K Kaijser
Impact in
- Developmental Biology top 10%
- Congenital limb and hand anomalies
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
Papers in
-
- Sexual Differentiation and Disorders 5
- Genetics 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- M. Fraccaro (10 shared papers)J. Lindsten (10 shared papers)D. Ikkos (2 shared papers)R Luft (2 shared papers)P.A. Öckerman (4 shared papers)G. Brante (2 shared papers)Arne Svedmyr (1 shared paper)Rolf Lundström (1 shared paper)
- Journals
- The Lancet (7 papers)Acta Paediatrica (6 papers)Annals of Human Genetics (2 papers)Clinical Genetics (2 papers)Nature (1 paper)
- Partner nations
- SwedenUnited KingdomHungary
In The Last Decade
K Kaijser
24 papers receiving 465 citations
Peers
Comparison fields: 5 of 75
- Developmental Biology 32
- Genetics 354
- Reproductive Medicine 41
- Molecular Biology 236
- Pediatrics, Perinatology and Child Health 56
Countries citing papers authored by K Kaijser
This map shows the geographic impact of K Kaijser'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 K Kaijser with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K Kaijser more than expected).
Fields of papers citing papers by K Kaijser
This network shows the impact of papers produced by K Kaijser. 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 K Kaijser. The network helps show where K Kaijser may publish in the future.
Co-authors
The 14 scholars most cited alongside K Kaijser, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1960 | 138 | |
| 2 | 1960 | 133 | |
| 3 | 1960 | 64 | |
| 4 | 1959 | 45 | |
| 5 | 1963 | 35 | |
| 6 | 1963 | 34 | |
| 7 | 1967 | 29 | |
| 8 | 1957 | 21 | |
| 9 | 1964 | 14 | |
| 10 | 1960 | 13 | |
| 11 | 1962 | 11 | |
| 12 | 1964 | 10 | |
| 13 | 1966 | 9 | |
| 14 | 1959 | 7 | |
| 15 | 1974 | 5 | |
| 16 | 1970 | 3 | |
| 17 | Congenital deficiency of abdominal musculature with associated genitourinary abnormalities. | 1953 | 2 |
| 18 | Chromosome studies in Laurence-Moon-Biedl's syndrome. | 1961 | 2 |
| 19 | [Incidence of gonadal dysgenesis in Sweden]. | 1959 | 1 |
| 20 | 1971 | 1 |
About K Kaijser
K Kaijser is a scholar working on Molecular Biology, Genetics, Surgery, Rheumatology and Plant Science, having authored 24 papers that have together received 581 indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Chromosomal and Genetic Variations (3 papers), Glycogen Storage Diseases and Myoclonus (3 papers), Sperm and Testicular Function (2 papers), Intestinal Malrotation and Obstruction Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Lysosomal Storage Disorders Research (2 papers). The work is most often cited by research in Developmental Biology (32 citations), Genetics (354 citations), Reproductive Medicine (41 citations), Molecular Biology (236 citations) and Pediatrics, Perinatology and Child Health (56 citations). K Kaijser has collaborated with scholars based in Sweden, United Kingdom and Hungary. Frequent co-authors include M. Fraccaro, J. Lindsten, D. Ikkos, R Luft, P.A. Öckerman, G. Brante, Arne Svedmyr, Rolf Lundström, H.P. Klinger and C. W. Gilbert. Their work appears in journals such as The Lancet, Acta Paediatrica, Annals of Human Genetics, Clinical Genetics and Nature.
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.