Vanita Berry

2.4k citations

38 papers · 1.7k indexed · h-index 19

Impact in

Ophthalmology top 1%
- Intraocular Surgery and Lenses
Genetics top 2%
- Yersinia bacterium, plague, ectoparasites research
- Ocular Disorders and Treatments

Papers in

Ophthalmology 12
- Intraocular Surgery and Lenses 10
Genetics 15
- Yersinia bacterium, plague, ectoparasites research 12
- Ocular Disorders and Treatments 2

Co-authors: Anthony T. Moore Shomi S. Bhattacharya Alan Shiels Donna S. Mackay Alexander Ionides Peter J. Francis M. Ashwin Reddy Roy A. Quinlan
Journals: The American Journal of Human Genetics (4 papers)Eye (4 papers)Ophthalmic Genetics (4 papers)European Journal of Human Genetics (2 papers)Human Molecular Genetics (2 papers)
Partner nations: United Kingdom United States Mexico

In The Last Decade

Vanita Berry

36 papers receiving 1.7k citations

Peers

Countries citing papers authored by Vanita Berry

Since Specialization

Citations

This map shows the geographic impact of Vanita Berry's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Vanita Berry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vanita Berry more than expected).

Fields of papers citing papers by Vanita Berry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vanita Berry. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Vanita Berry. The network helps show where Vanita Berry may publish in the future.

Co-authors

The 25 scholars most cited alongside Vanita Berry, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Vanita Berry Line = papers co-authored together Vanita Berry links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	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 ·Vanita Berry, Alexander Ionides, Michalis Georgiou, Roy A. Quinlan, Michel Michaelides	2023	3
2	Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts Eye ·Vanita Berry, Alex Ionides, Nikolas Pontikos, Anthony T. Moore, Roy A. Quinlan, Michel Michaelides	2021	4
3	The genetic landscape of crystallins in congenital cataract Orphanet Journal of Rare Diseases ·Vanita Berry, Alex Ionides, Nikolas Pontikos, Michalis Georgiou, Jing Yu, Louise Ocaka, Anthony T. Moore, Roy A. Quinlan, Michel Michaelides	2020	34
4	Inherited cataracts: molecular genetics, clinical features, disease mechanisms and novel therapeutic approaches British Journal of Ophthalmology ·Vanita Berry, Michalis Georgiou, Kaoru Fujinami, Roy A. Quinlan, Anthony T. Moore, Michel Michaelides	2020	47
5	The orphan nuclear receptor estrogen-related receptor beta (ERRβ) in triple-negative breast cancer Breast Cancer Research and Treatment ·Aileen I. Fernandez, Xue Geng, Krysta Chaldekas, Brent T. Harris, Anju Duttargi, Vanita Berry, Deborah L. Berry, Akanksha Mahajan, Luciane R. Cavalli, Balázs Győrffy, Ming Tan, Rebecca B. Riggins	2019	5
6	Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract Eye ·Vanita Berry, Alexander Ionides, Nikolas Pontikos, Ismail Moghul, Anthony T. Moore, Michael E. Cheetham, Michel Michaelides	2018	5
7	Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans European Journal of Human Genetics ·Vanita Berry, Cheryl Y. Gregory‐Evans, Warren Emmett, Naushin Waseem, Jacob Raby, Quincy Prescott, Anthony T. Moore, Shomi S. Bhattacharya	2013	47
8	A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q European Journal of Human Genetics ·Vanita Berry, Alexander Ionides, Anthony T. Moore, Shomi S. Bhattacharya	2011	2
9	A CRYGD mutation is associated with familial coralliform cataract Investigative Ophthalmology & Visual Science ·Anita Arora, A Rajashekar Reddy, Peter J. Francis, Alexander Ionides, Vanita Berry, Anthony T. Moore, S.S. Bhattacharya	2004	0
10	Recurrent 17 bp duplication in PITX3 is primarily associated with posterior polar cataract (CPP4) Journal of Medical Genetics ·Vanita Berry, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2004	48
11	Molecular genetic basis of inherited cataract and associated phenotypes Survey of Ophthalmology ·M. Ashwin Reddy, Peter J. Francis, Vanita Berry, Shomi S. Bhattacharya, Anthony T. Moore	2004	174
12	Visual outcome in patients with isolated autosomal dominant congenital cataract11None of the authors have any proprietary interest in this work. Ophthalmology ·Peter J. Francis, Alex Ionides, Vanita Berry, Shomi S. Bhattacharya, Anthony T. Moore	2001	12
13	Clinical and genetic heterogeneity in autosomal dominant cataract British Journal of Ophthalmology ·Alexander Ionides, Peter J. Francis, Vanita Berry, Donna S. Mackay, Siladitya Bhattacharya, Alan Shiels, Anthony T. Moore	1999	85
14	Connexin46 Mutations in Autosomal Dominant Congenital Cataract The American Journal of Human Genetics ·Donna S. Mackay, Alexander Ionides, Zoha Kibar, Guy A. Rouleau, Vanita Berry, Anthony T. Moore, Alan Shiels, Shomi S. Bhattacharya	1999	224
15	A Missense Mutation in the Human Connexin50 Gene (GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1q The American Journal of Human Genetics ·Alan Shiels, Donna S. Mackay, Alexander Ionides, Vanita Berry, Anthony T. Moore, Shomi S. Bhattacharya	1998	275
16	A New Locus for Dominant “Zonular Pulverulent” Cataract, on Chromosome 13 The American Journal of Human Genetics ·Donna S. Mackay, Alexander Ionides, Vanita Berry, Anthony T. Moore, Shomi Bhattacharya, Alan Shiels	1997	44
17	The clinical and genetic heterogeneity of autosomal dominant cataract Acta Ophthalmologica Scandinavica ·Alexander Ionides, Vanita Berry, Tony Moore, Shomi Bhattacharya, Alan Shiels	1996	13
18	IMMUNOFLUORESCENT EVIDENCE FOR THE ABUNDANCE OF FOCAL ADHESION KINASE IN THE HUMAN AND AVIAN OSTEOCLASTS AND ITS DOWN REGULATION BY CALCITONIN Journal of Endocrinology ·Vanita Berry, Hetal Rathod, L. B. Pulman, Harish K. Datta	1994	16
19	Characterization of a subtype of primary osteoclastoma: Extracellular calcium but not calcitonin inhibits aggressive HLA‐DR‐positive osteoclastoma possessing ‘functional’ calcitonin receptors The Journal of Pathology ·Hersha Rathod, ARCHIBALD J. MALCOLM, James Gillespie, Vanita Berry, J. Pooley, Nigel H. Piggott, Harish K. Datta	1994	5
20	Urinary excretion of histidine derivatives in megaloblastic anaemia and other conditions and a comparison with the folic acid clearance test Journal of Clinical Pathology ·I. Chanarin, M. C. Bennett, Vanita Berry	1962	51

About Vanita Berry

Vanita Berry is a scholar working on Ophthalmology, Genetics, Molecular Biology, Immunology and Allergy and Sensory Systems, having authored 38 papers that have together received 1.7k indexed citations. Recurring topics across this work include Connexins and lens biology (29 papers), Yersinia bacterium, plague, ectoparasites research (12 papers), Intraocular Surgery and Lenses (10 papers), RNA regulation and disease (5 papers), Cell Adhesion Molecules Research (2 papers), Ocular Disorders and Treatments (2 papers), Trace Elements in Health (2 papers) and Bone health and treatments (2 papers). The work is most often cited by research in Ophthalmology (480 citations), Genetics (716 citations), Molecular Biology (1.6k citations), Sensory Systems (40 citations) and Clinical Biochemistry (54 citations). Vanita Berry has collaborated with scholars based in United Kingdom, United States and Mexico. Frequent co-authors include Anthony T. Moore, Shomi S. Bhattacharya, Alan Shiels, Donna S. Mackay, Alexander Ionides, Peter J. Francis, M. Ashwin Reddy, Roy A. Quinlan, Siladitya Bhattacharya and Zoha Kibar. Their work appears in journals such as The American Journal of Human Genetics, Eye, Ophthalmic Genetics, European Journal of Human Genetics and Human Molecular Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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