Anand Giddabasappa

848 total citations
29 papers, 559 citations indexed

About

Anand Giddabasappa is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Oncology. According to data from OpenAlex, Anand Giddabasappa has authored 29 papers receiving a total of 559 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Radiology, Nuclear Medicine and Imaging and 7 papers in Oncology. Recurrent topics in Anand Giddabasappa's work include Retinal Development and Disorders (6 papers), Heavy Metal Exposure and Toxicity (5 papers) and CAR-T cell therapy research (3 papers). Anand Giddabasappa is often cited by papers focused on Retinal Development and Disorders (6 papers), Heavy Metal Exposure and Toxicity (5 papers) and CAR-T cell therapy research (3 papers). Anand Giddabasappa collaborates with scholars based in United States, United Kingdom and Switzerland. Anand Giddabasappa's co-authors include Donald A. Fox, J. E. Johnson, Jeetendra Eswaraka, K. Pothakos, J. Leigh Leasure, Weimin Xiao, James T. Dalton, Andrew D. White, Guy Perkins and Mark H. Ellisman and has published in prestigious journals such as PLoS ONE, Environmental Health Perspectives and Journal of Controlled Release.

In The Last Decade

Anand Giddabasappa

26 papers receiving 553 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anand Giddabasappa United States 11 306 118 114 94 89 29 559
Kosuke Noda Japan 8 217 0.7× 13 0.1× 226 2.0× 151 1.6× 50 0.6× 13 504
Mikiro Mori Japan 15 452 1.5× 8 0.1× 226 2.0× 134 1.4× 130 1.5× 35 836
Nomingerel Tserentsoodol United States 13 426 1.4× 7 0.1× 282 2.5× 121 1.3× 72 0.8× 19 677
Jing Bao China 11 158 0.5× 46 0.4× 82 0.7× 103 1.1× 6 0.1× 14 504
Katsuaki Miki Japan 12 293 1.0× 6 0.1× 209 1.8× 86 0.9× 66 0.7× 23 491
Munmun Chakraborty United States 13 450 1.5× 9 0.1× 51 0.4× 24 0.3× 130 1.5× 28 647
Yali Xu China 12 192 0.6× 15 0.1× 14 0.1× 26 0.3× 72 0.8× 26 454
Jianhong An China 15 251 0.8× 6 0.1× 148 1.3× 201 2.1× 42 0.5× 29 599
Séverine Leclerc Canada 13 351 1.1× 8 0.1× 17 0.1× 14 0.1× 79 0.9× 21 643
Małgorzata Goralska United States 12 242 0.8× 12 0.1× 48 0.4× 21 0.2× 19 0.2× 19 411

Countries citing papers authored by Anand Giddabasappa

Since Specialization
Citations

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

Fields of papers citing papers by Anand Giddabasappa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anand Giddabasappa

This figure shows the co-authorship network connecting the top 25 collaborators of Anand Giddabasappa. A scholar is included among the top collaborators of Anand Giddabasappa 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 Anand Giddabasappa. Anand Giddabasappa 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.
Colburg, Deana R.C., Ophir Vermesh, Anthony Chen, et al.. (2025). Advancing In Vivo Detection of T-Cell Function: Development and Preclinical Evaluation of 89Zr-Ivuxolimab, a Human OX40 PET Tracer. Journal of Nuclear Medicine. 66(9). 1449–1457.
2.
Jové, Veronica, Heather E. Wheeler, David R. Healy, et al.. (2024). Type I interferon regulation by USP18 is a key vulnerability in cancer. iScience. 27(4). 109593–109593. 6 indexed citations
3.
4.
Rakhilin, Nikolai, Bing Yang, Mary E. Spilker, et al.. (2023). Volumetric imaging of optically cleared and fluorescently labeled animal tissue (VIOLA) for quantifying the 3D biodistribution of nanoparticles at cellular resolution in tumor tissue. Journal of Controlled Release. 354. 244–259. 3 indexed citations
5.
Lee, Catherine, Ziyue Karen Jiang, Simon Planken, et al.. (2023). Efficacy and Imaging-Enabled Pharmacodynamic Profiling of KRAS G12C Inhibitors in Xenograft and Genetically Engineered Mouse Models of Cancer. Molecular Cancer Therapeutics. 22(7). 891–900.
6.
Montgomery, Mary K., et al.. (2023). Applying deep learning to segmentation of murine lung tumors in pre-clinical micro-computed tomography. Translational Oncology. 40. 101833–101833. 3 indexed citations
7.
Montgomery, Mary K., John David, Sripad Ram, et al.. (2021). Mouse lung automated segmentation tool for quantifying lung tumors after micro-computed tomography. PLoS ONE. 16(6). e0252950–e0252950. 10 indexed citations
8.
Gupta, Parul, Ziyue Karen Jiang, Bing Yang, et al.. (2021). Targeting and pharmacology of an anti-IL13Rα2 antibody and antibody-drug conjugate in a melanoma xenograft model. mAbs. 13(1). 1958662–1958662. 9 indexed citations
9.
Hwang, Seo‐Kyoung, et al.. (2021). Automated monitoring of respiratory rate as a novel humane endpoint: A refinement in mouse metastatic lung cancer models. PLoS ONE. 16(9). e0257694–e0257694. 7 indexed citations
10.
Giddabasappa, Anand, Vijay Gupta, Parul Gupta, et al.. (2016). Biodistribution and Targeting of Anti-5T4 Antibody–Drug Conjugate Using Fluorescence Molecular Tomography. Molecular Cancer Therapeutics. 15(10). 2530–2540. 26 indexed citations
11.
Giddabasappa, Anand, Hovhannes J. Gukasyan, D.A. Paterson, et al.. (2016). Axitinib inhibits retinal and choroidal neovascularization in in vitro and in vivo models. Experimental Eye Research. 145. 373–379. 50 indexed citations
12.
Peng, Qinghai, Anand Giddabasappa, John David, et al.. (2016). Editor's Highlight: Plasma miR-183/96/182 Cluster and miR-124 are Promising Biomarkers of Rat Retinal Toxicity. Toxicological Sciences. 152(2). 273–283. 14 indexed citations
13.
Eswaraka, Jeetendra, Anand Giddabasappa, Guangzhou Han, et al.. (2014). Axitinib and crizotinib combination therapy inhibits bone loss in a mouse model of castration resistant prostate cancer. BMC Cancer. 14(1). 742–742. 15 indexed citations
14.
Giddabasappa, Anand, Jeetendra Eswaraka, Christina M. Barrett, et al.. (2012). β-LGND2, an ERβ Selective Agonist, Inhibits Pathologic Retinal Neovascularization. Investigative Ophthalmology & Visual Science. 53(8). 5066–5066. 10 indexed citations
15.
Giddabasappa, Anand, et al.. (2010). Developmental Changes in Retinal Calcium (Ca2+) Signaling Mediate Increased Retinal Progenitor Cell (RPC) Proliferation During Gestational Lead Exposure (GLE). Investigative Ophthalmology & Visual Science. 51(13). 5948–5948. 1 indexed citations
16.
Giddabasappa, Anand, et al.. (2010). Low-Level Gestational Lead Exposure Increases Retinal Progenitor Cell Proliferation and Rod Photoreceptor and Bipolar Cell Neurogenesis in Mice. Environmental Health Perspectives. 119(1). 71–77. 19 indexed citations
17.
Giddabasappa, Anand, Christina M. Barrett, Christopher C. Coss, et al.. (2010). GTx-822, an ERβ-Selective Agonist, Protects Retinal Pigment Epithelium (ARPE-19) from Oxidative Stress by Activating MAPK and PI3-K Pathways. Investigative Ophthalmology & Visual Science. 51(11). 5934–5934. 9 indexed citations
18.
Leasure, J. Leigh, et al.. (2007). Low-Level Human Equivalent Gestational Lead Exposure Produces Sex-Specific Motor and Coordination Abnormalities and Late-Onset Obesity in Year-Old Mice. Environmental Health Perspectives. 116(3). 355–361. 108 indexed citations
19.
Johnson, J. E., et al.. (2005). Gestational Lead Exposure Switches Cell Fate Specification and Increases Proliferation in the Developing Mouse Retina. Investigative Ophthalmology & Visual Science. 46(13). 589–589. 1 indexed citations
20.
Johnson, J. E., et al.. (2005). Mouse Retinal Dopaminergic Amacrine Cell Density and Distribution Are Selectively Altered by Gestational Lead Exposure. Investigative Ophthalmology & Visual Science. 46(13). 567–567. 1 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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