Helga Sanner

4.2k total citations
42 papers, 714 citations indexed

About

Helga Sanner is a scholar working on Epidemiology, Rheumatology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Helga Sanner has authored 42 papers receiving a total of 714 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Epidemiology, 14 papers in Rheumatology and 10 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Helga Sanner's work include Inflammatory Myopathies and Dermatomyositis (25 papers), Eosinophilic Disorders and Syndromes (10 papers) and Autoimmune and Inflammatory Disorders Research (10 papers). Helga Sanner is often cited by papers focused on Inflammatory Myopathies and Dermatomyositis (25 papers), Eosinophilic Disorders and Syndromes (10 papers) and Autoimmune and Inflammatory Disorders Research (10 papers). Helga Sanner collaborates with scholars based in Norway, United States and Hungary. Helga Sanner's co-authors include Berit Flatø, Ivar Sjaastad, Thomas Schwartz, Jan Tore Gran, Ingrid E. Lundberg, Louise Pyndt Diederichsen, Trond Mogens Aaløkken, I. Sjaastad, Trygve Husebye and Ákos Koller and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Frontiers in Immunology.

In The Last Decade

Helga Sanner

41 papers receiving 704 citations

Peers

Helga Sanner
NJ McHugh United Kingdom
S. Maillard United Kingdom
J. A. Maldonado Cocco Argentina
Hisae Ichida Japan
B.A. Laing Australia
Kateřina Jarošová Czechia
R M Brouwer Netherlands
S. Vagnani Italy
Kizuku Watanabe Japan
Rita Jerath United States
NJ McHugh United Kingdom
Helga Sanner
Citations per year, relative to Helga Sanner Helga Sanner (= 1×) peers NJ McHugh

Countries citing papers authored by Helga Sanner

Since Specialization
Citations

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

Fields of papers citing papers by Helga Sanner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helga Sanner

This figure shows the co-authorship network connecting the top 25 collaborators of Helga Sanner. A scholar is included among the top collaborators of Helga Sanner 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 Helga Sanner. Helga Sanner 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.
Nicolai, Rebecca, Silvia Rosina, Brigitte Bader‐Meunier, et al.. (2025). Approach to Janus kinase inhibition for juvenile dermatomyositis among CARRA and PReS providers. Lara D. Veeken. 64(8). 4732–4737. 1 indexed citations
2.
Olarescu, Nicoleta Cristina, et al.. (2025). Visceral adipose tissue is related to interleukin 6 and resistin in juvenile idiopathic arthritis – a case-control study. Rheumatology International. 45(3). 63–63. 1 indexed citations
3.
Fominykh, Vera, Alexey Shadrin, Piotr Jahołkowski, et al.. (2025). Mapping the genetic landscape of immune-mediated disorders: potential implications for classification and therapeutic strategies. Frontiers in Immunology. 16. 1543781–1543781. 2 indexed citations
4.
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Jahołkowski, Piotr, Alexey Shadrin, Svend Andersen, et al.. (2024). Incidence and Genetic Risk of Juvenile Idiopathic Arthritis in Norway by Latitude. Arthritis & Rheumatology. 77(4). 458–467. 2 indexed citations
6.
Schwartz, Thomas, Helga Sanner, Vibke Lilleby, et al.. (2023). Cardiac dysfunction in mixed connective tissue disease: a nationwide observational study. Rheumatology International. 43(6). 1055–1065. 3 indexed citations
7.
Andersen, Svend, et al.. (2023). Antibiotic exposure in prenatal and early life and risk of juvenile idiopathic arthritis: a nationwide register-based cohort study. RMD Open. 9(3). e003333–e003333. 8 indexed citations
8.
Schwartz, Thomas, Eli Taraldsrud, May Brit Lund, et al.. (2022). Associations between cardiac and pulmonary involvement in patients with juvenile dermatomyositis—a cross-sectional study. Rheumatology International. 42(7). 1213–1220. 5 indexed citations
9.
Deakin, Claire T., John Bowes, Lisa G. Rider, et al.. (2022). Association with HLA-DRβ1 position 37 distinguishes juvenile dermatomyositis from adult-onset myositis. Human Molecular Genetics. 31(14). 2471–2481. 14 indexed citations
10.
Dijkhuizen, E. H. Pieter van, M. Mazzoni, Nuray Aktay Ayaz, et al.. (2022). Validity and Reliability of Four Parent/Patient–Reported Outcome Measures for Juvenile Idiopathic Arthritis Remote Monitoring. Arthritis Care & Research. 75(2). 391–400. 2 indexed citations
11.
Marstein, Henriette S., Kristin Godang, Berit Flatø, et al.. (2021). Bone mineral density and explanatory factors in children and adults with juvenile dermatomyositis at long term follow-up; a cross sectional study. Pediatric Rheumatology. 19(1). 56–56. 4 indexed citations
12.
Sanner, Helga, et al.. (2019). Effect on Cardiac Function of Longstanding Juvenile-onset Mixed Connective Tissue Disease: A Controlled Study. The Journal of Rheumatology. 46(7). 739–747. 8 indexed citations
13.
Schwartz, Thomas, Eva Kirkhus, Trond Mogens Aaløkken, et al.. (2017). Submaximal Exercise Capacity in Juvenile Dermatomyositis after Longterm Disease: The Contribution of Muscle, Lung, and Heart Involvement. The Journal of Rheumatology. 44(6). 827–834. 13 indexed citations
14.
Schwartz, Thomas, Eva Kirkhus, Trond Mogens Aaløkken, et al.. (2015). OP0151 The 6-Minute Walk Test Assessed in Juvenile Dermatomyositis After Long Term Follow-Up: The Impact of Muscle, Lung, and Heart Dysfunction. Annals of the Rheumatic Diseases. 74. 125–126. 1 indexed citations
15.
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Schwartz, Thomas, Ivar Sjaastad, Berit Flatø, et al.. (2014). In active juvenile dermatomyositis, elevated eotaxin and MCP-1 and cholesterol levels in the upper normal range are associated with cardiac dysfunction. Lara D. Veeken. 53(12). 2214–2222. 16 indexed citations
17.
Sanner, Helga, Ivar Sjaastad, & Berit Flatø. (2013). SAT0465 The Myositis Disease Activity Assessment Tool and the Printo Criteria for Clinically Inactive Disease Applied after Long-Term Follow-Up in Juvenile Onset Dermatomyositis.. Annals of the Rheumatic Diseases. 72. A738–A739. 3 indexed citations
18.
Sanner, Helga, et al.. (2012). Quality of life in adults with juvenile‐onset dermatomyositis: A case–control study. Arthritis Care & Research. 64(7). 1020–1027. 33 indexed citations
19.
Schwartz, Thomas, Helga Sanner, Trygve Husebye, Berit Flatø, & I. Sjaastad. (2011). Cardiac dysfunction in juvenile dermatomyositis: a case-control study. Annals of the Rheumatic Diseases. 70(5). 766–771. 54 indexed citations
20.
Sanner, Helga, Eva Kirkhus, Else Merckoll, et al.. (2010). Long‐term muscular outcome and predisposing and prognostic factors in juvenile dermatomyositis: A case–control study. Arthritis Care & Research. 62(8). 1103–1111. 50 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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