McKnight AJ - Search Results

1

A Formative Study of the Implementation of Whole Genome Sequencing in Northern Ireland.

Kerr K, McKenna C, Heggarty S, Bailie C, McMullan J, Crowe A, Kilner J, Donnelly M, Boyle S, Rea G, Flanagan C, McKee S, McKnight AJ. Kerr K, et al. Among authors: mcknight aj. Genes (Basel). 2022 Jun 21;13(7):1104. doi: 10.3390/genes13071104. Genes (Basel). 2022. PMID: 35885887 Free PMC article.

2

Variation in RTN3 and PPIL2 genes does not influence platelet membrane beta-secretase activity or susceptibility to alzheimer's disease in the northern Irish population.

Carson R, McKnight AJ, Todd S, Liu WW, Heggarty S, Craig D, McGuinness B, Irvine GB, Passmore AP, Johnston JA. Carson R, et al. Among authors: mcknight aj. Neuromolecular Med. 2009;11(4):337-44. doi: 10.1007/s12017-009-8080-3. Neuromolecular Med. 2009. PMID: 19669607

3

Resequencing of the CCL5 and CCR5 genes and investigation of variants for association with diabetic nephropathy.

Pettigrew KA, McKnight AJ, Patterson CC, Kilner J, Sadlier DM, Maxwell AP. Pettigrew KA, et al. Among authors: mcknight aj. J Hum Genet. 2010 Apr;55(4):248-51. doi: 10.1038/jhg.2010.15. Epub 2010 Mar 5. J Hum Genet. 2010. PMID: 20203694

4

Development of next generation sequencing panel for UMOD and association with kidney disease.

Bailie C, Kilner J, Maxwell AP, McKnight AJ. Bailie C, et al. Among authors: mcknight aj. PLoS One. 2017 Jun 13;12(6):e0178321. doi: 10.1371/journal.pone.0178321. eCollection 2017. PLoS One. 2017. PMID: 28609449 Free PMC article.

5

Design and implementation of a custom next generation sequencing panel for selected vitamin D associated genes.

Benson KA, Chand S, Maxwell AP, Smyth LJ, Kilner J, Borrows R, McKnight AJ. Benson KA, et al. Among authors: mcknight aj. BMC Res Notes. 2017 Jul 28;10(1):348. doi: 10.1186/s13104-017-2664-z. BMC Res Notes. 2017. PMID: 28754147 Free PMC article.

6

Validation of differentially methylated microRNAs identified from an epigenome-wide association study; Sanger and next generation sequencing approaches.

Smyth LJ, Maxwell AP, Benson KA, Kilner J, McKay GJ, McKnight AJ. Smyth LJ, et al. Among authors: mcknight aj. BMC Res Notes. 2018 Oct 29;11(1):767. doi: 10.1186/s13104-018-3872-x. BMC Res Notes. 2018. PMID: 30373632 Free PMC article.

7

Differential methylation in rare ophthalmic disorders: a systematic review protocol.

Kerr K, McAneney H, McKnight AJ. Kerr K, et al. Among authors: mcknight aj. Syst Rev. 2019 Apr 10;8(1):93. doi: 10.1186/s13643-019-0999-3. Syst Rev. 2019. PMID: 30971311 Free PMC article.

8

Communication strategies for rare cancers: a systematic review protocol.

Bell C, Kerr K, Moore K, McShane C, Anderson L, McKnight AJ, McAneney H. Bell C, et al. Among authors: mcknight aj. Syst Rev. 2019 Apr 23;8(1):102. doi: 10.1186/s13643-019-1017-5. Syst Rev. 2019. PMID: 31014400 Free PMC article.

9

Protocol for a scoping review of multi-omic analysis for rare diseases.

Kerr K, McAneney H, McKnight AJ. Kerr K, et al. Among authors: mcknight aj. BMJ Open. 2019 May 5;9(5):e026278. doi: 10.1136/bmjopen-2018-026278. BMJ Open. 2019. PMID: 31061034 Free PMC article.

10

Differential methylation as a diagnostic biomarker of rare renal diseases: a systematic review.

Kerr K, McAneney H, Flanagan C, Maxwell AP, McKnight AJ. Kerr K, et al. Among authors: mcknight aj. BMC Nephrol. 2019 Aug 16;20(1):320. doi: 10.1186/s12882-019-1517-5. BMC Nephrol. 2019. PMID: 31419951 Free PMC article.

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