Susanne E. Boonen
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Diabetes and associated disorders
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 13
- Genetic Syndromes and Imprinting 7
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 2
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- Epigenetics and DNA Methylation 5
- Co-authors
- Johanne M D Hahnemann (7 shared papers)Deborah Mackay (7 shared papers)I. Karen Temple (6 shared papers)David Robinson (3 shared papers)Helen White (3 shared papers)Jonathan L A Callaway (1 shared paper)Helen V. Firth (1 shared paper)Andrew T. Hattersley (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Human Genetics (2 papers)Biomolecules (1 paper)European Journal of Medical Genetics (1 paper)Scientific Reports (1 paper)
- Partner nations
- DenmarkUnited KingdomGermany
In The Last Decade
Susanne E. Boonen
18 papers receiving 764 citations
Peers
Comparison fields: 5 of 53
- Genetics 535
- Pediatrics, Perinatology and Child Health 260
- Molecular Biology 499
- Surgery 119
- Endocrinology, Diabetes and Metabolism 44
Countries citing papers authored by Susanne E. Boonen
This map shows the geographic impact of Susanne E. Boonen'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 Susanne E. Boonen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Susanne E. Boonen more than expected).
Fields of papers citing papers by Susanne E. Boonen
This network shows the impact of papers produced by Susanne E. Boonen. 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 Susanne E. Boonen. The network helps show where Susanne E. Boonen may publish in the future.
Co-authors
The 25 scholars most cited alongside Susanne E. Boonen, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 375 | |
| 2 | 2006 | 117 | |
| 3 | 2006 | 47 | |
| 4 | 2013 | 40 | |
| 5 | 2008 | 39 | |
| 6 | 2011 | 31 | |
| 7 | 2004 | 26 | |
| 8 | 2016 | 26 | |
| 9 | 2021 | 24 | |
| 10 | 2011 | 14 | |
| 11 | 2010 | 14 | |
| 12 | 2017 | 7 | |
| 13 | 2016 | 6 | |
| 14 | 2023 | 4 | |
| 15 | [Myalgic encephalomyelitis or chronic fatigue syndrome]. | 2019 | 4 |
| 16 | 2023 | 2 | |
| 17 | 2022 | 1 | |
| 18 | Myalgisk encefalomyelitis eller kronisk træthedssyndrom | 2019 | 1 |
| 19 | 2025 | 0 | |
| 20 | 2025 | 0 |
About Susanne E. Boonen
Susanne E. Boonen is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Pathology and Forensic Medicine, having authored 21 papers that have together received 778 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (7 papers), BRCA gene mutations in cancer (5 papers), Epigenetics and DNA Methylation (5 papers), Prenatal Screening and Diagnostics (4 papers), Genetic factors in colorectal cancer (3 papers), Pancreatic function and diabetes (3 papers), Genomics and Rare Diseases (2 papers) and Amyotrophic Lateral Sclerosis Research (2 papers). The work is most often cited by research in Genetics (535 citations), Pediatrics, Perinatology and Child Health (260 citations), Molecular Biology (499 citations), Surgery (119 citations) and Endocrinology, Diabetes and Metabolism (44 citations). Susanne E. Boonen has collaborated with scholars based in Denmark, United Kingdom and Germany. Frequent co-authors include Johanne M D Hahnemann, Deborah Mackay, I. Karen Temple, David Robinson, Helen White, Jonathan L A Callaway, Helen V. Firth, Andrew T. Hattersley, Judith A. Goodship and Carlo L. Acerini. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, Biomolecules, European Journal of Medical Genetics and Scientific Reports.
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.