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Matthew Carrigan, under-graduate - Publications

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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Whelan L, Dockery A, Wynne N, Zhu J, Stephenson K, Silvestri G, Turner J, O'Byrne JJ, Carrigan M, Humphries P, Keegan D, Kenna PF, Farrar GJ. Findings from a Genotyping Study of Over 1000 People with Inherited Retinal Disorders in Ireland. Genes. 11. PMID 31963381 DOI: 10.3390/Genes11010105  0.41
2019 Dockery A, Carrigan M, Wynne N, Stephenson K, Keegan D, Kenna PF, Farrar GJ. A Novel FLVCR1 Variant Implicated in Retinitis Pigmentosa. Advances in Experimental Medicine and Biology. 1185: 203-207. PMID 31884612 DOI: 10.1007/978-3-030-27378-1_33  0.357
2018 Byrne RP, Martiniano R, Cassidy LM, Carrigan M, Hellenthal G, Hardiman O, Bradley DG, McLaughlin RL. Insular Celtic population structure and genomic footprints of migration. Plos Genetics. 14: e1007152. PMID 29370172 DOI: 10.1371/Journal.Pgen.1007152  0.313
2017 Dockery A, Stephenson K, Keegan D, Wynne N, Silvestri G, Humphries P, Kenna PF, Carrigan M, Farrar GJ. Target 5000: Target Capture Sequencing for Inherited Retinal Degenerations. Genes. 8. PMID 29099798 DOI: 10.3390/Genes8110304  0.422
2017 Jane Farrar G, Carrigan M, Dockery A, Millington Ward S, Palfi A, Chadderton N, Humphries M, Kiang AS, Kenna PF, Humphries P. Toward an elucidation of the molecular genetics of inherited retinal degenerations. Human Molecular Genetics. PMID 28510639 DOI: 10.1093/Hmg/Ddx185  0.348
2016 Carrigan M, Duignan E, Malone CP, Stephenson K, Saad T, McDermott C, Green A, Keegan D, Humphries P, Kenna PF, Farrar GJ. Panel-Based Population Next-Generation Sequencing for Inherited Retinal Degenerations. Scientific Reports. 6: 33248. PMID 27624628 DOI: 10.1038/Srep33248  0.404
2015 Carrigan M, Duignan E, Humphries P, Palfi A, Kenna PF, Farrar GJ. A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration. The British Journal of Ophthalmology. PMID 26472407 DOI: 10.1136/Bjophthalmol-2015-306939  0.358
2011 Fiston-Lavier AS, Carrigan M, Petrov DA, González J. T-lex: a program for fast and accurate assessment of transposable element presence using next-generation sequencing data. Nucleic Acids Research. 39: e36. PMID 21177644 DOI: 10.1093/Nar/Gkq1291  0.42
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