tallózása szerző szerint "Karagiannidis I"

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  • Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort 
    Bertelsen B; Stefánsson H; Riff Jensen L; Melchior L; Mol Debes N; Groth C; Skov L; Werge T; Karagiannidis I; Tárnok, Zsanett; Barta, Csaba; Nagy, Péter; Farkas L; Brøndum-Nielsen K; Rizzo R; Gulisano M; Rujescu D; Kiemeney LA; Tosato S; Nawaz MS; Ingason A; Unnsteinsdottir U; Steinberg S; Ludvigsson P; Stefansson K; Kuss AW; Paschou P; Cath D; Hoekstra PJ; Müller-Vahl K; Stuhrmann M; Silahtaroglu A; Pfundt R; Tümer Z (2016)
    Background: Gilles de la Tourette syndrome (GTS) is a complex neuropsychiatric disorder with a strong genetic influence where copy number variations are suggested to play a role in disease pathogenesis. In a previous ...
  • Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology 
    Alexander J; Potamianou H; Xing JC; Deng L; Karagiannidis I; Tsetsos F; Drineas P; Tarnok Z; Rizzo R; Wolanczyk T; Farkas L; Nagy P; Szymanska U; Androutsos C; Tsironi V; Koumoulas A; Barta, Csaba; Sandor P; Barr CL; Tischfield J; Paschou P; Heiman GA; Georgitsi M (2016)
    Although the genetic basis of Tourette Syndrome (TS) remains unclear, several candidate genes have been implicated. Using a set of 382 TS individuals of European ancestry we investigated four candidate genes for TS (HDC, ...