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Refinement of 2q and 7p loci in a large multiplex NTD family.
Stamm DS, Siegel DG, Mehltretter L, Connelly JJ, Trott A, Ellis N, Zismann V, Stephan DA, George TM, Vekemans M, Ashley-Koch A, Gilbert JR, Gregory SG, Speer MC; NTD Collaborative Group. Stamm DS, et al. Birth Defects Res A Clin Mol Teratol. 2008 Jun;82(6):441-52. doi: 10.1002/bdra.20462. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18452155
SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.
Kollins SH, Anastopoulos AD, Lachiewicz AM, FitzGerald D, Morrissey-Kane E, Garrett ME, Keatts SL, Ashley-Koch AE. Kollins SH, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1580-8. doi: 10.1002/ajmg.b.30876. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18821566 Free PMC article.
Multiple rare SAPAP3 missense variants in trichotillomania and OCD.
Züchner S, Wendland JR, Ashley-Koch AE, Collins AL, Tran-Viet KN, Quinn K, Timpano KC, Cuccaro ML, Pericak-Vance MA, Steffens DC, Krishnan KR, Feng G, Murphy DL. Züchner S, et al. Mol Psychiatry. 2009 Jan;14(1):6-9. doi: 10.1038/mp.2008.83. Mol Psychiatry. 2009. PMID: 19096451 Free PMC article. Review. No abstract available.
Interactions between genotype and depressive symptoms on obesity.
Fuemmeler BF, Agurs-Collins T, McClernon FJ, Kollins SH, Garrett ME, Ashley-Koch AE. Fuemmeler BF, et al. Behav Genet. 2009 May;39(3):296-305. doi: 10.1007/s10519-009-9266-z. Epub 2009 Apr 1. Behav Genet. 2009. PMID: 19337825 Free PMC article.
272 results