Elisabet Andersson

5.3k total citations · 1 hit paper
48 papers, 3.7k citations indexed

About

Elisabet Andersson is a scholar working on Molecular Biology, Ecology and Immunology. According to data from OpenAlex, Elisabet Andersson has authored 48 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 13 papers in Ecology and 8 papers in Immunology. Recurrent topics in Elisabet Andersson's work include Developmental Biology and Gene Regulation (10 papers), Hydrology and Sediment Transport Processes (8 papers) and Pluripotent Stem Cells Research (7 papers). Elisabet Andersson is often cited by papers focused on Developmental Biology and Gene Regulation (10 papers), Hydrology and Sediment Transport Processes (8 papers) and Pluripotent Stem Cells Research (7 papers). Elisabet Andersson collaborates with scholars based in Sweden, United States and France. Elisabet Andersson's co-authors include Jonas Muhr, Johan Ericson, Christer Nilsson, Bennett G. Novitch, Mats E. Johansson, Zhanna Alekseenko, Thomas Perlmann, Qiaolin Deng, Takeshi Matsunaga and Roland Jansson and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Neuroscience.

In The Last Decade

Elisabet Andersson

47 papers receiving 3.6k citations

Hit Papers

Vertebrate neurogenesis is counteracted by Sox1–3 activity 2003 2026 2010 2018 2003 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabet Andersson Sweden 27 2.2k 703 666 621 614 48 3.7k
Jeremy W. Fox Canada 31 925 0.4× 587 0.8× 1.5k 2.2× 1.1k 1.8× 563 0.9× 71 5.3k
J. H. Brock United States 28 570 0.3× 1.4k 2.0× 643 1.0× 88 0.1× 740 1.2× 101 4.4k
M. J. Wiley Canada 21 590 0.3× 173 0.2× 476 0.7× 151 0.2× 89 0.1× 34 2.1k
Nicholas D. Holland United States 48 4.7k 2.2× 769 1.1× 1.0k 1.5× 1.1k 1.8× 123 0.2× 187 7.9k
William L. Perry United States 29 2.3k 1.0× 161 0.2× 944 1.4× 1.1k 1.7× 11 0.0× 63 4.5k
Kiyokazu Agata Japan 60 8.2k 3.8× 930 1.3× 651 1.0× 1.2k 1.9× 114 0.2× 231 10.5k
Jane Khudyakov United States 15 1.1k 0.5× 170 0.2× 253 0.4× 205 0.3× 381 0.6× 33 1.7k
Jayaraj Rajagopal United States 24 3.1k 1.4× 253 0.4× 74 0.1× 1.1k 1.8× 115 0.2× 36 5.3k
Daniel R. Buchholz United States 35 835 0.4× 232 0.3× 552 0.8× 1.0k 1.7× 19 0.0× 71 3.1k
Xiumin Yan China 26 1.1k 0.5× 69 0.1× 107 0.2× 666 1.1× 59 0.1× 61 1.7k

Countries citing papers authored by Elisabet Andersson

Since Specialization
Citations

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

Fields of papers citing papers by Elisabet Andersson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabet Andersson

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabet Andersson. A scholar is included among the top collaborators of Elisabet Andersson 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 Elisabet Andersson. Elisabet Andersson 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.
Harbut, Piotr, Francesca Campoccia Jalde, Anders Forsgren, et al.. (2023). Improved oxygenation in prone positioning of mechanically ventilated patients with COVID-19 acute respiratory distress syndrome is associated with decreased pulmonary shunt fraction: a prospective multicenter study. European journal of medical research. 28(1). 597–597. 3 indexed citations
2.
Finér, Leena, Samuli Joensuu, Elisabet Andersson, et al.. (2020). Manual for constructing water protection structures at ditch network maintenance sites and for water retention in forests. Jukuri (Natural Resources Institute Finland (Luke)). 1 indexed citations
3.
Fukusumi, Yoshiyasu, Martin Irmler, Ruth Beckervordersandforth, et al.. (2015). Dickkopf 3 Promotes the Differentiation of a Rostrolateral Midbrain Dopaminergic Neuronal SubsetIn Vivoand from Pluripotent Stem CellsIn Vitroin the Mouse. Journal of Neuroscience. 35(39). 13385–13401. 24 indexed citations
4.
Marklund, Ulrika, Zhanna Alekseenko, Elisabet Andersson, et al.. (2013). Detailed Expression Analysis of Regulatory Genes in the Early Developing Human Neural Tube. Stem Cells and Development. 23(1). 5–15. 26 indexed citations
5.
Panman, Lia, Elisabet Andersson, Zhanna Alekseenko, et al.. (2011). Transcription Factor-Induced Lineage Selection of Stem-Cell-Derived Neural Progenitor Cells. Cell stem cell. 8(6). 663–675. 53 indexed citations
6.
Andersson, Elisabet, Lachlan H. Thompson, Marie E. Jönsson, et al.. (2009). Efficient production of mesencephalic dopamine neurons by Lmx1a expression in embryonic stem cells. Proceedings of the National Academy of Sciences. 106(18). 7613–7618. 166 indexed citations
7.
Baudet, Christel, et al.. (2008). Retrograde Signaling onto Ret during Motor Nerve Terminal Maturation. Journal of Neuroscience. 28(4). 963–975. 55 indexed citations
8.
Andersson, Elisabet, Qiaolin Deng, Zhanna Alekseenko, et al.. (2006). Identification of Intrinsic Determinants of Midbrain Dopamine Neurons. Cell. 124(2). 393–405. 456 indexed citations
9.
Bailey, Peter J., Elisabet Andersson, Mattias Karlén, et al.. (2006). A global genomic transcriptional code associated with CNS-expressed genes. Experimental Cell Research. 312(16). 3108–3119. 37 indexed citations
10.
Alanentalo, Tomas, Fabrice Chatonnet, Mattias Karlén, et al.. (2005). Cloning and analysis of Nkx6.3 during CNS and gastrointestinal development. Gene Expression Patterns. 6(2). 162–170. 29 indexed citations
11.
Lundqvist, Elisabeth Åvall & Elisabet Andersson. (2004). Genetic Diversity in Populations of Plants with Different Breeding and Dispersal Strategies in a Free-Flowing Boreal River System. Hereditas. 135(1). 75–83. 36 indexed citations
12.
Andersson, Elisabet, et al.. (2003). Vertebrate neurogenesis is counteracted by Sox1–3 activity. Nature Neuroscience. 6(11). 1162–1168. 662 indexed citations breakdown →
13.
Stamataki, Despina, Elisabet Andersson, Jens Böse, et al.. (2002). Dorsal-ventral patterning of the spinal cord requires Gli3 transcriptional repressor activity. Genes & Development. 16(22). 2865–2878. 257 indexed citations
15.
16.
Andersson, Elisabet & Takeshi Matsunaga. (1996). Jaw, adaptive immunity and phylogeny of vertebrate antibody VH gene family. Research in Immunology. 147(4). 233–240. 16 indexed citations
17.
Charlemagne, Jacques, Takeshi Matsunaga, Elisabet Andersson, et al.. (1996). Unified nomenclature ofIg VH genes in rainbow trout (Oncorhynchus mykiss): definition of elevenVH families. Immunogenetics. 43(5). 325–326. 29 indexed citations
19.
Matsunaga, Takeshi, et al.. (1994). Evolution of Teleost Antibody Genes. Annals of the New York Academy of Sciences. 712(1). 42–54. 5 indexed citations
20.
Andersson, Elisabet, et al.. (1991). Evolution of a VH gene family in low Vertebrates. International Immunology. 3(6). 527–533. 18 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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