This map shows the geographic impact of Daljit Singh'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 Daljit Singh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daljit Singh more than expected).
This network shows the impact of papers produced by Daljit Singh. 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 Daljit Singh. The network helps show where Daljit Singh may publish in the future.
Co-authorship network of co-authors of Daljit Singh
This figure shows the co-authorship network connecting the top 25 collaborators of Daljit Singh.
A scholar is included among the top collaborators of Daljit Singh 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 Daljit Singh. Daljit Singh is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Vanita, Vanita, Jai Rup Singh, Daljit Singh, Raymonda Varon, & Karl Sperling. (2009). Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract.. PubMed. 15. 476–81.22 indexed citations
8.
Vanita, Vanita, Jai Rup Singh, Daljit Singh, Raymonda Varon, & Karl Sperling. (2008). A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin.. PubMed. 14. 1171–5.24 indexed citations
9.
Vanita, Vanita, Jai Rup Singh, Daljit Singh, Raymonda Varon, & Karl Sperling. (2008). A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin.. PubMed. 14. 323–6.36 indexed citations
10.
Guleria, Kamlesh, Vanita Vanita, Daljit Singh, & Jai Rup Singh. (2007). A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene.. PubMed. 13. 797–803.20 indexed citations
11.
Guleria, Kamlesh, Karl Sperling, Daljit Singh, et al.. (2007). A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.. PubMed. 13. 1657–65.32 indexed citations
12.
Vanita, Vanita, Hans Christian Hennies, Daljit Singh, et al.. (2006). A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.. PubMed. 12. 1217–22.35 indexed citations
Vanita, Vanita, Jai Rup Singh, J. Fielding Hejtmancik, et al.. (2006). A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.. PubMed. 12. 518–22.44 indexed citations
15.
Vanita, Vanita, J. Fielding Hejtmancik, Hans Christian Hennies, et al.. (2006). Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin.. PubMed. 12. 93–9.23 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.