Rachel L Taylor (R Taylor)

Years Active: 2019-2022
Publications (10 Years): 4

This page only lists publications with an associated author ORCID identifier.

Publications

Rachel L Taylor, Carla Sanjuro Soriano, Simon Williams, Denisa Dzulova, Jane Ashworth, Georgina Hall, Theodora Gale, I Christopher Lloyd, Chris F Inglehearn, Carmel Toomes, Sofia Douzgou, Graeme C Black
Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia. Orphanet journal of rare diseases 17 (1) (2022)
James E Self, Rachel L Taylor, A L Solebo, S Biswas, M Parulekar, A Dev Borman, J Ashworth, R McClenaghan, J Abbott, E O'Flynn, D Hildebrand, I C Lloyd
Cataract management in children: a review of the literature and current practice across five large UK centres. Eye (London, England) 34 (12) (2020)
Shalaw Rassul Sallah, Panagiotis I Sergouniotis, Stephanie Barton, Simon Ramsden, Rachel L Taylor, Amro Safadi, Mitra Kabir, Jamie M Ellingford, Nick Lench, Simon C Lovell, Graeme C M Black
Using an integrative machine learning approach utilising homology modelling to clinically interpret genetic variants: CACNA1F as an exemplar. European journal of human genetics : EJHG 28 (9) (2020)
Omamah A Jiman, Rachel L Taylor, Eva Lenassi, Jill Clayton Smith, Sofia Douzgou, Jamie M Ellingford, Stephanie Barton, Claire Hardcastle, Tracy Fletcher, Christopher Campbell, Jane Ashworth, Susmito Biswas, Simon C Ramsden, null null, Forbes D Manson, Graeme C Black
Diagnostic yield of panel-based genetic testing in syndromic inherited retinal disease. European journal of human genetics : EJHG 28 (5) (2019)

Rachel L Taylor.css-eqlu8i{font-size:small;padding-left:4px;} (R Taylor)