Mea Andersson
Impact in
- Reproductive Medicine top 5%
- Sperm and Testicular Function
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genomic variations and chromosomal abnormalities 2
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- Sexual Differentiation and Disorders 4
- Co-authors
- Albert de la Chapelle (5 shared papers)David C. Page (3 shared papers)Jan Böhme (1 shared paper)Lars Rask (1 shared paper)E Möller (1 shared paper)Gerhard Andersson (1 shared paper)A. de la Chapelle (1 shared paper)François Rouyer (1 shared paper)
- Journals
- Human Genetics (2 papers)The EMBO Journal (1 paper)The Journal of Immunology (1 paper)Science (1 paper)Genomics (1 paper)
- Partner nations
- FinlandUnited StatesFrance
In The Last Decade
Mea Andersson
7 papers receiving 470 citations
Peers
Comparison fields: 5 of 55
- Reproductive Medicine 98
- Genetics 328
- Immunology 125
- Molecular Biology 261
- Plant Science 136
Countries citing papers authored by Mea Andersson
This map shows the geographic impact of Mea Andersson'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 Mea Andersson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mea Andersson more than expected).
Fields of papers citing papers by Mea Andersson
This network shows the impact of papers produced by Mea Andersson. 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 Mea Andersson. The network helps show where Mea Andersson may publish in the future.
Co-authors
The 25 scholars most cited alongside Mea Andersson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 141 | |
| 2 | 1986 | 111 | |
| 3 | 1988 | 111 | |
| 4 | 1990 | 83 | |
| 5 | 1990 | 47 | |
| 6 | 1988 | 8 | |
| 7 | An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction. | 1987 | 8 |
About Mea Andersson
Mea Andersson is a scholar working on Genetics, Molecular Biology, Reproductive Medicine, Pediatrics, Perinatology and Child Health and Radiology, Nuclear Medicine and Imaging, having authored 7 papers that have together received 509 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Sexual Differentiation and Disorders (4 papers), Sperm and Testicular Function (2 papers), Genomic variations and chromosomal abnormalities (2 papers), T-cell and Retrovirus Studies (1 paper), Monoclonal and Polyclonal Antibodies Research (1 paper), T-cell and B-cell Immunology (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Reproductive Medicine (98 citations), Genetics (328 citations), Immunology (125 citations), Molecular Biology (261 citations) and Plant Science (136 citations). Mea Andersson has collaborated with scholars based in Finland, United States and France. Frequent co-authors include Albert de la Chapelle, David C. Page, Jan Böhme, Lars Rask, E Möller, Gerhard Andersson, A. de la Chapelle, François Rouyer, Jean Weissenbach and Dorothy Pettay. Their work appears in journals such as Human Genetics, The EMBO Journal, The Journal of Immunology, Science and Genomics.
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.