Lennart Iselius
Impact in
- Pharmacology top 0.5%
- Pharmacogenetics and Drug Metabolism
- Genetics top 2%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 27
- Genetic Associations and Epidemiology 12
- BRCA gene mutations in cancer 5
- Nutrition, Genetics, and Disease 4
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- J. Lindsten (14 shared papers)G. Alv�n (2 shared papers)Ursula Gundert‐Remy (1 shared paper)P Bechtel (1 shared paper)Kerstin Sluys (4 shared papers)Ulf dé Fairé (3 shared papers)Newton E. Morton (9 shared papers)Anders Hamsten (2 shared papers)
- Journals
- Human Genetics (10 papers)Clinical Genetics (10 papers)Hereditas (4 papers)European Journal of Clinical Pharmacology (3 papers)Acta Paediatrica (3 papers)
- Partner nations
- SwedenUnited StatesUnited Kingdom
In The Last Decade
Lennart Iselius
83 papers receiving 3.4k citations
Peers
Comparison fields: 5 of 139
- Pharmacology 515
- Genetics 759
- Pathology and Forensic Medicine 393
- Psychiatry and Mental health 256
- Pediatrics, Perinatology and Child Health 319
Countries citing papers authored by Lennart Iselius
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
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.
All Works
Showing the 20 most-cited of 85 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 327 | |
| 2 | 1990 | 315 | |
| 3 | 2001 | 174 | |
| 4 | 1987 | 163 | |
| 5 | 2001 | 161 | |
| 6 | 1986 | 141 | |
| 7 | 2005 | 135 | |
| 8 | 1997 | 135 | |
| 9 | 1985 | 112 | |
| 10 | 1984 | 103 | |
| 11 | 1995 | 102 | |
| 12 | 1986 | 96 | |
| 13 | 1993 | 75 | |
| 14 | 2001 | 73 | |
| 15 | 1976 | 63 | |
| 16 | 1991 | 62 | |
| 17 | Outcome after major trauma | 2003 | 60 |
| 18 | Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysis. | 1990 | 57 |
| 19 | 2001 | 54 | |
| 20 | 1983 | 47 |
About Lennart Iselius
Lennart Iselius is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine, having authored 85 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (12 papers), Prenatal Screening and Diagnostics (6 papers), BRCA gene mutations in cancer (5 papers), Genetic factors in colorectal cancer (5 papers), Acute Lymphoblastic Leukemia research (4 papers), Nutrition, Genetics, and Disease (4 papers), Trauma and Emergency Care Studies (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Pharmacology (515 citations), Genetics (759 citations), Pathology and Forensic Medicine (393 citations), Psychiatry and Mental health (256 citations) and Pediatrics, Perinatology and Child Health (319 citations). Lennart Iselius has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include J. Lindsten, G. Alv�n, Ursula Gundert‐Remy, P Bechtel, Kerstin Sluys, Ulf dé Fairé, Newton E. Morton, Anders Hamsten, Jes Olesen and Margareta Blombäck. Their work appears in journals such as Human Genetics, Clinical Genetics, Hereditas, European Journal of Clinical Pharmacology and Acta Paediatrica.
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.