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

Mandelll, Jeffrey D.; Mandell, Jeffrey D.; Wang, Sheng; Collaborative, Tourette Int; Morris, Montana T.; Kumarr, Yogesh; Kumar, Yogesh; Genetics, Tourette Syndrome; Sunn, Nawei; Sun, Nawei; Taaicg,; Jd, Mandell; Padmanabhuni, Shanmukha S.; Dongg, Shan; King, Robert A.; Arbelaez, Juan; Khalifa, Najah; Dahl, Niklas; Huang, Alden Y.; Duhnn, Clif; Nasello, Cara; Neale, Benjamin M.; Coppola, Giovanni; Mathews, Carol A.; Dong, Shan; Fernandez, Thomas V.; Scharf, Jeremiah M.; Buxbaum, Joseph D.; Grice, Dorothy E.; De Rubeis, Silvia; Duhn, Clif; Heiman, Gary A.; Xing, Jinchuan; Zhao, Xin; Abdulkadir, Mohamed; Tischfield, Jay A.; Bodmer, Benjamin; Yang, Zhiyu; Paschou, Peristera; Bromberg, Yana; Brown, Lawrence W.; State, Matthew W.; Willsey, A. Jeremy; Cheon, Keun-Ah; Coffey, Barbara J.; Dietrich, Andrea; Yu, Dongmei; Deng, Li; Mt, Morris; Elzerman, Lonneke; Fremer, Carolin; Garcia-Delgar, Blanca; Zinner, Samuel H.; Gilbert, Donald L.; Hagstrøm, Julie; Hedderly, Tammy; Heyman, Isobel; Hoekstra, Pieter J.; Hong, Hyun Ju; Huyser, Chaim; Kim, Eun-Joo; Kim, Young Key; Kim, Young-Shin; Koh, Yun-Joo; Kook, Sodahm; Kuperman, Samuel; Jeremy Willsey, A.; Leventhal, Bennett L.; Ludolph, Andrea G.; Madruga-Garrido, Marcos; Maras, Athanasios; Mir, Pablo; Morer, Astrid; MÃ¼ller-Vahl, K.; Münchau, Alexander; Müller-Vahl, Kirsten; Murphy, Tara L.; MÃ¼nchau, A.; Plessen, Kerstin J.; Poisner, Hannah; Roessner, Veit; Sanders, Stephan J.; Shin, Eun-Young; Song, Dong-Ho; Song, Jungeun; Thackray, Joshua K.; Tübing, Jennifer; Visscher, Frank; TÃ¼bing, J.; Wanderer, Sina; Woods, Martin; Mathewss, Carol A.; Zhang, Yeting; Androutsos, Christos; Barta, Csaba; Farkas, Luca; Fichna, Jakub; Georgitsi, Marianthi; Initiative (TSGENESEE), Tourette Syndrome Genetics Southern; Janik, Piotr; Karagiannidis, Iordanis; Koumoula, Anastasia; Nagy, Peter; Puchala, Joanna; Rizzo, Renata; Genetics (TAAICG), Tourette Association of America Int; Szejko, Natalia; Szymanska, Urszula; Tarnok, Zsanett; Ss, Padmanabhuni; Tsironi, Vaia; Wolanczyk, Tomasz; Zekanowski, Cezary; Barr, Cathy L.; Batterson, James R.; Berlin, Cheston; Bruun, Ruth D.; Budman, Cathy L.; Cath, Danielle C.; Chouinard, Sylvain; Cox, Nancy J.; Darrow, Sabrina; Davis, Lea K.; Dion, Yves; Freimer, Nelson B.; Grados, Marco A.; Hirschtritt, Matthew E.; Illmann, Cornelia; Ra, King; Xingg, Jinchuan; Kurlan, Roger; Leckman, James F.; Lyon, Gholson J.; Malaty, Irene A.; MacMahon, William M.; Heimann, Gary A.; Okun, Michael S.; Osiecki, Lisa; Pauls, David L.; Posthuma, Danielle; Ramensky, Vasily; Robertson, Mary M.; Rouleau, Guy A.; Sandor, Paul; Singer, Harvey S.; Smit, Jan; Mw, State; Sul, Jae-Hoon

Published in

Cell Press, Cell Reports, 12(25), p. 3544, 2018

DOI: 10.1016/j.celrep.2018.12.024

Cell Press, Cell Reports, 13(24), p. 3441-3454.e12, 2018

DOI: 10.1016/j.celrep.2018.08.082

SSRN Electronic Journal

DOI: 10.2139/ssrn.3188485

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

Journal article published in 2018 by Jeffrey D. Mandelll, Jeffrey D. Mandell, Sheng Wang, Tourette Int Collaborative, Montana T. Morris, Yogesh Kumarr, Yogesh Kumar, Tourette Syndrome Genetics, Nawei Sunn, Nawei Sun, Taaicg, Mandell Jd, Shanmukha S. Padmanabhuni, Shan Dongg, Robert A. King and other authors.