Martin Taylor, Ph.D.
Affiliations: | MRC Human Genetics Unit, Edinburgh, Scotland, United Kingdom |
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"Martin Taylor"Parents
Sign in to add mentor| Richard Mott | post-doc | 2004-2009 | Oxford |
| Nick Goldman | post-doc | 2006-2010 | European Bioinformatics Institute |
Children
Sign in to add trainee| Robert S. Young | post-doc | MRC Human Genetics Unit | |
| Alison M. Meynert | post-doc | 2010-2014 | MRC Human Genetics Unit |
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Publications
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| Young RS, Talmane L, Marion de Procé S, et al. (2022) The contribution of evolutionarily volatile promoters to molecular phenotypes and human trait variation. Genome Biology. 23: 89 |
| Younger NT, Wilson ML, Martinez Lyons A, et al. (2022) In vivo modeling of patient genetic heterogeneity identifies new ways to target cholangiocarcinoma. Cancer Research |
| Ramilowski JA, Yip CW, Agrawal S, et al. (2020) Functional annotation of human long noncoding RNAs via molecular phenotyping. Genome Research |
| Alam T, Agrawal S, Severin J, et al. (2020) Comparative transcriptomics of primary cells in vertebrates. Genome Research |
| Longman D, Jackson-Jones KA, Maslon MM, et al. (2020) Identification of a localized nonsense-mediated decay pathway at the endoplasmic reticulum. Genes & Development |
| Mordstein C, Savisaar R, Young RS, et al. (2020) Codon Usage and Splicing Jointly Influence mRNA Localization. Cell Systems |
| Halachev M, Meynert A, Taylor MS, et al. (2019) Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions. Plos Genetics. 15: e1008480 |
| Young RS, Kumar Y, Bickmore WA, et al. (2017) Bidirectional transcription initiation marks accessible chromatin and is not specific to enhancers. Genome Biology. 18: 242 |
| Moss CF, Dalla Rosa I, Hunt LE, et al. (2017) Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model. Nucleic Acids Research |
| Young RS, Hayashizaki Y, Andersson R, et al. (2015) The frequent evolutionary birth and death of functional promoters in mouse and human. Genome Research |