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Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion.
Poelmans G, Engelen JJ, Van Lent-Albrechts J, Smeets HJ, Schoenmakers E, Franke B, Buitelaar JK, Wuisman-Frerker M, Erens W, Steyaert J, Schrander-Stumpel C. Poelmans G, et al. Among authors: buitelaar jk. Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):140-7. doi: 10.1002/ajmg.b.30787. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18521840
Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth.
Brookes KJ, Neale B, Xu X, Thapar A, Gill M, Langley K, Hawi Z, Mill J, Taylor E, Franke B, Chen W, Ebstein R, Buitelaar J, Banaschewski T, Sonuga-Barke E, Eisenberg J, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Faraone SV, Asherson P. Brookes KJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):94-9. doi: 10.1002/ajmg.b.30562. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 17525975
Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder.
Sonuga-Barke EJ, Brookes KJ, Buitelaar J, Anney R, Bitsakou P, Baeyens D, Buschgens C, Chen W, Christiansen H, Eisenberg J, Kuntsi J, Manor I, Meliá A, Mulligan A, Rommelse N, Müller UC, Uebel H, Banaschewski T, Ebstein R, Franke B, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Thompson M, Taylor E, Asherson P, Faraone SV. Sonuga-Barke EJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Apr 5;147(3):316-9. doi: 10.1002/ajmg.b.30596. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18023044 Free article.
Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) program.
Anney RJ, Hawi Z, Sheehan K, Mulligan A, Pinto C, Brookes KJ, Xu X, Zhou K, Franke B, Buitelaar J, Vermeulen SH, Banaschewski T, Sonuga-Barke E, Ebstein R, Manor I, Miranda A, Mulas F, Oades RD, Roeyers H, Rommelse N, Rothenberger A, Sergeant J, Steinhausen HC, Taylor E, Thompson M, Asherson P, Faraone SV, Gill M. Anney RJ, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1495-500. doi: 10.1002/ajmg.b.30659. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18163388
DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage.
Chen W, Zhou K, Sham P, Franke B, Kuntsi J, Campbell D, Fleischman K, Knight J, Andreou P, Arnold R, Altink M, Boer F, Boholst MJ, Buschgens C, Butler L, Christiansen H, Fliers E, Howe-Forbes R, Gabriëls I, Heise A, Korn-Lubetzki I, Marco R, Medad S, Minderaa R, Müller UC, Mulligan A, Psychogiou L, Rommelse N, Sethna V, Uebel H, McGuffin P, Plomin R, Banaschewski T, Buitelaar J, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Thompson M, Faraone SV, Asherson P. Chen W, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1450-60. doi: 10.1002/ajmg.b.30672. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18189238
No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder.
Xu X, Duman EA, Anney R, Brookes K, Franke B, Zhou K, Buschgens C, Chen W, Christiansen H, Eisenberg J, Gabriëls I, Manor I, Marco R, Müller UC, Mulligan A, Rommelse N, Thompson M, Uebel H, Banaschewski T, Buitelaar J, Ebstein R, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Faraone SV, Asherson P. Xu X, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1306-9. doi: 10.1002/ajmg.b.30737. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18452186
814 results