Corinna Menzel
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cancer Research top 5%
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
Papers in
- Genetics 19
- Genomic variations and chromosomal abnormalities 14
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 3
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- Congenital heart defects research 4
- RNA Research and Splicing 4
- Co-authors
- Wei Chen (11 shared papers)Vera M. Kalscheuer (19 shared papers)Philipp Khaitovich (7 shared papers)Hans‐Hilger Ropers (17 shared papers)Ying Xu (5 shared papers)Hai Hu (4 shared papers)Niels Tommerup (7 shared papers)Reinhard Ullmann (11 shared papers)
- Journals
- BMC Genomics (3 papers)European Journal of Human Genetics (3 papers)The American Journal of Human Genetics (3 papers)Human Genetics (2 papers)Cytogenetic and Genome Research (2 papers)
- Partner nations
- GermanyNetherlandsChina
In The Last Decade
Corinna Menzel
28 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 101
- Genetics 881
- Cancer Research 422
- Aging 44
- Molecular Biology 1.2k
- Developmental Neuroscience 62
Countries citing papers authored by Corinna Menzel
This map shows the geographic impact of Corinna Menzel'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 Corinna Menzel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Corinna Menzel more than expected).
Fields of papers citing papers by Corinna Menzel
This network shows the impact of papers produced by Corinna Menzel. 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 Corinna Menzel. The network helps show where Corinna Menzel may publish in the future.
Co-authors
The 25 scholars most cited alongside Corinna Menzel, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 244 | |
| 2 | 2003 | 229 | |
| 3 | 2009 | 218 | |
| 4 | 2009 | 128 | |
| 5 | 2010 | 127 | |
| 6 | 2008 | 120 | |
| 7 | 2008 | 116 | |
| 8 | 2011 | 105 | |
| 9 | 2008 | 103 | |
| 10 | 2007 | 90 | |
| 11 | 1999 | 78 | |
| 12 | 2005 | 67 | |
| 13 | 2003 | 66 | |
| 14 | 2008 | 58 | |
| 15 | 2006 | 58 | |
| 16 | 2009 | 50 | |
| 17 | 2010 | 45 | |
| 18 | 2010 | 40 | |
| 19 | 2009 | 35 | |
| 20 | 2005 | 31 |
About Corinna Menzel
Corinna Menzel is a scholar working on Genetics, Molecular Biology, Plant Science, Cancer Research and Cellular and Molecular Neuroscience, having authored 28 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers), Chromosomal and Genetic Variations (7 papers), MicroRNA in disease regulation (5 papers), Congenital heart defects research (4 papers), RNA Research and Splicing (4 papers), Cancer-related molecular mechanisms research (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (881 citations), Cancer Research (422 citations), Aging (44 citations), Molecular Biology (1.2k citations) and Developmental Neuroscience (62 citations). Corinna Menzel has collaborated with scholars based in Germany, Netherlands and China. Frequent co-authors include Wei Chen, Vera M. Kalscheuer, Philipp Khaitovich, Hans‐Hilger Ropers, Ying Xu, Hai Hu, Niels Tommerup, Reinhard Ullmann, Ning Fu and Song Guo. Their work appears in journals such as BMC Genomics, European Journal of Human Genetics, The American Journal of Human Genetics, Human Genetics and Cytogenetic and Genome Research.
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.