K Kaijser

787 total citations
24 papers, 581 citations indexed

About

K Kaijser is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, K Kaijser has authored 24 papers receiving a total of 581 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Surgery. Recurrent topics in K Kaijser's work include Sexual Differentiation and Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). K Kaijser is often cited by papers focused on Sexual Differentiation and Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). K Kaijser collaborates with scholars based in Sweden, United Kingdom and Greece. K Kaijser's co-authors include J. Lindsten, M. Fraccaro, D. Ikkos, R Luft, P.A. Öckerman, G. Brante, Arne Svedmyr, Rolf Lundström, H.P. Klinger and Janet D. Rowley and has published in prestigious journals such as Nature, The Lancet and Acta Paediatrica.

In The Last Decade

K Kaijser

24 papers receiving 462 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
K Kaijser Sweden 11 358 245 115 60 44 24 581
Cantú Jm Mexico 12 259 0.7× 165 0.7× 83 0.7× 104 1.7× 16 0.4× 67 405
Mary Lucas United Kingdom 14 239 0.7× 152 0.6× 68 0.6× 186 3.1× 20 0.5× 24 475
Berta Santesson Sweden 12 171 0.5× 160 0.7× 82 0.7× 78 1.3× 12 0.3× 23 410
J Philip Denmark 6 183 0.5× 129 0.5× 56 0.5× 53 0.9× 33 0.8× 13 302
J. Rogers Byrd United States 12 288 0.8× 226 0.9× 55 0.5× 140 2.3× 180 4.1× 31 597
B Padeh Israel 13 139 0.4× 158 0.6× 44 0.4× 39 0.7× 22 0.5× 32 486
Catherine Palmer United States 8 125 0.3× 173 0.7× 21 0.2× 58 1.0× 10 0.2× 14 331
H.E. Wyandt United States 12 249 0.7× 206 0.8× 99 0.9× 89 1.5× 12 0.3× 25 405
JoyD.A. Delhanty United Kingdom 8 261 0.7× 97 0.4× 85 0.7× 225 3.8× 26 0.6× 8 482
G. Lefort France 16 377 1.1× 189 0.8× 217 1.9× 290 4.8× 49 1.1× 34 632

Countries citing papers authored by K Kaijser

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of K Kaijser

This figure shows the co-authorship network connecting the top 25 collaborators of K Kaijser. A scholar is included among the top collaborators of K Kaijser based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with K Kaijser. K Kaijser is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kaijser, K. (1974). Case report of an extra, small, acrocentric chromosome in a non‐mongoloid girl. Clinical Genetics. 5(3). 254–258. 5 indexed citations
2.
Kaijser, K & P.A. Öckerman. (1970). DIAGNOSTIC PROBLEMS IN GLUCOSE‐GALACTOSE MALABSORPTION: A Case Report. Acta Paediatrica. 59(2). 214–216. 3 indexed citations
3.
Lundström, Rolf, et al.. (1967). Rubella Immunity as Related to Age and History of Overt Disease. Acta Paediatrica. 56(3). 279–285. 29 indexed citations
4.
5.
Brante, G., K Kaijser, & P.A. Öckerman. (1964). Glycogenosis Type 1 (Lack of Glucose‐6‐Phosphatase) in Four Siblings. Acta Paediatrica. 53(5). 483–483. 14 indexed citations
6.
Lindsten, J., M. Fraccaro, D. Ikkos, et al.. (1963). Presumptive isochromosomes for the long arm of X in man. Analysis of five families. Annals of Human Genetics. 26(4). 383–406. 34 indexed citations
7.
Rowley, Janet D., S. Muldal, C. W. Gilbert, et al.. (1963). Synthesis of Deoxyribonucleic Acid on X-Chromosomes of an XXXXY Male. Nature. 197(4864). 251–252. 35 indexed citations
8.
Fraccaro, M., J. Lindsten, & K Kaijser. (1962). A CHILD WITH 49 CHROMOSOMES: FURTHER INVESTIGATIONS. The Lancet. 280(7254). 509–509. 11 indexed citations
9.
Kaijser, K. (1961). CONTAINER FOR CULTIVATING BLOOD FOR CHROMOSOME STUDIES. The Lancet. 278(7216). 1362–1362. 1 indexed citations
10.
Fraccaro, M., et al.. (1961). Chromosome studies in Laurence-Moon-Biedl's syndrome.. PubMed. 11. 23–33. 2 indexed citations
11.
Fraccaro, M., K Kaijser, & J. Lindsten. (1960). A CHILD WITH 49 CHROMOSOMES. The Lancet. 276(7156). 899–902. 137 indexed citations
12.
Fraccaro, M., K Kaijser, & J. Lindsten. (1960). CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILD. The Lancet. 275(7127). 724–727. 133 indexed citations
13.
Fraccaro, M., D. Ikkos, J. Lindsten, R Luft, & K Kaijser. (1960). A NEW TYPE OF CHROMOSOMAL ABNORMALITY IN GONADAL DYSGENESIS. The Lancet. 276(7160). 1144–1144. 64 indexed citations
14.
Fraccaro, M., K Kaijser, & J. Lindsten. (1960). Further cytogenetical observations in gonadal dysgenesis. Annals of Human Genetics. 24(3). 205–211. 13 indexed citations
15.
Kaijser, K, et al.. (1960). [Listeriosis--an additional case in infants].. PubMed. 57. 792–5. 1 indexed citations
16.
Kaijser, K, et al.. (1959). [Incidence of gonadal dysgenesis in Sweden].. PubMed. 61(3). 98–9. 1 indexed citations
17.
Fraccaro, M., K Kaijser, & J. Lindsten. (1959). CHROMOSOME COMPLEMENT IN GONADAL DYSGENESIS (TURNER'S SYNDROME). The Lancet. 273(7078). 886–886. 46 indexed citations
18.
Kaijser, K, et al.. (1959). Gonadal dysgenesis: an analysis of 15 cases.. PubMed. 64. 502–6. 1 indexed citations
19.
Kaijser, K, et al.. (1957). Ano‐Rectal Abnormalities as a Congenital Familial Incidence. Acta Paediatrica. 46(2). 199–200. 21 indexed citations
20.
Kaijser, K. (1953). Congenital deficiency of abdominal musculature with associated genitourinary abnormalities.. PubMed. 181(3). 173–6. 2 indexed citations

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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