Sunitha Nallur

1.9k total citations
20 papers, 855 citations indexed

About

Sunitha Nallur is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Sunitha Nallur has authored 20 papers receiving a total of 855 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 11 papers in Cancer Research and 3 papers in Oncology. Recurrent topics in Sunitha Nallur's work include MicroRNA in disease regulation (11 papers), RNA modifications and cancer (4 papers) and Cancer-related molecular mechanisms research (4 papers). Sunitha Nallur is often cited by papers focused on MicroRNA in disease regulation (11 papers), RNA modifications and cancer (4 papers) and Cancer-related molecular mechanisms research (4 papers). Sunitha Nallur collaborates with scholars based in United States, Ireland and Netherlands. Sunitha Nallur's co-authors include Joanne B. Weidhaas, Frank J. Slack, Trupti Paranjape, Erin F. Gillespie, Aurora Esquela‐Kerscher, Robert L. Ullrich, Masaomi Kato, David Tuck, David M. Eisenmann and Justin M. Holub and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Journal of Clinical Oncology.

In The Last Decade

Sunitha Nallur

19 papers receiving 839 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sunitha Nallur United States 15 638 575 99 56 50 20 855
Trupti Paranjape United States 13 863 1.4× 824 1.4× 91 0.9× 23 0.4× 46 0.9× 17 1.1k
Ruyi Xie China 8 288 0.5× 213 0.4× 113 1.1× 9 0.2× 29 0.6× 13 410
John M. Hinz United States 21 1.1k 1.7× 312 0.5× 198 2.0× 28 0.5× 72 1.4× 30 1.2k
Carlos Stahlhut United States 9 781 1.2× 680 1.2× 44 0.4× 18 0.3× 45 0.9× 15 951
Eelke Gort Netherlands 12 338 0.5× 197 0.3× 200 2.0× 20 0.4× 63 1.3× 29 561
Silvia Viaggi Italy 15 366 0.6× 271 0.5× 134 1.4× 8 0.1× 50 1.0× 35 664
Huacheng Luo United States 14 874 1.4× 274 0.5× 98 1.0× 19 0.3× 27 0.5× 29 1.1k
Paul Finnon United Kingdom 17 576 0.9× 362 0.6× 119 1.2× 32 0.6× 236 4.7× 32 1.1k
Kwon Tae You South Korea 13 651 1.0× 196 0.3× 97 1.0× 12 0.2× 66 1.3× 13 887
Delphine T. Marie‐Egyptienne Canada 9 378 0.6× 240 0.4× 183 1.8× 12 0.2× 55 1.1× 11 580

Countries citing papers authored by Sunitha Nallur

Since Specialization
Citations

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

Fields of papers citing papers by Sunitha Nallur

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sunitha Nallur

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

All Works

20 of 20 papers shown
1.
Nallur, Sunitha, et al.. (2020). Genome-Wide Identification of Genes Involved in General Acid Stress and Fluoride Toxicity in Saccharomyces cerevisiae. Frontiers in Microbiology. 11. 1410–1410. 16 indexed citations
2.
Hiller, David A., et al.. (2020). The Positively Charged Active Site of the Bacterial Toxin RelE Causes a Large Shift in the General Base pKa. Biochemistry. 59(17). 1665–1671. 3 indexed citations
3.
Hui, Pei, Stefan Gysler, Mohamed Uduman, et al.. (2018). MicroRNA signatures discriminate between uterine and ovarian serous carcinomas. Human Pathology. 76. 133–140. 8 indexed citations
4.
Berbasova, Tetyana, Sunitha Nallur, Kathryn D. Smith, et al.. (2017). Fluoride export (FEX) proteins from fungi, plants and animals are 'single barreled' channels containing one functional and one vestigial ion pore. PLoS ONE. 12(5). e0177096–e0177096. 28 indexed citations
5.
Salzman, David W., Kotoka Nakamura, Sunitha Nallur, et al.. (2016). miR-34 activity is modulated through 5′-end phosphorylation in response to DNA damage. Nature Communications. 7(1). 10954–10954. 66 indexed citations
6.
Metheetrairut, Chanatip, Brian D. Adams, Sunitha Nallur, Joanne B. Weidhaas, & Frank J. Slack. (2016). cel-mir-237 and its homologue, hsa-miR-125b, modulate the cellular response to ionizing radiation. Oncogene. 36(4). 512–524. 20 indexed citations
7.
McVeigh, Terri, Michael J. Kerin, David W. Salzman, et al.. (2015). Estrogen withdrawal, increased breast cancer risk and the KRAS-variant. Cell Cycle. 14(13). 2091–2099. 10 indexed citations
8.
Chung, Christine H., Ju‐Whei Lee, Robert J.C. Slebos, et al.. (2014). A 3′-UTR KRAS-variant is associated with cisplatin resistance in patients with recurrent and/or metastatic head and neck squamous cell carcinoma. Annals of Oncology. 25(11). 2230–2236. 32 indexed citations
9.
Paranjape, Trupti, Carlos Stahlhut, Terri McVeigh, et al.. (2014). Targeted resequencing of the microRNAome and 3′UTRome reveals functional germline DNA variants with altered prevalence in epithelial ovarian cancer. Oncogene. 34(16). 2125–2137. 24 indexed citations
10.
Weidhaas, Joanne B., Ju‐Whei Lee, Robbert J.C. Slebos, et al.. (2013). Association of the 3'-untranslated region KRAS-variant with cisplatin resistance in patients with recurrent and/or metastatic head and neck squamous cell carcinoma.. Journal of Clinical Oncology. 31(15_suppl). 6016–6016. 2 indexed citations
11.
Kundu, Samrat T., Sunitha Nallur, Trupti Paranjape, et al.. (2012). KRAS alleles: The LCS6 3′UTR variant and KRAS coding sequence mutations in the NCI-60 panel. Cell Cycle. 11(2). 361–366. 21 indexed citations
12.
Smits, Kim M., Trupti Paranjape, Sunitha Nallur, et al.. (2011). A Let-7 MicroRNA SNP in the KRAS 3′UTR Is Prognostic in Early-Stage Colorectal Cancer. Clinical Cancer Research. 17(24). 7723–7731. 85 indexed citations
13.
Paranjape, Trupti, Helen Heneghan, Robert Lindner, et al.. (2011). A 3′-untranslated region KRAS variant and triple-negative breast cancer: a case-control and genetic analysis. The Lancet Oncology. 12(4). 377–386. 101 indexed citations
14.
Chan, Elcie, Rajeshvari Patel, Sunitha Nallur, et al.. (2011). MicroRNA signatures differentiate melanoma subtypes. Cell Cycle. 10(11). 1845–1852. 75 indexed citations
15.
Weidhaas, Joanne B., Frank J. Slack, Nicola Miller, et al.. (2011). Association between KRAS rs61764370 and triple-negative breast cancer—a false positive? – Authors' reply. The Lancet Oncology. 12(8). 724–724.
16.
Godshalk, Sirie E., Trupti Paranjape, Sunitha Nallur, et al.. (2010). A Variant in a MicroRNA complementary site in the 3′ UTR of the KIT oncogene increases risk of acral melanoma. Oncogene. 30(13). 1542–1550. 32 indexed citations
17.
Ratner, Elena, David Tuck, C. Richter, et al.. (2010). MicroRNA signatures differentiate uterine cancer tumor subtypes. Gynecologic Oncology. 118(3). 251–257. 78 indexed citations
18.
Kato, Masaomi, Trupti Paranjape, Robert L. Ullrich, et al.. (2009). The mir-34 microRNA is required for the DNA damage response in vivo in C. elegans and in vitro in human breast cancer cells. Oncogene. 28(25). 2419–2424. 188 indexed citations
19.
Weidhaas, Joanne B., David M. Eisenmann, Justin M. Holub, & Sunitha Nallur. (2006). A Conserved RAS/Mitogen-Activated Protein Kinase Pathway Regulates DNA Damage–Induced Cell Death Postirradiation in Radelegans. Cancer Research. 66(21). 10434–10438. 23 indexed citations
20.
Weidhaas, Joanne B., David M. Eisenmann, Justin M. Holub, & Sunitha Nallur. (2006). A Caenorhabditis elegans tissue model of radiation-induced reproductive cell death. Proceedings of the National Academy of Sciences. 103(26). 9946–9951. 43 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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