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
- Genetics 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genomic variations and chromosomal abnormalities 2
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- Glycogen Storage Diseases and Myoclonus 3
- Co-authors
- Jan Lindsten (10 shared papers)M. Fraccaro (10 shared papers)D. Ikkos (2 shared papers)Radoslaw Luft (2 shared papers)Per Arne 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 KingdomItaly
In The Last Decade
K Kaijser
24 papers receiving 505 citations
Peers
Comparison fields: 5 of 76
- Developmental Biology 34
- Genetics 403
- Reproductive Medicine 49
- Molecular Biology 268
- Pediatrics, Perinatology and Child Health 66
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 | 159 | |
| 2 | 1960 | 145 | |
| 3 | 1960 | 72 | |
| 4 | 1959 | 51 | |
| 5 | 1963 | 43 | |
| 6 | 1963 | 38 | |
| 7 | 1967 | 30 | |
| 8 | 1957 | 23 | |
| 9 | 1960 | 16 | |
| 10 | 1964 | 15 | |
| 11 | 1962 | 12 | |
| 12 | 1964 | 11 | |
| 13 | 1959 | 11 | |
| 14 | 1966 | 9 | |
| 15 | 1974 | 5 | |
| 16 | 1970 | 3 | |
| 17 | Congenital deficiency of abdominal musculature with associated genitourinary abnormalities. | 1953 | 2 |
| 18 | 1961 | 2 | |
| 19 | Chromosome studies in Laurence-Moon-Biedl's syndrome. | 1961 | 2 |
| 20 | [SEX CHROMOSOME ABERRATIONS XXXXY]. | 1964 | 1 |
About K Kaijser
K Kaijser is a scholar working on Genetics, Rheumatology, Molecular Biology, Reproductive Medicine and Surgery, having authored 24 papers that have together received 654 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), Glycogen Storage Diseases and Myoclonus (3 papers), Chromosomal and Genetic Variations (3 papers), Biochemical and Molecular Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Intestinal Malrotation and Obstruction Disorders (2 papers) and Lysosomal Storage Disorders Research (2 papers). The work is most often cited by research in Developmental Biology (34 citations), Genetics (403 citations), Reproductive Medicine (49 citations), Molecular Biology (268 citations) and Pediatrics, Perinatology and Child Health (66 citations). K Kaijser has collaborated with scholars based in Sweden, United Kingdom and Italy. Frequent co-authors include Jan Lindsten, M. Fraccaro, D. Ikkos, Radoslaw Luft, Per Arne Öckerman, G. Brante, Arne Svedmyr, Rolf Lundström, C. W. Gilbert and L. G. Lajtha. 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.