Kenny E - Search Results

1

Genetic variants in XRRC5 may predict development of venous thrombotic events in myeloma patients on thalidomide.

Tewari P, Kenny E, Staines A, Chanock S, Browne P, Lawler M. Tewari P, et al. Among authors: kenny e. Blood. 2009 May 28;113(22):5691-2. doi: 10.1182/blood-2009-03-211177. Blood. 2009. PMID: 19478055 Free article. No abstract available.

2

The future of genomics in Ireland - focus on genomics for health.

Seoighe C, Bracken AP, Buckley P, Doran P, Green R, Healy S, Kavanagh D, Kenny E, Lawler M, Lowery M, Morris D, Morrissey D, O'Byrne JJ, Shields D, Smith O, Steward CA, Sweeney B, Kolch W. Seoighe C, et al. Among authors: kenny e. HRB Open Res. 2020 Dec 4;3:89. doi: 10.12688/hrbopenres.13187.1. eCollection 2020. HRB Open Res. 2020. PMID: 33855271 Free PMC article.

3

Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility.

O'Dushlaine C, Kenny E, Heron E, Donohoe G, Gill M, Morris D; International Schizophrenia Consortium; Corvin A. O'Dushlaine C, et al. Among authors: kenny e. Mol Psychiatry. 2011 Mar;16(3):286-92. doi: 10.1038/mp.2010.7. Epub 2010 Feb 16. Mol Psychiatry. 2011. PMID: 20157312

4

Next-generation sequencing of the mitochondrial genome and association with IgA nephropathy in a renal transplant population.

Douglas AP, Vance DR, Kenny EM, Morris DW, Maxwell AP, McKnight AJ. Douglas AP, et al. Sci Rep. 2014 Dec 9;4:7379. doi: 10.1038/srep07379. Sci Rep. 2014. PMID: 25488329 Free PMC article.

5

Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing.

Kenna KP, McLaughlin RL, Byrne S, Elamin M, Heverin M, Kenny EM, Cormican P, Morris DW, Donaghy CG, Bradley DG, Hardiman O. Kenna KP, et al. J Med Genet. 2013 Nov;50(11):776-83. doi: 10.1136/jmedgenet-2013-101795. Epub 2013 Jul 23. J Med Genet. 2013. PMID: 23881933 Free PMC article.

6

Identification of mechanosensitive genes during skeletal development: alteration of genes associated with cytoskeletal rearrangement and cell signalling pathways.

Rolfe RA, Nowlan NC, Kenny EM, Cormican P, Morris DW, Prendergast PJ, Kelly D, Murphy P. Rolfe RA, et al. BMC Genomics. 2014 Jan 20;15:48. doi: 10.1186/1471-2164-15-48. BMC Genomics. 2014. PMID: 24443808 Free PMC article.

7

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. PLoS One. 2013;8(3):e58815. doi: 10.1371/journal.pone.0058815. Epub 2013 Mar 26. PLoS One. 2013. PMID: 23555596 Free PMC article.

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. 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

Translation of 5' leaders is pervasive in genes resistant to eIF2 repression.

Andreev DE, O'Connor PB, Fahey C, Kenny EM, Terenin IM, Dmitriev SE, Cormican P, Morris DW, Shatsky IN, Baranov PV. Andreev DE, et al. Among authors: kenny em. Elife. 2015 Jan 26;4:e03971. doi: 10.7554/eLife.03971. Elife. 2015. PMID: 25621764 Free PMC article.

10

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. Kenny EM, et al. Among authors: kenny g. Mol Psychiatry. 2014 Aug;19(8):872-9. doi: 10.1038/mp.2013.127. Epub 2013 Oct 15. Mol Psychiatry. 2014. PMID: 24126926

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