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An international multicenter association study of the serotonin transporter gene in persistent ADHD.
Landaas ET, Johansson S, Jacobsen KK, Ribasés M, Bosch R, Sánchez-Mora C, Jacob CP, Boreatti-Hümmer A, Kreiker S, Lesch KP, Kiemeney LA, Kooij JJ, Kan C, Buitelaar JK, Faraone SV, Halmøy A, Ramos-Quiroga JA, Cormand B, Reif A, Franke B, Mick E, Knappskog PM, Haavik J. Landaas ET, et al. Among authors: kiemeney la. Genes Brain Behav. 2010 Jul;9(5):449-58. doi: 10.1111/j.1601-183X.2010.00567.x. Epub 2010 Jan 25. Genes Brain Behav. 2010. PMID: 20113357 Free article.
Meta-analysis of the DRD5 VNTR in persistent ADHD.
Klein M, Berger S, Hoogman M, Dammers J, Makkinje R, Heister AJGAM, Galesloot TE, Kiemeney LALM, Weber H, Kittel-Schneider S, Lesch KP, Reif A, Ribase S M, Ramos-Quiroga JA, Cormand B, Zayats T, Hegvik TA, Jacobsen KK, Johansson S, Haavik J, Mota NR, Bau CHD, Grevet EH, Doyle A, Faraone SV, Arias-Va Squez A, Franke B. Klein M, et al. Eur Neuropsychopharmacol. 2016 Sep;26(9):1527-1532. doi: 10.1016/j.euroneuro.2016.06.012. Epub 2016 Jul 29. Eur Neuropsychopharmacol. 2016. PMID: 27480019
Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.
Corominas J, Klein M, Zayats T, Rivero O, Ziegler GC, Pauper M, Neveling K, Poelmans G, Jansch C, Svirin E, Geissler J, Weber H, Reif A, Arias Vasquez A, Galesloot TE, Kiemeney LALM, Buitelaar JK, Ramos-Quiroga JA, Cormand B, Ribasés M, Hveem K, Gabrielsen ME, Hoffmann P, Cichon S, Haavik J, Johansson S, Jacob CP, Romanos M, Franke B, Lesch KP. Corominas J, et al. Mol Psychiatry. 2020 Sep;25(9):2047-2057. doi: 10.1038/s41380-018-0210-6. Epub 2018 Aug 16. Mol Psychiatry. 2020. PMID: 30116028 Free PMC article.
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: kiemeney la. 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
A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms.
Arias-Vásquez A, Groffen AJ, Spijker S, Ouwens KG, Klein M, Vojinovic D, Galesloot TE, Bralten J, Hottenga JJ, van der Most PJ, Kattenberg VM, Pool R, Nolte IM, Penninx BWJH, Fedko IO, Dolan CV, Nivard MG, den Braber A, van Duijn CM, Hoekstra PJ, Buitelaar JK, Kiemeney LA, Hoogman M, Middeldorp CM, Draisma HHM, Vermeulen SH, Sánchez-Mora C, Ramos-Quiroga JA, Ribasés M; EAGLE-ADHD Consortium; Hartman CA, Kooij JJS, Amin N, Smit AB, Franke B, Boomsma DI. Arias-Vásquez A, et al. Among authors: kiemeney la. Behav Genet. 2019 May;49(3):270-285. doi: 10.1007/s10519-018-09947-2. Epub 2019 Jan 18. Behav Genet. 2019. PMID: 30659475
Association of the dopamine transporter (SLC6A3/DAT1) gene 9-6 haplotype with adult ADHD.
Franke B, Hoogman M, Arias Vasquez A, Heister JG, Savelkoul PJ, Naber M, Scheffer H, Kiemeney LA, Kan CC, Kooij JJ, Buitelaar JK. Franke B, et al. Among authors: kiemeney la. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1576-9. doi: 10.1002/ajmg.b.30861. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18802924
DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders.
Reif A, Nguyen TT, Weissflog L, Jacob CP, Romanos M, Renner TJ, Buttenschon HN, Kittel-Schneider S, Gessner A, Weber H, Neuner M, Gross-Lesch S, Zamzow K, Kreiker S, Walitza S, Meyer J, Freitag CM, Bosch R, Casas M, Gómez N, Ribasès M, Bayès M, Buitelaar JK, Kiemeney LA, Kooij JJ, Kan CC, Hoogman M, Johansson S, Jacobsen KK, Knappskog PM, Fasmer OB, Asherson P, Warnke A, Grabe HJ, Mahler J, Teumer A, Völzke H, Mors ON, Schäfer H, Ramos-Quiroga JA, Cormand B, Haavik J, Franke B, Lesch KP. Reif A, et al. Among authors: kiemeney la. Neuropsychopharmacology. 2011 Oct;36(11):2318-27. doi: 10.1038/npp.2011.120. Epub 2011 Jul 13. Neuropsychopharmacology. 2011. PMID: 21750579 Free PMC article.
Shared and unique genetic contributions to attention deficit/hyperactivity disorder and substance use disorders: a pilot study of six candidate genes.
Carpentier PJ, Arias Vasquez A, Hoogman M, Onnink M, Kan CC, Kooij JJ, Makkinje R, Iskandar S, Kiemeney LA, de Jong CA, Franke B, Buitelaar JK. Carpentier PJ, et al. Among authors: kiemeney la. Eur Neuropsychopharmacol. 2013 Jun;23(6):448-57. doi: 10.1016/j.euroneuro.2012.07.003. Epub 2012 Jul 26. Eur Neuropsychopharmacol. 2013. PMID: 22841130 Free article.
Autism spectrum disorders and autistic traits share genetics and biology.
Bralten J, van Hulzen KJ, Martens MB, Galesloot TE, Arias Vasquez A, Kiemeney LA, Buitelaar JK, Muntjewerff JW, Franke B, Poelmans G. Bralten J, et al. Among authors: kiemeney la. Mol Psychiatry. 2018 May;23(5):1205-1212. doi: 10.1038/mp.2017.98. Epub 2017 May 16. Mol Psychiatry. 2018. PMID: 28507316 Free PMC article.
GLRB allelic variation associated with agoraphobic cognitions, increased startle response and fear network activation: a potential neurogenetic pathway to panic disorder.
Deckert J, Weber H, Villmann C, Lonsdorf TB, Richter J, Andreatta M, Arias-Vasquez A, Hommers L, Kent L, Schartner C, Cichon S, Wolf C, Schaefer N, von Collenberg CR, Wachter B, Blum R, Schümann D, Scharfenort R, Schumacher J, Forstner AJ, Baumann C, Schiele MA, Notzon S, Zwanzger P, Janzing JGE, Galesloot T, Kiemeney LA, Gajewska A, Glotzbach-Schoon E, Mühlberger A, Alpers G, Fydrich T, Fehm L, Gerlach AL, Kircher T, Lang T, Ströhle A, Arolt V, Wittchen HU, Kalisch R, Büchel C, Hamm A, Nöthen MM, Romanos M, Domschke K, Pauli P, Reif A. Deckert J, et al. Among authors: kiemeney la. Mol Psychiatry. 2017 Oct;22(10):1431-1439. doi: 10.1038/mp.2017.2. Epub 2017 Feb 7. Mol Psychiatry. 2017. PMID: 28167838
688 results