Morris DW - Search Results

1

Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies.

Anney RJ, Kenny E, O'Dushlaine CT, Lasky-Su J, Franke B, Morris DW, Neale BM, Asherson P, Faraone SV, Gill M. Anney RJ, et al. Among authors: morris dw. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1379-86. doi: 10.1002/ajmg.b.30836. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18663727 Free PMC article.

2

The SNP ratio test: pathway analysis of genome-wide association datasets.

O'Dushlaine C, Kenny E, Heron EA, Segurado R, Gill M, Morris DW, Corvin A. O'Dushlaine C, et al. Among authors: morris dw. Bioinformatics. 2009 Oct 15;25(20):2762-3. doi: 10.1093/bioinformatics/btp448. Epub 2009 Jul 20. Bioinformatics. 2009. PMID: 19620097

3

Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation.

Hill MJ, Kenny E, Roche S, Morris DW, Corvin A, Hawi Z, Gill M, Anney RJ. Hill MJ, et al. Among authors: morris dw. Psychiatr Genet. 2011 Dec;21(6):281-6. doi: 10.1097/YPG.0b013e328348045b. Psychiatr Genet. 2011. PMID: 21642896

4

Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness.

Bigdeli TB, Ripke S, Bacanu SA, Lee SH, Wray NR, Gejman PV, Rietschel M, Cichon S, St Clair D, Corvin A, Kirov G, McQuillin A, Gurling H, Rujescu D, Andreassen OA, Werge T, Blackwood DH, Pato CN, Pato MT, Malhotra AK, O'Donovan MC, Kendler KS, Fanous AH; Schizophrenia Working Group of the Psychiatric Genomics Consortium. Bigdeli TB, et al. Am J Med Genet B Neuropsychiatr Genet. 2016 Mar;171B(2):276-89. doi: 10.1002/ajmg.b.32402. Epub 2015 Dec 11. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 26663532 Free PMC article.

5

Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.

Harold D, Connolly S, Riley BP, Kendler KS, McCarthy SE, McCombie WR, Richards A, Owen MJ, O'Donovan MC, Walters J; Wellcome Trust Case Control Consortium 2; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Donohoe G, Gill M, Corvin A, Morris DW. Harold D, et al. Among authors: morris dw. Am J Med Genet B Neuropsychiatr Genet. 2019 Apr;180(3):223-231. doi: 10.1002/ajmg.b.32716. Epub 2019 Feb 23. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30801977 Free PMC article.

6

An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases.

O'Dushlaine CT, Dolan C, Weale ME, Stanton A, Croke DT, Kalviainen R, Eriksson K, Kantanen AM, Gibson RA, Hosford D, Sisodiya SM, Gill M, Corvin AP, Morris DW, Delanty N, Cavalleri GL. O'Dushlaine CT, et al. Among authors: morris dw. Eur J Hum Genet. 2008 Feb;16(2):176-83. doi: 10.1038/sj.ejhg.5201938. Epub 2007 Oct 31. Eur J Hum Genet. 2008. PMID: 17971835

7

Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression.

Quinn EM, Hill M, Anney R, Gill M, Corvin AP, Morris DW. Quinn EM, et al. Among authors: morris dw. Bipolar Disord. 2010 Jun;12(4):440-5. doi: 10.1111/j.1399-5618.2010.00817.x. Bipolar Disord. 2010. PMID: 20636642

8

Multiplex target enrichment using DNA indexing for ultra-high throughput SNP detection.

Kenny EM, Cormican P, Gilks WP, Gates AS, O'Dushlaine CT, Pinto C, Corvin AP, Gill M, Morris DW. Kenny EM, et al. Among authors: morris dw. DNA Res. 2011 Feb;18(1):31-8. doi: 10.1093/dnares/dsq029. Epub 2010 Dec 16. DNA Res. 2011. PMID: 21163834 Free PMC article.

9

A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia.

Jia P, Wang L, Fanous AH, Chen X, Kendler KS; International Schizophrenia Consortium; Zhao Z. Jia P, et al. J Med Genet. 2012 Feb;49(2):96-103. doi: 10.1136/jmedgenet-2011-100397. Epub 2011 Dec 20. J Med Genet. 2012. PMID: 22187495

10

Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 Genomes data.

Quinn EM, Cormican P, Kenny EM, Hill M, Anney R, Gill M, Corvin AP, Morris DW. Quinn EM, et al. Among authors: morris dw. PLoS One. 2013;8(3):e58815. doi: 10.1371/journal.pone.0058815. Epub 2013 Mar 26. PLoS One. 2013. PMID: 23555596 Free PMC article.

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