BETA: Related publications
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| Whelan L, Dockery A, Wynne N, et al. (2020) Findings from a Genotyping Study of Over 1000 People with Inherited Retinal Disorders in Ireland. Genes. 11 |
| Dockery A, Carrigan M, Wynne N, et al. (2019) A Novel FLVCR1 Variant Implicated in Retinitis Pigmentosa. Advances in Experimental Medicine and Biology. 1185: 203-207 |
| Byrne RP, Martiniano R, Cassidy LM, et al. (2018) Insular Celtic population structure and genomic footprints of migration. Plos Genetics. 14: e1007152 |
| Dockery A, Stephenson K, Keegan D, et al. (2017) Target 5000: Target Capture Sequencing for Inherited Retinal Degenerations. Genes. 8 |
| Jane Farrar G, Carrigan M, Dockery A, et al. (2017) Toward an elucidation of the molecular genetics of inherited retinal degenerations. Human Molecular Genetics |
| Carrigan M, Duignan E, Malone CP, et al. (2016) Panel-Based Population Next-Generation Sequencing for Inherited Retinal Degenerations. Scientific Reports. 6: 33248 |
| Carrigan M, Duignan E, Humphries P, et al. (2015) A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration. The British Journal of Ophthalmology |
| Fiston-Lavier AS, Carrigan M, Petrov DA, et al. (2011) T-lex: a program for fast and accurate assessment of transposable element presence using next-generation sequencing data. Nucleic Acids Research. 39: e36 |