Srirangan Sampath

523 citations
12 papers · 246 indexed · h-index 8
Topics
Retinal Development and Disorders (3 papers)Genomic variations and chromosomal abnormalities (3 papers)Genomics and Rare Diseases (2 papers)

In The Last Decade

Srirangan Sampath

12 papers receiving 241 citations

Peers

Srirangan Sampath
Comparison fields: 5 of 49
  • Molecular Biology 165
  • Genetics 102
  • Ophthalmology 36
  • Cell Biology 35
  • Sensory Systems 27
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Countries citing papers authored by Srirangan Sampath

Since Specialization
Citations

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

Fields of papers citing papers by Srirangan Sampath

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Srirangan Sampath. 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 Srirangan Sampath. The network helps show where Srirangan Sampath may publish in the future.

Co-authorship network of co-authors of Srirangan Sampath

This figure shows the co-authorship network connecting the top 25 collaborators of Srirangan Sampath. A scholar is included among the top collaborators of Srirangan Sampath 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 Srirangan Sampath. Srirangan Sampath is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
#WorkIndexed citations
1 9
2 9
3 1
4 35
5 3
6 31
7 2
8 48
9 2
10 37
11
Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India.
42
12
Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly.
27

About Srirangan Sampath

Srirangan Sampath is a scholar working on Ophthalmology, Genetics and Sensory Systems, having authored 12 papers that have together received 246 indexed citations. Recurring topics across this work include Retinal Development and Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Sensory Systems (27 citations), Ophthalmology (36 citations) and Genetics (102 citations). Srirangan Sampath has collaborated with scholars based in United States, Australia and India. Frequent co-authors include Shirly G. Panicker, Anil K. Mandal, Aramati B. M. Reddy, Yves Lacassie, Subhabrata Chakrabarti, Dorairajan Balasubramanian, Anne L. Estep, Andrew B. West, William E. Tidyman and Seyed E. Hasnain. Their work appears in journals such as PLoS ONE, Human Mutation and European Journal of Human 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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