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
- Genetics 17
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Craniofacial Disorders and Treatments 2
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- Prenatal Screening and Diagnostics 6
- Co-authors
- Niels Tommerup (10 shared papers)Guo-Liang Xu (1 shared paper)James J. Russo (1 shared paper)E. Viégas-Pèquignot (1 shared paper)Timothy H. Bestor (1 shared paper)Chih-Lin Hsieh (1 shared paper)Déborah Bourc’his (1 shared paper)Maj A. Hultén (1 shared paper)
- Journals
- European Journal of Human Genetics (5 papers)Human Genetics (2 papers)Clinical Genetics (2 papers)The Cleft Palate-Craniofacial Journal (1 paper)The Lancet (1 paper)
- Partner nations
- DenmarkGermanyUnited States
In The Last Decade
Merete Bugge
19 papers receiving 1.3k citations
Merete Bugge's Hit Papers
Peers
Comparison fields: 5 of 85
- Genetics 670
- Molecular Biology 996
- Pediatrics, Perinatology and Child Health 184
- Developmental Biology 23
- Cancer Research 67
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 | 963 |
| 2 | 2007 | 107 | |
| 3 | 2004 | 53 | |
| 4 | 2000 | 40 | |
| 5 | 2004 | 36 | |
| 6 | 1996 | 36 | |
| 7 | 2006 | 33 | |
| 8 | 2022 | 29 | |
| 9 | 1983 | 26 | |
| 10 | 2002 | 24 | |
| 11 | 1997 | 20 | |
| 12 | 1999 | 17 | |
| 13 | 1996 | 13 | |
| 14 | 1997 | 9 | |
| 15 | 2011 | 7 | |
| 16 | 2011 | 7 | |
| 17 | 2004 | 6 | |
| 18 | 2005 | 6 | |
| 19 | 1998 | 2 |
About Merete Bugge
Merete Bugge is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Developmental Biology, Plant Science and Molecular Biology, having authored 19 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (6 papers), Prenatal Screening and Diagnostics (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Congenital limb and hand anomalies (2 papers), RNA modifications and cancer (2 papers) and Craniofacial Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (670 citations), Molecular Biology (996 citations), Pediatrics, Perinatology and Child Health (184 citations), Developmental Biology (23 citations) and Cancer Research (67 citations). Merete Bugge has collaborated with scholars based in Denmark, Germany and United States. Frequent co-authors include Niels Tommerup, Guo-Liang Xu, James J. Russo, E. Viégas-Pèquignot, Timothy H. Bestor, Chih-Lin Hsieh, Déborah Bourc’his, Maj A. Hultén, Xiaoyan Qu and Michael Bjorn Petersen. Their work appears in journals such as European Journal of Human Genetics, Human Genetics, Clinical Genetics, The Cleft Palate-Craniofacial Journal and The Lancet.
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.