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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 8, 2024. (Total: 233355Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Tourette Syndrome and HDC[original query]
Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Jan 159B (1): 72-6.
Lei Jing, Deng Xiong, Zhang Jie, Su Linyan, Xu Hongbo, Liang Hui, Huang Xian, Song Zhi, Deng H
[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
Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families.
Journal of medical genetics 2013 Nov 50 (11): 760-4.
Karagiannidis Iordanis, Dehning Sandra, Sandor Paul, Tarnok Zsanett, Rizzo Renata, Wolanczyk Tomasz, Madruga-Garrido Marcos, Hebebrand Johannes, Nöthen Markus M, Lehmkuhl Gerd, Farkas Luca, Nagy Peter, Szymanska Urszula, Anastasiou Zachos, Stathias Vasileios, Androutsos Christos, Tsironi Vaia, Koumoula Anastasia, Barta Csaba, Zill Peter, Mir Pablo, Müller Norbert, Barr Cathy, Paschou Periste
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 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
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