Michael Abbott – Research output — The University of Aberdeen Research Portal

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2023
Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing: implications for future testing
Hocking, L., Andrews, C., Armstrong, C., Ansari, M., Baty, D., Berg, J., Bradley, T., Clark, C., Diamond, A., Doherty, J., Lampe, A., McGowan, R., Moore, D. J., O'Sullivan, D., Purvis, A., Santoyo-Lopez, J., Westwood, P., Abbott, M., Williams, N., Scottish Genomes Partnership, & 2 othersAitman, T. J. & Miedzybrodzka, Z., 1 Feb 2023, In: European Journal of Human Genetics. 31, 2, p. 231-238 8 p.
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2022
Continuing the sequence? Towards an Economic Evaluation of Whole Genome Sequencing for the Diagnosis of Rare Diseases in Scotland
Abbott, M., McKenzie, L., Moran, B., Heidenreich, S., Hernández, R., Hocking- Mennie, L., Clark, C., Clark, C., Gomes, J., Lampe, A., Baty, D., McGowan, R., Miedzybrodzka, Z. & Ryan, M., Oct 2022, In: Journal of Community Genetics. 13, p. 487-501 16 p.
Research output: Contribution to journal › Article › peer-review

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5 Citations (Scopus)

14 Downloads (Pure)