O Jensson

2.2k total citations
41 papers, 1.7k citations indexed

About

O Jensson is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, O Jensson has authored 41 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 13 papers in Genetics and 12 papers in Physiology. Recurrent topics in O Jensson's work include Amyloidosis: Diagnosis, Treatment, Outcomes (9 papers), Alzheimer's disease research and treatments (9 papers) and Iron Metabolism and Disorders (4 papers). O Jensson is often cited by papers focused on Amyloidosis: Diagnosis, Treatment, Outcomes (9 papers), Alzheimer's disease research and treatments (9 papers) and Iron Metabolism and Disorders (4 papers). O Jensson collaborates with scholars based in Iceland, United Kingdom and Sweden. O Jensson's co-authors include Blas Frangione, Anders Grubb, Ástríður Pálsdóttir, Magnus Abrahamson, Ísleifur Ólafsson, Jorge Ghiso, Magnus Ulvsbäck, Åke Lundwall, Árni Árnason and Leifur Thorsteinsson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nucleic Acids Research.

In The Last Decade

O Jensson

39 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
O Jensson Iceland 17 662 661 421 236 216 41 1.7k
Helge Löfberg Sweden 19 450 0.7× 495 0.7× 288 0.7× 134 0.6× 201 0.9× 32 1.6k
Akiko Ishii Japan 24 249 0.4× 738 1.1× 231 0.5× 205 0.9× 182 0.8× 75 1.6k
Martha Konieczkowski United States 24 221 0.3× 835 1.3× 541 1.3× 31 0.1× 158 0.7× 41 1.8k
Hitomi Imachi Japan 25 257 0.4× 736 1.1× 89 0.2× 145 0.6× 154 0.7× 112 2.0k
Takashi Oite Japan 26 175 0.3× 979 1.5× 913 2.2× 16 0.1× 138 0.6× 117 2.2k
Berardino Porfirio Italy 19 84 0.1× 718 1.1× 89 0.2× 159 0.7× 214 1.0× 69 1.3k
Muriel Gaudry France 25 307 0.5× 909 1.4× 106 0.3× 22 0.1× 95 0.4× 36 1.9k
G. Aßmann Germany 23 237 0.4× 377 0.6× 32 0.1× 102 0.4× 167 0.8× 98 1.8k
Björn Hartleben Germany 24 186 0.3× 1.1k 1.7× 1.2k 2.9× 36 0.2× 416 1.9× 52 2.8k
Yasushi Nakamoto Japan 18 95 0.1× 356 0.5× 487 1.2× 62 0.3× 60 0.3× 78 1.2k

Countries citing papers authored by O Jensson

Since Specialization
Citations

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

Fields of papers citing papers by O Jensson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of O Jensson

This figure shows the co-authorship network connecting the top 25 collaborators of O Jensson. A scholar is included among the top collaborators of O Jensson 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 O Jensson. O Jensson 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.
Haan, J., Marion L. C. Maat–Schieman, Sjoerd G. van Duinen, et al.. (2009). Co-localization of β/A4 and cystatin C in cortical blood vessels in Dutch, but not in Icelandic hereditary cerebral hemorrhage with amyloidosis. Acta Neurologica Scandinavica. 89(5). 367–371. 11 indexed citations
2.
Hol, Frans A., M.P.A. Geurds, O Jensson, et al.. (1994). Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family. Human Genetics. 93(4). 452–6. 9 indexed citations
3.
Jensson, O, et al.. (1994). Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutation. Journal of Internal Medicine. 235(5). 443–450. 2 indexed citations
4.
Ögmundsdóttir, Helga M., Leifur Thorsteinsson, Ásbjörn Sigfússon, et al.. (1992). Natural killer cell function and malignant cell phenotype in hairy cell leukaemia. Apmis. 100(1-6). 10–20. 2 indexed citations
5.
Ólafsson, Ísleifur, Gunnar Guðmundsson, Magnus Abrahamson, O Jensson, & Anders Grubb. (1990). The amino terminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated: direct sequence analysis from agarose gel electropherograms. Scandinavian Journal of Clinical and Laboratory Investigation. 50(1). 85–93. 10 indexed citations
6.
Thorsteinsson, Leifur, Helga M. Ögmundsdóttir, Ásbjörn Sigfússon, et al.. (1990). The First Icelandic Family with X‐Linked Agammaglobulinemia: Studies of Genetic Markers and Immune Function. Scandinavian Journal of Immunology. 32(3). 273–280. 2 indexed citations
7.
Pálsdóttir, Ástríður, S Jónsdóttir, Magnus Abrahamson, Anders Grubb, & O Jensson. (1990). Three RFLPs at the 3′ end of the cystatin C gene, the disease gene in hereditary cystatin C amyloid angiopathy (HCCAA) in Iceland. Nucleic Acids Research. 18(24). 7471–7471. 2 indexed citations
8.
Ólafsson, Ísleifur, Gunnar Guðmundsson, Magnus Abrahamson, O Jensson, & Anders Grubb. (1990). The amino terminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated: direct sequence analysis from agarose gel electropherograms. Scandinavian Journal of Clinical and Laboratory Investigation. 50(1). 85–93. 27 indexed citations
9.
Abrahamson, Magnus, Ísleifur Ólafsson, Ástríður Pálsdóttir, et al.. (1990). Structure and expression of the human cystatin C gene. Biochemical Journal. 268(2). 287–294. 494 indexed citations
10.
Jensson, O, et al.. (1989). [Norwegian propositions for blood transfusion practices].. PubMed. 104(3). 83–4.
11.
Yamada, Masahito, Hiroshi Tsukagoshi, Yoshiaki Wada, et al.. (1989). Absence of the cystatin C amyloid in the cerebral amyloid angiopathy, senile plaque, and extra-CNS amyloid deposits of aged Japanese. Acta Neurologica Scandinavica. 79(6). 504–509. 7 indexed citations
12.
Pálsdóttir, Ástríður, Leifur Thorsteinsson, Ísleifur Ólafsson, et al.. (1988). MUTATION IN CYSTATIN C GENE CAUSES HEREDITARY BRAIN HAEMORRHAGE. The Lancet. 332(8611). 603–604. 158 indexed citations
13.
Ivens, Alasdair, et al.. (1988). X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17. Human Genetics. 78(4). 356–358. 15 indexed citations
14.
Jensson, O, Gunnar Guðmundsson, Árni Árnason, et al.. (1987). Hereditary cystatin C (γ-trace) amyloid angiopathy of the CNS causing cerebral hemorrhage. Acta Neurologica Scandinavica. 76(2). 102–114. 90 indexed citations
15.
Pálsdóttir, Ástríður, Ragnheiður Fossdal, O Jensson, & Allen C. Amason. (1987). Bgl II polymorphic site upstream to the human complement component C4A gene. Nucleic Acids Research. 15(5). 2395–2395. 4 indexed citations
16.
Pálsdóttir, Ástríður, Árni Árnason, Ragnheiður Fossdal, & O Jensson. (1987). Gene organization of haplotypes expressing two different C4A allotypes. Human Genetics. 76(3). 220–4. 25 indexed citations
17.
Árnason, Árni, et al.. (1986). Genetic markers in families with hereditary cerebral hemorrhage with amyloidosis. Acta Neurologica Scandinavica. 73(3). 314. 1 indexed citations
18.
Cohen, David H., Helen Feiner, O Jensson, & Blas Frangione. (1983). Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastroentero-pancreatic neuroendocrine protein, gamma trace.. The Journal of Experimental Medicine. 158(2). 623–628. 150 indexed citations
19.
Kaur, Jasbir, Daniel Catovsky, Helgi Valdimarsson, O Jensson, & A. S. D. Spiers. (1972). Familial Acute Myeloid Leukaemia with Acquired Pelger-Huet Anomaly and Aneuploidy of C Group. BMJ. 4(5836). 327–331. 33 indexed citations
20.
Jensson, O & Kristján Árnason. (1963). [AN ICELANDIC PELGER ANOMALY FAMILY].. PubMed. 47. 97–101.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Helge Löfberg Breakdown of academic impact, for papers by Akiko Ishii Breakdown of academic impact, for papers by Martha Konieczkowski Breakdown of academic impact, for papers by Hitomi Imachi Breakdown of academic impact, for papers by Takashi Oite Breakdown of academic impact, for papers by Berardino Porfirio Breakdown of academic impact, for papers by Muriel Gaudry Breakdown of academic impact, for papers by G. Aßmann Breakdown of academic impact, for papers by Björn Hartleben Breakdown of academic impact, for papers by Yasushi Nakamoto
Rankless by CCL
2026