K.‐H. Gustavson
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Developmental Biology top 10%
Papers in
- Genetics 12
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genomic variations and chromosomal abnormalities 3
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- Sexual Differentiation and Disorders 3
- Mitochondrial Function and Pathology 3
- Co-authors
- Bengt Hagberg (4 shared papers)G Hagberg (2 shared papers)Bengt Björkstén (2 shared papers)Gösta Holmgren (4 shared papers)Ingrid Nordenson (2 shared papers)Hans K son Blomquist (2 shared papers)H. Wilbrand (1 shared paper)Gunnar Sanner (3 shared papers)
- Journals
- Acta Paediatrica (10 papers)Clinical Genetics (10 papers)Human Heredity (2 papers)Human Molecular Genetics (1 paper)Human Genetics (1 paper)
- Partner nations
- SwedenNetherlandsDenmark
In The Last Decade
K.‐H. Gustavson
36 papers receiving 842 citations
Peers
Comparison fields: 5 of 94
- Genetics 343
- Developmental Biology 20
- Pediatrics, Perinatology and Child Health 162
- Rheumatology 118
- Neurology 49
Countries citing papers authored by K.‐H. Gustavson
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
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-authors
The 25 scholars most cited alongside K.‐H. Gustavson, 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 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1980 | 87 | |
| 2 | 1982 | 78 | |
| 3 | 1977 | 72 | |
| 4 | 1977 | 65 | |
| 5 | 1971 | 62 | |
| 6 | 1979 | 59 | |
| 7 | 1969 | 52 | |
| 8 | 1964 | 48 | |
| 9 | 1981 | 40 | |
| 10 | 1983 | 38 | |
| 11 | 1974 | 37 | |
| 12 | Familial Menière's disease: a genetic investigation. | 1987 | 35 |
| 13 | 1989 | 31 | |
| 14 | 1973 | 29 | |
| 15 | 1992 | 26 | |
| 16 | 1985 | 23 | |
| 17 | 1961 | 22 | |
| 18 | Body height and dental development in patients with Turner's syndrome. | 1974 | 20 |
| 19 | 1985 | 17 | |
| 20 | 1983 | 16 |
About K.‐H. Gustavson
K.‐H. Gustavson is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Clinical Biochemistry, having authored 36 papers that have together received 938 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Metabolism and Genetic Disorders (4 papers), Adolescent and Pediatric Healthcare (3 papers), Selenium in Biological Systems (3 papers), Sexual Differentiation and Disorders (3 papers), Mitochondrial Function and Pathology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (343 citations), Developmental Biology (20 citations), Pediatrics, Perinatology and Child Health (162 citations), Rheumatology (118 citations) and Neurology (49 citations). K.‐H. Gustavson has collaborated with scholars based in Sweden, Netherlands and Denmark. Frequent co-authors include Bengt Hagberg, G Hagberg, Bengt Björkstén, Gösta Holmgren, Ingrid Nordenson, Hans K son Blomquist, H. Wilbrand, Gunnar Sanner, Göran Hallmans and Arne Tärnvik. Their work appears in journals such as Acta Paediatrica, Clinical Genetics, Human Heredity, Human Molecular 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.