Vineeta Bajaj

417 total citations
9 papers, 325 citations indexed

About

Vineeta Bajaj is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Vineeta Bajaj has authored 9 papers receiving a total of 325 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 Pediatrics, Perinatology and Child Health. Recurrent topics in Vineeta Bajaj's work include Epigenetics and DNA Methylation (4 papers), Genetic Syndromes and Imprinting (3 papers) and RNA modifications and cancer (2 papers). Vineeta Bajaj is often cited by papers focused on Epigenetics and DNA Methylation (4 papers), Genetic Syndromes and Imprinting (3 papers) and RNA modifications and cancer (2 papers). Vineeta Bajaj collaborates with scholars based in United States, India and Israel. Vineeta Bajaj's co-authors include Karen S. Christopherson, Melanie R. Mark, Paul J. Godowski, Arun Kumar, Abdullah Mahmood Ali, Izabela A. Malinowska, Paul D. Kaufman, David J. Kwiatkowski, Laura E. MacConaill and James Spoonamore and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Gene.

In The Last Decade

Vineeta Bajaj

9 papers receiving 313 citations

Peers

Vineeta Bajaj
Mark E. Ireland United States
Julia M. D. Grandjean United States
Nagarekha Pasupuleti United States
Anne B. Carlson United States
V. Rao United States
Mark E. Ireland United States
Vineeta Bajaj
Citations per year, relative to Vineeta Bajaj Vineeta Bajaj (= 1×) peers Mark E. Ireland

Countries citing papers authored by Vineeta Bajaj

Since Specialization
Citations

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

Fields of papers citing papers by Vineeta Bajaj

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vineeta Bajaj

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

All Works

9 of 9 papers shown
1.
Bajaj, Vineeta, et al.. (2021). Evaluation of Hsp90 and mTOR inhibitors as potential drugs for the treatment of TSC1/TSC2 deficient cancer. PLoS ONE. 16(4). e0248380–e0248380. 8 indexed citations
2.
Ichikawa, Yuichi, Caitlin Connelly, Thomas C. R. Miller, et al.. (2017). A synthetic biology approach to probing nucleosome symmetry. eLife. 6. 18 indexed citations
3.
Bajaj, Vineeta, et al.. (2013). A small molecule inhibitor of fungal histone acetyltransferase Rtt109. Bioorganic & Medicinal Chemistry Letters. 23(10). 2853–2859. 29 indexed citations
4.
Qin, Wei, Vineeta Bajaj, Izabela A. Malinowska, et al.. (2011). Angiomyolipoma Have Common Mutations in TSC2 but No Other Common Genetic Events. PLoS ONE. 6(9). e24919–e24919. 48 indexed citations
5.
Bajaj, Vineeta, Pooja Singhmar, & Arun Kumar. (2008). Promoter characterization and regulation of expression of an imprinted gene SLC22A18AS. Gene. 424(1-2). 40–47. 9 indexed citations
6.
Ali, Abdullah Mahmood, Vineeta Bajaj, KS Gopinath, & Arun Kumar. (2008). Characterization of the human SLC22A18 gene promoter and its regulation by the transcription factor Sp1. Gene. 429(1-2). 37–43. 8 indexed citations
7.
Kumar, Arun, et al.. (2007). Role of CYP1B1, MYOC, OPTN, and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients.. PubMed. 13. 667–76. 72 indexed citations
8.
Bajaj, Vineeta, et al.. (2004). Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5. BMC Genetics. 5(1). 13–13. 7 indexed citations
9.
Christopherson, Karen S., Melanie R. Mark, Vineeta Bajaj, & Paul J. Godowski. (1992). Ecdysteroid-dependent regulation of genes in mammalian cells by a Drosophila ecdysone receptor and chimeric transactivators.. Proceedings of the National Academy of Sciences. 89(14). 6314–6318. 126 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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