Jan Lindsten
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Associations and Epidemiology
- Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
Papers in
- Genetics 109
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 63
- Genomic variations and chromosomal abnormalities 47
- Genetic Associations and Epidemiology 12
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- Prenatal Screening and Diagnostics 15
- Co-authors
- M. Fraccaro (53 shared papers)Lore Zech (24 shared papers)K Kaijser (10 shared papers)Lennart Iselius (14 shared papers)Maj A. Hultén (30 shared papers)Nils R. Ringertz (2 shared papers)Gösta Gahrton (10 shared papers)T.O. Caspersson (11 shared papers)
- Journals
- The Lancet (19 papers)Hereditas (18 papers)Clinical Genetics (15 papers)Annals of Human Genetics (12 papers)Human Genetics (10 papers)
- Partner nations
- SwedenItalyUnited States
In The Last Decade
Jan Lindsten
183 papers receiving 4.7k citations
Peers
Comparison fields: 5 of 145
- Genetics 2.7k
- Cancer Research 551
- Pediatrics, Perinatology and Child Health 476
- Hematology 329
- Developmental Biology 35
Countries citing papers authored by Jan Lindsten
This map shows the geographic impact of Jan Lindsten'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 Jan Lindsten with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jan Lindsten more than expected).
Fields of papers citing papers by Jan Lindsten
This network shows the impact of papers produced by Jan Lindsten. 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 Jan Lindsten. The network helps show where Jan Lindsten may publish in the future.
Co-authors
The 25 scholars most cited alongside Jan Lindsten, 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 190 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 240 | |
| 2 | 1986 | 183 | |
| 3 | 1980 | 181 | |
| 4 | 1981 | 170 | |
| 5 | 1960 | 156 | |
| 6 | 1970 | 147 | |
| 7 | 1977 | 147 | |
| 8 | 1960 | 146 | |
| 9 | 1983 | 137 | |
| 10 | 1984 | 116 | |
| 11 | 1985 | 116 | |
| 12 | 1970 | 109 | |
| 13 | 1975 | 97 | |
| 14 | 1964 | 93 | |
| 15 | 1974 | 90 | |
| 16 | 1972 | 89 | |
| 17 | 1970 | 83 | |
| 18 | 1977 | 83 | |
| 19 | 1965 | 75 | |
| 20 | 1960 | 71 |
About Jan Lindsten
Jan Lindsten is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Hematology, Cancer Research and Plant Science, having authored 190 papers that have together received 5.6k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (63 papers), Genomic variations and chromosomal abnormalities (47 papers), Chromosomal and Genetic Variations (22 papers), Prenatal Screening and Diagnostics (15 papers), Carcinogens and Genotoxicity Assessment (14 papers), Down syndrome and intellectual disability research (13 papers), Genetic Associations and Epidemiology (12 papers) and Chronic Myeloid Leukemia Treatments (7 papers). The work is most often cited by research in Genetics (2.7k citations), Cancer Research (551 citations), Pediatrics, Perinatology and Child Health (476 citations), Hematology (329 citations) and Developmental Biology (35 citations). Jan Lindsten has collaborated with scholars based in Sweden, Italy and United States. Frequent co-authors include M. Fraccaro, Lore Zech, K Kaijser, Lennart Iselius, Maj A. Hultén, Nils R. Ringertz, Gösta Gahrton, T.O. Caspersson, L. Tiepolo and Kenneth Berglund. Their work appears in journals such as The Lancet, Hereditas, Clinical Genetics, Annals of Human Genetics and Human Genetics.
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.