Vanita Berry

9PUBLICATIONS
8CO-AUTHORS
Gene mappingVision scienceCell and nuclear divisionGene expression (incl. microarray and other genome-wide approaches)
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Publications (9)

|Sep 26, 2026
STOML1 as an Exploratory Candidate Gene for Autosomal Dominant Iris and Chorioretinal Coloboma in a British Family.

|Jul 03, 2024
A novel frameshift variant in BCOR causes congenital nuclear cataract.

Vanita Berry, Manav B Ponnekanti, Nikolas Pontikos

|Jul 26, 2023
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.

Vanita Berry, Alexander Ionides, Michalis Georgiou

|Jun 23, 2022
A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family.

Vanita Berry, Kaoru Fujinami, Kiyofumi Mochizuki

|Nov 08, 2021
Pathogenic variants in the CYP21A2 gene cause isolated autosomal dominant congenital posterior polar cataracts.

Vanita Berry, Nikolas Pontikos, Alex Ionides

|Aug 04, 2021
Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts.

Vanita Berry, Alex Ionides, Nikolas Pontikos

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Frequent Collaborators

5 joint publications

Nikolas Pontikos

4 joint publications

Michel Michaelides

2 joint publications

Michalis Georgiou

2 joint publications

Roy A Quinlan