Research output per year
Research output per year
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Dive into the research topics where Amy Findlay is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Research output
- 3 Article
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A Mouse Model of Brittle Cornea Syndrome caused by mutation in Zfp469
Stanton, C., Findlay, A., Drake, C., Mustafa, Z., Gautier, P., McKie, L., Jackson, I. J. & Vitart, V., 22 Sept 2021, In: Disease Models and Mechanisms.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function
Findlay, A., McKie, L., Keighren, M., Clementson-Mobbs, S., Sanchez-Pulido, L., Wells, S., Cross, S. & Jackson, I., 16 Jan 2020, In: Scientific Reports. 10, 437.Research output: Contribution to journal › Article › peer-review
Open AccessFile -
Mouse Idh3a Mutations Cause Retinal Degeneration and Reduced Mitochondrial Function
Findlay, A., Carter, R. N., Starbuck, B., McKie, L., Novakova, K., Budd, P. S., Keighren, M., Marsh, J. A., Cross, S., Simon, M., Potter, P., Morton, N. M. & Jackson, I. J., Dec 2018, In: Disease Models and Mechanisms.Research output: Contribution to journal › Article › peer-review
Open AccessFile
Projects
- 4 Finished
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Wound healing in the embryonic chick cornea; an eggcellent opportunity
1/07/23 → 31/03/24
Project: Research
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Specialised phenotype training and collaborative project building for myopia research
1/03/22 → 31/03/24
Project: Research
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Specialised phenotype training and collaborative project building for myopia research
1/03/22 → 31/05/22
Project: Research
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Establishing a role for genetic variants associated with myopia and retinal detachment at the BMP3 locus
1/07/19 → 31/03/21
Project: Research