Hanne E. Akselsen

1.5k total citations
28 papers, 1.2k citations indexed

About

Hanne E. Akselsen is a scholar working on Genetics, Immunology and Surgery. According to data from OpenAlex, Hanne E. Akselsen has authored 28 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 11 papers in Immunology and 7 papers in Surgery. Recurrent topics in Hanne E. Akselsen's work include Diabetes and associated disorders (13 papers), T-cell and B-cell Immunology (8 papers) and Immune Cell Function and Interaction (7 papers). Hanne E. Akselsen is often cited by papers focused on Diabetes and associated disorders (13 papers), T-cell and B-cell Immunology (8 papers) and Immune Cell Function and Interaction (7 papers). Hanne E. Akselsen collaborates with scholars based in Norway, Sweden and United Kingdom. Hanne E. Akselsen's co-authors include Dag E. Undlien, Erik Thorsby, Kjersti S. Rønningen, Benedicte A. Lie, Knut Dahl‐Jørgensen, Geir Joner, John A. Todd, D E Undlien, Jørn Nerup and Flemming Pociot and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Diabetes and Genome Research.

In The Last Decade

Hanne E. Akselsen

28 papers receiving 1.2k citations

Peers

Hanne E. Akselsen

GENET

IMMUN

SURGE

EDM

H. Donner Germany

Helen E. Stevens United Kingdom

Sunanda Babu United States

J. Braun Germany

I Deschamps France

Beate Skinningsrud Norway

A Florin-Christensen Argentina

Kalle Kisand Estonia

Jose Zapardiel‐Gonzalo United States

Johanna Aaltonen Finland

H. Donner Germany

Hanne E. Akselsen

1.1k ×1.6

GENET

781 ×1.5

IMMUN

256 ×0.7

SURGE

535 ×1.5

EDM

187 ×1.4

Citations per year, relative to Hanne E. Akselsen Hanne E. Akselsen (= 1×) peers H. Donner

Countries citing papers authored by Hanne E. Akselsen

Since Specialization

Citations

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

Fields of papers citing papers by Hanne E. Akselsen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hanne E. Akselsen. 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 Hanne E. Akselsen. The network helps show where Hanne E. Akselsen may publish in the future.

Co-authorship network of co-authors of Hanne E. Akselsen

This figure shows the co-authorship network connecting the top 25 collaborators of Hanne E. Akselsen. A scholar is included among the top collaborators of Hanne E. Akselsen 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 Hanne E. Akselsen. Hanne E. Akselsen 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

Rasmussen, Trond, et al.. (2014). HLA associated type 1 diabetes risk in children of Pakistani migrants to Norway. Medical Hypotheses. 83(6). 664–667. 1 indexed citations

Gervin, Kristina, Hanne E. Akselsen, Ingunn Brandt, et al.. (2011). Extensive variation and low heritability of DNA methylation identified in a twin study. Genome Research. 21(11). 1813–1821. 45 indexed citations

Skinningsrud, Beate, Benedicte A. Lie, Ewa Lavant, et al.. (2011). Multiple Loci in the HLA Complex Are Associated with Addison's Disease. The Journal of Clinical Endocrinology & Metabolism. 96(10). E1703–E1708. 43 indexed citations

Rønningen, Kjersti S., et al.. (2011). HLA‐DRB1, ‐DQA1 and ‐DQB1 Alleles and Haplotypes in First‐Generation Pakistani Immigrants in Norway. Scandinavian Journal of Immunology. 75(4). 426–430. 6 indexed citations

Wangensteen, Teresia, Hanne E. Akselsen, Jostein Holmen, Dag E. Undlien, & Lars Retterstøl. (2010). A Common Haplotype in NAPEPLD Is Associated With Severe Obesity in a Norwegian Population‐Based Cohort (the HUNT Study). Obesity. 19(3). 612–617. 28 indexed citations

Wangensteen, Teresia, T Egeland, Hanne E. Akselsen, et al.. (2010). FTO Genotype and Weight Gain in Obese and Normal Weight Adults From a Norwegian Population Based Cohort (the HUNT Study). Experimental and Clinical Endocrinology & Diabetes. 118(9). 649–652. 10 indexed citations

Bjørnvold, Marit, D E Undlien, Geir Joner, et al.. (2008). Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes. Diabetologia. 51(4). 589–596. 47 indexed citations

Lie, Benedicte A., Marte K. Viken, Hanne E. Akselsen, et al.. (2007). Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease. Human Immunology. 68(7). 592–598. 6 indexed citations

Munthe‐Kaas, Monica Cheng, Kai-Häkon Carlsen, K. H. Carlsen, et al.. (2007). HLA Dr‐Dq haplotypes and the TNFA‐308 polymorphism: associations with asthma and allergy. Allergy. 62(9). 991–998. 28 indexed citations

10.

Blomhoff, Anne, Marita Olsson, Stefan Johansson, et al.. (2006). Linkage disequilibrium and haplotype blocks in the MHC vary in an HLA haplotype specific manner assessed mainly by DRB1*03 and DRB1*04 haplotypes. Genes and Immunity. 7(2). 130–140. 40 indexed citations

11.

Bjørnvold, Marit, Silja Svanstrøm Amundsen, Lars C. Stene, et al.. (2006). FOXP3 polymorphisms in type 1 diabetes and coeliac disease. Journal of Autoimmunity. 27(2). 140–144. 37 indexed citations

12.

Blomhoff, Anne, E. Helen Kemp, David J. Gawkrodger, et al.. (2005). CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases. Pigment Cell Research. 18(1). 55–58. 56 indexed citations

13.

Johansson, Stefan, Benedicte A. Lie, John A. Todd, et al.. (2003). Evidence of at least two type 1 diabetes susceptibility genes in the HLA complex distinct from HLA-DQB1, -DQA1 and –DRB1. Genes and Immunity. 4(1). 46–53. 59 indexed citations

14.

Lie, Benedicte A., Hanne E. Akselsen, Christopher L. Bowlus, et al.. (2002). Polymorphisms in the gene encoding thymus-specific serine protease in the extended HLA complex: a potential candidate gene for autoimmune and HLA-associated diseases. Genes and Immunity. 3(5). 306–312. 18 indexed citations

15.

Lie, Benedicte A., Kjersti S. Rønningen, Hanne E. Akselsen, Erik Thorsby, & Dag E. Undlien. (2000). Application and Interpretation of Transmission/Disequilibrium Tests: Transmission of HLA-DQ Haplotypes to Unaffected Siblings in 526 Families with Type 1 Diabetes. The American Journal of Human Genetics. 66(2). 740–743. 17 indexed citations

16.

Lie, Benedicte A., Ludvig M. Sollid, Henry Ascher, et al.. (1999). A gene telomeric of the HLA class I region is involved in predisposition to both type 1 diabetes and coeliac disease. Tissue Antigens. 54(2). 162–168. 99 indexed citations

17.

Undlien, D E, Ingrid Kockum, Kjersti S. Rønningen, et al.. (1999). HLA associations in type 1 diabetes among patients not carrying high‐risk DR3‐DQ2 or DR4‐DQ8 haplotypes. Tissue Antigens. 54(6). 543–551. 29 indexed citations

18.

Lie, Benedicte A., John A. Todd, Flemming Pociot, et al.. (1999). The Predisposition to Type 1 Diabetes Linked to the Human Leukocyte Antigen Complex Includes at Least One Non–Class II Gene. The American Journal of Human Genetics. 64(3). 793–800. 153 indexed citations

19.

Undlien, D E, H. Bell, Hans Erik Heier, Hanne E. Akselsen, & E Thørsby. (1998). [Genetic diagnostic test for hemochromatosis].. PubMed. 118(2). 238–40. 5 indexed citations

20.

Lie, Benedicte A., Hanne E. Akselsen, Geir Joner, et al.. (1997). HLA Associations in Insulin-Dependent Diabetes Mellitus: No Independent Association to Particular DP Genes. Human Immunology. 55(2). 170–175. 25 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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