| Toward an elucidation of the molecular genetics of inherited retinal degenerations GJ Farrar, M Carrigan, A Dockery, S Millington-Ward, A Palfi, ... Human molecular genetics 26 (R1), R2-R11, 2017 | 91 | 2017 |
| Intravitreal delivery of AAV-NDI1 provides functional benefit in a murine model of Leber hereditary optic neuropathy N Chadderton, A Palfi, S Millington-Ward, O Gobbo, N Overlack, ... European Journal of Human Genetics 21 (1), 62-68, 2013 | 91 | 2013 |
| T-lex: a program for fast and accurate assessment of transposable element presence using next-generation sequencing data AS Fiston-Lavier, M Carrigan, DA Petrov, J González Nucleic acids research 39 (6), e36-e36, 2011 | 65 | 2011 |
| Panel-based population next-generation sequencing for inherited retinal degenerations M Carrigan, E Duignan, CPG Malone, K Stephenson, T Saad, ... Scientific reports 6 (1), 33248, 2016 | 62 | 2016 |
| Target 5000: target capture sequencing for inherited retinal degenerations A Dockery, K Stephenson, D Keegan, N Wynne, G Silvestri, P Humphries, ... Genes 8 (11), 304, 2017 | 54 | 2017 |
| Insular Celtic population structure and genomic footprints of migration RP Byrne, R Martiniano, LM Cassidy, M Carrigan, G Hellenthal, ... PLoS Genetics 14 (1), e1007152, 2018 | 46 | 2018 |
| Findings from a genotyping study of over 1000 people with inherited retinal disorders in Ireland L Whelan, A Dockery, N Wynne, J Zhu, K Stephenson, G Silvestri, ... Genes 11 (1), 105, 2020 | 44 | 2020 |
| A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration M Carrigan, E Duignan, P Humphries, A Palfi, PF Kenna, GJ Farrar British Journal of Ophthalmology 100 (4), 495-500, 2016 | 41 | 2016 |
| microRNA regulatory circuits in a mouse model of inherited retinal degeneration A Palfi, K Hokamp, SM Hauck, S Vencken, S Millington-Ward, ... Scientific Reports 6 (1), 31431, 2016 | 29 | 2016 |
| Gene expression changes during retinal development and rod specification FC Mansergh, M Carrigan, K Hokamp, GJ Farrar Molecular vision 21, 61, 2015 | 13 | 2015 |
| Novel 199 base pair NEFH promoter drives expression in retinal ganglion cells S Millington-Ward, N Chadderton, M Berkeley, LK Finnegan, KS Hanlon, ... Scientific Reports 10 (1), 16515, 2020 | 12 | 2020 |
| A novel FLVCR1 variant implicated in retinitis pigmentosa A Dockery, M Carrigan, N Wynne, K Stephenson, D Keegan, PF Kenna, ... Retinal Degenerative Diseases: Mechanisms and Experimental Therapy, 203-207, 2019 | 7 | 2019 |
| Assessing cone photoreceptor structure in patients with mutations in the OPN1LW/OPN1MW gene array EJ Patterson, M Kasilian, A Kalitzeos, CP Malone, M Carrigan, A Green, ... Investigative Ophthalmology & Visual Science 58 (8), 1257-1257, 2017 | 7 | 2017 |
| RPE-directed gene therapy improves mitochondrial function in murine dry AMD models S Millington-Ward, N Chadderton, LK Finnegan, IJM Post, M Carrigan, ... International Journal of Molecular Sciences 24 (4), 3847, 2023 | 6 | 2023 |
| AAV‐mediated gene therapy improving mitochondrial function provides benefit in age‐related macular degeneration models S Millington‐Ward, N Chadderton, LK Finnegan, IJM Post, M Carrigan, ... Clinical and Translational Medicine 12 (8), 2022 | 6 | 2022 |
| Multimodal imaging in a pedigree of X-linked Retinoschisis with a novel RS1 variant K Stephenson, A Dockery, N Wynne, M Carrigan, P Kenna, G Jane Farrar, ... BMC Medical Genetics 19, 1-10, 2018 | 6 | 2018 |
| Optimisation of AAV-NDI1 Significantly Enhances Its Therapeutic Value for Correcting Retinal Mitochondrial Dysfunction N Chadderton, A Palfi, DM Maloney, M Carrigan, LK Finnegan, ... Pharmaceutics 15 (2), 322, 2023 | 4 | 2023 |
| Variants of yeast NDI1 gene, and uses thereof in the treatment of disease associated with mitochondrial dysfunction GJ Farrar, S Millington-Ward, N Chadderton, MA Carrigan, P Kenna US Patent 10,220,102, 2019 | 2 | 2019 |
| Intrafamilial Phenotype Variation Associated with BBS1 Met390Arg CP Malone, M Carrigan, K Collins, H Dempsey, A Dockery, GJ Farrar, ... Investigative Ophthalmology & Visual Science 58 (8), 3257-3257, 2017 | 1 | 2017 |
| Genetic Diagnosis and Treatment of Inherited Retinopathies M Carrigan Trinity College Dublin, 2014 | 1 | 2014 |
