Neeta Mathur

1.5k total citations
18 papers, 1.2k citations indexed

About

Neeta Mathur is a scholar working on Molecular Biology, Plant Science and Biochemistry. According to data from OpenAlex, Neeta Mathur has authored 18 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 6 papers in Plant Science and 4 papers in Biochemistry. Recurrent topics in Neeta Mathur's work include Photosynthetic Processes and Mechanisms (13 papers), Mitochondrial Function and Pathology (4 papers) and Peroxisome Proliferator-Activated Receptors (4 papers). Neeta Mathur is often cited by papers focused on Photosynthetic Processes and Mechanisms (13 papers), Mitochondrial Function and Pathology (4 papers) and Peroxisome Proliferator-Activated Receptors (4 papers). Neeta Mathur collaborates with scholars based in Canada and Germany. Neeta Mathur's co-authors include Jaideep Mathur, Martin Hülskamp, Bhylahalli Purushottam Srinivas, Kiah A. Barton, John S. Greenwood, Michael R. Wozny, Victor Kirik, Martin Schattat, Firas Bou Daher and Geoffrey O. Wasteneys and has published in prestigious journals such as The Plant Cell, Development and PLANT PHYSIOLOGY.

In The Last Decade

Neeta Mathur

18 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Neeta Mathur Canada	15	1.0k	711	249	131	56	18	1.2k
Boris Voigt Germany	16	805 0.8×	796 1.1×	345 1.4×	33 0.3×	35 0.6×	25	1.2k
Lawrence R. Griffing United States	20	770 0.8×	654 0.9×	324 1.3×	29 0.2×	17 0.3×	39	1.2k
Robert C. Augustine United States	13	795 0.8×	705 1.0×	204 0.8×	76 0.6×	19 0.3×	14	1.1k
Kiah A. Barton Canada	12	493 0.5×	321 0.5×	46 0.2×	101 0.8×	31 0.6×	15	574
Michael B. Sheahan Australia	12	848 0.8×	761 1.1×	200 0.8×	43 0.3×	50 0.9×	15	1.1k
Tonglin Mao China	22	1.1k 1.1×	1.3k 1.9×	317 1.3×	55 0.4×	14 0.3×	41	1.6k
Cristina Ruberti Italy	19	732 0.7×	739 1.0×	217 0.9×	54 0.4×	7 0.1×	27	1.2k
T. KATO Japan	27	1.8k 1.8×	2.0k 2.8×	383 1.5×	65 0.5×	15 0.3×	59	2.5k
Songguang Yang China	22	1.4k 1.4×	1.3k 1.9×	204 0.8×	64 0.5×	14 0.3×	43	1.9k
Kateřina Schwarzerová Czechia	17	997 1.0×	1.2k 1.6×	145 0.6×	36 0.3×	17 0.3×	31	1.4k

Countries citing papers authored by Neeta Mathur

Since Specialization

Citations

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

Fields of papers citing papers by Neeta Mathur

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neeta Mathur

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

All Works

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18 of 18 papers shown

Mathur, Jaideep, et al.. (2023). Membrane contacts with the endoplasmic reticulum modulate plastid morphology and behaviour. Frontiers in Plant Science. 14. 1293906–1293906. 8 indexed citations

Mathur, Jaideep, et al.. (2022). The ER Is a Common Mediator for the Behavior and Interactions of Other Organelles. Frontiers in Plant Science. 13. 846970–846970. 18 indexed citations

Mathur, Jaideep, et al.. (2018). Peroxisome Mitochondria Inter-relations in Plants. Sub-cellular biochemistry. 89. 417–433. 10 indexed citations

Wozny, Michael R., et al.. (2018). Plastid Envelope-Localized Proteins Exhibit a Stochastic Spatiotemporal Relationship to Stromules. Frontiers in Plant Science. 9. 754–754. 8 indexed citations

Barton, Kiah A., et al.. (2017). Chloroplast behaviour and interactions with other organelles in Arabidopsis thaliana pavement cells. Journal of Cell Science. 131(2). 48 indexed citations

Mathur, Neeta, et al.. (2016). High Light Intensity Leads to Increased Peroxule-Mitochondria Interactions in Plants. Frontiers in Cell and Developmental Biology. 4. 6–6. 53 indexed citations

Wozny, Michael R., et al.. (2016). Photo‐convertible fluorescent proteins as tools for fresh insights on subcellular interactions in plants. Journal of Microscopy. 263(2). 148–157. 14 indexed citations

Barton, Kiah A., et al.. (2015). Mitochondrial pleomorphy in plant cells is driven by contiguous ER dynamics. Frontiers in Plant Science. 6. 783–783. 72 indexed citations

Barton, Kiah A., et al.. (2013). Simultaneous live-imaging of peroxisomes and the ER in plant cells suggests contiguity but no luminal continuity between the two organelles. Frontiers in Physiology. 4. 196–196. 37 indexed citations

10.

Schattat, Martin, Sarah Griffiths, Neeta Mathur, et al.. (2012). Differential Coloring Reveals That Plastids Do Not Form Networks for Exchanging Macromolecules. The Plant Cell. 24(4). 1465–1477. 67 indexed citations

11.

Wozny, Michael R., et al.. (2011). Color Recovery after Photoconversion of H2B::mEosFP Allows Detection of Increased Nuclear DNA Content in Developing Plant Cells . PLANT PHYSIOLOGY. 158(1). 95–106. 16 indexed citations

12.

Mathur, Jaideep, et al.. (2010). mEosFP-Based Green-to-Red Photoconvertible Subcellular Probes for Plants . PLANT PHYSIOLOGY. 154(4). 1573–1587. 50 indexed citations

13.

Mathur, Neeta, et al.. (2009). Peroxule extension over ER‐defined paths constitutes a rapid subcellular response to hydroxyl stress. The Plant Journal. 59(2). 231–242. 107 indexed citations

14.

Saedler, Rainer, et al.. (2004). Actin Control Over Microtubules Suggested by DISTORTED2 Encoding the Arabidopsis ARPC2 Subunit Homolog. Plant and Cell Physiology. 45(7). 813–822. 59 indexed citations

15.

Mathur, Jaideep, et al.. (2003). A Novel Localization Pattern for an EB1-like Protein Links Microtubule Dynamics to Endomembrane Organization. Current Biology. 13(22). 1991–1997. 109 indexed citations

16.

Mathur, Jaideep, et al.. (2003). Arabidopsis CROOKEDencodes for the smallest subunit of the ARP2/3 complex and controls cell shape by region specific fine F-actin formation. Development. 130(14). 3137–3146. 148 indexed citations

17.

Mathur, Jaideep, et al.. (2003). Mutations in Actin-Related Proteins 2 and 3 Affect Cell Shape Development in Arabidopsis. The Plant Cell. 15(7). 1632–1645. 194 indexed citations

18.

Mathur, Jaideep, Neeta Mathur, & Martin Hülskamp. (2002). Simultaneous Visualization of Peroxisomes and Cytoskeletal Elements Reveals Actin and Not Microtubule-Based Peroxisome Motility in Plants,. PLANT PHYSIOLOGY. 128(3). 1031–1045. 151 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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