Benedicte A. Lie

2.5k total citations
35 papers, 1.4k citations indexed

About

Benedicte A. Lie is a scholar working on Immunology, Rheumatology and Genetics. According to data from OpenAlex, Benedicte A. Lie has authored 35 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Immunology, 10 papers in Rheumatology and 10 papers in Genetics. Recurrent topics in Benedicte A. Lie's work include T-cell and B-cell Immunology (12 papers), Diabetes and associated disorders (9 papers) and Systemic Lupus Erythematosus Research (7 papers). Benedicte A. Lie is often cited by papers focused on T-cell and B-cell Immunology (12 papers), Diabetes and associated disorders (9 papers) and Systemic Lupus Erythematosus Research (7 papers). Benedicte A. Lie collaborates with scholars based in Norway, Sweden and United States. Benedicte A. Lie's co-authors include Ludvig M. Sollid, Erik Thorsby, Marte K. Viken, Tom H. Karlsen, Kirsten Muri Boberg, Gry B. N. Nordang, Erik Schrumpf, Hanne F. Harbo, Dag E. Undlien and Berit Flatø and has published in prestigious journals such as Gastroenterology, PLoS ONE and Hepatology.

In The Last Decade

Benedicte A. Lie

35 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Benedicte A. Lie Norway	22	571	300	269	266	235	35	1.4k
Maria Giovanna Danieli Italy	28	497 0.9×	187 0.6×	230 0.9×	637 2.4×	339 1.4×	79	1.8k
Arno R. van der Slik Netherlands	26	1.3k 2.2×	547 1.8×	412 1.5×	183 0.7×	142 0.6×	47	2.0k
Mauro Congia Italy	25	1.0k 1.8×	1.1k 3.6×	653 2.4×	476 1.8×	113 0.5×	50	2.7k
Marzia Dolcino Italy	20	316 0.6×	110 0.4×	314 1.2×	327 1.2×	184 0.8×	35	1.3k
Elisa Tinazzi Italy	25	415 0.7×	110 0.4×	187 0.7×	175 0.7×	202 0.9×	63	1.5k
G. F. Bottazzo United Kingdom	30	986 1.7×	1.1k 3.7×	596 2.2×	310 1.2×	146 0.6×	65	3.2k
Yaron Tomer United States	24	604 1.1×	1.0k 3.5×	164 0.6×	172 0.6×	135 0.6×	30	1.9k
Britt Nakken Norway	27	980 1.7×	236 0.8×	160 0.6×	280 1.1×	425 1.8×	54	2.0k
Simona Fisogni Italy	20	144 0.3×	98 0.3×	501 1.9×	276 1.0×	147 0.6×	56	1.5k
J. Bertrams Germany	24	948 1.7×	943 3.1×	750 2.8×	165 0.6×	203 0.9×	88	2.2k

Countries citing papers authored by Benedicte A. Lie

Since Specialization

Citations

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

Fields of papers citing papers by Benedicte A. Lie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Benedicte A. Lie. 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 Benedicte A. Lie. The network helps show where Benedicte A. Lie may publish in the future.

Co-authorship network of co-authors of Benedicte A. Lie

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

Viken, Marte K., Benedicte A. Lie, Per Medbøe Thorsby, et al.. (2021). High nocturnal sleep fragmentation is associated with low T lymphocyte P2Y11 protein levels in narcolepsy type 1. SLEEP. 44(8). 7 indexed citations

Andreassen, Ole A., Yunpeng Wang, Wesley K. Thompson, et al.. (2015). Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms. PLoS ONE. 10(4). e0123057–e0123057. 33 indexed citations

Provan, Sella Aarrestad, D. P. C. de Rooy, Annette H M van der Helm–van Mil, et al.. (2013). Associations between APOE Genotypes and Disease Susceptibility, Joint Damage and Lipid Levels in Patients with Rheumatoid Arthritis. PLoS ONE. 8(4). e60970–e60970. 19 indexed citations

Maniaol, Angelina, Ahmed Elsais, Åslaug Rudjord Lorentzen, et al.. (2012). Late Onset Myasthenia Gravis Is Associated with HLA DRB1*15:01 in the Norwegian Population. PLoS ONE. 7(5). e36603–e36603. 97 indexed citations

Martín, Jose‐Ezequiel, Behrooz Z. Alizadeh, Miguel Á. González‐Gay, et al.. (2011). Evidence for PTPN22 R620W Polymorphism As the Sole Common Risk Variant for Rheumatoid Arthritis in the 1p13.2 Region. The Journal of Rheumatology. 38(11). 2290–2296. 18 indexed citations

Nordang, Gry B. N., Marte K. Viken, Silja Svanstrøm Amundsen, et al.. (2011). Interferon regulatory factor 5 gene polymorphism confers risk to several rheumatic diseases and correlates with expression of alternative thymic transcripts. Lara D. Veeken. 51(4). 619–626. 32 indexed citations

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

Link, Jenny, Åslaug Rudjord Lorentzen, Ingrid Kockum, et al.. (2010). Two HLA class I genes independently associated with multiple sclerosis. Journal of Neuroimmunology. 226(1-2). 172–176. 19 indexed citations

Ramagopalan, S V, Jenny Link, Jake Byrnes, et al.. (2009). HLA-DRB1 and month of birth in multiple sclerosis. Neurology. 73(24). 2107–2111. 38 indexed citations

10.

Harbo, Hanne F., Åslaug Rudjord Lorentzen, Kjell‐Morten Myhr, et al.. (2009). Norwegian Sami differs significantly from other Norwegians according to their HLA profile. Tissue Antigens. 75(3). 207–217. 14 indexed citations

11.

Skinningsrud, Beate, Benedicte A. Lie, Eystein S. Husebye, et al.. (2009). A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis. Annals of the Rheumatic Diseases. 69(8). 1471–1474. 48 indexed citations

12.

Eike, Morten Christoph, Tim Becker, Keith Humphreys, Martin L. Olsson, & Benedicte A. Lie. (2008). Conditional analyses on the T1DGC MHC dataset: novel associations with type 1 diabetes around HLA-G and confirmation of HLA-B. Genes and Immunity. 10(1). 56–67. 26 indexed citations

13.

Viken, Marte K., Martin L. Olsson, Siri T. Flåm, et al.. (2007). The PTPN22 promoter polymorphism –1123G>C association cannot be distinguished from the 1858C>T association in a Norwegian rheumatoid arthritis material. Tissue Antigens. 70(3). 190–197. 53 indexed citations

14.

Harbo, Hanne F., Åslaug Rudjord Lorentzen, Margitta T. Kampman, et al.. (2007). Low frequency of the disease‐associated DRB1*15‐DQB1*06 haplotype may contribute to the low prevalence of multiple sclerosis in Sami. Tissue Antigens. 69(4). 299–304. 32 indexed citations

15.

Viken, Marte K., Geir Joner, Knut Dahl‐Jørgensen, et al.. (2007). Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis. Human Immunology. 68(9). 748–755. 28 indexed citations

16.

Smestad, C., Boel Brynedal, Gudrun Jonasdottir, et al.. (2007). The impact of HLA‐A and ‐DRB1 on age at onset, disease course and severity in Scandinavian multiple sclerosis patients. European Journal of Neurology. 14(8). 835–840. 55 indexed citations

17.

Melum, Espen, Tom H. Karlsen, Ulrika Broomé, et al.. (2006). The 32‐base pair deletion of the chemokine receptor 5 gene (CCR5‐Δ32) is not associated with primary sclerosing cholangitis in 363 Scandinavian patients. Tissue Antigens. 68(1). 78–81. 13 indexed citations

18.

Karlsen, Tom H., Benedicte A. Lie, Kathrine Frey Frøslie, et al.. (2006). Polymorphisms in the Steroid and Xenobiotic Receptor Gene Influence Survival in Primary Sclerosing Cholangitis. Gastroenterology. 131(3). 781–787. 49 indexed citations

19.

Sollid, Ludvig M. & Benedicte A. Lie. (2005). Celiac Disease Genetics: Current Concepts and Practical Applications. Clinical Gastroenterology and Hepatology. 3(9). 843–851. 166 indexed citations

20.

Louka, A.S., Benedicte A. Lie, Bente A. Talseth‐Palmer, et al.. (2003). Coeliac disease patients carry conserved HLA-DR3-DQ2 haplotypes revealed by association of TNF alleles. Immunogenetics. 55(5). 339–343. 26 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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