Sameer Paithankar

656 total citations
8 papers, 354 citations indexed

About

Sameer Paithankar is a scholar working on Molecular Biology, Genetics and Computer Networks and Communications. According to data from OpenAlex, Sameer Paithankar has authored 8 papers receiving a total of 354 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Computer Networks and Communications. Recurrent topics in Sameer Paithankar's work include Genomics and Rare Diseases (3 papers), Scientific Computing and Data Management (2 papers) and Parasitic Diseases Research and Treatment (1 paper). Sameer Paithankar is often cited by papers focused on Genomics and Rare Diseases (3 papers), Scientific Computing and Data Management (2 papers) and Parasitic Diseases Research and Treatment (1 paper). Sameer Paithankar collaborates with scholars based in United States, Netherlands and India. Sameer Paithankar's co-authors include Aleksandar Milosavljevic, Cristian Coarfa, Andrew R. Jackson, Fuli Yu, Danny Challis, Uday S. Evani, Jin Yu, Richard A. Gibbs, Kevin Riehle and Viren Amin and has published in prestigious journals such as Nature Communications, BMC Bioinformatics and BMC Genomics.

In The Last Decade

Sameer Paithankar

8 papers receiving 346 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sameer Paithankar United States 7 246 142 101 24 21 8 354
Chuan Chen China 11 272 1.1× 108 0.8× 130 1.3× 23 1.0× 18 0.9× 26 383
Jennifer Li‐Pook‐Than Canada 7 363 1.5× 113 0.8× 48 0.5× 21 0.9× 25 1.2× 7 468
Sirawit Ittisoponpisan United Kingdom 5 226 0.9× 113 0.8× 20 0.2× 18 0.8× 17 0.8× 7 352
Justin Warner United Kingdom 4 322 1.3× 89 0.6× 123 1.2× 14 0.6× 11 0.5× 6 423
Pauline A. Fujita United States 5 432 1.8× 103 0.7× 84 0.8× 21 0.9× 18 0.9× 5 537
Maayan Amit Israel 8 578 2.3× 62 0.4× 84 0.8× 19 0.8× 9 0.4× 8 656
Kenneth Kuhn United States 7 365 1.5× 162 1.1× 21 0.2× 17 0.7× 24 1.1× 7 527
Jaehoon Lee South Korea 9 323 1.3× 86 0.6× 46 0.5× 45 1.9× 38 1.8× 16 431
Dan Sheppard United Kingdom 5 214 0.9× 107 0.8× 58 0.6× 17 0.7× 13 0.6× 11 376
Florence Salmon United Kingdom 8 259 1.1× 227 1.6× 44 0.4× 13 0.5× 28 1.3× 12 459

Countries citing papers authored by Sameer Paithankar

Since Specialization
Citations

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

Fields of papers citing papers by Sameer Paithankar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sameer Paithankar

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

All Works

8 of 8 papers shown
1.
Patel, Ronak Y., Andrew R. Jackson, Chris Bizon, et al.. (2018). ClinGen Allele Registry links information about genetic variants. Human Mutation. 39(11). 1690–1701. 25 indexed citations
2.
Amin, Viren, R. Alan Harris, Vitor Onuchic, et al.. (2015). Epigenomic footprints across 111 reference epigenomes reveal tissue-specific epigenetic regulation of lincRNAs. Nature Communications. 6(1). 6370–6370. 57 indexed citations
3.
Coarfa, Cristian, Andrew P. Jackson, Arpit Tandon, et al.. (2014). Analysis of interactions between the epigenome and structural mutability of the genome using Genboree workbench tools. BMC Bioinformatics. 15(S7). S2–S2. 17 indexed citations
4.
Riehle, Kevin, Cristian Coarfa, Andrew P. Jackson, et al.. (2012). The Genboree Microbiome Toolset and the analysis of 16S rRNA microbial sequences. BMC Bioinformatics. 13(S13). S11–S11. 44 indexed citations
5.
Challis, Danny, Jin Yu, Uday S. Evani, et al.. (2012). An integrative variant analysis suite for whole exome next-generation sequencing data. BMC Bioinformatics. 13(1). 8–8. 160 indexed citations
6.
Evani, Uday S., Danny Challis, Jin Yu, et al.. (2012). Atlas2 Cloud: a framework for personal genome analysis in the cloud. BMC Genomics. 13(S6). 39 indexed citations
7.
Evani, Uday S., Danny Challis, Jin Yu, et al.. (2011). Enabling Atlas2 personal genome analysis on the cloud. 26. 117–120. 1 indexed citations
8.
Dangi, Anil, Sameer Paithankar, Mahendra Pratap Singh, et al.. (2009). Tetracycline treatment targeting Wolbachia affects expression of an array of proteins in Brugia malayi parasite. PROTEOMICS. 9(17). 4192–4208. 11 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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