Berta Santesson
Impact in
- Developmental Biology top 10%
- Congenital limb and hand anomalies
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
-
- Sexual Differentiation and Disorders 4
- DNA Repair Mechanisms 2
- Genetics 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- J.A. Böök (10 shared papers)PER ZETTERQVIST (2 shared papers)Kerstin Lindahl‐Kiessling (3 shared papers)Anita Mattsson (1 shared paper)K. H. Gustavson (4 shared papers)L. Atkins (1 shared paper)Hartmut Voss (1 shared paper)Hans Olof Åkesson (1 shared paper)
- Journals
- Hereditas (4 papers)Clinical Genetics (4 papers)Acta Paediatrica (3 papers)The Lancet (3 papers)Human Genetics (1 paper)
- Partner nations
- SwedenUnited StatesHungary
In The Last Decade
Berta Santesson
21 papers receiving 373 citations
Peers
Comparison fields: 5 of 69
- Developmental Biology 30
- Genetics 193
- Pediatrics, Perinatology and Child Health 92
- Cancer Research 66
- Chemical Health and Safety 2
Countries citing papers authored by Berta Santesson
This map shows the geographic impact of Berta Santesson'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 Berta Santesson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Berta Santesson more than expected).
Fields of papers citing papers by Berta Santesson
This network shows the impact of papers produced by Berta Santesson. 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 Berta Santesson. The network helps show where Berta Santesson may publish in the future.
Co-authors
The 20 scholars most cited alongside Berta Santesson, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1960 | 99 | |
| 2 | 1979 | 74 | |
| 3 | 1961 | 60 | |
| 4 | 1972 | 28 | |
| 5 | 1962 | 25 | |
| 6 | 1965 | 25 | |
| 7 | 1961 | 24 | |
| 8 | 1969 | 18 | |
| 9 | 1986 | 18 | |
| 10 | 1973 | 15 | |
| 11 | 1967 | 15 | |
| 12 | 1985 | 12 | |
| 13 | 1961 | 11 | |
| 14 | 1970 | 9 | |
| 15 | 1968 | 8 | |
| 16 | 1974 | 7 | |
| 17 | 1972 | 4 | |
| 18 | 1980 | 3 | |
| 19 | 1973 | 2 | |
| 20 | 2009 | 2 |
About Berta Santesson
Berta Santesson is a scholar working on Molecular Biology, Genetics, Plant Science, Pediatrics, Perinatology and Child Health and Surgery, having authored 23 papers that have together received 460 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Chromosomal and Genetic Variations (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Sexual Differentiation and Disorders (4 papers), Prenatal Screening and Diagnostics (4 papers), Congenital Anomalies and Fetal Surgery (3 papers), DNA Repair Mechanisms (2 papers) and T-cell and B-cell Immunology (2 papers). The work is most often cited by research in Developmental Biology (30 citations), Genetics (193 citations), Pediatrics, Perinatology and Child Health (92 citations), Cancer Research (66 citations) and Chemical Health and Safety (2 citations). Berta Santesson has collaborated with scholars based in Sweden, United States and Hungary. Frequent co-authors include J.A. Böök, PER ZETTERQVIST, Kerstin Lindahl‐Kiessling, Anita Mattsson, K. H. Gustavson, L. Atkins, Hartmut Voss, Hans Olof Åkesson, Theodor Weber and Valdemar Skoog. Their work appears in journals such as Hereditas, Clinical Genetics, Acta Paediatrica, The Lancet 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.