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Results: 1 to 20 of 40

1.

Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci.

Coleman C, Quinn EM, Ryan AW, Conroy J, Trimble V, Mahmud N, Kennedy N, Corvin AP, Morris DW, Donohoe G, O'Morain C, MacMathuna P, Byrnes V, Kiat C, Trynka G, Wijmenga C, Kelleher D, Ennis S, Anney RJ, McManus R.

Eur J Hum Genet. 2015 Apr 29. doi: 10.1038/ejhg.2015.87. [Epub ahead of print]

PMID:
25920553
2.

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.

Merikangas AK, Segurado R, Heron EA, Anney RJ, Paterson AD, Cook EH, Pinto D, Scherer SW, Szatmari P, Gill M, Corvin AP, Gallagher L.

Mol Psychiatry. 2014 Nov 25. doi: 10.1038/mp.2014.150. [Epub ahead of print]

PMID:
25421404
3.

Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients.

Mothersill O, Morris DW, Kelly S, Rose EJ, Bokde A, Reilly R, Gill M, Corvin AP, Donohoe G.

Schizophr Res. 2014 Aug;157(1-3):225-30. doi: 10.1016/j.schres.2014.05.023. Epub 2014 Jun 2.

PMID:
24888525
4.

Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants.

Kelly S, Morris DW, Mothersill O, Rose EJ, Fahey C, O'Brien C, O'Hanlon E, Gill M, Corvin AP, Donohoe G.

Neurosci Lett. 2014 Jun 27;574:6-10. doi: 10.1016/j.neulet.2014.05.002. Epub 2014 May 10.

PMID:
24820543
5.

No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset.

Heron EA, Cormican P, Donohoe G, O'Neill FA, Kendler KS, Riley BP; Wellcome Trust Case Control Consortium 2, Gill M, Corvin AP, Morris DW.

Schizophr Res. 2014 Apr;154(1-3):79-82. doi: 10.1016/j.schres.2014.01.038. Epub 2014 Feb 20.

6.

Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample.

Fahey C, Byrne S, McLaughlin R, Kenna K, Shatunov A, Donohoe G, Gill M, Al-Chalabi A, Bradley DG, Hardiman O, Corvin AP, Morris DW.

Neurobiol Aging. 2014 Jun;35(6):1510.e1-5. doi: 10.1016/j.neurobiolaging.2013.12.003. Epub 2013 Dec 12.

PMID:
24411481
7.

Effects of MIR137 on fronto-amygdala functional connectivity.

Mothersill O, Morris DW, Kelly S, Rose EJ, Fahey C, O'Brien C, Lyne R, Reilly R, Gill M, Corvin AP, Donohoe G.

Neuroimage. 2014 Apr 15;90:189-95. doi: 10.1016/j.neuroimage.2013.12.019. Epub 2013 Dec 19.

PMID:
24361663
8.

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.

Kenny EM, Cormican P, Furlong S, Heron E, Kenny G, Fahey C, Kelleher E, Ennis S, Tropea D, Anney R, Corvin AP, Donohoe G, Gallagher L, Gill M, Morris DW.

Mol Psychiatry. 2014 Aug;19(8):872-9. doi: 10.1038/mp.2013.127. Epub 2013 Oct 15.

PMID:
24126926
9.

Genome-wide association analysis identifies 13 new risk loci for schizophrenia.

Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, Williams S, Wray NR, Xia K, Bettella F, Borglum AD, Bulik-Sullivan BK, Cormican P, Craddock N, de Leeuw C, Durmishi N, Gill M, Golimbet V, Hamshere ML, Holmans P, Hougaard DM, Kendler KS, Lin K, Morris DW, Mors O, Mortensen PB, Neale BM, O'Neill FA, Owen MJ, Milovancevic MP, Posthuma D, Powell J, Richards AL, Riley BP, Ruderfer D, Rujescu D, Sigurdsson E, Silagadze T, Smit AB, Stefansson H, Steinberg S, Suvisaari J, Tosato S, Verhage M, Walters JT; Multicenter Genetic Studies of Schizophrenia Consortium, Levinson DF, Gejman PV, Kendler KS, Laurent C, Mowry BJ, O'Donovan MC, Owen MJ, Pulver AE, Riley BP, Schwab SG, Wildenauer DB, Dudbridge F, Holmans P, Shi J, Albus M, Alexander M, Campion D, Cohen D, Dikeos D, Duan J, Eichhammer P, Godard S, Hansen M, Lerer FB, Liang KY, Maier W, Mallet J, Nertney DA, Nestadt G, Norton N, O'Neill FA, Papadimitriou GN, Ribble R, Sanders AR, Silverman JM, Walsh D, Williams NM, Wormley B; Psychosis Endophenotypes International Consortium, Arranz MJ, Bakker S, Bender S, Bramon E, Collier D, Crespo-Facorro B, Hall J, Iyegbe C, Jablensky A, Kahn RS, Kalaydjieva L, Lawrie S, Lewis CM, Lin K, Linszen DH, Mata I, McIntosh A, Murray RM, Ophoff RA, Powell J, Rujescu D, Van Os J, Walshe M, Weisbrod M, Wiersma D; Wellcome Trust Case Control Consortium 2, Donnelly P, Barroso I, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin AP, Deloukas P, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Spencer CC, Band G, Bellenguez C, Freeman C, Hellenthal G, Giannoulatou E, Pirinen M, Pearson RD, Strange A, Su Z, Vukcevic D, Donnelly P, Langford C, Hunt SE, Edkins S, Gwilliam R, Blackburn H, Bumpstead SJ, Dronov S, Gillman M, Gray E, Hammond N, Jayakumar A, McCann OT, Liddle J, Potter SC, Ravindrarajah R, Ricketts M, Tashakkori-Ghanbaria A, Waller MJ, Weston P, Widaa S, Whittaker P, Barroso I, Deloukas P, Mathew CG, Blackwell JM, Brown MA, Corvin AP, McCarthy MI, Spencer CC, Bramon E, Corvin AP, O'Donovan MC, Stefansson K, Scolnick E, Purcell S, McCarroll SA, Sklar P, Hultman CM, Sullivan PF.

Nat Genet. 2013 Oct;45(10):1150-9. doi: 10.1038/ng.2742. Epub 2013 Aug 25.

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.

PLoS One. 2013;8(3):e58815. doi: 10.1371/journal.pone.0058815. Epub 2013 Mar 26.

11.

The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function.

Rose EJ, Morris DW, Fahey C, Robertson IH, Greene C, O'Doherty J, Newell FN, Garavan H, McGrath J, Bokde A, Tropea D, Gill M, Corvin AP, Donohoe G.

Twin Res Hum Genet. 2012 Jun;15(3):296-303. doi: 10.1017/thg.2012.7.

PMID:
22856365
12.

Insulin-like growth factor 1 (IGF1) and its active peptide (1-3)IGF1 enhance the expression of synaptic markers in neuronal circuits through different cellular mechanisms.

Corvin AP, Molinos I, Little G, Donohoe G, Gill M, Morris DW, Tropea D.

Neurosci Lett. 2012 Jun 27;520(1):51-6. doi: 10.1016/j.neulet.2012.05.029. Epub 2012 May 17.

PMID:
22609570
13.

Functional investigation of a schizophrenia GWAS signal at the CDC42 gene.

Gilks WP, Hill M, Gill M, Donohoe G, Corvin AP, Morris DW.

World J Biol Psychiatry. 2012 Oct;13(7):550-4. doi: 10.3109/15622975.2012.666359. Epub 2012 Mar 5.

PMID:
22385474
14.

The NOS1 variant rs6490121 is associated with variation in prefrontal function and grey matter density in healthy individuals.

Rose EJ, Greene C, Kelly S, Morris DW, Robertson IH, Fahey C, Jacobson S, O'Doherty J, Newell FN, McGrath J, Bokde A, Garavan H, Frodl T, Gill M, Corvin AP, Donohoe G.

Neuroimage. 2012 Mar;60(1):614-22. doi: 10.1016/j.neuroimage.2011.12.054. Epub 2011 Dec 29.

PMID:
22227051
15.

Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathology.

Rünker AE, O'Tuathaigh C, Dunleavy M, Morris DW, Little GE, Corvin AP, Gill M, Henshall DC, Waddington JL, Mitchell KJ.

PLoS One. 2011;6(11):e26488. doi: 10.1371/journal.pone.0026488. Epub 2011 Nov 21.

16.

Two patients walk into a clinic...a genomics perspective on the future of schizophrenia.

Corvin AP.

BMC Biol. 2011 Nov 11;9:77. doi: 10.1186/1741-7007-9-77. Review.

17.

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.

DNA Res. 2011 Feb;18(1):31-8. doi: 10.1093/dnares/dsq029. Epub 2010 Dec 16.

18.

ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia.

Donohoe G, Rose E, Frodl T, Morris D, Spoletini I, Adriano F, Bernardini S, Caltagirone C, Bossù P, Gill M, Corvin AP, Spalletta G.

Neuroimage. 2011 Feb 1;54(3):2132-7. doi: 10.1016/j.neuroimage.2010.09.089. Epub 2010 Oct 8.

PMID:
20934520
19.

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

Quinn EM, Hill M, Anney R, Gill M, Corvin AP, Morris DW.

Bipolar Disord. 2010 Jun;12(4):440-5. doi: 10.1111/j.1399-5618.2010.00817.x. Erratum in: Bipolar Disord. 2012 Nov;14(7):792.

PMID:
20636642
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