Inger Jonasson

2.3k total citations
8 papers, 426 citations indexed

About

Inger Jonasson is a scholar working on Rheumatology, Genetics and Immunology. According to data from OpenAlex, Inger Jonasson has authored 8 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Rheumatology, 3 papers in Genetics and 3 papers in Immunology. Recurrent topics in Inger Jonasson's work include Systemic Lupus Erythematosus Research (3 papers), T-cell and B-cell Immunology (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Inger Jonasson is often cited by papers focused on Systemic Lupus Erythematosus Research (3 papers), T-cell and B-cell Immunology (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Inger Jonasson collaborates with scholars based in Sweden, United States and Portugal. Inger Jonasson's co-authors include R. B. R. Persson, E Fries, Michael Wassler, Ulf Gyllensten, Gerður Gröndal, Elisabet Svenungsson, Bo Johanneson, Helga Kristjánsdóttir, Marta E. Alarcón‐Riquelme and Ingrid E. Lundberg and has published in prestigious journals such as PLoS ONE, Biochemical Journal and Journal of Medical Genetics.

In The Last Decade

Inger Jonasson

7 papers receiving 422 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Inger Jonasson Sweden 6 175 161 156 137 45 8 426
Arianne C. van Sechel Netherlands 6 263 1.5× 241 1.5× 83 0.5× 42 0.3× 40 0.9× 9 614
T Sarr United States 8 192 1.1× 139 0.9× 54 0.3× 16 0.1× 28 0.6× 8 431
Yoshiko Kawasaki Japan 11 32 0.2× 125 0.8× 45 0.3× 41 0.3× 8 0.2× 18 325
Bartholomew J. Naughton United States 8 41 0.2× 269 1.7× 20 0.1× 81 0.6× 13 0.3× 11 464
M.M. Morris United Kingdom 5 292 1.7× 96 0.6× 72 0.5× 29 0.2× 49 1.1× 9 491
S A McCormick United States 10 34 0.2× 210 1.3× 39 0.3× 14 0.1× 83 1.8× 12 477
Anja Schlecht Germany 16 175 1.0× 279 1.7× 22 0.1× 38 0.3× 265 5.9× 37 885
Patrizia Ferrara France 10 82 0.5× 296 1.8× 15 0.1× 32 0.2× 10 0.2× 13 428
Markus Thiel Germany 8 125 0.7× 142 0.9× 37 0.2× 25 0.2× 12 0.3× 10 339
Maha Mustafa Sweden 10 329 1.9× 71 0.4× 98 0.6× 27 0.2× 29 0.6× 16 549

Countries citing papers authored by Inger Jonasson

Since Specialization
Citations

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

Fields of papers citing papers by Inger Jonasson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inger Jonasson

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

All Works

8 of 8 papers shown
1.
Lopes, Fátima, Mafalda Barbosa, Adam Ameur, et al.. (2016). Identification of novel genetic causes of Rett syndrome-like phenotypes. Journal of Medical Genetics. 53(3). 190–199. 126 indexed citations
2.
Lopes, Fátima, Mafalda Barbosa, Teresa Temudo, et al.. (2015). ISDN2014_0322: REMOVED: Identification of novel genetic causes of Rett syndrome‐like phenotypes by whole exome sequencing. International Journal of Developmental Neuroscience. 47(Part_A). 99–99.
3.
Johansson, Åsa, Inger Jonasson, & Ulf Gyllensten. (2009). Extended Haplotypes in the Growth Hormone Releasing Hormone Receptor Gene (GHRHR) Are Associated with Normal Variation in Height. PLoS ONE. 4(2). e4464–e4464. 8 indexed citations
4.
Lindqvist, Anna-Karin B., Kristján Steinsson, Bo Johanneson, et al.. (2000). A Susceptibility Locus for Human Systemic Lupus Erythematosus (hSLE1) on Chromosome 2q. Journal of Autoimmunity. 14(2). 169–178. 153 indexed citations
5.
Johanneson, Bo, Kristján Steinsson, Helga Kristjánsdóttir, et al.. (1999). A Comparison of Genome-scans Performed in Multicase Families with Systemic Lupus Erythematosus from Different Population Groups. Journal of Autoimmunity. 13(1). 137–141. 19 indexed citations
6.
Alarcón‐Riquelme, Marta E., Inger Jonasson, Bo Johanneson, et al.. (1999). Genetic analysis of the contribution of IL10 to systemic lupus erythematosus.. PubMed. 26(10). 2148–52. 30 indexed citations
7.
Fries, E, et al.. (1988). Labelling of proteins with [35S]methionine in monolayer cultures of rat hepatocytes.. PubMed. 16(4). 737–45. 1 indexed citations
8.
Wassler, Michael, Inger Jonasson, R. B. R. Persson, & E Fries. (1987). Differential permeabilization of membranes by saponin treatment of isolated rat hepatocytes. Release of secretory proteins. Biochemical Journal. 247(2). 407–415. 89 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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