Folyóiratcikkek tallózása szerző szerint "Paschou P"

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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 ...
  • Epigenome-Wide Association Study of Tic Disorders 
    Zilhão NR; Padmanabhuni SS; Pagliaroli, Luca; Barta, Csaba; BIOS Consortium; Smit DJA; Cath D; Nivard MG; Baselmans BML; Van Dongen J; Paschou P; Boomsma DI (2015)
    Tic disorders are moderately heritable common psychiatric disorders that can be highly troubling, both in childhood and in adulthood. In this study, we report results obtained in the first epigenome-wide association study ...
  • Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome 
    Huang AY; Yu D; Davis LK; Sul JH; Tsetsos F; Ramensky V; Zelaya I; Ramos EM; Osiecki L; Chen JA; McGrath LM; Illmann C; Sandor P; Barr CL; Grados M; Singer HS; Nothen MM; Hebebrand J; King RA; Dion Y; Rouleau G; Budman CL; Depienne C; Worbe Y; Hartmann A; Muller-Vahl KR; Stuhrmann M; Aschauer H; Stamenkovic M; Schloegelhofer M; Konstantinidis A; Lyon GJ; McMahon WM; Barta, Csaba; Tárnok, Zsanett; Nagy, Péter; Batterson JR; Rizzo R; Cath DC; Wolanczyk T; Berlin C; Malaty IA; Okun MS; Woods DW; Rees E; Pato CN; Pato MT; Knowles JA; Posthuma D; Pauls DL; Cox NJ; Neale BM; Freimer NB; Paschou P; Mathews CA; Scharf JM; Coppola G; Tourette Syndrome Association International Consortium for Genetics (TSAICG); Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI) (2017)
    Tourette syndrome (TS) is a model neuropsychiatric disorder thought to arise from abnormal development and/or maintenance of cortico-striato-thalamo-cortical circuits. TS is highly heritable, but its underlying genetic ...
  • 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, ...
  • TS-EUROTRAIN: A European-wide investigation and training network on the etiology and pathophysiology of Gilles de la Tourette Syndrome 
    Forde NJ; Kanaan AS; Widomska J; Padmanabhuni SS; Nespoli E; Alexander J; Rodriguez Arranz JI; Fan S; Houssari R; Nawaz MS; Rizzo F; Pagliaroli, Luca; Zilhäo NR; Arányi, Tamás; Barta, Csaba; Boeckers TM; Boomsma DI; Buisman WR; Buitelaar JK; Cath D; Dietrich A; Driessen N; Drineas P; Dunlap M; Gerasch S; Glennon J; Hengerer B; Van den Heuvel OA; Jespersgaard C; Möller HE; Müller-Vahl KR; Openneer TJC; Poelmans G; Pouwels PJW; Scharf JM; Stefansson H; Tümer Z; Veltman DJ; Van der Werf YD; Hoekstra PJ; Ludolph A; Paschou P (2016)
    Gilles de la Tourette Syndrome (GTS) is characterized by the presence of multiple motor and phonic tics with a fluctuating course of intensity, frequency, and severity. Up to 90% of patients with GTS present with comorbid ...