Jonathan M. Blagburn

1.7k total citations
59 papers, 1.3k citations indexed

About

Jonathan M. Blagburn is a scholar working on Cellular and Molecular Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, Jonathan M. Blagburn has authored 59 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Cellular and Molecular Neuroscience, 29 papers in Genetics and 16 papers in Molecular Biology. Recurrent topics in Jonathan M. Blagburn's work include Neurobiology and Insect Physiology Research (38 papers), Insect and Arachnid Ecology and Behavior (29 papers) and Nerve injury and regeneration (14 papers). Jonathan M. Blagburn is often cited by papers focused on Neurobiology and Insect Physiology Research (38 papers), Insect and Arachnid Ecology and Behavior (29 papers) and Nerve injury and regeneration (14 papers). Jonathan M. Blagburn collaborates with scholars based in Puerto Rico, United Kingdom and Italy. Jonathan M. Blagburn's co-authors include Jonathan P. Bacon, Paolo Domenici, David B. Sattelle, Rosa E. Blanco, David J. Beadle, Bruno Marie, Ileana Soto, David T. Booth, Jane A. Davies and Harry Alexopoulos and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Development.

In The Last Decade

Jonathan M. Blagburn

57 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jonathan M. Blagburn Puerto Rico 20 740 374 356 340 135 59 1.3k
O. Trujillo‐Cenóz Uruguay 26 1.0k 1.4× 183 0.5× 625 1.8× 209 0.6× 131 1.0× 59 1.8k
Richard C. Goris Japan 22 705 1.0× 270 0.7× 288 0.8× 205 0.6× 345 2.6× 94 1.4k
David T. Moran United States 25 699 0.9× 237 0.6× 324 0.9× 422 1.2× 161 1.2× 44 2.0k
Jonathan P. Bacon United Kingdom 19 762 1.0× 445 1.2× 435 1.2× 343 1.0× 189 1.4× 41 1.4k
Leila Maria Pessôa Brazil 15 408 0.6× 332 0.9× 560 1.6× 248 0.7× 340 2.5× 60 2.1k
Eric D. Hoopfer United States 15 1.3k 1.8× 498 1.3× 511 1.4× 590 1.7× 111 0.8× 17 2.0k
John Palka United States 28 1.5k 2.0× 687 1.8× 748 2.1× 665 2.0× 163 1.2× 55 2.1k
Maximiliano L. Suster Japan 20 629 0.8× 117 0.3× 1.1k 3.1× 562 1.7× 161 1.2× 22 2.1k
Renate Sandeman Australia 23 1.3k 1.7× 319 0.9× 215 0.6× 277 0.8× 688 5.1× 28 1.7k
Thomas O. Auer Switzerland 19 516 0.7× 194 0.5× 771 2.2× 436 1.3× 66 0.5× 29 1.5k

Countries citing papers authored by Jonathan M. Blagburn

Since Specialization
Citations

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

Fields of papers citing papers by Jonathan M. Blagburn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jonathan M. Blagburn. 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 Jonathan M. Blagburn. The network helps show where Jonathan M. Blagburn may publish in the future.

Co-authorship network of co-authors of Jonathan M. Blagburn

This figure shows the co-authorship network connecting the top 25 collaborators of Jonathan M. Blagburn. A scholar is included among the top collaborators of Jonathan M. Blagburn 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 Jonathan M. Blagburn. Jonathan M. Blagburn 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.
Eichler, Katharina, Stefanie Hampel, Steven A. Calle-Schuler, et al.. (2024). Somatotopic organization among parallel sensory pathways that promote a grooming sequence in Drosophila. eLife. 12.
2.
Eichler, Katharina, Stefanie Hampel, Steven A. Calle-Schuler, et al.. (2023). Somatotopic organization among parallel sensory pathways that promote a grooming sequence in Drosophila. eLife. 12. 2 indexed citations
3.
Blagburn, Jonathan M., et al.. (2021). Retinoic acid treatment recruits macrophages and increases axonal regeneration after optic nerve injury in the frog Rana pipiens. PLoS ONE. 16(11). e0255196–e0255196. 5 indexed citations
4.
5.
Jezzini, Sami H., Amelia Merced, & Jonathan M. Blagburn. (2018). Shaking-B misexpression increases the formation of gap junctions but not chemical synapses between auditory sensory neurons and the giant fiber of Drosophila melanogaster. PLoS ONE. 13(8). e0198710–e0198710. 3 indexed citations
6.
Blagburn, Jonathan M., et al.. (2016). Optic nerve injury upregulates retinoic acid signaling in the adult frog visual system. Journal of Chemical Neuroanatomy. 77. 80–92. 9 indexed citations
7.
Jezzini, Sami H., et al.. (2016). Shaking B Mediates Synaptic Coupling between Auditory Sensory Neurons and the Giant Fiber of Drosophila melanogaster. PLoS ONE. 11(4). e0152211–e0152211. 18 indexed citations
8.
Blagburn, Jonathan M., et al.. (2013). Auditory Responses of Engrailed and Invected-Expressing Johnston’s Organ Neurons in Drosophila melanogaster. PLoS ONE. 8(8). e71419–e71419. 10 indexed citations
9.
Blagburn, Jonathan M., et al.. (2012). Changes in fibroblast growth factor-2 and FGF receptors in the frog visual system during optic nerve regeneration. Journal of Chemical Neuroanatomy. 46(1-2). 35–44. 7 indexed citations
10.
11.
Blagburn, Jonathan M.. (2008). Engrailed expression in subsets of adult Drosophila sensory neurons: an enhancer-trap study. Invertebrate Neuroscience. 8(3). 133–146. 11 indexed citations
12.
Blagburn, Jonathan M.. (2006). Co-factors and co-repressors of Engrailed: expression in the central nervous system and cerci of the cockroach, Periplaneta americana. Cell and Tissue Research. 327(1). 177–187. 1 indexed citations
13.
14.
Soto, Ileana, et al.. (2002). Changes in brain‐derived neurotrophic factor and trkB receptor in the adult Rana pipiens retina and optic tectum after optic nerve injury. The Journal of Comparative Neurology. 454(4). 456–469. 25 indexed citations
15.
Blagburn, Jonathan M., et al.. (2001). Presynaptic effects of biogenic amines modulating synaptic transmission between identified sensory neurons and giant interneurons in the first instar cockroach. Journal of Comparative Physiology A. 187(8). 633–645. 9 indexed citations
16.
Stern, Michael, et al.. (1997). Regeneration of cercal filiform hair sensory neurons in the first‐instar cockroach restores escape behavior. Journal of Neurobiology. 33(4). 439–458. 2 indexed citations
17.
Blagburn, Jonathan M., María A. Sosa, & Rosa E. Blanco. (1996). Specificity of identified central synapses in the embryonic cockroach: Appropriate connections form before the onset of spontaneous afferent activity. The Journal of Comparative Neurology. 373(4). 511–528. 12 indexed citations
18.
Thompson, Kevin S. J., et al.. (1992). Correlation of filiform hair position with sensory afferent morphology and synaptic connections in the second instar cockroach. The Journal of Comparative Neurology. 320(2). 213–227. 18 indexed citations
19.
Blagburn, Jonathan M. & Kevin S. J. Thompson. (1990). Specificity of filiform hair afferent synapses onto giant interneurons in Periplaneta americana: Anatomy is not a sufficient determinant. The Journal of Comparative Neurology. 302(2). 255–271. 15 indexed citations
20.
Blagburn, Jonathan M.. (1989). Synaptic specificity in the first instar cockroach: patterns of monosynaptic input from filiform hair afferents to giant interneurons. Journal of Comparative Physiology A. 166(1). 133–42. 23 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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