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Recent Submissions

  • Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination 
    Eszlári, Nóra; Millinghoffer, András Dániel; Petschner, Péter; Gonda, Xénia; Baksa, Dániel; Pulay, Attila József; Réthelyi, János; Breen Gerome; Deakin John Francis William; Antal, Péter; Bagdy, György; Juhász, Gabriella (2019)
    Ruminative response style is a passive and repetitive way of responding to stress, associated with several disorders. Although twin and candidate gene studies have proven the genetic underpinnings of rumination, no genome-wide ...
  • 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 (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 ...
  • 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 ...
  • Variability in the prevalence of adult ADHD in treatment seeking substance use disorder patients: Results from an international multi-center study exploring DSM-IV and DSM-5 criteria 
    van de Glind G; Konstenius M; Koeter MWJ; van Emmerik-van Oortmerssen K; Carpentier P-J; Kaye S; Degenhardt L; Skutle A; Franck J; Bu E-T; Moggi F; Dom G; Verspreet S; Demetrovics, Zsolt; Kapitány-Fövény, Máté; Fatséas M; Auriacombe M; Schillinger A; Møller M; Johnson B; Faraone SV; Ramos-Quiroga JA; Casas M; Allsop S; Carruthers S; Schoevers RA; Wallhed S; Barta, Csaba; Alleman P; Levin FR; van den Brink W; IASP Research Group (2014)
    Background: Available studies vary in their estimated prevalence of attention deficit/hyperactivity disorder (ADHD) in substance use disorder (SUD) patients, ranging from 2 to 83%. A better understanding of the possible ...

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