Birgit Jepsen
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Congenital heart defects research
- Chromatin Remodeling and Cancer
Papers in
- Genetics 4
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 2
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- Chromosomal and Genetic Variations 2
- Co-authors
- Maria Kirchhoff (3 shared papers)Flemming Skovby (2 shared papers)Anne‐Marie Bisgaard (2 shared papers)Thue Bryndorf (1 shared paper)Karen Brøndum‐Nielsen (1 shared paper)Monika Cohen (1 shared paper)Zeynep Tümer (1 shared paper)Niels Tommerup (1 shared paper)
In The Last Decade
Birgit Jepsen
4 papers receiving 95 citations
Peers
Comparison fields: 5 of 31
- Genetics 77
- Molecular Biology 53
- Pediatrics, Perinatology and Child Health 14
- Cognitive Neuroscience 11
- Genetics 6
Countries citing papers authored by Birgit Jepsen
This map shows the geographic impact of Birgit Jepsen'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 Birgit Jepsen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birgit Jepsen more than expected).
Fields of papers citing papers by Birgit Jepsen
This network shows the impact of papers produced by Birgit Jepsen. 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 Birgit Jepsen. The network helps show where Birgit Jepsen may publish in the future.
Co-authors
The 25 scholars most cited alongside Birgit Jepsen, 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 | 2006 | 47 | |
| 2 | 2007 | 30 | |
| 3 | 2010 | 10 | |
| 4 | 2023 | 8 |
About Birgit Jepsen
Birgit Jepsen is a scholar working on Genetics, Plant Science, Molecular Biology, Infectious Diseases and Organic Chemistry, having authored 4 papers that have together received 95 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers), Chromosomal and Genetic Variations (2 papers) and Congenital heart defects research (1 paper). The work is most often cited by research in Genetics (77 citations), Molecular Biology (53 citations), Pediatrics, Perinatology and Child Health (14 citations), Cognitive Neuroscience (11 citations) and Genetics (6 citations). Birgit Jepsen has collaborated with scholars based in Denmark, Germany and Finland. Frequent co-authors include Maria Kirchhoff, Flemming Skovby, Anne‐Marie Bisgaard, Thue Bryndorf, Karen Brøndum‐Nielsen, Monika Cohen, Zeynep Tümer, Niels Tommerup, Reinhard Ullmann and Tim Jensen. Their work appears in journals such as European Journal of Medical Genetics, Frontiers in Neuroscience and American Journal of Medical Genetics Part A.
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.