Countries citing papers authored by Radha Ayyagari
Since
Specialization
Citations
This map shows the geographic impact of Radha Ayyagari'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 Radha Ayyagari with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Radha Ayyagari more than expected).
This network shows the impact of papers produced by Radha Ayyagari. 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 Radha Ayyagari. The network helps show where Radha Ayyagari may publish in the future.
Co-authorship network of co-authors of Radha Ayyagari
This figure shows the co-authorship network connecting the top 25 collaborators of Radha Ayyagari.
A scholar is included among the top collaborators of Radha Ayyagari 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 Radha Ayyagari. Radha Ayyagari is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Chavali, Venkata Ramana Murthy, et al.. (2016). Role of Complement-1q Tumor Necrosis Factor Related Protein 5 (CTRP5/C1QTNF5) in Late-Onset Retinal Degeneration (L-ORD) Pathology. Investigative Ophthalmology & Visual Science. 57(12). 3181–3181.
Naeem, Muhammad Asif, Inayat Ullah, Shaheen N. Khan, et al.. (2015). Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness.. PubMed Central. 21. 1261–71.6 indexed citations
Biswas, Pooja, Pauline Lee, Shahid Y. Khan, et al.. (2013). Identification of causative mutations in consanguineous pedigrees from Pakistan with recessive retinal degeneration by whole exome analysis. Investigative Ophthalmology & Visual Science. 54(15). 3349–3349.3 indexed citations
12.
Duncan, Jacque L., et al.. (2012). Exome Analysis Identified A Novel Mutation In A Family With Recessive Retinal Degeneration. Investigative Ophthalmology & Visual Science. 53(14). 4523–4523.1 indexed citations
Ayyagari, Radha, Rando Allikmets, H. Okamoto, et al.. (2004). Linkage and mutation analysis to identify the gene associated with macular degeneration segregating in a cynomolgus monkey (Macaca fascicularis) pedigree.. Investigative Ophthalmology & Visual Science. 45(13). 1825–1825.1 indexed citations
16.
Ambasudhan, Rajesh, Monica M. Jablonski, Robert N. Fariss, et al.. (2003). Subcellular Localization of ELOVL4 Gene Product in Cultured Cells and Mammalian Retinae and Intracellular Misrouting of its Mutant. Investigative Ophthalmology & Visual Science. 44(13). 5096–5096.1 indexed citations
Padma, T., Radha Ayyagari, Surendra Basti, et al.. (1995). Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.. PubMed. 57(4). 840–5.49 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.