Lotta Borgius

2.1k total citations · 1 hit paper
17 papers, 1.5k citations indexed

About

Lotta Borgius is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Molecular Biology. According to data from OpenAlex, Lotta Borgius has authored 17 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 10 papers in Cell Biology and 7 papers in Molecular Biology. Recurrent topics in Lotta Borgius's work include Zebrafish Biomedical Research Applications (9 papers), Neurogenesis and neuroplasticity mechanisms (7 papers) and Axon Guidance and Neuronal Signaling (4 papers). Lotta Borgius is often cited by papers focused on Zebrafish Biomedical Research Applications (9 papers), Neurogenesis and neuroplasticity mechanisms (7 papers) and Axon Guidance and Neuronal Signaling (4 papers). Lotta Borgius collaborates with scholars based in Sweden, Japan and Austria. Lotta Borgius's co-authors include Ole Kiehn, Kimberly J. Dougherty, Martin Hägglund, Adolfo E. Talpalar, Julien Bouvier, Alessandra Pierani, Gilles Fortin, Carlos E. Restrepo, Shigeyoshi Itohara and Takuji Iwasato and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Lotta Borgius

17 papers receiving 1.5k citations

Hit Papers

Neuronal atlas of the dorsal horn defines its architectur... 2018 2026 2020 2023 2018 50 100 150 200 250

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lotta Borgius Sweden 16 637 494 398 307 277 17 1.5k
Tomoko Velasquez United States 9 681 1.1× 581 1.2× 680 1.7× 232 0.8× 338 1.2× 9 1.6k
Frédéric Brocard France 25 866 1.4× 667 1.4× 503 1.3× 395 1.3× 184 0.7× 49 1.8k
Raúl E. Russo Uruguay 19 695 1.1× 214 0.4× 327 0.8× 207 0.7× 273 1.0× 37 1.1k
Simon Gosgnach Canada 18 748 1.2× 918 1.9× 477 1.2× 468 1.5× 79 0.3× 32 1.8k
Jianren Song China 14 404 0.6× 369 0.7× 269 0.7× 179 0.6× 147 0.5× 24 970
George Z. Mentis United States 34 1.1k 1.7× 620 1.3× 1.7k 4.2× 274 0.9× 183 0.7× 65 3.2k
Adolfo E. Talpalar Sweden 15 482 0.8× 373 0.8× 319 0.8× 212 0.7× 160 0.6× 20 1.8k
Jonas Broman Sweden 26 727 1.1× 210 0.4× 533 1.3× 217 0.7× 596 2.2× 53 1.6k
Sandrine S. Bertrand France 20 651 1.0× 189 0.4× 422 1.1× 230 0.7× 273 1.0× 47 1.2k
Christopher A. Hinckley United States 14 350 0.5× 322 0.7× 308 0.8× 189 0.6× 58 0.2× 16 888

Countries citing papers authored by Lotta Borgius

Since Specialization
Citations

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

Fields of papers citing papers by Lotta Borgius

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lotta Borgius

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

All Works

17 of 17 papers shown
1.
Caldeira, Vanessa, et al.. (2024). Excitatory spinal Lhx9-derived interneurons modulate locomotor frequency in mice. Journal of Neuroscience. 44(18). e1607232024–e1607232024. 2 indexed citations
2.
Häring, Martin, Amit Zeisel, Hannah Hochgerner, et al.. (2018). Neuronal atlas of the dorsal horn defines its architecture and links sensory input to transcriptional cell types. Nature Neuroscience. 21(6). 869–880. 297 indexed citations breakdown →
3.
Zhang, Ming-Dong, Jie Su, Csaba Ádori, et al.. (2018). Ca2+-binding protein NECAB2 facilitates inflammatory pain hypersensitivity. Journal of Clinical Investigation. 128(9). 3757–3768. 21 indexed citations
4.
Caldeira, Vanessa, Kimberly J. Dougherty, Lotta Borgius, & Ole Kiehn. (2017). Spinal Hb9::Cre-derived excitatory interneurons contribute to rhythm generation in the mouse. Scientific Reports. 7(1). 41369–41369. 57 indexed citations
5.
Borgius, Lotta, Hiroshi Nishimaru, Vanessa Caldeira, et al.. (2014). Spinal Glutamatergic Neurons Defined by EphA4 Signaling Are Essential Components of Normal Locomotor Circuits. Journal of Neuroscience. 34(11). 3841–3853. 43 indexed citations
6.
Zhang, Ming-Dong, Giuseppe Tortoriello, Brian Hsueh, et al.. (2014). Neuronal calcium-binding proteins 1/2 localize to dorsal root ganglia and excitatory spinal neurons and are regulated by nerve injury. Proceedings of the National Academy of Sciences. 111(12). E1149–58. 49 indexed citations
7.
Talpalar, Adolfo E., Julien Bouvier, Lotta Borgius, et al.. (2013). Dual-mode operation of neuronal networks involved in left–right alternation. Nature. 500(7460). 85–88. 244 indexed citations
8.
Hägglund, Martin, Kimberly J. Dougherty, Lotta Borgius, et al.. (2013). Optogenetic dissection reveals multiple rhythmogenic modules underlying locomotion. Proceedings of the National Academy of Sciences. 110(28). 11589–11594. 138 indexed citations
9.
Restrepo, Carlos E., et al.. (2011). Change in the balance of excitatory and inhibitory midline fiber crossing as an explanation for the hopping phenotype in EphA4 knockout mice. European Journal of Neuroscience. 34(7). 1102–1112. 25 indexed citations
10.
Talpalar, Adolfo E., Toshiaki Endo, Peter Löw, et al.. (2011). Identification of Minimal Neuronal Networks Involved in Flexor-Extensor Alternation in the Mammalian Spinal Cord. Neuron. 71(6). 1071–1084. 73 indexed citations
11.
Leão, Richardson N., Luis V. Colom, Lotta Borgius, Ole Kiehn, & André Fisahn. (2011). Medial septal dysfunction by Aβ-induced KCNQ channel-block in glutamatergic neurons. Neurobiology of Aging. 33(9). 2046–2061. 30 indexed citations
12.
Borgius, Lotta, et al.. (2010). A transgenic mouse line for molecular genetic analysis of excitatory glutamatergic neurons. Molecular and Cellular Neuroscience. 45(3). 245–257. 77 indexed citations
13.
Kiehn, Ole, Kimberly J. Dougherty, Martin Hägglund, et al.. (2010). Probing spinal circuits controlling walking in mammals. Biochemical and Biophysical Research Communications. 396(1). 11–18. 44 indexed citations
14.
Hägglund, Martin, Lotta Borgius, Kimberly J. Dougherty, & Ole Kiehn. (2010). Activation of groups of excitatory neurons in the mammalian spinal cord or hindbrain evokes locomotion. Nature Neuroscience. 13(2). 246–252. 181 indexed citations
15.
Kiehn, Ole, Katharina A. Quinlan, Carlos E. Restrepo, et al.. (2007). Excitatory components of the mammalian locomotor CPG. Brain Research Reviews. 57(1). 56–63. 52 indexed citations
16.
Borgius, Lotta, et al.. (2006). Neuropilin1 is a direct downstream target of Nurr1 in the developing brain stem. Journal of Neurochemistry. 97(5). 1403–1411. 31 indexed citations
17.
Borgius, Lotta, Knut R. Steffensen, Jan-Ακε Gustafsson, & Eckardt Treuter. (2002). Glucocorticoid Signaling Is Perturbed by the Atypical Orphan Receptor and Corepressor SHP. Journal of Biological Chemistry. 277(51). 49761–49766. 109 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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