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Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study.
Foley C, Heron EA, Harold D, Walters J, Owen M, O'Donovan M, Sebat J, Kelleher E, Mooney C, Durand A, Pinto C, Cormican P, Morris D, Donohoe G, Gill M, Gallagher L, Corvin A. Foley C, et al. Among authors: morris d. Br J Psychiatry. 2020 May;216(5):275-279. doi: 10.1192/bjp.2019.262. Br J Psychiatry. 2020. PMID: 31964429
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
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
4,552 results