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| Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2022 Dec . Abdulkadir Mohamed, Tischfield Jay A, Heiman Gary A, Hoekstra Pieter J, Dietrich Andr |
| Investigating Direct and Indirect Genetic Effects in Attention-Deficit/Hyperactivity Disorder Using Parent-Offspring Trios. Biological psychiatry 2022 Jun . Martin Joanna, Wray Matthew, Agha Sharifah Shameem, Lewis Katie J S, Anney Richard J L, O'Donovan Michael C, Thapar Anita, Langley Ka |
| Synaptic processes and immune-related pathways implicated in Tourette syndrome. Translational psychiatry 2021 01 11 (1): 56. Tsetsos Fotis, Yu Dongmei, Sul Jae Hoon, Huang Alden Y, Illmann Cornelia, Osiecki Lisa, Darrow Sabrina M, Hirschtritt Matthew E, Greenberg Erica, Muller-Vahl Kirsten R, Stuhrmann Manfred, Dion Yves, Rouleau Guy A, Aschauer Harald, Stamenkovic Mara, Schlögelhofer Monika, Sandor Paul, Barr Cathy L, Grados Marco A, 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, Wagner Michael, Knowles James A, Jeremy Willsey A, Tischfield Jay A, Heiman Gary A, Cox Nancy J, Freimer Nelson B, Neale Benjamin M, Davis Lea K, Coppola Giovanni, Mathews Carol A, Scharf Jeremiah M, Paschou Peristera, , Barr Cathy L, Batterson James R, Berlin Cheston, Budman Cathy L, Cath Danielle C, Coppola Giovanni, Cox Nancy J, Darrow Sabrina, Davis Lea K, Dion Yves, Freimer Nelson B, Grados Marco A, Greenberg Erica, Hirschtritt Matthew E, Huang Alden Y, Illmann Cornelia, King Robert A, Kurlan Roger, Leckman James F, Lyon Gholson J, Malaty Irene A, Mathews Carol A, McMahon William M, Neale Benjamin M, Okun Michael S, Osiecki Lisa, Robertson Mary M, Rouleau Guy A, Sandor Paul, Scharf Jeremiah M, Singer Harvey S, Smit Jan H, Sul Jae Hoon, Yu Dongmei, , Aschauer Harald Aschauer Harald, Barta Csaba, Budman Cathy L, Cath Danielle C, Depienne Christel, Hartmann Andreas, Hebebrand Johannes, Konstantinidis Anastasios, Mathews Carol A, Müller-Vahl Kirsten, Nagy Peter, Nöthen Markus M, Paschou Peristera, Rizzo Renata, Rouleau Guy A, Sandor Paul, Scharf Jeremiah M, Schlögelhofer Monika, Stamenkovic Mara, Stuhrmann Manfred, Tsetsos Fotis, Tarnok Zsanett, Wolanczyk Tomasz, Worbe Yulia, , Brown Lawrence, Cheon Keun-Ah, Coffey Barbara J, Dietrich Andrea, Fernandez Thomas V, Garcia-Delgar Blanca, Gilbert Donald, Grice Dorothy E, Hagstrøm Julie, Hedderly Tammy, Heiman Gary A, Heyman Isobel, Hoekstra Pieter J, Huyser Chaim, Kim Young Key, Kim Young-Shin, King Robert A, Koh Yun-Joo, Kook Sodahm, Kuperman Samuel, Leventhal Bennett L, Madruga-Garrido Marcos, Mir Pablo, Morer Astrid, Münchau Alexander, Plessen Kerstin J, Roessner Veit, Shin Eun-Young, Song Dong-Ho, Song Jungeun, Tischfield Jay A, Willsey A Jeremy, Zinner Samuel, , Aschauer Harald, Barr Cathy L, Barta Csaba, Batterson James R, Berlin Cheston, Brown Lawrence, Budman Cathy L, Cath Danielle C, Coffey Barbara J, Coppola Giovanni, Cox Nancy J, Darrow Sabrina, Davis Lea K, Depienne Christel, Dietrich Andrea, Dion Yves, Fernandez Thomas, Freimer Nelson B, Gilbert Donald, Grados Marco A, Greenberg Erica, Hartmann Andreas, Hebebrand Johannes, Heiman Gary, Hirschtritt Matthew E, Hoekstra Pieter, Huang Alden Y, Illmann Cornelia, Jankovic Joseph, King Robert A, Kuperman Samuel, Lee Paul C, Lyon Gholson J, Malaty Irene A, Mathews Carol A, McMahon William M, Müller-Vahl Kirsten, Nagy Peter, Neale Benjamin M, Nöthen Markus M, Okun Michael S, Osiecki Lisa, Paschou Peristera, Rizzo Renata, Robertson Mary M, Rouleau Guy A, Sandor Paul, Scharf Jeremiah M, Schlögelhofer Monika, Singer Harvey S, Stamenkovic Mara, Stuhrmann Manfred, Sul Jae Hoon, Tarnok Zsanett, Tischfield Jay, Tsetsos Fotis, Willsey A Jeremy, Woods Douglas, Worbe Yulia, Yu Dongmei, Zinner Samu |
| The role of SLITRK6 in the pathogenesis of Tourette syndrome: From the conclusion of a family-based study in the Chinese Han population. The journal of gene medicine 2020 Feb e3173. Liu Wenmiao, Zhang Xuzhan, Deng Ziwen, Li Guixia, Zhang Ru, Yang Zongjun, Che Fengyuan, Liu Shiguo, Li H |
| Association of a Variant of CNR1 Gene Encoding Cannabinoid Receptor 1 With Gilles de la Tourette Syndrome. Frontiers in genetics 2020 11 125. Szejko Natalia, Fichna Jakub Piotr, Safranow Krzysztof, Dziuba Tomasz, Zekanowski Cezary, Janik Pio |
| Family-Based Analysis Combined with Case-Controls Study Implicate Roles of PCNT in Tourette Syndrome. Neuropsychiatric disease and treatment 2020 16 349-354. Liu Wenmiao, Guo Yixia, Liu Xiumei, Zhang Ru, Dong Jicheng, Deng Hao, He Fan, Che Fengyuan, Liu Shiguo, Yi Ming |
Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.
Nature human behaviour 2020 12 5 (4): 482-496. Wendt Frank R, Pathak Gita A, Lencz Todd, Krystal John H, Gelernter Joel, Polimanti Rena |
| Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.
Cell 2019 Dec 179 (7): 1469-1482.e11. , |
| Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Translational psychiatry 2019 Mar 9 (1): 120. Mufford Mary, Cheung Josh, Jahanshad Neda, van der Merwe Celia, Ding Linda, Groenewold Nynke, Koen Nastassja, Chimusa Emile R, Dalvie Shareefa, Ramesar Raj, , Knowles James A, Lochner Christine, Hibar Derrek P, Paschou Peristera, van den Heuvel Odile A, Medland Sarah E, Scharf Jeremiah M, Mathews Carol A, Thompson Paul M, Stein Dan |
| Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome. Tremor and other hyperkinetic movements (New York, N.Y.) 2019 9 . Depienne Christel, Ciura Sorana, Trouillard Oriane, Bouteiller Delphine, Leitã O Elsa, Nava Caroline, Keren Boris, Marie Yannick, Guegan Justine, Forlani Sylvie, Brice Alexis, Anheim Mathieu, Agid Yves, Krack Paul, Damier Philippe, Viallet François, Houeto Jean-Luc, Durif Franck, Vidailhet Marie, Worbe Yulia, Roze Emmanuel, Kabashi Edor, Hartmann Andre |
| Hyperactivity in mice lacking one allele of the glutamic acid decarboxylase 67 gene. Attention deficit and hyperactivity disorders 2018 Dec 10 (4): 267-271. Smith Karen Müll |
| Genome wide analysis of rare copy number variations in alcohol abuse or dependence. Journal of psychiatric research 2018 Jun 103 212-218. Rodríguez-López Julio, Flórez Gerardo, Blanco Vanessa, Pereiro César, Fernández José Manuel, Fariñas Emilio, Estévez Valentín, Gómez-Trigo Jesús, Gurriarán Xaquín, Calvo Raquel, Sáiz Pilar, , Vázquez Fernando Lino, Arrojo Manuel, Costas Javi |
| Association of the AADAC gene and Tourette syndrome in a Han Chinese cohort. Neuroscience letters 2017 Dec 666 24-27. Yuan Lamei, Zheng Wen, Yang Zuocheng, Deng Xiong, Song Zhi, Deng H |
| Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Nov . Zhang Yanqing, Liu Yi, Zarrei Mehdi, Tong Winnie, Dong Rui, Wang Ying, Zhang Haiyan, Yang Xiaomeng, MacDonald Jeffrey R, Uddin Mohammed, Scherer Stephen W, Gai Zhongt |
| Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population. Neuroscience letters 2017 Aug . Guan Hongzai, Liu Wenmiao, Gao Chuanping, Wu Xingfu, Wang Guiju, Liu Shiguo, Liu Jinshe |
| Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron 2017 Jun 94 (6): 1101-1111.e7. 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, , |
| De Novo Coding Variants Are Strongly Associated with Tourette Disorder. Neuron 2017 May 94 (3): 486-499.e9. Willsey A Jeremy, Fernandez Thomas V, Yu Dongmei, King Robert A, Dietrich Andrea, Xing Jinchuan, Sanders Stephan J, Mandell Jeffrey D, Huang Alden Y, Richer Petra, Smith Louw, Dong Shan, Samocha Kaitlin E, , , Neale Benjamin M, Coppola Giovanni, Mathews Carol A, Tischfield Jay A, Scharf Jeremiah M, State Matthew W, Heiman Gary |
| Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. European archives of psychiatry and clinical neuroscience 2017 May . Abdulkadir Mohamed, Londono Douglas, Gordon Derek, Fernandez Thomas V, Brown Lawrence W, Cheon Keun-Ah, Coffey Barbara J, Elzerman Lonneke, Fremer Carolin, Fründt Odette, Garcia-Delgar Blanca, Gilbert Donald L, Grice Dorothy E, Hedderly Tammy, Heyman Isobel, Hong Hyun Ju, Huyser Chaim, Ibanez-Gomez Laura, Jakubovski Ewgeni, Kim Young Key, Kim Young Shin, Koh Yun-Joo, Kook Sodahm, Kuperman Samuel, Leventhal Bennett, Ludolph Andrea G, Madruga-Garrido Marcos, Maras Athanasios, Mir Pablo, Morer Astrid, Müller-Vahl Kirsten, Münchau Alexander, Murphy Tara L, Plessen Kerstin J, Roessner Veit, Shin Eun-Young, Song Dong-Ho, Song Jungeun, Tübing Jennifer, van den Ban Els, Visscher Frank, Wanderer Sina, Woods Martin, Zinner Samuel H, King Robert A, Tischfield Jay A, Heiman Gary A, Hoekstra Pieter J, Dietrich Andr |
| Choline acetyltransferase may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control study. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2017 Jan 1-21. Yang Xiuling, Liu Wenmiao, Yi Mingji, Zhang Ru, Xu Yinglei, Huang Zuzhou, Liu Shiguo, Li Ta |
| BDNF and LTP-/LTD-like plasticity of the primary motor cortex in Gilles de la Tourette syndrome. Experimental brain research 2016 Nov . Marsili L, Suppa A, Di Stasio F, Belvisi D, Upadhyay N, Berardelli I, Pasquini M, Petrucci S, Ginevrino M, Fabbrini G, Cardona F, Defazio G, Berardelli |
| Investigation of a Possible Role for the Histidine Decarboxylase Gene in Tourette Syndrome in the Chinese Han Population: A Family-Based Study. PloS one 2016 11 (8): e0160265. Dong He, Liu Wenmiao, Liu Meixin, Xu Longqiang, Li Qiang, Zhang Ru, Zhang Xin, Liu Shig |
| Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort. Frontiers in neuroscience 2016 10 531. Padmanabhuni Shanmukha S, Houssari Rayan, Esserlind Ann-Louise, Olesen Jes, Werge Thomas M, Hansen Thomas F, Bertelsen Birgitte, Tsetsos Fotis, Paschou Peristera, Tümer Zeyn |
| Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology. Frontiers in neuroscience 2016 10 428. Alexander John, Potamianou Hera, Xing Jinchuan, Deng Li, Karagiannidis Iordanis, Tsetsos Fotis, Drineas Petros, Tarnok Zsanett, Rizzo Renata, Wolanczyk Tomasz, Farkas Luca, Nagy Peter, Szymanska Urszula, Androutsos Christos, Tsironi Vaia, Koumoula Anastasia, Barta Csaba, , Sandor Paul, Barr Cathy L, Tischfield Jay, Paschou Peristera, Heiman Gary A, Georgitsi Mariant |
| Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort. Biological psychiatry 2015 Sep . Bertelsen Birgitte, Stefánsson Hreinn, Riff Jensen Lars, Melchior Linea, Mol Debes Nanette, Groth Camilla, Skov Liselotte, Werge Thomas, Karagiannidis Iordanis, Tarnok Zsanett, Barta Csaba, Nagy Peter, Farkas Luca, Brøndum-Nielsen Karen, Rizzo Renata, Gulisano Mariangela, Rujescu Dan, Kiemeney Lambertus A, Tosato Sarah, Nawaz Muhammad Sulaman, Ingason Andres, Unnsteinsdottir Unnur, Steinberg Stacy, Ludvigsson Pétur, Stefansson Kari, Kuss Andreas Walter, Paschou Peristera, Cath Danielle, Hoekstra Pieter J, Müller-Vahl Kirsten, Stuhrmann Manfred, Silahtaroglu Asli, Pfundt Rolph, Tümer Zeyn |
| Analysis of SLITRK1 in Japanese patients with Tourette syndrome using a next-generation sequencer. Psychiatric genetics 2015 Aug . Inai Aya, Tochigi Mamoru, Kuwabara Hitoshi, Nishimura Fumichika, Kato Kayoko, Eriguchi Yosuke, Shimada Takafumi, Furukawa Masaomi, Kawamura Yoshiya, Sasaki Tsukasa, Kakiuchi Chihiro, Kasai Kiyoto, Kano Yuki |
| The role of GRIN2B in Tourette syndrome: Results from a transmission disequilibrium study. Journal of affective disorders 2015 Aug 187 62-65. Che Fengyuan, Zhang Ying, Wang Guiju, Heng Xueyuan, Liu Shiguo, Du Yife |
| Association between the polymorphism of C861G (rs6296) in the serotonin 1B receptor gene and Tourette syndrome in Han Chinese people. Asia-Pacific psychiatry : official journal of the Pacific Rim College of Psychiatrists 2015 Jun . Yi Mingji, Zhang Ying, Wang Yujie, Su Nailun, Liu Shig |
| Association between DRD2/ANKK1 TaqIA Polymorphism and Susceptibility with Tourette Syndrome: A Meta-Analysis. PloS one 2015 10 (6): e0131060. Yuan Aihua, Su Liang, Yu Shunying, Li Chunbo, Yu Tao, Sun Jinh |
| Association of ADORA1 rs2228079 and ADORA2A rs5751876 Polymorphisms with Gilles de la Tourette Syndrome in the Polish Population. PloS one 2015 10 (8): e0136754. Janik Piotr, Berdy?ski Mariusz, Safranow Krzysztof, ?ekanowski Ceza |
| Support of positive association in family-based genetic analysis between COL27A1 and Tourette syndrome. Scientific reports 2015 5 12687. Liu Shiguo, Yu Xiaoxia, Xu Quanchen, Cui Jiajia, Yi Mingji, Zhang Xinhua, Ge Yinlin, Ma |
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- Page last updated:Jan 26, 2023
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