Tejasvi Niranjan

726 total citations
11 papers, 477 citations indexed

About

Tejasvi Niranjan is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Tejasvi Niranjan has authored 11 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Tejasvi Niranjan's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Chromosomal and Genetic Variations (2 papers). Tejasvi Niranjan is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Chromosomal and Genetic Variations (2 papers). Tejasvi Niranjan collaborates with scholars based in United States, Australia and Russia. Tejasvi Niranjan's co-authors include Tao Wang, Charles E. Schwartz, Sarah J. Wheelan, Cindy Skinner, Curt I. Civin, Jef D. Boeke, Tao Wang, Jared P. Steranka, Peilin Shen and Hongkai Ji and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Tejasvi Niranjan

11 papers receiving 471 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tejasvi Niranjan United States 8 380 161 142 64 59 11 477
Dayong Qiu United States 6 287 0.8× 49 0.3× 34 0.2× 45 0.7× 37 0.6× 7 410
David Yao United States 10 479 1.3× 56 0.3× 95 0.7× 34 0.5× 96 1.6× 12 642
Seungshin Ha United States 7 220 0.6× 29 0.2× 83 0.6× 50 0.8× 24 0.4× 9 315
Stefan R. Kassabov United States 8 700 1.8× 81 0.5× 51 0.4× 89 1.4× 37 0.6× 12 804
Sailaja Peddada United States 5 431 1.1× 29 0.2× 394 2.8× 28 0.4× 28 0.5× 7 569
Stephen Tran United States 9 634 1.7× 38 0.2× 117 0.8× 57 0.9× 33 0.6× 11 768
Katarina Kapuralin Croatia 7 234 0.6× 31 0.2× 35 0.2× 186 2.9× 47 0.8× 12 400
Pascal E. D. Lachance Canada 6 439 1.2× 40 0.2× 42 0.3× 175 2.7× 63 1.1× 9 550
Juergen K. Naggert United States 6 334 0.9× 63 0.4× 105 0.7× 74 1.2× 18 0.3× 8 547

Countries citing papers authored by Tejasvi Niranjan

Since Specialization
Citations

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

Fields of papers citing papers by Tejasvi Niranjan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tejasvi Niranjan

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

All Works

11 of 11 papers shown
1.
Niranjan, Tejasvi, Melanie May, Patrick Tarpey, et al.. (2019). Dysregulations of sonic hedgehog signaling in MED12‐related X‐linked intellectual disability disorders. Molecular Genetics & Genomic Medicine. 7(4). e00569–e00569. 10 indexed citations
2.
Pirooznia, Mehdi, Tejasvi Niranjan, Yun-Ching Chen, et al.. (2019). Affected Sib-Pair Analyses Identify Signaling Networks Associated With Social Behavioral Deficits in Autism. Frontiers in Genetics. 10. 1186–1186. 1 indexed citations
3.
Stavrovskaya, Elena, Tejasvi Niranjan, Elana J. Fertig, et al.. (2017). StereoGene: rapid estimation of genome-wide correlation of continuous or interval feature data. Bioinformatics. 33(20). 3158–3165. 14 indexed citations
4.
Niranjan, Tejasvi, Chin Fen Teo, Melanie May, et al.. (2017). Identification and characterization of a missense mutation in the O-linked β-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability. Journal of Biological Chemistry. 292(21). 8948–8963. 80 indexed citations
5.
Chiu, Shu‐Ling, Graham H. Diering, Bing Ye, et al.. (2017). GRASP1 Regulates Synaptic Plasticity and Learning through Endosomal Recycling of AMPA Receptors. Neuron. 93(6). 1405–1419.e8. 45 indexed citations
6.
Niranjan, Tejasvi, et al.. (2016). A distinct X‐linked syndrome involving joint contractures, keloids, large optic cup‐to‐disc ratio, and renal stones results from a filamin A (FLNA) mutation. American Journal of Medical Genetics Part A. 170(4). 881–890. 10 indexed citations
7.
Niranjan, Tejasvi, Cindy Skinner, Melanie May, et al.. (2015). Affected Kindred Analysis of Human X Chromosome Exomes to Identify Novel X-Linked Intellectual Disability Genes. PLoS ONE. 10(2). e0116454–e0116454. 39 indexed citations
8.
Niranjan, Tejasvi, Héctor Corrada Bravo, Margaret A. Taub, et al.. (2011). Effective detection of rare variants in pooled DNA samples using Cross-pool tailcurve analysis. Genome biology. 12(9). R93–R93. 7 indexed citations
9.
Mejı́as, Rebeca, Victor Anggono, Tejasvi Niranjan, et al.. (2011). Gain-of-function glutamate receptor interacting protein 1 variants alter GluA2 recycling and surface distribution in patients with autism. Proceedings of the National Academy of Sciences. 108(12). 4920–4925. 73 indexed citations
10.
Niranjan, Tejasvi, Héctor Corrada Bravo, Margaret A. Taub, et al.. (2011). Effective detection of rare variants in pooled DNA samples using cross-pool tail-curve analysis. Genome biology. 12(S1). 1 indexed citations
11.
Huang, Cheng Ran Lisa, A.M. Schneider, Tejasvi Niranjan, et al.. (2010). Mobile Interspersed Repeats Are Major Structural Variants in the Human Genome. Cell. 141(7). 1171–1182. 197 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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