Vanita Berry

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 8

Top Venues

Ophthalmic genetics

BMJ open ophthalmology

The British journal of ophthalmology

Eye (London, England)

UCL, Institute of Ophthalmology, University College London

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

Affiliation History

UCL, Institute of Ophthalmology, University College London

United Kingdom

Senior Research Fellow/ Dr :: Genetics

Publications

Vanita Berry, Manav B Ponnekanti, Nikolas Pontikos, Roy A Quinlan, Michel Michaelides
A novel frameshift variant in BCOR causes congenital nuclear cataract. Ophthalmic genetics (2024)
Vanita Berry, Alexander Ionides, Michalis Georgiou, Roy A Quinlan, Michel Michaelides
Multimorbidity due to novel pathogenic variants in the WFS1/RP1/NOD2 genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British family. BMJ open ophthalmology 8 (1) (2023)
Vanita Berry, Kaoru Fujinami, Kiyofumi Mochizuki, Takeshi Iwata, Nikolas Pontikos, Roy A Quinlan, Michel Michaelides
A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family. Ophthalmic genetics 43 (5) (2022)
Vanita Berry, Nikolas Pontikos, Alex Ionides, Angelos Kalitzeos, Roy A Quinlan, Michel Michaelides
Pathogenic variants in the CYP21A2 gene cause isolated autosomal dominant congenital posterior polar cataracts. Ophthalmic genetics (2021)
Vanita Berry, Alex Ionides, Nikolas Pontikos, Anthony T Moore, Roy A Quinlan, Michel Michaelides
Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts. Eye (London, England) (2021)
Vanita Berry, Michalis Georgiou, Kaoru Fujinami, Roy Quinlan, Anthony Moore, Michel Michaelides
Inherited cataracts: molecular genetics, clinical features, disease mechanisms and novel therapeutic approaches. The British journal of ophthalmology 104 (10) (2020)
Vanita Berry, Nikolas Pontikos, Lubica Dudakova, Anthony T Moore, Roy Quinlan, Petra Liskova, Michel Michaelides
A novel missense mutation in LIM2 causing isolated autosomal dominant congenital cataract. Ophthalmic genetics 41 (2) (2020)
Vanita Berry, Alex Ionides, Nikolas Pontikos, Michalis Georgiou, Jing Yu, Louise A Ocaka, Anthony T Moore, Roy A Quinlan, Michel Michaelides
The genetic landscape of crystallins in congenital cataract. Orphanet journal of rare diseases 15 (1) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Vanita Berry