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Employment (1)

UCL, Institute of Ophthalmology, University College London: London, London, GB

Senior Research Fellow/ Dr (Genetics)
Employment
Source: Self-asserted source
Vanita Berry

Works (10)

A novel frameshift variant in BCOR causes congenital nuclear cataract

Ophthalmic Genetics
2024-11 | Journal article
DOI: 10.1080/13816810.2024.2373248
Contributors: Vanita Berry; Manav B. Ponnekanti; Nikolas Pontikos; Roy A. Quinlan; Michel Michaelides
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Crossref

Multimorbidity due to novel pathogenic variants in theWFS1/RP1/NOD2genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn’s disease in a British family

BMJ Open Ophthalmology
2023-07 | Journal article
DOI: 10.1136/bmjophth-2023-001252
Contributors: Vanita Berry; Alexander Ionides; Michalis Georgiou; Roy A Quinlan; Michel Michaelides
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Crossref

A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family

Ophthalmic Genetics
2022-09-03 | Journal article
DOI: 10.1080/13816810.2022.2090010
Contributors: Vanita Berry; Kaoru Fujinami; Kiyofumi Mochizuki; Takeshi Iwata; Nikolas Pontikos; Roy A. Quinlan; Michel Michaelides
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Crossref

Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts

Eye
2022-08 | Journal article
DOI: 10.1038/s41433-021-01711-x
Contributors: Vanita Berry; Alex Ionides; Nikolas Pontikos; Anthony T. Moore; Roy A. Quinlan; Michel Michaelides
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Crossref

Pathogenic variants in the CYP21A2 gene cause isolated autosomal dominant congenital posterior polar cataracts

Ophthalmic Genetics
2022-03-04 | Journal article
DOI: 10.1080/13816810.2021.1998556
Contributors: Vanita Berry; Nikolas Pontikos; Alex Ionides; Angelos Kalitzeos; Roy A. Quinlan; Michel Michaelides
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Crossref

Variants in PAX6, PITX3 and HSF4 Causing Autosomal Dominant Congenital Cataract

2021-04-05 | Other
DOI: 10.21203/rs.3.rs-367664/v1
Contributors: Vanita Berry; Alex Ionides; Nikolas Pontikos; Anthony T Moore; Roy A Quinlan; Michel Michaelides
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Crossref

The genetic landscape of crystallins in congenital cataract

Orphanet Journal of Rare Diseases
2020-12 | Journal article
DOI: 10.1186/s13023-020-01613-3
Contributors: Vanita Berry; Alex Ionides; Nikolas Pontikos; Michalis Georgiou; Jing Yu; Louise A. Ocaka; Anthony T. Moore; Roy A. Quinlan; Michel Michaelides
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Crossref
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Inherited cataracts: molecular genetics, clinical features, disease mechanisms and novel therapeutic approaches

British Journal of Ophthalmology
2020-10-25 | Journal article
DOI: 10.1136/bjophthalmol-2019-315282
Contributors: Vanita Berry; Michalis Georgiou; Kaoru Fujinami; Roy Quinlan; Anthony Moore; Michel Michaelides
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Crossref
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Preferred source (of 2)‎

A novel missense mutation in LIM2 causing isolated autosomal dominant congenital cataract

Ophthalmic Genetics
2020-03-03 | Journal article
DOI: 10.1080/13816810.2020.1737950
Contributors: Vanita Berry; Nikolas Pontikos; Lubica Dudakova; Anthony T. Moore; Roy Quinlan; Petra Liskova; Michel Michaelides
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Crossref

Whole Exome Sequencing Reveals Novel and Recurrent Disease-Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital Cataract.

Genes
2020-01 | Journal article
DOI: 10.3390/genes11050512
PMID: 32384692
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