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9. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Williams NM; Zaharieva I; Martin A; Langley K; Mantripragada K; Fossdal R; Stefansson H; Stefansson K; Magnusson P; Gudmundsson OO; Gustafsson O; Holmans P; Owen MJ; O'Donovan M; Thapar A Lancet; 2010 Oct; 376(9750):1401-8. PubMed ID: 20888040 [TBL] [Abstract][Full Text] [Related]
10. Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder. Rajagopal VM; Duan J; Vilar-Ribó L; Grove J; Zayats T; Ramos-Quiroga JA; Satterstrom FK; Artigas MS; Bybjerg-Grauholm J; Bækvad-Hansen M; Als TD; Rosengren A; Daly MJ; Neale BM; Nordentoft M; Werge T; Mors O; Hougaard DM; Mortensen PB; Ribasés M; Børglum AD; Demontis D Nat Genet; 2022 Aug; 54(8):1117-1124. PubMed ID: 35927488 [TBL] [Abstract][Full Text] [Related]
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12. Polymorphisms of the dopamine transporter gene: influence on response to methylphenidate in attention deficit-hyperactivity disorder. Roman T; Rohde LA; Hutz MH Am J Pharmacogenomics; 2004; 4(2):83-92. PubMed ID: 15059031 [TBL] [Abstract][Full Text] [Related]
13. Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies. Bonvicini C; Faraone SV; Scassellati C Mol Psychiatry; 2016 Jul; 21(7):872-84. PubMed ID: 27217152 [TBL] [Abstract][Full Text] [Related]
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16. Significant association between rare IPO11-HTR1A variants and attention deficit hyperactivity disorder in Caucasians. Zuo L; Saba L; Lin X; Tan Y; Wang K; Krystal JH; Tabakoff B; Luo X Am J Med Genet B Neuropsychiatr Genet; 2015 Oct; 168(7):544-56. PubMed ID: 26079129 [TBL] [Abstract][Full Text] [Related]
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