Andreas Dufke
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 44
- Genomic variations and chromosomal abnormalities 26
- Genetic Syndromes and Imprinting 11
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 4
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- Genomics and Chromatin Dynamics 6
- Epigenetics and DNA Methylation 5
- Co-authors
- H. Enders (12 shared papers)Thomas Liehr (10 shared papers)Thomas Eggermann (7 shared papers)Michael von Bonin (7 shared papers)Olaf Rieß (11 shared papers)Ute Grasshoff (7 shared papers)Karl Oliver Kagan (10 shared papers)Ulrike A. Mau‐Holzmann (8 shared papers)
- Journals
- Cytogenetic and Genome Research (9 papers)Prenatal Diagnosis (7 papers)European Journal of Human Genetics (4 papers)Human Mutation (2 papers)Fertility and Sterility (1 paper)
- Partner nations
- GermanyUnited StatesFrance
In The Last Decade
Andreas Dufke
58 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 86
- Genetics 802
- Pediatrics, Perinatology and Child Health 275
- Molecular Biology 600
- Genetics 67
- Plant Science 250
Countries citing papers authored by Andreas Dufke
This map shows the geographic impact of Andreas Dufke'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 Andreas Dufke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Dufke more than expected).
Fields of papers citing papers by Andreas Dufke
This network shows the impact of papers produced by Andreas Dufke. 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 Andreas Dufke. The network helps show where Andreas Dufke may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Dufke, 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 174 | |
| 2 | 2005 | 132 | |
| 3 | 2008 | 103 | |
| 4 | 2004 | 71 | |
| 5 | 2012 | 69 | |
| 6 | 2007 | 63 | |
| 7 | 2010 | 57 | |
| 8 | 2005 | 44 | |
| 9 | 2005 | 42 | |
| 10 | 2005 | 38 | |
| 11 | 2011 | 34 | |
| 12 | 2007 | 32 | |
| 13 | 2006 | 31 | |
| 14 | 2015 | 28 | |
| 15 | 2001 | 28 | |
| 16 | 2017 | 27 | |
| 17 | 2003 | 26 | |
| 18 | 2010 | 25 | |
| 19 | 2013 | 25 | |
| 20 | 2017 | 24 |
About Andreas Dufke
Andreas Dufke is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 61 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (26 papers), Prenatal Screening and Diagnostics (20 papers), Chromosomal and Genetic Variations (14 papers), Genetic Syndromes and Imprinting (11 papers), Genomics and Rare Diseases (7 papers), Genomics and Chromatin Dynamics (6 papers), Epigenetics and DNA Methylation (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Genetics (802 citations), Pediatrics, Perinatology and Child Health (275 citations), Molecular Biology (600 citations), Genetics (67 citations) and Plant Science (250 citations). Andreas Dufke has collaborated with scholars based in Germany, United States and France. Frequent co-authors include H. Enders, Thomas Liehr, Thomas Eggermann, Michael von Bonin, Olaf Rieß, Ute Grasshoff, Karl Oliver Kagan, Ulrike A. Mau‐Holzmann, Heike Starke and Dagmar Wieczorek. Their work appears in journals such as Cytogenetic and Genome Research, Prenatal Diagnosis, European Journal of Human Genetics, Human Mutation and Fertility and Sterility.
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.