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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. Among authors: rommelse n. 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
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.
Brookes K, Xu X, Chen W, Zhou K, Neale B, Lowe N, Anney R, Franke B, Gill M, Ebstein R, Buitelaar J, Sham P, Campbell D, Knight J, Andreou P, Altink M, Arnold R, Boer F, Buschgens C, Butler L, Christiansen H, Feldman L, Fleischman K, Fliers E, Howe-Forbes R, Goldfarb A, Heise A, Gabriëls I, Korn-Lubetzki I, Johansson L, Marco R, Medad S, Minderaa R, Mulas F, Müller U, Mulligan A, Rabin K, Rommelse N, Sethna V, Sorohan J, Uebel H, Psychogiou L, Weeks A, Barrett R, Craig I, Banaschewski T, Sonuga-Barke E, Eisenberg J, Kuntsi J, Manor I, McGuffin P, Miranda A, Oades RD, Plomin R, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Taylor E, Thompson M, Faraone SV, Asherson P. Brookes K, et al. Among authors: rommelse n. Mol Psychiatry. 2006 Oct;11(10):934-53. doi: 10.1038/sj.mp.4001869. Epub 2006 Aug 8. Mol Psychiatry. 2006. PMID: 16894395 Free article.
Are motor inhibition and cognitive flexibility dead ends in ADHD?
Rommelse NN, Altink ME, de Sonneville LM, Buschgens CJ, Buitelaar J, Oosterlaan J, Sergeant JA. Rommelse NN, et al. J Abnorm Child Psychol. 2007 Dec;35(6):957-67. doi: 10.1007/s10802-007-9146-z. Epub 2007 May 15. J Abnorm Child Psychol. 2007. PMID: 17503173 Free article.
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. Among authors: rommelse n. 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.
A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.
Asherson P, Zhou K, Anney RJ, Franke B, Buitelaar J, Ebstein R, Gill M, Altink M, Arnold R, Boer F, Brookes K, Buschgens C, Butler L, Cambell D, Chen W, Christiansen H, Feldman L, Fleischman K, Fliers E, Howe-Forbes R, Goldfarb A, Heise A, Gabriëls I, Johansson L, Lubetzki I, Marco R, Medad S, Minderaa R, Mulas F, Müller U, Mulligan A, Neale B, Rijsdijk F, Rabin K, Rommelse N, Sethna V, Sorohan J, Uebel H, Psychogiou L, Weeks A, Barrett R, Xu X, Banaschewski T, Sonuga-Barke E, Eisenberg J, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Taylor E, Thompson M, Faraone SV. Asherson P, et al. Among authors: rommelse n. Mol Psychiatry. 2008 May;13(5):514-21. doi: 10.1038/sj.mp.4002140. Epub 2008 Jan 8. Mol Psychiatry. 2008. PMID: 18180756 Free article.
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. Among authors: rommelse n. 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
195 results