Øivind Nilssen

1.7k total citations
47 papers, 1.2k citations indexed

About

Øivind Nilssen is a scholar working on Molecular Biology, Physiology and Epidemiology. According to data from OpenAlex, Øivind Nilssen has authored 47 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 15 papers in Physiology and 13 papers in Epidemiology. Recurrent topics in Øivind Nilssen's work include Lysosomal Storage Disorders Research (15 papers), Poxvirus research and outbreaks (9 papers) and Carbohydrate Chemistry and Synthesis (8 papers). Øivind Nilssen is often cited by papers focused on Lysosomal Storage Disorders Research (15 papers), Poxvirus research and outbreaks (9 papers) and Carbohydrate Chemistry and Synthesis (8 papers). Øivind Nilssen collaborates with scholars based in Norway, United States and Denmark. Øivind Nilssen's co-authors include Dag Malm, Lisbeth Tranebjærg, Thomas Berg, Terje Traavik, Thomas Rosenberg, Ole Kristian Tollersrud, Malachy Ifeanyi Okeke, Claes Möller, Hilde Monica Frostad Riise Stensland and Michael D. Weston and has published in prestigious journals such as PLoS ONE, Brain and Biochemical Journal.

In The Last Decade

Øivind Nilssen

47 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Øivind Nilssen Norway 21 641 395 217 190 160 47 1.2k
Sylvie Rouquier France 19 887 1.4× 130 0.3× 104 0.5× 183 1.0× 549 3.4× 36 2.0k
Betsy M. Ohlsson‐Wilhelm United States 19 511 0.8× 106 0.3× 100 0.5× 57 0.3× 37 0.2× 41 1.3k
Dominique Giorgi France 20 825 1.3× 144 0.4× 100 0.5× 176 0.9× 571 3.6× 44 2.0k
Ritsuko Koga Japan 20 978 1.5× 336 0.9× 315 1.5× 155 0.8× 50 0.3× 30 1.9k
Karima Kissa France 21 1.4k 2.1× 275 0.7× 267 1.2× 1.7k 8.8× 22 0.1× 38 3.2k
Keiichiro Susuki Japan 26 610 1.0× 379 1.0× 88 0.4× 272 1.4× 28 0.2× 71 3.0k
Tyler Hickman United States 12 1.6k 2.5× 37 0.1× 210 1.0× 169 0.9× 183 1.1× 14 2.1k
Karen Ehrenman United States 22 1.3k 2.0× 96 0.2× 183 0.8× 103 0.5× 85 0.5× 29 2.0k
Donald L. Ewert United States 20 654 1.0× 45 0.1× 348 1.6× 87 0.5× 188 1.2× 45 1.6k
Niels C. Adams United States 14 1.2k 1.8× 105 0.3× 465 2.1× 182 1.0× 129 0.8× 16 2.8k

Countries citing papers authored by Øivind Nilssen

Since Specialization
Citations

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

Fields of papers citing papers by Øivind Nilssen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Øivind Nilssen

This figure shows the co-authorship network connecting the top 25 collaborators of Øivind Nilssen. A scholar is included among the top collaborators of Øivind Nilssen 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 Øivind Nilssen. Øivind Nilssen 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.
Løseth, Sissel, Helle Høyer, Eric Delpire, et al.. (2022). Late-onset sensory-motor axonal neuropathy, a novelSLC12A6-related phenotype. Brain. 146(3). 912–922. 3 indexed citations
2.
Rendtorff, Nanna Dahl, Lisbeth Tranebjærg, Karen Grønskov, et al.. (2016). Usher syndrome in Denmark: mutation spectrum and some clinical observations. Molecular Genetics & Genomic Medicine. 4(5). 527–539. 20 indexed citations
3.
4.
Nilssen, Øivind, Hilde Monica Frostad Riise Stensland, & Dag Malm. (2011). Clinical utility gene card for: α-Mannosidosis. European Journal of Human Genetics. 19(7). 832–832. 2 indexed citations
5.
Stensland, Hilde Monica Frostad Riise, et al.. (2011). Molecular and cellular characterization of novel α-mannosidosis mutations. Human Molecular Genetics. 20(13). 2651–2661. 12 indexed citations
6.
Okeke, Malachy Ifeanyi, Øivind Nilssen, Ugo Moens, Morten Tryland, & Terje Traavik. (2009). In vitro host range, multiplication and virion forms of recombinant viruses obtained from co-infection in vitro with a vaccinia-vectored influenza vaccine and a naturally occurring cowpox virus isolate. Virology Journal. 6(1). 55–55. 11 indexed citations
7.
Hansen, Hilde, Malachy Ifeanyi Okeke, Øivind Nilssen, & Terje Traavik. (2009). Comparison and phylogenetic analysis of cowpox viruses isolated from cats and humans in Fennoscandia. Archives of Virology. 154(8). 1293–1302. 12 indexed citations
8.
Okeke, Malachy Ifeanyi, Olayiwola A. Adekoya, Ugo Moens, et al.. (2009). Comparative sequence analysis of A-type inclusion (ATI) and P4c proteins of orthopoxviruses that produce typical and atypical ATI phenotypes. Virus Genes. 39(2). 200–209. 12 indexed citations
9.
Ingebretsen, Ole C., et al.. (2008). Real-time detection and quantification of mitochondrial mutations with oligonucleotide primers containing locked nucleic acid. Clinica Chimica Acta. 390(1-2). 126–133. 12 indexed citations
10.
Malm, Dag & Øivind Nilssen. (2008). Alpha-mannosidosis. Orphanet Journal of Rare Diseases. 3(1). 21–21. 122 indexed citations
11.
Tranebjærg, Lisbeth, et al.. (2008). Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II. Human Mutation. 29(3). 451–451. 92 indexed citations
12.
Urushihara, Maki, Shoji Kagami, Koji Yasutomo, et al.. (2004). Sisters with a-mannosidosis and systemic lupus erythematosus. European Journal of Pediatrics. 163(4-5). 192–195. 26 indexed citations
13.
Tranebjærg, Lisbeth, Thomas Rosenberg, Claes Möller, et al.. (2001). A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation. The American Journal of Human Genetics. 69(1). 228–234. 67 indexed citations
14.
Berg, Thomas, et al.. (1999). Spectrum of Mutations in α-Mannosidosis. The American Journal of Human Genetics. 64(1). 77–88. 57 indexed citations
15.
Tollersrud, Ole Kristian, et al.. (1999). Characterization of a novel α-mannosidosis-causing mutation and its use in leukocyte genotyping after bone marrow transplantation. Human Genetics. 104(1). 106–107. 5 indexed citations
16.
Berg, Thomas, et al.. (1997). Genomic Structure of the Human Lysosomal α-Mannosidase Gene (MANB). Genomics. 42(2). 200–207. 35 indexed citations
17.
Nilssen, Øivind, Carl Gunnar Fossdal, B.V. Johansen, & Bjørn H. Lindqvist. (1996). Bacteriophage P4 Capsid-Size Determination and Its Relationship to P2 Helper Interference. Virology. 219(2). 443–452. 6 indexed citations
18.
Nilssen, Øivind, Erich W. Six, Melvin G. Sunshine, & Bjørn H. Lindqvist. (1996). Mutational Analysis of the Bacteriophage P4 Capsid-Size-Determining Gene. Virology. 219(2). 432–442. 10 indexed citations
19.
Jacobsen, Erik, Erich W. Six, Øivind Nilssen, et al.. (1995). Bacteriophage P2: Genes Involved in Baseplate Assembly. Virology. 213(1). 109–121. 32 indexed citations
20.
Nilssen, Øivind, Ole Kristian Tollersrud, O. Borud, & Lisbeth Tranebjærg. (1993). A simple and rapid PCR based method for AGUFin determination. Human Molecular Genetics. 2(4). 484–484. 4 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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