M. Ashwin Reddy

981 total citations
10 papers, 673 citations indexed

About

M. Ashwin Reddy is a scholar working on Genetics, Molecular Biology and Ophthalmology. According to data from OpenAlex, M. Ashwin Reddy has authored 10 papers receiving a total of 673 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Ophthalmology. Recurrent topics in M. Ashwin Reddy's work include Connexins and lens biology (4 papers), Retinal Development and Disorders (3 papers) and Yersinia bacterium, plague, ectoparasites research (3 papers). M. Ashwin Reddy is often cited by papers focused on Connexins and lens biology (4 papers), Retinal Development and Disorders (3 papers) and Yersinia bacterium, plague, ectoparasites research (3 papers). M. Ashwin Reddy collaborates with scholars based in United Kingdom, Mexico and Belgium. M. Ashwin Reddy's co-authors include Shomi S. Bhattacharya, Anthony T. Moore, Peter J. Francis, Vanita Berry, Roy A. Quinlan, Eranga N. Vithana, Ian Mackay, Alisoun H. Carey, Elias I. Traboulsi and Graeme C. Black and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Investigative Ophthalmology & Visual Science.

In The Last Decade

M. Ashwin Reddy

8 papers receiving 654 citations

Peers

M. Ashwin Reddy

MB

GENET

OPHTH

CB

RNMI

Diego Cantalapiedra Spain

Katsuhiro Hosono Japan

Sharola Dharmaraj United States

Daniel Navarro-Gomez United States

Jeaneen L. Andorf United States

Béatrice Bocquet France

Keiko Miyadera United States

Xunlun Sheng China

Maria E Sousa United States

Luísa Coutinho Santos Portugal

Diego Cantalapiedra Spain

M. Ashwin Reddy

622 ×1.1

MB

171 ×0.6

GENET

366 ×1.4

OPHTH

74 ×1.0

CB

101 ×2.0

RNMI

Citations per year, relative to M. Ashwin Reddy M. Ashwin Reddy (= 1×) peers Diego Cantalapiedra

Countries citing papers authored by M. Ashwin Reddy

Since Specialization

Citations

This map shows the geographic impact of M. Ashwin Reddy'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 M. Ashwin Reddy with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Ashwin Reddy more than expected).

Fields of papers citing papers by M. Ashwin Reddy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Ashwin Reddy. 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 M. Ashwin Reddy. The network helps show where M. Ashwin Reddy may publish in the future.

Co-authorship network of co-authors of M. Ashwin Reddy

This figure shows the co-authorship network connecting the top 25 collaborators of M. Ashwin Reddy. A scholar is included among the top collaborators of M. Ashwin Reddy based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. Ashwin Reddy. M. Ashwin Reddy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

1.

Kelly, Cormac, et al.. (2024). Decolonising the ‘red’ reflex test: transitioning from terminology based on colour to anatomy. Eye. 39(2). 379–381.

2.

Hogg, Chris R., et al.. (2014). Electroretinogram assessment of children with sensorineural hearing loss: implications for screening. Journal of American Association for Pediatric Ophthalmology and Strabismus. 18(4). e24–e24.

3.

Chandra, Aman, José Antonio Aragon-Martin, Sabiha Gati, et al.. (2012). A Genotype-Phenotype Comparison ofADAMTSL4andFBN1in Isolated Ectopia Lentis. Investigative Ophthalmology & Visual Science. 53(8). 4889–4889. 46 indexed citations

4.

Joyce, Sarah, et al.. (2010). Cerebrotendinous Xanthomatosis (CTX): An Association of Pulverulent Cataracts and Pseudo-Dominant Developmental Delay in a Family with a Splice Site Mutation inCYP27A1— A Case Report. Ophthalmic Genetics. 31(2). 73–76. 6 indexed citations

5.

Leroy, Bart P., Niki Hart‐Holden, B. A. Lafaut, et al.. (2004). Mutations of VMD2 Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC). Investigative Ophthalmology & Visual Science. 45(10). 3683–3683. 163 indexed citations

6.

Meredith, Sarah, M. Ashwin Reddy, Louise Allen, Anthony T. Moore, & Keith Bradshaw. (2004). Full-field ERG responses recorded with skin electrodes in paediatric patients with retinal dystrophy. Documenta Ophthalmologica. 109(1). 57–66. 13 indexed citations

7.

Reddy, M. Ashwin, Peter J. Francis, Vanita Berry, Shomi S. Bhattacharya, & Anthony T. Moore. (2004). Molecular genetic basis of inherited cataract and associated phenotypes. Survey of Ophthalmology. 49(3). 300–315. 174 indexed citations

8.

Reddy, M. Ashwin. (2004). Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract. Human Molecular Genetics. 13(9). 945–953. 53 indexed citations

9.

Reddy, M. Ashwin. (2003). A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma. British Journal of Ophthalmology. 87(2). 197–202. 30 indexed citations

10.

Berry, Vanita, Peter J. Francis, M. Ashwin Reddy, et al.. (2001). Alpha-B Crystallin Gene (CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans. The American Journal of Human Genetics. 69(5). 1141–1145. 188 indexed citations

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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