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Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder.
Sánchez-Mora C, Ramos-Quiroga JA, Bosch R, Corrales M, Garcia-Martínez I, Nogueira M, Pagerols M, Palomar G, Richarte V, Vidal R, Arias-Vasquez A, Bustamante M, Forns J, Gross-Lesch S, Guxens M, Hinney A, Hoogman M, Jacob C, Jacobsen KK, Kan CC, Kiemeney L, Kittel-Schneider S, Klein M, Onnink M, Rivero O, Zayats T, Buitelaar J, Faraone SV, Franke B, Haavik J, Johansson S, Lesch KP, Reif A, Sunyer J, Bayés M, Casas M, Cormand B, Ribasés M. Sánchez-Mora C, et al. Among authors: casas m. Neuropsychopharmacology. 2015 Mar;40(4):915-26. doi: 10.1038/npp.2014.267. Epub 2014 Oct 6. Neuropsychopharmacology. 2015. PMID: 25284319 Free PMC article.
Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorder.
Ribasés M, Bosch R, Hervás A, Ramos-Quiroga JA, Sánchez-Mora C, Bielsa A, Gastaminza X, Guijarro-Domingo S, Nogueira M, Gómez-Barros N, Kreiker S, Gross-Lesch S, Jacob CP, Lesch KP, Reif A, Johansson S, Plessen KJ, Knappskog PM, Haavik J, Estivill X, Casas M, Bayés M, Cormand B. Ribasés M, et al. Among authors: casas m. Biol Psychiatry. 2009 Nov 15;66(10):926-34. doi: 10.1016/j.biopsych.2009.06.024. Epub 2009 Sep 5. Biol Psychiatry. 2009. PMID: 19733838
Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD.
Franke B, Vasquez AA, Johansson S, Hoogman M, Romanos J, Boreatti-Hümmer A, Heine M, Jacob CP, Lesch KP, Casas M, Ribasés M, Bosch R, Sánchez-Mora C, Gómez-Barros N, Fernàndez-Castillo N, Bayés M, Halmøy A, Halleland H, Landaas ET, Fasmer OB, Knappskog PM, Heister AJ, Kiemeney LA, Kooij JJ, Boonstra AM, Kan CC, Asherson P, Faraone SV, Buitelaar JK, Haavik J, Cormand B, Ramos-Quiroga JA, Reif A. Franke B, et al. Among authors: casas m. Neuropsychopharmacology. 2010 Feb;35(3):656-64. doi: 10.1038/npp.2009.170. Epub 2009 Nov 4. Neuropsychopharmacology. 2010. PMID: 19890261 Free PMC article.
Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations.
Johansson S, Halmøy A, Mavroconstanti T, Jacobsen KK, Landaas ET, Reif A, Jacob C, Boreatti-Hümmer A, Kreiker S, Lesch KP, Kan CC, Kooij JJ, Kiemeney LA, Buitelaar JK, Franke B, Ribasés M, Bosch R, Bayés M, Casas M, Ramos-Quiroga JA, Cormand B, Knappskog P, Haavik J. Johansson S, et al. Among authors: casas m. Am J Med Genet B Neuropsychiatr Genet. 2010 Jul;153B(5):1008-15. doi: 10.1002/ajmg.b.31067. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20213726
Evaluation of common variants in 16 genes involved in the regulation of neurotransmitter release in ADHD.
Sánchez-Mora C, Cormand B, Ramos-Quiroga JA, Hervás A, Bosch R, Palomar G, Nogueira M, Gómez-Barros N, Richarte V, Corrales M, Garcia-Martinez I, Corominas R, Guijarro S, Bigorra A, Bayés M, Casas M, Ribasés M. Sánchez-Mora C, et al. Among authors: casas m. Eur Neuropsychopharmacol. 2013 Jun;23(6):426-35. doi: 10.1016/j.euroneuro.2012.07.014. Epub 2012 Aug 30. Eur Neuropsychopharmacol. 2013. PMID: 22939005
Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.
Yang L, Neale BM, Liu L, Lee SH, Wray NR, Ji N, Li H, Qian Q, Wang D, Li J, Faraone SV, Wang Y; Psychiatric GWAS Consortium: ADHD Subgroup. Yang L, et al. Am J Med Genet B Neuropsychiatr Genet. 2013 Jul;162B(5):419-430. doi: 10.1002/ajmg.b.32169. Epub 2013 May 31. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23728934 Free PMC article.
881 results