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Page 1
Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four European populations.
Sánchez-Mora C, Ribasés M, Casas M, Bayés M, Bosch R, Fernàndez-Castillo N, Brunso L, Jacobsen KK, Landaas ET, Lundervold AJ, Gross-Lesch S, Kreiker S, Jacob CP, Lesch KP, Buitelaar JK, Hoogman M, Kiemeney LA, Kooij JJ, Mick E, Asherson P, Faraone SV, Franke B, Reif A, Johansson S, Haavik J, Ramos-Quiroga JA, Cormand B. Sánchez-Mora C, et al. Among authors: bayes m. Am J Med Genet B Neuropsychiatr Genet. 2011 Jul;156B(5):600-12. doi: 10.1002/ajmg.b.31202. Epub 2011 May 18. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21595008
Meta-analysis of brain-derived neurotrophic factor p.Val66Met in adult ADHD in four European populations.
Sánchez-Mora C, Ribasés M, Ramos-Quiroga JA, Casas M, Bosch R, Boreatti-Hümmer A, Heine M, Jacob CP, Lesch KP, Fasmer OB, Knappskog PM, Kooij JJS, Kan C, Buitelaar JK, Mick E, Asherson P, Faraone SV, Franke B, Johansson S, Haavik J, Reif A, Bayés M, Cormand B. Sánchez-Mora C, et al. Among authors: bayes m. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):512-523. doi: 10.1002/ajmg.b.31008. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19603419
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: bayes 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: bayes 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: bayes 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
Candidate system analysis in ADHD: evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1.
Ribasés M, Ramos-Quiroga JA, Hervás A, Sánchez-Mora C, Bosch R, Bielsa A, Gastaminza X, Lesch KP, Reif A, Renner TJ, Romanos M, Warnke A, Walitza S, Freitag C, Meyer J, Palmason H, Casas M, Bayés M, Cormand B. Ribasés M, et al. Among authors: bayes m. World J Biol Psychiatry. 2012 Apr;13(4):281-92. doi: 10.3109/15622975.2011.584905. Epub 2012 Mar 9. World J Biol Psychiatry. 2012. PMID: 22404661
An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples.
Ribasés M, Sánchez-Mora C, Ramos-Quiroga JA, Bosch R, Gómez N, Nogueira M, Corrales M, Palomar G, Jacob CP, Gross-Lesch S, Kreiker S, Reif A, Lesch KP, Cormand B, Casas M, Bayés M. Ribasés M, et al. Among authors: bayes m. Psychiatr Genet. 2012 Aug;22(4):155-60. doi: 10.1097/YPG.0b013e328353957e. Psychiatr Genet. 2012. PMID: 22504457
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: bayes 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.
Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB.
Ribasés M, Ramos-Quiroga JA, Hervás A, Bosch R, Bielsa A, Gastaminza X, Artigas J, Rodriguez-Ben S, Estivill X, Casas M, Cormand B, Bayés M. Ribasés M, et al. Among authors: bayes m. Mol Psychiatry. 2009 Jan;14(1):71-85. doi: 10.1038/sj.mp.4002100. Epub 2007 Oct 16. Mol Psychiatry. 2009. PMID: 17938636
176 results