First person – Amy Findlay
Publication year - 2018
Publication title -
disease models and mechanisms
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.327
H-Index - 83
eISSN - 1754-8411
pISSN - 1754-8403
DOI - 10.1242/dmm.038265
Subject(s) - retinal degeneration , selection (genetic algorithm) , function (biology) , human disease , degeneration (medical) , biology , disease , gerontology , genetics , medicine , ophthalmology , pathology , computer science , gene , artificial intelligence
First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms, helping early-career researchers promote themselves alongside their papers. Amy Findlay is first author on ‘ Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function ’, published in DMM. Amy is a postdoc in the lab of Ian Jackson at MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK. The focus of her research is using mouse models of human disease to investigate the genetic causes of retinal degeneration.
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