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Vision for good
Home
What we do
History
Case for Support
Donate
Contact us
Thank you
More
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  • What we do
  • History
  • Case for Support
  • Donate
  • Contact us
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  • What we do
  • History
  • Case for Support
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  • Contact us
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The difference our work makes to one family

Barry Stickings MBE, talks about his son, Toby who is affected with bilateral anophthalmia and the support that Prof Nicky Ragge has given the whole family over the last 30 years. 


Barry enthusiastically supports the Vision for Good goal to create a leading UK Centre that combines research with supporting families. 


Barry is ex-Chairman of charity MACS (Microphthalmia, Anophthalmia & Coloboma Support) and Founder of the new worldwide support group BAAM (Bilateral Anophthalmia and Me ) 

About Vision for good

Observe magazine: "Funding boost for world-leading research"

Observe magazine: "Funding boost for world-leading research"

Observe magazine: "Funding boost for world-leading research"

In 2021, eye genetics research at Oxford Brookes University  received a gift of £2 million from investment business Baillie Gifford. The pledge supports the work of Professor Nicola Ragge who has spearheaded a national eye genetics service and led pioneering research into eye development problems in children. 

Radio interview: ABC Science Show

Observe magazine: "Funding boost for world-leading research"

Observe magazine: "Funding boost for world-leading research"

In this radio interview, Nicky Ragge describes some of the conditions which occur in babies’ eyes caused by genetic problems, and some treatments which can be applied.

Listen to the interview

Our work at Oxford Brookes University

Follow this link to our Oxford Brookes web pages

Our research papers

Follow this link to read our papers

The group's collaborators within europe and across the world

Our collaborators

Recent posters (European Society for Human Genetics, Berlin

ESHG 2024: Novel cases with biallelic variants in Wnt ligand secretion mediator (WLS) (pdf)Download
ESHG 2024: Optical Genome Mapping facilitates rapid characterisation developmental eye anomalies (pdf)Download

Recent open access publications

Holt et al. 2019: De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes (pdf)Download
Kesim et al. 2023: Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1 (pdf)Download
Caron et al. 2023: heterogeneity associated with the disruption of retinoic acid receptor beta (pdf)Download
Ceroni et al. 2022: Analysis of Fibroblast Growth Factor 14 (FGF14) (pdf)Download
Holt et al. 2022: heterozygous variants in the Wnt-signalling pathway gene FZD5 (pdf)Download
Zha et al .2020: Biallelic variants in the small optic lobe calpain CAPN15 (pdf)Download

All about our work ...

POSTER CREATED BY KARTHIKA JEGANATHAN

A member of Professor Nicky Ragge’s team

Download PDF

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