Natasha N. Kumar

1.6k total citations
34 papers, 1.2k citations indexed

About

Natasha N. Kumar is a scholar working on Endocrine and Autonomic Systems, Social Psychology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Natasha N. Kumar has authored 34 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Endocrine and Autonomic Systems, 15 papers in Social Psychology and 8 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Natasha N. Kumar's work include Neuroscience of respiration and sleep (19 papers), Neuroendocrine regulation and behavior (15 papers) and Sleep and Wakefulness Research (7 papers). Natasha N. Kumar is often cited by papers focused on Neuroscience of respiration and sleep (19 papers), Neuroendocrine regulation and behavior (15 papers) and Sleep and Wakefulness Research (7 papers). Natasha N. Kumar collaborates with scholars based in Australia, United States and China. Natasha N. Kumar's co-authors include Ann K. Goodchild, Douglas A. Bayliss, Simon McMullan, Patrice G. Guyenet, Yingtang Shi, William Y.S. Wang, Brian J. Morris, Adam Benjafield, Paul M. Pilowsky and Nissar A. Darmani and has published in prestigious journals such as Science, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

Natasha N. Kumar

34 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natasha N. Kumar Australia 17 583 321 296 282 234 34 1.2k
Pamela J. Davern Australia 22 555 1.0× 165 0.5× 484 1.6× 191 0.7× 276 1.2× 43 1.5k
Takato Kunitake Japan 20 475 0.8× 283 0.9× 259 0.9× 413 1.5× 235 1.0× 44 1.2k
Flavia Carreño United States 20 249 0.4× 276 0.9× 135 0.5× 281 1.0× 214 0.9× 29 1.1k
Donghai Huangfu United States 13 571 1.0× 254 0.8× 272 0.9× 175 0.6× 134 0.6× 17 860
Sylvie Laforest Canada 21 334 0.6× 254 0.8× 93 0.3× 578 2.0× 266 1.1× 28 1.4k
P.G. Guertzenstein Brazil 14 642 1.1× 159 0.5× 484 1.6× 361 1.3× 236 1.0× 18 1.2k
Monica M. Caverson Canada 19 724 1.2× 214 0.7× 296 1.0× 357 1.3× 121 0.5× 28 1.2k
Timothy W. Bailey United States 18 759 1.3× 361 1.1× 188 0.6× 562 2.0× 428 1.8× 20 1.6k
Massako Kadekaro United States 24 565 1.0× 227 0.7× 171 0.6× 646 2.3× 350 1.5× 63 1.8k
Mark M. Knuepfer United States 23 362 0.6× 136 0.4× 685 2.3× 542 1.9× 365 1.6× 84 1.7k

Countries citing papers authored by Natasha N. Kumar

Since Specialization
Citations

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

Fields of papers citing papers by Natasha N. Kumar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natasha N. Kumar. 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 Natasha N. Kumar. The network helps show where Natasha N. Kumar may publish in the future.

Co-authorship network of co-authors of Natasha N. Kumar

This figure shows the co-authorship network connecting the top 25 collaborators of Natasha N. Kumar. A scholar is included among the top collaborators of Natasha N. Kumar 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 Natasha N. Kumar. Natasha N. Kumar 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.
McMullan, Simon, et al.. (2024). Galaninergic and hypercapnia-activated neuronal projections to the ventral respiratory column. Brain Structure and Function. 229(5). 1121–1142. 4 indexed citations
2.
Kumar, Natasha N., et al.. (2024). Expression of Endogenous Epitope-Tagged GPR4 in the Mouse Brain. eNeuro. 11(3). ENEURO.0002–24.2024. 4 indexed citations
3.
Chen, Jessica, Eun A Choi, Philip Jean-Richard-dit-Bressel, et al.. (2024). Chemogenetic activation of arcuate nucleus NPY and NPY/AgRP neurons increases feeding behaviour in mice. Neuropeptides. 107. 102454–102454. 8 indexed citations
4.
Burke, Peter G.R., Natasha N. Kumar, Ann K. Goodchild, et al.. (2022). Upregulated Angiotensin Ia Receptors in the Hypothalamic Paraventricular Nucleus Sensitize Neuroendocrine Vasopressin Release and Blood Pressure in a Rodent Model of Polycystic Kidney Disease. Neuroendocrinology. 112(12). 1200–1213. 7 indexed citations
6.
Menuet, Clément, Angela A. Connelly, Jaspreet K. Bassi, et al.. (2020). PreBötzinger complex neurons drive respiratory modulation of blood pressure and heart rate. eLife. 9. 61 indexed citations
7.
Carrive, Pascal, et al.. (2019). Adaptation of Respiratory-Related Brain Regions to Long-Term Hypercapnia: Focus on Neuropeptides in the RTN. Frontiers in Neuroscience. 13. 1343–1343. 9 indexed citations
8.
Sun, Qi‐Jian, Natasha N. Kumar, Sheng Le, et al.. (2019). Neurons in the Intermediate Reticular Nucleus Coordinate Postinspiratory Activity, Swallowing, and Respiratory-Sympathetic Coupling in the Rat. Journal of Neuroscience. 39(49). 9757–9766. 48 indexed citations
9.
Guyenet, Patrice G., Douglas A. Bayliss, Ruth L. Stornetta, et al.. (2016). Proton detection and breathing regulation by the retrotrapezoid nucleus. The Journal of Physiology. 594(6). 1529–1551. 65 indexed citations
10.
Kumar, Natasha N., Ana Velić, Jorge Soliz, et al.. (2015). Regulation of breathing by CO 2 requires the proton-activated receptor GPR4 in retrotrapezoid nucleus neurons. Science. 348(6240). 1255–1260. 180 indexed citations
11.
Zhou, Cheng, Jennifer E. Douglas, Natasha N. Kumar, et al.. (2013). Forebrain HCN1 Channels Contribute to Hypnotic Actions of Ketamine. Anesthesiology. 118(4). 785–795. 59 indexed citations
12.
Wang, Sheng, Najate Benamer, Sébastien Zanella, et al.. (2013). TASK-2 Channels Contribute to pH Sensitivity of Retrotrapezoid Nucleus Chemoreceptor Neurons. Journal of Neuroscience. 33(41). 16033–16044. 105 indexed citations
13.
Parker, Lindsay M., Vikram J. Tallapragada, Natasha N. Kumar, & Ann K. Goodchild. (2012). Distribution and localisation of Gα proteins in the rostral ventrolateral medulla of normotensive and hypertensive rats: Focus on catecholaminergic neurons. Neuroscience. 218. 20–34. 6 indexed citations
14.
Kumar, Natasha N., et al.. (2012). Brain sources of inhibitory input to the rat rostral ventrolateral medulla. The Journal of Comparative Neurology. 521(1). 213–232. 52 indexed citations
16.
Pilowsky, Paul M., Stephen B.G. Abbott, Peter G.R. Burke, et al.. (2008). METABOTROPIC NEUROTRANSMISSION AND INTEGRATION OF SYMPATHETIC NERVE ACTIVITY BY THE ROSTRAL VENTROLATERAL MEDULLA IN THE RAT. Clinical and Experimental Pharmacology and Physiology. 35(4). 508–511. 16 indexed citations
18.
Kumar, Natasha N., Ann K. Goodchild, Qun Li, & Paul M. Pilowsky. (2006). AN ALDOSTERONE‐RELATED SYSTEM IN THE VENTROLATERAL MEDULLA OBLONGATA OF SPONTANEOUSLY HYPERTENSIVE AND WISTAR‐KYOTO RATS. Clinical and Experimental Pharmacology and Physiology. 33(1-2). 71–75. 9 indexed citations
19.
Speirs, H. J. L., et al.. (2004). Association of G-protein-coupled receptor kinase 4 haplotypes, but not HSD3B1 or PTP1B polymorphisms, with essential hypertension. Journal of Hypertension. 22(5). 931–936. 80 indexed citations
20.
Darmani, Nissar A., et al.. (2003). Behaviorally active doses of the CB1 receptor antagonist SR 141716A increase brain serotonin and dopamine levels and turnover. Pharmacology Biochemistry and Behavior. 75(4). 777–787. 79 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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