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Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1).
Williams NM, Preece A, Morris DW, Spurlock G, Bray NJ, Stephens M, Norton N, Williams H, Clement M, Dwyer S, Curran C, Wilkinson J, Moskvina V, Waddington JL, Gill M, Corvin AP, Zammit S, Kirov G, Owen MJ, O'Donovan MC. Williams NM, et al. Among authors: morris dw. Arch Gen Psychiatry. 2004 Apr;61(4):336-44. doi: 10.1001/archpsyc.61.4.336. Arch Gen Psychiatry. 2004. PMID: 15066891
Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.
Turic D, Robinson L, Duke M, Morris DW, Webb V, Hamshere M, Milham C, Hopkin E, Pound K, Fernando S, Grierson A, Easton M, Williams N, Van Den Bree M, Chowdhury R, Gruen J, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J. Turic D, et al. Among authors: morris dw. Mol Psychiatry. 2003 Feb;8(2):176-85. doi: 10.1038/sj.mp.4001216. Mol Psychiatry. 2003. PMID: 12610650
Confirming RGS4 as a susceptibility gene for schizophrenia.
Morris DW, Rodgers A, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP. Morris DW, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):50-3. doi: 10.1002/ajmg.b.20109. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755443
Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample.
Corvin A, McGhee KA, Murphy K, Donohoe G, Nangle JM, Schwaiger S, Kenny N, Clarke S, Meagher D, Quinn J, Scully P, Baldwin P, Browne D, Walsh C, Waddington JL, Morris DW, Gill M. Corvin A, et al. Among authors: morris dw. Am J Med Genet B Neuropsychiatr Genet. 2007 Oct 5;144B(7):949-53. doi: 10.1002/ajmg.b.30452. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17492767
335 results