Birgitte Bertelsen
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- Cancer Genomics and Diagnostics
Papers in
-
- DNA Repair Mechanisms 3
- Genetics 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- BRCA gene mutations in cancer 2
- Co-authors
- Zeynep Tümer (12 shared papers)Karen Brøndum‐Nielsen (5 shared papers)Finn Cilius Nielsen (4 shared papers)Lusine Nazaryan‐Petersen (2 shared papers)Liselotte Skov (5 shared papers)Kirstine Ravn (1 shared paper)Nanette Mol Debes (5 shared papers)Miyako Kodama (1 shared paper)
- Journals
- Familial Cancer (2 papers)Human Mutation (2 papers)European Journal of Human Genetics (1 paper)npj Genomic Medicine (1 paper)Frontiers in Neuroscience (1 paper)
- Partner nations
- DenmarkUnited StatesUnited Kingdom
In The Last Decade
Birgitte Bertelsen
26 papers receiving 510 citations
Birgitte Bertelsen's Hit Papers
Peers
Comparison fields: 5 of 80
- Genetics 195
- Cancer Research 73
- Molecular Biology 244
- Pathology and Forensic Medicine 63
- Genetics 32
Countries citing papers authored by Birgitte Bertelsen
This map shows the geographic impact of Birgitte Bertelsen'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 Birgitte Bertelsen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birgitte Bertelsen more than expected).
Fields of papers citing papers by Birgitte Bertelsen
This network shows the impact of papers produced by Birgitte Bertelsen. 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 Birgitte Bertelsen. The network helps show where Birgitte Bertelsen may publish in the future.
Co-authors
The 25 scholars most cited alongside Birgitte Bertelsen, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 56 | |
| 2 | Whole genome sequencing in clinical practice Hit paper breakdown → | 2024 | 56 |
| 3 | 2015 | 54 | |
| 4 | 2019 | 54 | |
| 5 | 2011 | 46 | |
| 6 | 2016 | 42 | |
| 7 | 2011 | 37 | |
| 8 | 2013 | 26 | |
| 9 | 2015 | 21 | |
| 10 | 2020 | 20 | |
| 11 | 2013 | 14 | |
| 12 | 2014 | 13 | |
| 13 | 2021 | 13 | |
| 14 | 2020 | 11 | |
| 15 | 2015 | 8 | |
| 16 | 2019 | 8 | |
| 17 | 2018 | 8 | |
| 18 | 2023 | 7 | |
| 19 | 2022 | 7 | |
| 20 | 2022 | 6 |
About Birgitte Bertelsen
Birgitte Bertelsen is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Clinical Psychology and Surgery, having authored 26 papers that have together received 525 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (6 papers), Obsessive-Compulsive Spectrum Disorders (6 papers), Cancer Genomics and Diagnostics (4 papers), Autism Spectrum Disorder Research (3 papers), DNA Repair Mechanisms (3 papers), Nutritional Studies and Diet (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Genetics (195 citations), Cancer Research (73 citations), Molecular Biology (244 citations), Pathology and Forensic Medicine (63 citations) and Genetics (32 citations). Birgitte Bertelsen has collaborated with scholars based in Denmark, United States and United Kingdom. Frequent co-authors include Zeynep Tümer, Karen Brøndum‐Nielsen, Finn Cilius Nielsen, Lusine Nazaryan‐Petersen, Liselotte Skov, Kirstine Ravn, Nanette Mol Debes, Miyako Kodama, Frederik Otzen Bagger and Line Borgwardt. Their work appears in journals such as Familial Cancer, Human Mutation, European Journal of Human Genetics, npj Genomic Medicine and Frontiers in Neuroscience.
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.