HuGE Literature Finder
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| Gene variations in PBX1, LMX1A and SLITRK1 are associated with obsessive-compulsive disorder and its clinical features. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2019 Mar 61 180-185. Melo-Felippe Fernanda B, Fontenelle Leonardo F, Kohlrausch Fabiana |
| 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 |
| 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 |
| Glutamate system genes and brain volume alterations in pediatric obsessive-compulsive disorder: a preliminary study. Psychiatry research 2012 Nov . Wu K, Hanna GL, Easter P, Kennedy JL, Rosenberg DR, Arnold PD |
| SERT Ileu425Val in autism, Asperger syndrome and obsessive-compulsive disorder. Psychiatric genetics 2008 Feb 18 (1): 31-9. Wendland Jens R, DeGuzman Theresa B, McMahon Francis, Rudnick Gary, Detera-Wadleigh Sevilla D, Murphy Dennis |
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