Snehalata A. Pawar

648 total citations
20 papers, 525 citations indexed

About

Snehalata A. Pawar is a scholar working on Radiology, Nuclear Medicine and Imaging, Molecular Biology and Oncology. According to data from OpenAlex, Snehalata A. Pawar has authored 20 papers receiving a total of 525 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Radiology, Nuclear Medicine and Imaging, 9 papers in Molecular Biology and 5 papers in Oncology. Recurrent topics in Snehalata A. Pawar's work include Effects of Radiation Exposure (10 papers), Ubiquitin and proteasome pathways (4 papers) and DNA Repair Mechanisms (3 papers). Snehalata A. Pawar is often cited by papers focused on Effects of Radiation Exposure (10 papers), Ubiquitin and proteasome pathways (4 papers) and DNA Repair Mechanisms (3 papers). Snehalata A. Pawar collaborates with scholars based in United States, Germany and Taiwan. Snehalata A. Pawar's co-authors include Viraj Deshpande, Martin Hauer‐Jensen, Esta Sterneck, Marilyn N. Szentirmay, Sudeep Banerjee, Michèle Sawadogo, Shikha Sharan, Tapasree Roy Sarkar, Sumit K. Shah and Kimberly J. Krager and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Snehalata A. Pawar

20 papers receiving 521 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Snehalata A. Pawar United States	14	286	109	82	67	59	20	525
Ognoon Mungunsukh United States	15	228 0.8×	143 1.3×	51 0.6×	63 0.9×	106 1.8×	25	596
Carly M. Sayers United States	9	307 1.1×	85 0.8×	58 0.7×	88 1.3×	108 1.8×	12	540
Ming Yan China	14	248 0.9×	86 0.8×	86 1.0×	96 1.4×	45 0.8×	51	546
Sangeeta Adak United States	12	214 0.7×	46 0.4×	70 0.9×	39 0.6×	32 0.5×	18	406
Karunakaran Coral India	17	192 0.7×	69 0.6×	64 0.8×	56 0.8×	27 0.5×	28	504
Emiko Yamada Japan	17	344 1.2×	97 0.9×	92 1.1×	111 1.7×	80 1.4×	38	743
Lu Xue China	10	181 0.6×	84 0.8×	71 0.9×	52 0.8×	56 0.9×	34	513
Suguru Matsumoto Japan	11	308 1.1×	83 0.8×	65 0.8×	25 0.4×	43 0.7×	25	576
Benito Casanova Spain	13	307 1.1×	50 0.5×	129 1.6×	66 1.0×	29 0.5×	16	751
Hua Gu China	13	216 0.8×	56 0.5×	115 1.4×	57 0.9×	54 0.9×	32	487

Countries citing papers authored by Snehalata A. Pawar

Since Specialization

Citations

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

Fields of papers citing papers by Snehalata A. Pawar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Snehalata A. Pawar. 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 Snehalata A. Pawar. The network helps show where Snehalata A. Pawar may publish in the future.

Co-authorship network of co-authors of Snehalata A. Pawar

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

All Works

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20 of 20 papers shown

Gawali, Basveshwar, Vijayalakshmi Sridharan, Kimberly J. Krager, Marjan Boerma, & Snehalata A. Pawar. (2023). TLR4—A Pertinent Player in Radiation-Induced Heart Disease?. Genes. 14(5). 1002–1002. 10 indexed citations

Sridharan, Vijayalakshmi, Kimberly J. Krager, Snehalata A. Pawar, et al.. (2023). Effects of Whole and Partial Heart Irradiation on Collagen, Mast Cells, and Toll-like Receptor 4 in the Mouse Heart. Cancers. 15(2). 406–406. 2 indexed citations

Boerma, Marjan, Vijayalakshmi Sridharan, Kimberly J. Krager, & Snehalata A. Pawar. (2022). Small animal models of localized heart irradiation. Methods in cell biology. 168. 221–234. 4 indexed citations

Pietras, Eric M., et al.. (2021). Analysis of Radiation‐Induced Changes in Cell Cycle and DNA Damage of Murine Hematopoietic Stem Cells by Multi‐Color Flow Cytometry. Current Protocols. 1(8). 1 indexed citations

Sadhukhan, Ratan, Sarita Garg, Reid D. Landes, et al.. (2020). Simultaneous exposure to chronic irradiation and simulated microgravity differentially alters immune cell phenotype in mouse thymus and spleen. Life Sciences in Space Research. 28. 66–73. 13 indexed citations

Garg, Sarita, Ratan Sadhukhan, Sudeep Banerjee, et al.. (2019). Gamma-Tocotrienol Protects the Intestine from Radiation Potentially by Accelerating Mesenchymal Immune Cell Recovery. Antioxidants. 8(3). 57–57. 13 indexed citations

Banerjee, Sudeep, Qiang Fu, Sumit K. Shah, et al.. (2019). C/EBPδ protects from radiation-induced intestinal injury and sepsis by suppression of inflammatory and nitrosative stress. Scientific Reports. 9(1). 13953–13953. 24 indexed citations

Banerjee, Sudeep, Tyler Alexander, Thomas Groves, et al.. (2019). Loss of C/EBPδ Exacerbates Radiation-Induced Cognitive Decline in Aged Mice due to Impaired Oxidative Stress Response. International Journal of Molecular Sciences. 20(4). 885–885. 13 indexed citations

Banerjee, Sudeep, Sumit K. Shah, Stepan Melnyk, et al.. (2018). Cebpd Is Essential for Gamma-Tocotrienol Mediated Protection against Radiation-Induced Hematopoietic and Intestinal Injury. Antioxidants. 7(4). 55–55. 17 indexed citations

10.

Banerjee, Sudeep, Nükhet Aykin‐Burns, Kimberly J. Krager, et al.. (2016). Loss of C/EBPδ enhances IR-induced cell death by promoting oxidative stress and mitochondrial dysfunction. Free Radical Biology and Medicine. 99. 296–307. 35 indexed citations

11.

Pawar, Snehalata A., Lijian Shao, Jianhui Chang, et al.. (2014). C/EBPδ Deficiency Sensitizes Mice to Ionizing Radiation-Induced Hematopoietic and Intestinal Injury. PLoS ONE. 9(4). e94967–e94967. 26 indexed citations

12.

Aykin‐Burns, Nükhet, et al.. (2014). C/EBPδ Modulates Reactive Oxygen Species to Protect againstIR-Induced Cell Death. Free Radical Biology and Medicine. 76. S145–S145. 1 indexed citations

13.

Pathak, Rupak, Snehalata A. Pawar, Qiang Fu, et al.. (2013). Characterization of Transgenic Gfrp Knock-In Mice: Implications for Tetrahydrobiopterin in Modulation of Normal Tissue Radiation Responses. Antioxidants and Redox Signaling. 20(9). 1436–1446. 22 indexed citations

14.

Geiger, Hartmut, Snehalata A. Pawar, E. J. Kerschen, et al.. (2012). Pharmacological targeting of the thrombomodulin–activated protein C pathway mitigates radiation toxicity. Nature Medicine. 18(7). 1123–1129. 86 indexed citations

15.

Sarkar, Tapasree Roy, Shikha Sharan, Jun Wang, et al.. (2011). Identification of a Src Tyrosine Kinase/SIAH2 E3 Ubiquitin Ligase Pathway That Regulates C/EBPδ Expression and Contributes to Transformation of Breast Tumor Cells. Molecular and Cellular Biology. 32(2). 320–332. 57 indexed citations

16.

Pawar, Snehalata A., Tapasree Roy Sarkar, Kuppusamy Balamurugan, et al.. (2010). C/EBPδ targets cyclin D1 for proteasome-mediated degradation via induction of CDC27/APC3 expression. Proceedings of the National Academy of Sciences. 107(20). 9210–9215. 59 indexed citations

17.

Szentirmay, Marilyn N., Snehalata A. Pawar, Mario Sirito, et al.. (2005). Tumor-suppression function of transcription factor USF2 in prostate carcinogenesis. Oncogene. 25(4). 579–587. 29 indexed citations

18.

Pawar, Snehalata A., Marilyn N. Szentirmay, Heiko Hermeking, & Michèle Sawadogo. (2004). Evidence for a cancer-specific switch at the CDK4 promoter with loss of control by both USF and c-Myc. Oncogene. 23(36). 6125–6135. 29 indexed citations

19.

Szentirmay, Marilyn N., Huixin Yang, Snehalata A. Pawar, Charles Vinson, & Michèle Sawadogo. (2003). The IGF2 Receptor Is a USF2-specific Target in Nontumorigenic Mammary Epithelial Cells but Not in Breast Cancer Cells. Journal of Biological Chemistry. 278(39). 37231–37240. 33 indexed citations

20.

Pawar, Snehalata A. & Viraj Deshpande. (2000). Characterization of acid‐induced unfolding intermediates of glucose/xylose isomerase. European Journal of Biochemistry. 267(21). 6331–6338. 51 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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