Ólafur Jensson

799 total citations
20 papers, 617 citations indexed

About

Ólafur Jensson is a scholar working on Molecular Biology, Physiology and Hematology. According to data from OpenAlex, Ólafur Jensson has authored 20 papers receiving a total of 617 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Physiology and 5 papers in Hematology. Recurrent topics in Ólafur Jensson's work include Alzheimer's disease research and treatments (7 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (5 papers) and Chronic Kidney Disease and Diabetes (3 papers). Ólafur Jensson is often cited by papers focused on Alzheimer's disease research and treatments (7 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (5 papers) and Chronic Kidney Disease and Diabetes (3 papers). Ólafur Jensson collaborates with scholars based in Iceland, United States and Sweden. Ólafur Jensson's co-authors include Leifur Thorsteinsson, Alfreð Árnason, Anders Grubb, Ísleifur Ólafsson, Gunnar Guðmundsson, Helge Löfberg, Johan Malm, Alasdair Ivens, Robert Williamson and Gudrun E. Moore and has published in prestigious journals such as Nature, New England Journal of Medicine and Development.

In The Last Decade

Ólafur Jensson

20 papers receiving 590 citations

Peers

Countries citing papers authored by Ólafur Jensson

Since Specialization

Citations

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

Fields of papers citing papers by Ólafur Jensson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ólafur Jensson

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

#	Work	Indexed citations
1	Microvascular degeneration in hereditary cystatin C amyloid angiopathy of the brain 1997 ·Apmis ·Zhen Zhen Wang, Ólafur Jensson, Leifur Thorsteinsson, Harry V. Vinters	28
2	The Molecular Pathology of Hereditary Cystatin C Amyloid Angiopathy Causing Brain Hemorrhage 1996 ·Brain Pathology ·Ísleifur Ólafsson, Leifur Thorsteinsson, Ólafur Jensson	45
3	Immune Reactions Associated With Cerebral Amyloid Angiopathy 1996 ·Stroke ·Masahito Yamada, Yoshinori Itoh, Masayuki Shintaku, Junichiro Kawamura, Ólafur Jensson, Leifur Thorsteinsson, Naomi Suematsu, Masaaki Matsushita, E Otomo	104
4	Human cystatin C expression and regulation by TGF-β1: Implications for the pathogenesis of hereditary cystatin C amyloid angiopathy causing brain hemorrhage 1996 ·Amyloid ·Valur Emilsson, Leifur Thorsteinsson, Ólafur Jensson, (unknown)	6
5	Mapping the locus of atrophia areata, a helicoid peripapillary chorioretinal degeneration with autosomal dominant inheritance, to chromosome 11p15 1995 ·Human Molecular Genetics ·Ragnheiður Fossdal, (unknown), James L. Weber, Ólafur Jensson	18
6	Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresis 1992 ·Human Mutation ·S Jónsdóttir, Carol Diamond, Barbara Levinson, (unknown), Ólafur Jensson, Jane Gitschier	7
7	On the role of monocytes/macrophages in the pathogenesis of central nervous system lesions in hereditary cystatin C amyloid angiopathy 1992 ·Journal of the Neurological Sciences ·Leifur Thorsteinsson, G. Georgsson, Bjarni Ãsgeirsson, María Bjarnadóttir, Ísleifur Ólafsson, Ólafur Jensson, Gunnar Guðmundsson	26
8	Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis 1992 ·Human Genetics ·Magnus Abrahamson, S Jónsdóttir, Ísleifur Ólafsson, Ólafur Jensson, Anders Grubb	55
9	X Chromosome Genes Involved in the Regulation of Facial Clefting and Spina Bifida 1990 ·The Cleft Palate-Craniofacial Journal ·(unknown), Alasdair Ivens, Robert Newton, (unknown), Deborah J. Henderson, Ólafur Jensson	8
10	causing amyloid angiopathy and brain hemorrhage ‐ clinical genetics in Iceland 1989 ·Clinical Genetics ·Ólafur Jensson, Ástríður Pálsdóttir, Leifur Thorsteinsson, Alfreð Árnason	16
11	An Isolate of Families with Hereditary Cystatin C Amyloid Angiopathy and Cerebral Haemorrhage in the South of Iceland 1988 ·Ólafur Jensson, Leifur Thorsteinsson, Ástríður Pálsdóttir, Gunnar Guðmundsson, Alfreð Árnason, (unknown), Magnus Abrahamson, Anders Grubb, Ísleifur Ólafsson, Åke Lundwall	1
12	The application of molecular genetics to detection of craniofacial abnormality 1988 ·Development ·Gudrun E. Moore, Alasdair Ivens, (unknown), Árni Björnsson, Alfreð Árnason, Ólafur Jensson, Robert Williamson	21
13	Linkage of an X-chromosome cleft palate gene 1987 ·Nature ·Gudrun E. Moore, Alasdair Ivens, (unknown), (unknown), Robert Williamson, David C. Page, (unknown), Alfreð Árnason, Ólafur Jensson	95
14	Abnormal Metabolism of γ-Trace Alkaline Microprotein 1984 ·New England Journal of Medicine ·Anders Grubb, Ólafur Jensson, Gunnar Guðmundsson, Alfreð Árnason, Helge Löfberg, Johan Malm	117
15	An unusual Rhesus haplotype, —D—, in Iceland 1983 ·Forensic Science International ·(unknown), Ólafur Jensson, Gudmundur Thórdarson, Sunna Sigurðardóttir	7
16	Macroglobulinaemia in an Icelandic Family 1978 ·Acta Medica Scandinavica ·(unknown), (unknown), (unknown), Ólafur Jensson, Snorri Ólafsson, Helgi Valdimarsson	24
17	Studies on the Pelger Anomaly in Iceland 1977 ·Acta Medica Scandinavica ·Ólafur Jensson, (unknown), Gudmundur Jóhannesson, (unknown)	3
18	FREQUENCY OF IgA DEFICIENCY IN BLOOD DONORS AND Rh NEGATIVE WOMEN IN ICELAND 1977 ·Acta Pathologica Microbiologica Scandinavica Section C Immunology ·Sigurður Guðmundsson, Ólafur Jensson	13
19	Studies on Hereditary Spherocytosis in Iceland 1977 ·Acta Medica Scandinavica ·Ólafur Jensson, (unknown), (unknown)	14
20	Serum esterases of Icelanders 1. A “silent” pseudocholinesterase gene in an icelandic family 1975 ·Clinical Genetics ·Alfreð Árnason, Ólafur Jensson, Sigurður Guðmundsson	9

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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