Runa NJÅLSSON

586 total citations
11 papers, 438 citations indexed

About

Runa NJÅLSSON is a scholar working on Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Runa NJÅLSSON has authored 11 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Biochemistry, 7 papers in Molecular Biology and 2 papers in Rheumatology. Recurrent topics in Runa NJÅLSSON's work include Sulfur Compounds in Biology (11 papers), Glutathione Transferases and Polymorphisms (7 papers) and Redox biology and oxidative stress (3 papers). Runa NJÅLSSON is often cited by papers focused on Sulfur Compounds in Biology (11 papers), Glutathione Transferases and Polymorphisms (7 papers) and Redox biology and oxidative stress (3 papers). Runa NJÅLSSON collaborates with scholars based in Sweden, United States and Australia. Runa NJÅLSSON's co-authors include Svante Norgren, Agne Larsson, Katarina Steen Carlsson, Ellinor Ristoff, Andreas Winkler, Christina Hebert, Olav Rooyackers, Michael W. Lieberman, Nuran Erçal and Linu Abraham and has published in prestigious journals such as Biochemical Journal, Biochemical and Biophysical Research Communications and Cellular and Molecular Life Sciences.

In The Last Decade

Runa NJÅLSSON

11 papers receiving 424 citations

Peers

Runa NJÅLSSON
Karim Zuhra Switzerland
Gleb Martovetsky United States
P P Sokol United States
Anil G. Palekar United States
Runa NJÅLSSON
Citations per year, relative to Runa NJÅLSSON Runa NJÅLSSON (= 1×) peers Mariana Panayotova‐Heiermann

Countries citing papers authored by Runa NJÅLSSON

Since Specialization
Citations

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

Fields of papers citing papers by Runa NJÅLSSON

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Runa NJÅLSSON

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

All Works

11 of 11 papers shown
1.
Winkler, Andreas, Runa NJÅLSSON, Katarina Steen Carlsson, et al.. (2011). Glutathione is essential for early embryogenesis – Analysis of a glutathione synthetase knockout mouse. Biochemical and Biophysical Research Communications. 412(1). 121–126. 39 indexed citations
2.
NJÅLSSON, Runa. (2005). Glutathione synthetase deficiency. Cellular and Molecular Life Sciences. 62(17). 1938–1945. 68 indexed citations
3.
Garganta, Cheryl, et al.. (2005). Recurrent High Anion Gap Metabolic Acidosis Secondary to 5-Oxoproline (Pyroglutamic Acid). American Journal of Kidney Diseases. 46(1). e4–e10. 29 indexed citations
4.
NJÅLSSON, Runa & Svante Norgren. (2005). Physiological and pathological aspects of GSH metabolism. Acta Paediatrica. 94(2). 132–137. 113 indexed citations
5.
NJÅLSSON, Runa & Svante Norgren. (2005). Physiological and pathological aspects of GSH metabolism. Acta Paediatrica. 94(2). 132–137. 70 indexed citations
6.
NJÅLSSON, Runa, Katarina Steen Carlsson, Jiali Luo, et al.. (2004). Human hereditary glutathione synthetase deficiency: kinetic properties of mutant enzymes. Biochemical Journal. 381(2). 489–494. 6 indexed citations
7.
NJÅLSSON, Runa, Katarina Steen Carlsson, Andreas Winkler, Agne Larsson, & Svante Norgren. (2003). Diagnostics in patients with glutathione synthetase deficiency but without mutations in the exons of the GSS gene. Human Mutation. 22(6). 497–497. 21 indexed citations
8.
Ristoff, Ellinor, Christina Hebert, Runa NJÅLSSON, et al.. (2002). Glutathione synthetase deficiency: Is γ‐glutamylcysteine accumulation a way to cope with oxidative stress in cells with insufficient levels of glutathione?. Journal of Inherited Metabolic Disease. 25(7). 577–584. 36 indexed citations
9.
NJÅLSSON, Runa, et al.. (2001). Cooperative Binding of γ-Glutamyl Substrate to Human Glutathione Synthetase. Biochemical and Biophysical Research Communications. 289(1). 80–84. 20 indexed citations
10.
NJÅLSSON, Runa, Katarina Steen Carlsson, B. Olin, et al.. (2000). Kinetic properties of missense mutations in patients with glutathione synthetase deficiency. Biochemical Journal. 349(1). 275–275. 24 indexed citations
11.
NJÅLSSON, Runa, Katarina Steen Carlsson, B. Olin, et al.. (2000). Kinetic properties of missense mutations in patients with glutathione synthetase deficiency. Biochemical Journal. 349(1). 275–279. 12 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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