Erik Salaneck

1.5k total citations
26 papers, 1.0k citations indexed

About

Erik Salaneck is a scholar working on Cellular and Molecular Neuroscience, Infectious Diseases and Molecular Biology. According to data from OpenAlex, Erik Salaneck has authored 26 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 10 papers in Infectious Diseases and 8 papers in Molecular Biology. Recurrent topics in Erik Salaneck's work include Neuropeptides and Animal Physiology (8 papers), Vector-borne infectious diseases (6 papers) and Viral Infections and Vectors (5 papers). Erik Salaneck is often cited by papers focused on Neuropeptides and Animal Physiology (8 papers), Vector-borne infectious diseases (6 papers) and Viral Infections and Vectors (5 papers). Erik Salaneck collaborates with scholars based in Sweden, United Kingdom and United States. Erik Salaneck's co-authors include Dan Larhammar, Åke Lundkvist, Tove Hoffman, Karolina Nissen, Dario Akaberi, Janina Krambrich, Magnus Berglund, Tomas Larsson, Earl T. Larson and Thomas G. T. Jaenson and has published in prestigious journals such as PLoS ONE, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Erik Salaneck

26 papers receiving 1.0k citations

Peers

Erik Salaneck

CMN

EAS

PARAS

Azhar Maqbool United Kingdom

Rui Chen China

Timothy Boswell United Kingdom

Rachel Kaletsky United States

F. Sánchez Spain

James B. Wood United States

Agnès Fleury Mexico

Pooja Rao India

Nick J. Edwards United Kingdom

Tetsuo Nasu Japan

Azhar Maqbool United Kingdom

Erik Salaneck

194 ×0.5

CMN

79 ×0.2

288 ×1.1

182 ×0.9

EAS

248 ×1.6

PARAS

Citations per year, relative to Erik Salaneck Erik Salaneck (= 1×) peers Azhar Maqbool

Countries citing papers authored by Erik Salaneck

Since Specialization

Citations

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

Fields of papers citing papers by Erik Salaneck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erik Salaneck

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

All Works

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20 of 20 papers shown

Nissen, Karolina, Johanna Berg, Andreas Bråve, et al.. (2021). Civil–Military Collaboration to Facilitate Rapid Deployment of a Mobile Laboratory in Early Response to COVID-19: A High-Readiness Exercise. Health Security. 19(5). 488–497. 5 indexed citations

Hoffman, Tove, Karolina Nissen, Janina Krambrich, et al.. (2020). Evaluation of a COVID-19 IgM and IgG rapid test; an efficient tool for assessment of past exposure to SARS-CoV-2. Infection Ecology & Epidemiology. 10(1). 1754538–1754538. 140 indexed citations

Schmidt, Sabine, Cornelia Silaghi, Jasmin Skuballa, et al.. (2020). The absence of the drhm gene is not a marker for human-pathogenicity in European Anaplasma phagocytophilum strains. Parasites & Vectors. 13(1). 238–238. 13 indexed citations

Nissen, Karolina, Janina Krambrich, Dario Akaberi, et al.. (2020). Long-distance airborne dispersal of SARS-CoV-2 in COVID-19 wards. Scientific Reports. 10(1). 19589–19589. 136 indexed citations

Tolf, Conny, Sara Larsson, Peter Wilhelmsson, et al.. (2015). Candidatus Neoehrlichia mikurensis in Ticks from Migrating Birds in Sweden. PLoS ONE. 10(7). e0133250–e0133250. 29 indexed citations

Barboutis, Christos, Thord Fransson, Thomas G. T. Jaenson, et al.. (2014). Spotted fever Rickettsia species in Hyalomma and Ixodes ticks infesting migratory birds in the European Mediterranean area. Parasites & Vectors. 7(1). 318–318. 86 indexed citations

Salaneck, Erik, et al.. (2013). Soft tissue infection caused byLegionella bozemaniiin a patient with ongoing immunosuppressive treatment. Infection Ecology & Epidemiology. 3(1). 20739–20739. 9 indexed citations

Salaneck, Erik, Tomas Larsson, Earl T. Larson, & Dan Larhammar. (2007). Birth and death of neuropeptide Y receptor genes in relation to the teleost fish tetraploidization. Gene. 409(1-2). 61–71. 42 indexed citations

Fredriksson, Robert, Tim Boswell, Tomas Larsson, et al.. (2006). Neuropeptide Y‐family receptors Y₆and Y₇in chicken. FEBS Journal. 273(9). 2048–2063. 52 indexed citations

10.

Salaneck, Erik, Earl T. Larson, Tomas Larsson, & Dan Larhammar. (2005). Effects of a Teleost Tetraploidization on Neuropeptide Y Receptor Gene Repertoire in Ray‐Finned Fishes. Annals of the New York Academy of Sciences. 1040(1). 457–459. 12 indexed citations

11.

Ruuskanen, Jori O., Henri Xhaard, Anne Marjamäki, et al.. (2004). Identification of Duplicated Fourth α2-Adrenergic Receptor Subtype by Cloning and Mapping of Five Receptor Genes in Zebrafish. Molecular Biology and Evolution. 21(1). 14–28. 59 indexed citations

12.

Larhammar, Dan & Erik Salaneck. (2004). Molecular evolution of NPY receptor subtypes. Neuropeptides. 38(4). 141–151. 170 indexed citations

13.

Salaneck, Erik. (2003). Three Neuropeptide Y Receptor Genes in the Spiny Dogfish, Squalus acanthias, Support en Bloc Duplications in Early Vertebrate Evolution. Molecular Biology and Evolution. 20(8). 1271–1280. 21 indexed citations

14.

Berglund, Magnus, Robert Fredriksson, Erik Salaneck, & Dan Larhammar. (2002). Reciprocal mutations of neuropeptide Y receptor Y2 in human and chicken identify amino acids important for antagonist binding. FEBS Letters. 518(1-3). 5–9. 24 indexed citations

15.

Salaneck, Erik, Robert Fredriksson, Earl T. Larson, J. Michael Conlon, & Dan Larhammar. (2001). A neuropeptide Y receptor Y1‐subfamily gene from an agnathan, the European river lamprey. European Journal of Biochemistry. 268(23). 6146–6154. 23 indexed citations

16.

Salaneck, Erik, Sara K.S. Holmberg, Magnus Berglund, Timothy Boswell, & Dan Larhammar. (2000). Chicken neuropeptide Y receptor Y2: structural and pharmacological differences to mammalian Y2¹. FEBS Letters. 484(3). 229–234. 41 indexed citations

17.

Risinger, Carl, et al.. (1998). Cloning of two loci for synapse protein Snap25 in zebrafish: Comparison of paralogous linkage groups suggests loss of one locus in the mammalian lineage. Journal of Neuroscience Research. 54(5). 563–573. 16 indexed citations

18.

Lundell, Ingrid, et al.. (1997). Cloning and Characterization of a Novel Neuropeptide Y Receptor Subtype in the Zebrafish. DNA and Cell Biology. 16(11). 1357–1363. 53 indexed citations

19.

Larhammar, Dan, Ingrid Lundell, Erik Salaneck, et al.. (1997). Evolution of neuropeptide Y and its receptors. 551. 2 indexed citations

20.

Lorens, James B., et al.. (1995). Embryonic Expression and DNA-Binding Properties of Zebrafish Pax-6. Biochemical and Biophysical Research Communications. 215(1). 122–128. 19 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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