Publications: Keegan, Niall

2022

Keegan, N.P., Wilton, S.D. and Fletcher, S. (2022) Analysis of pathogenic pseudoexons reveals novel mechanisms driving cryptic splicing. Frontiers in Genetics, 12 . Art. 806946.

Keegan, N.P., Wilton, S.D. and Fletcher, S. (2022) Corrigendum: Analysis of pathogenic pseudoexons reveals novel mechanisms driving cryptic splicing. Frontiers in Genetics, 13 . Art. 943044.

Keegan, Niall Patrick (2022) Hidden stitches: RNA cryptic splicing and its role in human disease. PhD thesis, Murdoch University.

2021

Ham, K.ORCID: 0000-0002-7036-5334, Keegan, N., McIntosh, C., Aung-Htut, M., Zaw, K.ORCID: 0000-0002-4121-1985, Greer, K., Fletcher, S. and Wilton, S. (2021) Cryptic U2-dependent pre-mRNASplice site usage induced by splice switching antisense oligonucleotides. Research Square . In Review.

Ham, K.A.ORCID: 0000-0002-7036-5334, Keegan, N.P., McIntosh, C.S., Aung-Htut, M.T., Zaw, K.ORCID: 0000-0002-4121-1985, Greer, K., Fletcher, S. and Wilton, S.D. (2021) Induction of cryptic pre-mRNA splice-switching by antisense oligonucleotides. Scientific Reports, 11 (1). Article 15137.

Keegan, N.P. and Fletcher, S. (2021) A spotter’s guide to SNPtic exons: The common splice variants underlying some SNP–phenotype correlations. Molecular Genetics & Genomic Medicine, 10 (1). Art. e1840.

2020

Keegan, N.P. (2020) Pseudoexons of the DMD Gene. Journal of Neuromuscular Diseases, 7 (2). pp. 77-95.

2019

Keegan, N.P., Wilton, S.D. and Fletcher, S. (2019) Breakpoint junction features of seven DMD deletion mutations. Human Genome Variation, 6 (1).

2017

Keegan, Niall (2017) Splicing behaviour and exotic mutations in the DMD gene. Masters by Research thesis, Murdoch University.

2015

Keegan, N.P., Wilton, S. and Fletcher, S. (2015) PCR‐based strategies for delimiting large mutations in the DMD gene. The Journal of Gene Medicine, 17 (8-9). PO2.