Sangeetha Sukumari‐Ramesh

1.4k total citations
29 papers, 1.1k citations indexed

About

Sangeetha Sukumari‐Ramesh is a scholar working on Neurology, Molecular Biology and Epidemiology. According to data from OpenAlex, Sangeetha Sukumari‐Ramesh has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 15 papers in Molecular Biology and 7 papers in Epidemiology. Recurrent topics in Sangeetha Sukumari‐Ramesh's work include Intracerebral and Subarachnoid Hemorrhage Research (15 papers), Neuroinflammation and Neurodegeneration Mechanisms (6 papers) and Kruppel-like factors research (6 papers). Sangeetha Sukumari‐Ramesh is often cited by papers focused on Intracerebral and Subarachnoid Hemorrhage Research (15 papers), Neuroinflammation and Neurodegeneration Mechanisms (6 papers) and Kruppel-like factors research (6 papers). Sangeetha Sukumari‐Ramesh collaborates with scholars based in United States, Czechia and India. Sangeetha Sukumari‐Ramesh's co-authors include Krishnan M. Dhandapani, Frederick Bonsack, Cargill H. Alleyne, John R. Vender, Melissa D. Laird, N. E. Yanasak, Patrick Youssef, Richard D. Fessler, Steffen E. Meiler and Nagendra Singh and has published in prestigious journals such as Brain Research, International Journal of Molecular Sciences and Journal of Neurochemistry.

In The Last Decade

Sangeetha Sukumari‐Ramesh

29 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sangeetha Sukumari‐Ramesh United States 18 528 454 268 164 157 29 1.1k
Huangde Fu China 11 459 0.9× 158 0.3× 256 1.0× 155 0.9× 123 0.8× 19 984
Larissa Khoutorova United States 21 427 0.8× 177 0.4× 495 1.8× 195 1.2× 123 0.8× 33 1.5k
Kaifu Ke China 22 628 1.2× 257 0.6× 285 1.1× 159 1.0× 192 1.2× 72 1.3k
Ryan D. Readnower United States 13 555 1.1× 382 0.8× 88 0.3× 262 1.6× 98 0.6× 15 1.1k
Wei Yin United States 15 740 1.4× 164 0.4× 360 1.3× 212 1.3× 109 0.7× 34 1.5k
Nanshan Song China 11 510 1.0× 118 0.3× 193 0.7× 135 0.8× 107 0.7× 14 899
Bao Wang China 15 384 0.7× 269 0.6× 133 0.5× 300 1.8× 42 0.3× 42 977
Sylvia F. Chen United States 14 741 1.4× 300 0.7× 337 1.3× 151 0.9× 73 0.5× 16 1.5k
Jinning Song China 16 315 0.6× 167 0.4× 142 0.5× 100 0.6× 65 0.4× 43 802
Pak H. Chan United States 12 564 1.1× 188 0.4× 404 1.5× 125 0.8× 70 0.4× 13 1.2k

Countries citing papers authored by Sangeetha Sukumari‐Ramesh

Since Specialization
Citations

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

Fields of papers citing papers by Sangeetha Sukumari‐Ramesh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sangeetha Sukumari‐Ramesh. 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 Sangeetha Sukumari‐Ramesh. The network helps show where Sangeetha Sukumari‐Ramesh may publish in the future.

Co-authorship network of co-authors of Sangeetha Sukumari‐Ramesh

This figure shows the co-authorship network connecting the top 25 collaborators of Sangeetha Sukumari‐Ramesh. A scholar is included among the top collaborators of Sangeetha Sukumari‐Ramesh 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 Sangeetha Sukumari‐Ramesh. Sangeetha Sukumari‐Ramesh 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.
Zhi, Wenbo, et al.. (2025). Brain proteome changes after intracerebral hemorrhage in aged male and female mice. Neurobiology of Disease. 212. 106936–106936. 1 indexed citations
2.
Bonsack, Frederick, et al.. (2022). Intracerebral Hemorrhage: The Effects of Aging on Brain Injury. Frontiers in Aging Neuroscience. 14. 859067–859067. 16 indexed citations
3.
4.
Bonsack, Frederick, et al.. (2020). Brain injury and repair after intracerebral hemorrhage: The role of microglia and brain-infiltrating macrophages. Neurochemistry International. 142. 104923–104923. 25 indexed citations
5.
Bonsack, Frederick & Sangeetha Sukumari‐Ramesh. (2019). Differential Cellular Expression of Galectin-1 and Galectin-3 After Intracerebral Hemorrhage. Frontiers in Cellular Neuroscience. 13. 157–157. 27 indexed citations
6.
Bonsack, Frederick, et al.. (2019). Intracerebral Hemorrhage: Blood Components and Neurotoxicity. Brain Sciences. 9(11). 316–316. 47 indexed citations
7.
Bonsack, Frederick & Sangeetha Sukumari‐Ramesh. (2018). TSPO: An Evolutionarily Conserved Protein with Elusive Functions. International Journal of Molecular Sciences. 19(6). 1694–1694. 72 indexed citations
8.
Bonsack, Frederick, Catherine A. Foss, Ali S. Arbab, et al.. (2018). [125 I]IodoDPA-713 Binding to 18 kDa Translocator Protein (TSPO) in a Mouse Model of Intracerebral Hemorrhage: Implications for Neuroimaging. Frontiers in Neuroscience. 12. 66–66. 4 indexed citations
9.
Bonsack, Frederick, Cargill H. Alleyne, & Sangeetha Sukumari‐Ramesh. (2017). Resveratrol Attenuates Neurodegeneration and Improves Neurological Outcomes after Intracerebral Hemorrhage in Mice. Frontiers in Cellular Neuroscience. 11. 228–228. 42 indexed citations
10.
Sukumari‐Ramesh, Sangeetha & Cargill H. Alleyne. (2016). Post-Injury Administration of Tert-butylhydroquinone Attenuates Acute Neurological Injury After Intracerebral Hemorrhage in Mice. Journal of Molecular Neuroscience. 58(4). 525–531. 34 indexed citations
11.
Bonsack, Frederick, Cargill H. Alleyne, & Sangeetha Sukumari‐Ramesh. (2016). Augmented expression of TSPO after intracerebral hemorrhage: a role in inflammation?. Journal of Neuroinflammation. 13(1). 151–151. 75 indexed citations
12.
Patel, Chintan, S. Priya Narayanan, Wenbo Zhang, et al.. (2014). Activation of the Endothelin System Mediates Pathological Angiogenesis during Ischemic Retinopathy. American Journal Of Pathology. 184(11). 3040–3051. 30 indexed citations
13.
Sukumari‐Ramesh, Sangeetha, Cargill H. Alleyne, & Krishnan M. Dhandapani. (2012). Astrogliosis: a Target for Intervention in Intracerebral Hemorrhage?. Translational Stroke Research. 3(S1). 80–87. 21 indexed citations
14.
Sukumari‐Ramesh, Sangeetha, Cargill H. Alleyne, & Krishnan M. Dhandapani. (2012). Astrocyte-Specific Expression of Survivin after Intracerebral Hemorrhage in Mice: A Possible Role in Reactive Gliosis?. Journal of Neurotrauma. 29(18). 2798–2804. 47 indexed citations
15.
Sukumari‐Ramesh, Sangeetha, J. Nicole Bentley, Melissa D. Laird, et al.. (2011). Dietary phytochemicals induce p53‐ and caspase‐independent cell death in human neuroblastoma cells. International Journal of Developmental Neuroscience. 29(7). 701–710. 40 indexed citations
16.
Yanasak, N. E., et al.. (2011). Therapeutic Targeting of Astrocytes After Traumatic Brain Injury. Translational Stroke Research. 2(4). 633–642. 12 indexed citations
17.
Wakade, Chandramohan, Sangeetha Sukumari‐Ramesh, Melissa D. Laird, Krishnan M. Dhandapani, & John R. Vender. (2010). Delayed reduction in hippocampal postsynaptic density protein-95 expression temporally correlates with cognitive dysfunction following controlled cortical impact in mice. Journal of neurosurgery. 113(6). 1195–1201. 87 indexed citations
18.
Sukumari‐Ramesh, Sangeetha, Melissa D. Laird, Nagendra Singh, et al.. (2010). Astrocyte‐derived glutathione attenuates hemin‐induced apoptosis in cerebral microvascular cells. Glia. 58(15). 1858–1870. 32 indexed citations
19.
Laird, Melissa D., et al.. (2010). Curcumin attenuates cerebral edema following traumatic brain injury in mice: a possible role for aquaporin‐4?. Journal of Neurochemistry. 113(3). 637–648. 118 indexed citations
20.
Sukumari‐Ramesh, Sangeetha & Ellen K. LeMosy. (2009). Gastrulation Defective Protease Interacts with Anionic Components of the Drosophila Ovary Extracellular Matrix. Protein and Peptide Letters. 16(4). 437–443. 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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