Erkki Juronen

876 total citations
36 papers, 656 citations indexed

About

Erkki Juronen is a scholar working on Molecular Biology, Genetics and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Erkki Juronen has authored 36 papers receiving a total of 656 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Erkki Juronen's work include Glutathione Transferases and Polymorphisms (12 papers), Connexins and lens biology (6 papers) and Genomics, phytochemicals, and oxidative stress (4 papers). Erkki Juronen is often cited by papers focused on Glutathione Transferases and Polymorphisms (12 papers), Connexins and lens biology (6 papers) and Genomics, phytochemicals, and oxidative stress (4 papers). Erkki Juronen collaborates with scholars based in Estonia, Sweden and United Kingdom. Erkki Juronen's co-authors include Gunnar Tasa, Aavo‐Valdur Mikelsaar, Margus Pooga, Madeleine Zetterberg, Henrik Zetterberg, Kaj Blennow, Ingrid Liiv, Mona Seibt Palmér, Sulev Ingerpuu and Kai Kisand and has published in prestigious journals such as Journal of Biological Chemistry, Blood and PLoS ONE.

In The Last Decade

Erkki Juronen

36 papers receiving 623 citations

Peers

Erkki Juronen

OPHTH

IMMUN

RNMI

GENET

Kaiser Alam Saudi Arabia

Alessia Lamolinara Italy

Danish Saleh United States

Jeanette Hamlington United States

J Wojcierowski Poland

Nadia Akawi United Arab Emirates

Catherine Prades France

Nobuhiko Kubo Japan

Saara Aittomäki Finland

Akash Gupta United States

Kaiser Alam Saudi Arabia

Erkki Juronen

253 ×0.7

225 ×1.8

OPHTH

138 ×1.1

IMMUN

86 ×1.0

RNMI

16 ×0.2

GENET

Citations per year, relative to Erkki Juronen Erkki Juronen (= 1×) peers Kaiser Alam

Countries citing papers authored by Erkki Juronen

Since Specialization

Citations

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

Fields of papers citing papers by Erkki Juronen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erkki Juronen

This figure shows the co-authorship network connecting the top 25 collaborators of Erkki Juronen. A scholar is included among the top collaborators of Erkki Juronen 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 Erkki Juronen. Erkki Juronen 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

Nacer, Adéla, Erkki Juronen, Pavlo Holenya, et al.. (2022). Expanding the Malaria Antibody Toolkit: Development and Characterisation of Plasmodium falciparum RH5, CyRPA, and CSP Recombinant Human Monoclonal Antibodies. Frontiers in Cellular and Infection Microbiology. 12. 901253–901253. 3 indexed citations

Celojevic, Dragana, Alexandra Abramsson, Mona Seibt Palmér, et al.. (2014). EPHA2 polymorphisms in Estonian patients with age-related cataract. Ophthalmic Genetics. 37(1). 1–5. 13 indexed citations

Celojevic, Dragana, Staffan Nilsson, Gunnar Tasa, et al.. (2013). Genetic Variation of Superoxide Dismutases in Patients with Primary Open-angle Glaucoma. Ophthalmic Genetics. 35(2). 79–84. 9 indexed citations

Mikelsaar, Aavo‐Valdur, et al.. (2012). Epitope of titin A-band-specific monoclonal antibody Tit1 5 H1.1 is highly conserved in several Fn3 domains of the titin molecule. Centriole staining in human, mouse and zebrafish cells. Cell Division. 7(1). 21–21. 8 indexed citations

Palmér, Mona Seibt, Lennart Minthon, Anders Wallin, et al.. (2011). Ubiquitin Carboxyl-Terminal Esterase L1(UCHL1)S18Y Polymorphism In Patients With Cataracts. Ophthalmic Genetics. 32(2). 75–79. 4 indexed citations

Mikelsaar, Aavo‐Valdur, et al.. (2010). Titin A-band-specific Monoclonal Antibody Tit1 5H1.1. Cellular Titin As a Centriolar Protein in Non-muscle Cells. Hybridoma. 29(5). 391–401. 2 indexed citations

Juronen, Erkki, et al.. (2008). Functional Characterization of Fingers Subdomain-specific Monoclonal Antibodies Inhibiting the Hepatitis C Virus RNA-dependent RNA Polymerase. Journal of Biological Chemistry. 283(35). 24089–24102. 10 indexed citations

Zetterberg, Madeleine, Gunnar Tasa, Mona Seibt Palmér, et al.. (2007). Apolipoprotein E Polymorphisms in Patients With Primary Open-Angle Glaucoma. American Journal of Ophthalmology. 143(6). 1059–1060. 29 indexed citations

Zetterberg, Madeleine, Gunnar Tasa, Mona Seibt Palmér, et al.. (2007). Methylenetetrahydrofolate Reductase Genetic Polymorphisms in Patients with Primary Open-Angle Glaucoma. Ophthalmic Genetics. 28(2). 47–50. 18 indexed citations

10.

Liiv, Ingrid, Ana Rebane, Tõnis Org, et al.. (2007). DNA-PK contributes to the phosphorylation of AIRE: Importance in transcriptional activity. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1783(1). 74–83. 65 indexed citations

11.

Juronen, Erkki, et al.. (2004). Eye Lens Crystallins: A Component of Intraocular Pseudoexfoliative Material. Ophthalmic Research. 36(1). 51–54. 3 indexed citations

12.

Tasa, Gunnar, et al.. (2003). Dietary Sugar and Salt Represent Real Risk Factors for Cataract Development. Ophthalmologica. 217(4). 302–307. 3 indexed citations

13.

Yan, Fengxiang, M. Chris Langub, Carlton A. Hornung, et al.. (2003). CYP2D6, GST‐M1 and GST‐T1 enzymes: expression in parathyroid gland and association with the parathyroid hormone concentration during early renal replacement therapy. British Journal of Clinical Pharmacology. 56(1). 68–77. 8 indexed citations

14.

Alexandrie, Anna-Karin, Agneta Rannug, Erkki Juronen, Gunnar Tasa, & Margareta Warholm. (2002). Detection and characterization of a novel functional polymorphism in the GSTT1 gene. Pharmacogenetics. 12(8). 613–619. 23 indexed citations

15.

Tasa, Gunnar, Jaak Kals, Kai Muru, et al.. (2001). A novel mutation in the M1S1 gene responsible for gelatinous droplike corneal dystrophy.. PubMed. 42(12). 2762–4. 40 indexed citations

16.

Juronen, Erkki, et al.. (2000). Polymorphic Glutathione S-transferase M1 is a Risk Factor of Primary Open-angle Glaucoma among Estonians. Experimental Eye Research. 71(5). 447–452. 69 indexed citations

17.

Tasa, Gunnar, et al.. (1995). Phenotyping of glutathione S-transferase M1 in the Estonian population by ELISA using GSTM1a and GSTM1b specific monoclonal antibodies. Clinica Chimica Acta. 239(2). 191–196. 1 indexed citations

18.

Sikut, Rein, et al.. (1994). No Immunoglobulins in Cataractous Lenses. Ophthalmic Research. 26(5). 261–263. 1 indexed citations

19.

Juronen, Erkki, et al.. (1991). FPLC purification of mouse monoclonal antibodies from ascitic fluid using blue DEAE and thiophilic sorbents. Journal of Immunological Methods. 136(1). 103–109. 14 indexed citations

20.

Juronen, Erkki, et al.. (1988). Rapid, simple and sensitive antigen capture ELISA for the quantitation of myoglobin using monoclonal antibodies. Journal of Immunological Methods. 111(1). 109–115. 10 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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