Human Genome Epidemiology Literature Finder
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Query Trace: Tourette syndrome[original query] |
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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 |
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 |
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 |
Genetic correlations among psychiatric and immune-related phenotypes based on genome-wide association data. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2018 10 177 (7): 641-657. Tylee Daniel S, Sun Jiayin, Hess Jonathan L, Tahir Muhammad A, Sharma Esha, Malik Rainer, Worrall Bradford B, Levine Andrew J, Martinson Jeremy J, Nejentsev Sergey, Speed Doug, Fischer Annegret, Mick Eric, Walker Brian R, Crawford Andrew, Grant Struan F A, Polychronakos Constantin, Bradfield Jonathan P, Sleiman Patrick M A, Hakonarson Hakon, Ellinghaus Eva, Elder James T, Tsoi Lam C, Trembath Richard C, Barker Jonathan N, Franke Andre, Dehghan Abbas, , , , , , , Faraone Stephen V, Glatt Stephen |
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 J, |
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.
Cell 2019 Dec 179 (7): 1469-1482.e11. , |
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, Leitão 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 |
Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome. Frontiers in neurology 2020 9 11 803. Pagliaroli Luca, Vereczkei Andrea, Padmanabhuni Shanmukha Sampath, Tarnok Zsanett, Farkas Luca, Nagy Peter, Rizzo Renata, Wolanczyk Tomasz, Szymanska Urszula, Kapisyzi Mira, Basha Entela, Koumoula Anastasia, Androutsos Christos, Tsironi Vaia, Karagiannidis Iordanis, Paschou Peristera, Barta Csa |
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, ?ekanowski 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 |
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 |
A Rare Novel CLCN2 Variation and Risk of Gilles de la Tourette Syndrome: Whole-Exome Sequencing in a Multiplex Family and a Follow-Up Study in a Chinese Population. Frontiers in psychiatry 2020 12 11 543911. Yuan Aihua, Wang Zengge, Xu Wen, Ding Qiang, Zhao Ying, Han Jingjing, Sun Jinh |
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 |
Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree. Molecular psychiatry 2021 9 26 (12): 7522-7529. 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 |
Investigation of gene-environment interactions in relation to tic severity. Journal of neural transmission (Vienna, Austria : 1996) 2021 8 128 (11): 1757-1765. 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 |
Concordance and comorbidities among monozygotic twins with tic disorders. Journal of psychiatric research 2021 11 146 297-303. Pedersen Julie Holst, Skytthe Axel, Bybjerg-Grauholm Jonas, Kucukyildiz Asli Sena, Skov Liselotte, Debes Nanette Mol, Tümer Zeyn |
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 |
Elevated Expression of SLC6A4 Encoding the Serotonin Transporter (SERT) in Gilles de la Tourette Syndrome. Genes 2021 1 12 (1): . Hildonen Mathis, Levy Amanda M, Dahl Christina, Bjerregaard Victoria A, Birk Møller Lisbeth, Guldberg Per, Debes Nanette M, Tümer Zeyn |
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 |
Increased prevalence of minor physical anomalies in patients with epilepsy. Scientific reports 2022 8 12 (1): 13707. Tényi Dalma, Tényi Tamás, Csábi Györgyi, Jeges Sára, Bóné Beáta, L?rincz Katalin, Kovács Norbert, Janszky Józs |
Tics: neurological disorders determined by a deficit in sensorimotor gating processes. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 7 43 (10): 5839-5850. Schilke Edoardo Dalmato, Tremolizzo Lucio, Appollonio Ildebrando, Ferrarese Car |
In Silico Analysis Identified Putative Pathogenic Missense nsSNPs in Human SLITRK1 Gene. Genes 2022 4 13 (4): . Ali Muhammad Zeeshan, Farid Arshad, Ahmad Safeer, Muzammal Muhammad, Mohaini Mohammed Al, Alsalman Abdulkhaliq J, Al Hawaj Maitham A, Alhashem Yousef N, Alsaleh Abdulmonem A, Almusalami Eman M, Maryam Mahpara, Khan Muzammil Ahm |
ASH1L may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control study. Brain and behavior 2022 3 12 (4): e2539. Liu Wenmiao, Xu Lulu, Zhang Cheng, Shen Lu, Dong Jicheng, Zhang Han, Liu Shiguo, Che Fengyuan, Zheng Xuepi |
Association between plasma proteome and childhood neurodevelopmental disorders: A two-sample Mendelian randomization analysis. EBioMedicine 2022 3 78 103948. Yang Jian, He Xiaoyan, Qian Li, Zhao Binbin, Fan Yajuan, Gao Fengjie, Yan Bin, Zhu Feng, Ma Xianca |
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 |
Correction: Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome. Tremor and other hyperkinetic movements (New York, N.Y.) 2023 7 13 22. Christel Depienne, Sorana Ciura, Oriane Trouillard, Delphine Bouteiller, Elsa Leitão, Caroline Nava, Boris Keren, Yannick Marie, Justine Guegan, Sylvie Forlani, Alexis Brice, Mathieu Anheim, Yves Agid, Paul Krack, Philippe Damier, François Viallet, Jean-Luc Houeto, Franck Durif, Marie Vidailhet, Yulia Worbe, Emmanuel Roze, Edor Kabashi, Andreas Hartma |
Convergent imaging-transcriptomic evidence for disturbed iron homeostasis in Gilles de la Tourette syndrome. medRxiv : the preprint server for health sciences 2023 6 . Ahmad Seif Kanaan, Dongmei Yu, Riccardo Metere, Andreas Schäfer, Torsten Schlumm, Berkin Bilgic, Alfred Anwander, Carol A Mathews, Jeremiah M Scharf, Kirsten Müller-Vahl, Harald E Möll |
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD. Nature communications 2023 12 14 (1): 8077. Sheng Wang, Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo, Juan Arbelaez, Clif Duhn, , Vanessa H Bal, Kate Langley, Joanna Martin, Pieter J Hoekstra, Andrea Dietrich, Jinchuan Xing, Gary A Heiman, Jay A Tischfield, Thomas V Fernandez, Michael J Owen, Michael C O'Donovan, Anita Thapar, Matthew W State, A Jeremy Wills |
Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene. PloS one 2023 10 18 (10): e0291978. Thomas V Fernandez, Zsanett P Williams, Tina Kline, Shreenath Rajendran, Farhan Augustine, Nicole Wright, Catherine A W Sullivan, Emily Olfson, Sarah B Abdallah, Wenzhong Liu, Ellen J Hoffman, Abha R Gupta, Harvey S Sing |
Genome-wide association study identifies DRAM1 associated with Tourette syndrome in Taiwan. Biomedical journal 2024 4 100725. Wei-De Lin, Ting-Yuan Liu, Yu-Chia Chen, I-Ching Chou, Fuu-Jen Ts |
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- Page last updated:Apr 22, 2024
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