Eeva Therman
Impact in
- Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Developmental Biology top 2%
Papers in
-
- DNA Repair Mechanisms 15
- Genomics and Chromatin Dynamics 11
- Sexual Differentiation and Disorders 6
-
- Chromosomal and Genetic Variations 32
- Plant Genetic and Mutation Studies 7
- Co-authors
- Klaus Pätau (17 shared papers)Gloria E. Sarto (23 shared papers)Evelyn M. Kuhn (16 shared papers)Carter Denniston (10 shared papers)Stanley L. Inhorn (6 shared papers)David W. Smith (5 shared papers)David W. Smith (4 shared papers)Robert DeMars (4 shared papers)
- Journals
- Human Genetics (19 papers)Chromosoma (11 papers)Hereditas (5 papers)Physiologia Plantarum (4 papers)American Journal of Botany (4 papers)
- Partner nations
- United StatesFinlandBrazil
In The Last Decade
Eeva Therman
87 papers receiving 2.8k citations
Eeva Therman's Hit Papers
Peers
Comparison fields: 5 of 115
- Genetics 1.9k
- Developmental Biology 148
- Pediatrics, Perinatology and Child Health 642
- Plant Science 895
- Molecular Biology 1.4k
Countries citing papers authored by Eeva Therman
This map shows the geographic impact of Eeva Therman'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 Eeva Therman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eeva Therman more than expected).
Fields of papers citing papers by Eeva Therman
This network shows the impact of papers produced by Eeva Therman. 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 Eeva Therman. The network helps show where Eeva Therman may publish in the future.
Co-authors
The 25 scholars most cited alongside Eeva Therman, 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 89 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | MULTIPLE CONGENITAL ANOMALY CAUSED BY AN EXTRA AUTOSOME Hit paper breakdown → | 1960 | 473 |
| 2 | 1990 | 156 | |
| 3 | 1960 | 153 | |
| 4 | 1989 | 137 | |
| 5 | 1974 | 119 | |
| 6 | 1963 | 112 | |
| 7 | 1962 | 109 | |
| 8 | Apparently isodicentric but functionally monocentric X chromosome in man. | 1974 | 105 |
| 9 | X inactivation in man: a woman with t(Xq--;12q+). | 1973 | 104 |
| 10 | The D triisomy syndrome and XO gonadal dysgenesis in two sisters. | 1961 | 88 |
| 11 | 1990 | 79 | |
| 12 | 1974 | 78 | |
| 13 | 1987 | 71 | |
| 14 | 1961 | 69 | |
| 15 | 1980 | 66 | |
| 16 | 1986 | 57 | |
| 17 | 1986 | 53 | |
| 18 | 1979 | 51 | |
| 19 | 1981 | 46 | |
| 20 | 1982 | 44 |
About Eeva Therman
Eeva Therman is a scholar working on Molecular Biology, Plant Science, Genetics, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 89 papers that have together received 3.2k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (32 papers), Genomic variations and chromosomal abnormalities (20 papers), DNA Repair Mechanisms (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Genomics and Chromatin Dynamics (11 papers), Plant Genetic and Mutation Studies (7 papers), Carcinogens and Genotoxicity Assessment (7 papers) and Sexual Differentiation and Disorders (6 papers). The work is most often cited by research in Genetics (1.9k citations), Developmental Biology (148 citations), Pediatrics, Perinatology and Child Health (642 citations), Plant Science (895 citations) and Molecular Biology (1.4k citations). Eeva Therman has collaborated with scholars based in United States, Finland and Brazil. Frequent co-authors include Klaus Pätau, Gloria E. Sarto, Evelyn M. Kuhn, Carter Denniston, Stanley L. Inhorn, David W. Smith, David W. Smith, Robert DeMars, Renata Laxová and E Tammisalo. Their work appears in journals such as Human Genetics, Chromosoma, Hereditas, Physiologia Plantarum and American Journal of Botany.
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.