Lennart Iselius

5k citations
89 papers · 4.2k · h-index 33

Impact in

  • Pharmacology top 0.5%
    • Pharmacogenetics and Drug Metabolism
  • Genetics top 2%
    • Genetic Associations and Epidemiology
    • Genomic variations and chromosomal abnormalities

Papers in

    • Genetic Associations and Epidemiology 20
    • Genomic variations and chromosomal abnormalities 8
    • BRCA gene mutations in cancer 4
    • Pharmacogenetics and Drug Metabolism 7

Lennart Iselius

88 papers receiving 3.8k citations

Peers

Lennart Iselius
Comparison fields: 5 of 123
  • Pharmacology 736
  • Genetics 1.1k
  • Pathology and Forensic Medicine 352
  • Pediatrics, Perinatology and Child Health 230
  • Emergency Medicine 130
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Citations per field
00.5×5×10×15×21.7×
Toby Andrew · 1×
Citations per year

Countries citing papers authored by Lennart Iselius

Since Specialization
Citations

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

Fields of papers citing papers by Lennart Iselius

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Lennart Iselius, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Lennart Iselius Line = papers co-authored together Lennart Iselius links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 89 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1992343
2 1990323
3 2001188
4 1980181
5 2001171
6 1987162
7 1986155
8 1997148
9 1983137
10 2005134
11 1984116
12 1985116
13 1995107
14 198697
15 200184
16 199381
17 197672
18 199161
19 200161
20
Outcome after major trauma
200360

About Lennart Iselius

Lennart Iselius is a scholar working on Genetics, Pharmacology, Pathology and Forensic Medicine, Emergency Medicine and Surgery, having authored 89 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (20 papers), Genomic variations and chromosomal abnormalities (8 papers), Lipoproteins and Cardiovascular Health (7 papers), Genetic factors in colorectal cancer (7 papers), Pharmacogenetics and Drug Metabolism (7 papers), Down syndrome and intellectual disability research (4 papers), Trauma and Emergency Care Studies (4 papers) and BRCA gene mutations in cancer (4 papers). The work is most often cited by research in Pharmacology (736 citations), Genetics (1.1k citations), Pathology and Forensic Medicine (352 citations), Pediatrics, Perinatology and Child Health (230 citations) and Emergency Medicine (130 citations). Lennart Iselius has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include Jan Lindsten, Gunnar Alv�n, Pierre R Bechtel, Ursula Gundert‐Remy, Newton E. Morton, Ulf dé Fairé, Kerstin Prignitz Sluys, Anders Hamsten, Folke Sjöqvist and Jes Olesen. Their work appears in journals such as Human Genetics, Clinical Genetics, Hereditas, Acta Paediatrica and European Journal of Clinical Pharmacology.

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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