Kerr K - Search Results

1

Systematic review of differential methylation in rare ophthalmic diseases.

Kerr K, McAneney H, Smyth L, Flanagan C, Silvestri J, Nesbitt MA, Wooster C, McKnight AJ. Kerr K, et al. BMJ Open Ophthalmol. 2019 Nov 13;4(1):e000342. doi: 10.1136/bmjophth-2019-000342. eCollection 2019. BMJ Open Ophthalmol. 2019. PMID: 31799411 Free PMC article. Review.

2

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

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

3

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: kerr k. Syst Rev. 2019 Apr 23;8(1):102. doi: 10.1186/s13643-019-1017-5. Syst Rev. 2019. PMID: 31014400 Free PMC article.

4

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

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

5

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. BMC Nephrol. 2019 Aug 16;20(1):320. doi: 10.1186/s12882-019-1517-5. BMC Nephrol. 2019. PMID: 31419951 Free PMC article.

6

Genetic Strategies to Understand Human Diabetic Nephropathy: Wet-Lab Approaches.

Smyth LJ, Kerr K, Duffy S, Kilner J, McKnight AJ. Smyth LJ, et al. Among authors: kerr k. Methods Mol Biol. 2020;2067:205-240. doi: 10.1007/978-1-4939-9841-8_15. Methods Mol Biol. 2020. PMID: 31701455 Review.

7

Genetic Strategies to Understand Human Diabetic Nephropathy: In Silico Strategies for Molecular Data-Association Studies.

Canadas-Garre M, Smyth LJ, Anderson K, Kerr K, McKnight AJ. Canadas-Garre M, et al. Among authors: kerr k. Methods Mol Biol. 2020;2067:241-275. doi: 10.1007/978-1-4939-9841-8_16. Methods Mol Biol. 2020. PMID: 31701456

8

A scoping review and proposed workflow for multi-omic rare disease research.

Kerr K, McAneney H, Smyth LJ, Bailie C, McKee S, McKnight AJ. Kerr K, et al. 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.

9

Assessment of differentially methylated loci in individuals with end-stage kidney disease attributed to diabetic kidney disease: an exploratory study.

Smyth LJ, Kilner J, Nair V, Liu H, Brennan E, Kerr K, Sandholm N, Cole J, Dahlström E, Syreeni A, Salem RM, Nelson RG, Looker HC, Wooster C, Anderson K, McKay GJ, Kee F, Young I, Andrews D, Forsblom C, Hirschhorn JN, Godson C, Groop PH, Maxwell AP, Susztak K, Kretzler M, Florez JC, McKnight AJ. Smyth LJ, et al. Among authors: kerr k. Clin Epigenetics. 2021 May 1;13(1):99. doi: 10.1186/s13148-021-01081-x. Clin Epigenetics. 2021. PMID: 33933144 Free PMC article.

10

Identification and validation of a novel pathogenic variant in GDF2 (BMP9) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations.

Balachandar S, Graves TJ, Shimonty A, Kerr K, Kilner J, Xiao S, Slade R, Sroya M, Alikian M, Curetean E, Thomas E, McConnell VPM, McKee S, Boardman-Pretty F, Devereau A, Fowler TA, Caulfield MJ, Alton EW, Ferguson T, Redhead J, McKnight AJ, Thomas GA; Genomics England Research Consortium; Aldred MA, Shovlin CL. Balachandar S, et al. Among authors: kerr k. Am J Med Genet A. 2022 Mar;188(3):959-964. doi: 10.1002/ajmg.a.62584. Epub 2021 Dec 13. Am J Med Genet A. 2022. PMID: 34904380 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,125 results

Search Page

Filters