K.‐H. Gustavson

1.3k total citations
36 papers, 938 citations indexed

About

K.‐H. Gustavson is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, K.‐H. Gustavson has authored 36 papers receiving a total of 938 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in K.‐H. Gustavson's work include Genetics and Neurodevelopmental Disorders (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Metabolism and Genetic Disorders (4 papers). K.‐H. Gustavson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Metabolism and Genetic Disorders (4 papers). K.‐H. Gustavson collaborates with scholars based in Sweden, Denmark and Netherlands. K.‐H. Gustavson's co-authors include Bengt Hagberg, G Hagberg, Bengt Björkstén, Gösta Holmgren, Hans K son Blomquist, Ingrid Nordenson, H. Wilbrand, Gunnar Sanner, Bruno Hägglöf and Ove Bäck and has published in prestigious journals such as The Lancet, Human Molecular Genetics and Acta Psychiatrica Scandinavica.

In The Last Decade

K.‐H. Gustavson

36 papers receiving 842 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.‐H. Gustavson Sweden 18 343 247 162 118 107 36 938
Salvador Castells United States 17 380 1.1× 153 0.6× 111 0.7× 88 0.7× 78 0.7× 51 813
Henry G. Dunn Canada 26 522 1.5× 459 1.9× 237 1.5× 174 1.5× 109 1.0× 65 1.5k
L. Crome Nigeria 22 232 0.7× 460 1.9× 293 1.8× 97 0.8× 174 1.6× 71 1.2k
M. F. Niermeijer Netherlands 18 212 0.6× 300 1.2× 189 1.2× 87 0.7× 299 2.8× 44 902
Piero Pirazzoli Italy 25 430 1.3× 686 2.8× 301 1.9× 70 0.6× 101 0.9× 64 1.7k
Carol E. Anderson United States 20 563 1.6× 364 1.5× 156 1.0× 55 0.5× 51 0.5× 45 1.2k
Werner F. Blum Germany 16 242 0.7× 299 1.2× 213 1.3× 20 0.2× 171 1.6× 20 1.1k
Richard Lindenberg United States 22 101 0.3× 396 1.6× 238 1.5× 101 0.9× 164 1.5× 37 1.4k
Pierre J. Vinken Netherlands 12 77 0.2× 238 1.0× 136 0.8× 67 0.6× 93 0.9× 37 1.1k
R. W. Hornabrook United Kingdom 17 103 0.3× 133 0.5× 72 0.4× 117 1.0× 113 1.1× 55 1.1k

Countries citing papers authored by K.‐H. Gustavson

Since Specialization
Citations

This map shows the geographic impact of K.‐H. Gustavson'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.‐H. Gustavson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K.‐H. Gustavson more than expected).

Fields of papers citing papers by K.‐H. Gustavson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by K.‐H. Gustavson. 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.‐H. Gustavson. The network helps show where K.‐H. Gustavson may publish in the future.

Co-authorship network of co-authors of K.‐H. Gustavson

This figure shows the co-authorship network connecting the top 25 collaborators of K.‐H. Gustavson. A scholar is included among the top collaborators of K.‐H. Gustavson 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.‐H. Gustavson. K.‐H. Gustavson 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.
Gustavson, K.‐H., et al.. (1994). Dermatoglyphics in Individuals with Asocial Behaviour. Upsala Journal of Medical Sciences. 99(1). 63–67. 4 indexed citations
2.
Dahl, Niklas, T. Tønnesen, Wim J. Kleijer, et al.. (1992). Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene. Human Molecular Genetics. 1(3). 195–198. 26 indexed citations
3.
Dahl, Niklas, P. Goonewardena, Claes Wadelius, et al.. (1989). Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome. Human Genetics. 82(3). 216–218. 31 indexed citations
4.
Dahl, Niklas, et al.. (1988). A Case of Complete Trisomy 2p/Triploidy Mosaicism. Acta Paediatrica. 77(6). 925–929. 1 indexed citations
5.
Gustavson, K.‐H., et al.. (1987). New type of spinocerebellar degeneration syndrome in a northern Swedish population. Clinical Genetics. 32(5). 306–312. 4 indexed citations
6.
Iselius, L & K.‐H. Gustavson. (1984). Spatial Distribution of the Gene for Infantile Genetic Agranulocytosis. Human Heredity. 34(6). 358–363. 6 indexed citations
7.
Gustavson, K.‐H.. (1981). The Epidemiology of Severe Mental Retardation in Sweden. International Journal of Mental Health. 10(1). 37–46. 2 indexed citations
8.
Björkstén, Bengt, Ove Bäck, K.‐H. Gustavson, et al.. (1980). ZINC AND IMMUNE FUNCTION IN DOWN'S SYNDROME. Acta Paediatrica. 69(2). 183–187. 87 indexed citations
9.
Gustavson, K.‐H. & J. Wahlström. (1977). Trisomy 9p syndrome and XYY syndrome in siblings. Clinical Genetics. 11(1). 67–72. 10 indexed citations
10.
11.
Gustavson, K.‐H., et al.. (1977). Severe Mental Retardation in a Swedish County – II. Etiologic and Pathogenetic Aspects of Children Born 1959–1970. Neuropediatrics. 8(3). 293–304. 72 indexed citations
12.
Lindsten, J., et al.. (1974). Body height and dental development in patients with Turner's syndrome.. PubMed. Suppl 34. 33–46. 20 indexed citations
13.
Gustavson, K.‐H. & H. Wilbrand. (1974). Chronic Symmetric Osteomyelitis. Acta Radiologica Diagnosis. 15(5). 551–557. 37 indexed citations
14.
Gustavson, K.‐H., Lennart Wetterberg, Maria Bäckström, & Svante B. Ross. (1973). Catechol‐O‐methyltransferase activity in erythrocytes in Down's syndrome. Clinical Genetics. 4(3). 279–280. 29 indexed citations
15.
Santesson, Berta, J.A. Böök, & K.‐H. Gustavson. (1972). DNA synthesis of human XYY cells. Clinical Genetics. 3(1). 73–81. 4 indexed citations
16.
Gustavson, K.‐H., Bengt Hagberg, & Gunnar Sanner. (1969). [Causes of cerebral palsy. 4. The CP-syndrome with genetic background].. PubMed. 66(17). 1773–9. 1 indexed citations
17.
Gustavson, K.‐H., et al.. (1969). IDENTICAL SYNDROMES OF CEREBRAL PALSY IN THE SAME FAMILY. Acta Paediatrica. 58(4). 330–340. 52 indexed citations
18.
Gustavson, K.‐H., Stefan Johansson, & L Wranne. (1968). IMMUNOGLOBULINS IN 13–15 TRISOMY SYNDROME DUE TO A TRANSLOCATION. Acta Paediatrica. 57(5). 436–440. 5 indexed citations
19.
Gustavson, K.‐H., et al.. (1963). THE KARYOTYPE IN T. SJÖGREN'S SYNDROME: (Mental Defect, Ichthyosis and Spastic Paralysis.). Acta Psychiatrica Scandinavica. 39(1). 114–118. 2 indexed citations
20.
Lundin, Lennart & K.‐H. Gustavson. (1962). Urinary BAIB Excretion in Down’s Syndrome (Mongolism). Human Heredity. 12(2). 156–163. 3 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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