Mette Viuff
Impact in
Papers in
- Genetics 21
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 21
- Estrogen and related hormone effects 1
- Genetic Mapping and Diversity in Plants and Animals 1
-
- Sexual Differentiation and Disorders 11
- Co-authors
- Claus Højbjerg Gravholt (26 shared papers)Kirstine Stochholm (12 shared papers)N.H. Andersen (9 shared papers)Agnethe Berglund (10 shared papers)Anne Skakkebæk (8 shared papers)Simon Chang (4 shared papers)Svend Juul (5 shared papers)Jens Fedder (4 shared papers)
- Journals
- The Journal of Clinical Endocrinology & Metabolism (4 papers)Human Reproduction (2 papers)European Journal of Human Genetics (2 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (2 papers)Orphanet Journal of Rare Diseases (2 papers)
- Partner nations
- DenmarkUnited StatesUnited Kingdom
In The Last Decade
Mette Viuff
25 papers receiving 876 citations
Peers
Comparison fields: 5 of 58
- Genetics 582
- Urology 70
- Reproductive Medicine 81
- Pediatrics, Perinatology and Child Health 90
- Molecular Biology 349
Countries citing papers authored by Mette Viuff
This map shows the geographic impact of Mette Viuff'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 Mette Viuff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mette Viuff more than expected).
Fields of papers citing papers by Mette Viuff
This network shows the impact of papers produced by Mette Viuff. 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 Mette Viuff. The network helps show where Mette Viuff may publish in the future.
Co-authors
The 25 scholars most cited alongside Mette Viuff, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 190 | |
| 2 | 2019 | 124 | |
| 3 | 2016 | 73 | |
| 4 | 2022 | 71 | |
| 5 | 2015 | 50 | |
| 6 | 2019 | 44 | |
| 7 | 2019 | 40 | |
| 8 | 2016 | 32 | |
| 9 | 2017 | 29 | |
| 10 | 2020 | 28 | |
| 11 | 2018 | 26 | |
| 12 | 2022 | 24 | |
| 13 | 2022 | 23 | |
| 14 | 2021 | 20 | |
| 15 | 2020 | 20 | |
| 16 | 2017 | 18 | |
| 17 | 2022 | 16 | |
| 18 | 2023 | 16 | |
| 19 | 2021 | 14 | |
| 20 | 2023 | 10 |
About Mette Viuff
Mette Viuff is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Gender Studies and Cardiology and Cardiovascular Medicine, having authored 28 papers that have together received 884 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Sexual Differentiation and Disorders (11 papers), Gender Studies in Language (3 papers), Reproductive Biology and Fertility (3 papers), Estrogen and related hormone effects (1 paper), MicroRNA in disease regulation (1 paper), Genetic Mapping and Diversity in Plants and Animals (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Genetics (582 citations), Urology (70 citations), Reproductive Medicine (81 citations), Pediatrics, Perinatology and Child Health (90 citations) and Molecular Biology (349 citations). Mette Viuff has collaborated with scholars based in Denmark, United States and United Kingdom. Frequent co-authors include Claus Højbjerg Gravholt, Kirstine Stochholm, N.H. Andersen, Agnethe Berglund, Anne Skakkebæk, Simon Chang, Svend Juul, Jens Fedder, Trine Holm Johannsen and Katharina M. Main. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Human Reproduction, European Journal of Human Genetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics and Orphanet Journal of Rare Diseases.
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.