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Year | Number of Results |
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2020 | 2 |
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Page 1
A scoping review and proposed workflow for multi-omic rare disease research.
Orphanet J Rare Dis. 2020 Apr 28;15(1):107. doi: 10.1186/s13023-020-01376-x.
Orphanet J Rare Dis. 2020.
PMID: 32345347
Free PMC article.
Review.
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: bailie c.
Genes (Basel). 2022 Jun 21;13(7):1104. doi: 10.3390/genes13071104.
Genes (Basel). 2022.
PMID: 35885887
Free PMC article.
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Evaluating the impact of COVID-19 on rare disease support groups.
McMullan J, Crowe AL, Bailie C, McKnight AJ.
McMullan J, et al. Among authors: bailie c.
BMC Res Notes. 2021 May 6;14(1):168. doi: 10.1186/s13104-021-05579-8.
BMC Res Notes. 2021.
PMID: 33957984
Free PMC article.
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Improvements needed to support people living and working with a rare disease in Northern Ireland: current rare disease support perceived as inadequate.
McMullan J, Crowe AL, Bailie C, Moore K, McMullan LS, Shamandi N, McAneney H, McKnight AJ.
McMullan J, et al. Among authors: bailie c.
Orphanet J Rare Dis. 2020 Nov 9;15(1):315. doi: 10.1186/s13023-020-01559-6.
Orphanet J Rare Dis. 2020.
PMID: 33168042
Free PMC article.
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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.
PLoS One. 2017 Jun 13;12(6):e0178321. doi: 10.1371/journal.pone.0178321. eCollection 2017.
PLoS One. 2017.
PMID: 28609449
Free PMC article.
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