dietrich, Andrea, Hoekstra, Pieter J.

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