Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Tourette Syndrome and SLITRK1[original query] |
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| Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome. Acta neurologica Scandinavica 2006 Dec 114 (6): 400-2. Deng H, Le W D, Xie W J, Jankovic |
| Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses. Human molecular genetics 2006 Nov 15 (22): 3324-8. 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 |
| Association study between Gilles de la Tourette Syndrome and two genes in the Robo-Slit pathway located in the chromosome 11q24 linked/associated region. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Jan 147B (1): 68-72. Miranda D M, Wigg K, Feng Y, Sandor P, Barr C |
| [Searching for Tourette's syndrome gene. Part 2. Patient's genome variability]. Post?py higieny i medycyny do?wiadczalnej (Online) 2012 66 (0): 89-95. Kowalska Anna, Midro Alina T, Janik Piotr, Gogol Anna, S?u?ewski Wojciech, Rajewski Andrz |
| Characterization of SLITRK1 variation in obsessive-compulsive disorder. PloS one 2013 8 (8): e70376. Ozomaro Uzoezi, Cai Guiqing, Kajiwara Yuji, Yoon Seungtai, Makarov Vladimir, Delorme Richard, Betancur Catalina, Ruhrmann Stephan, Falkai Peter, Grabe Hans Jörgen, Maier Wolfgang, Wagner Michael, Lennertz Leonhard, Moessner Rainald, Murphy Dennis L, Buxbaum Joseph D, Züchner Stephan, Grice Dorothy |
| 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 |
| 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 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 |
| 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 |
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