Merete Bugge
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Molecular Biology top 10%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Cancer-related gene regulation
- Genomics and Chromatin Dynamics
Papers in ⓘ
-
- Congenital limb and hand anomalies 2
- Genetics 15
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 4
- Craniofacial Disorders and Treatments 2
- Co-authors
- Niels Tommerup (10 shared papers)Maj Hultén (1 shared paper)Chih-Lin Hsieh (1 shared paper)Déborah Bourc’his (1 shared paper)James J. Russo (1 shared paper)Xiaoyan Qu (1 shared paper)E. Viégas-Pèquignot (1 shared paper)Timothy H. Bestor (1 shared paper)
In The Last Decade
Merete Bugge
15 papers receiving 1.1k citations
Hit Papers
Peers
Comparison fields: 5 of 81
- Genetics 584
- Molecular Biology 935
- Developmental Biology 20
- Pediatrics, Perinatology and Child Health 146
- Cancer Research 71
Countries citing papers authored by Merete Bugge
This map shows the geographic impact of Merete Bugge'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 Merete Bugge with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Merete Bugge more than expected).
Fields of papers citing papers by Merete Bugge
This network shows the impact of papers produced by Merete Bugge. 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 Merete Bugge. The network helps show where Merete Bugge may publish in the future.
Co-authors
The 25 scholars most cited alongside Merete Bugge, 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 | Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene Hit paper breakdown → | 1999 | 884 |
| 2 | 2007 | 88 | |
| 3 | 2000 | 38 | |
| 4 | 1996 | 33 | |
| 5 | 2002 | 22 | |
| 6 | 2004 | 21 | |
| 7 | 1997 | 19 | |
| 8 | 2006 | 19 | |
| 9 | 1999 | 16 | |
| 10 | 1996 | 10 | |
| 11 | 1997 | 8 | |
| 12 | 2011 | 7 | |
| 13 | 2011 | 7 | |
| 14 | 2004 | 5 | |
| 15 | 2005 | 5 |
About Merete Bugge
Merete Bugge is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Molecular Biology, having authored 15 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromosomal and Genetic Variations (4 papers), Craniofacial Disorders and Treatments (2 papers), RNA modifications and cancer (2 papers), Congenital limb and hand anomalies (2 papers) and Telomeres, Telomerase, and Senescence (1 paper). The work is most often cited by research in Genetics (584 citations), Molecular Biology (935 citations), Developmental Biology (20 citations), Pediatrics, Perinatology and Child Health (146 citations) and Cancer Research (71 citations). Merete Bugge has collaborated with scholars based in Denmark, Germany and Greece. Frequent co-authors include Niels Tommerup, Maj Hultén, Chih-Lin Hsieh, Déborah Bourc’his, James J. Russo, Xiaoyan Qu, E. Viégas-Pèquignot, Timothy H. Bestor, Guoliang Xu and Reinhard Ullmann. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, Human Mutation, The Cleft Palate-Craniofacial Journal and European Journal of Medical Genetics.
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.