Moritz Menzel
Impact in
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- Wnt/β-catenin signaling in development and cancer
- Cancer-related gene regulation
- Melanoma and MAPK Pathways
Papers in
- Genetics 4
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
- Genetic and Kidney Cyst Diseases 1
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- Wnt/β-catenin signaling in development and cancer 3
- Cancer-related gene regulation 2
- Co-authors
- Michael Schwarz (3 shared papers)Birgit Sauer (2 shared papers)Claus Garbe (2 shared papers)Tobias Sinnberg (2 shared papers)Birgit Schittek (2 shared papers)Saskia Biskup (5 shared papers)Max Schubach (3 shared papers)Dennis Döcker (3 shared papers)
- Journals
- European Journal of Human Genetics (3 papers)FEBS Journal (1 paper)Journal of Translational Medicine (1 paper)Zoomorphology (1 paper)Cancer Research (1 paper)
- Partner nations
- GermanyFinlandSaudi Arabia
In The Last Decade
Moritz Menzel
9 papers receiving 346 citations
Peers
Comparison fields: 5 of 71
- Molecular Biology 221
- Developmental Neuroscience 11
- Hepatology 17
- Genetics 65
- Oncology 55
Countries citing papers authored by Moritz Menzel
This map shows the geographic impact of Moritz 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 Moritz Menzel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Moritz Menzel more than expected).
Fields of papers citing papers by Moritz Menzel
This network shows the impact of papers produced by Moritz 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 Moritz Menzel. The network helps show where Moritz Menzel may publish in the future.
Co-authors
The 25 scholars most cited alongside Moritz 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
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 94 | |
| 2 | 2013 | 69 | |
| 3 | 2010 | 64 | |
| 4 | 2007 | 46 | |
| 5 | 2015 | 33 | |
| 6 | 2018 | 28 | |
| 7 | 2014 | 13 | |
| 8 | 2021 | 3 | |
| 9 | 2018 | 2 |
About Moritz Menzel
Moritz Menzel is a scholar working on Genetics, Molecular Biology, Surgery, Genetics and Neurology, having authored 9 papers that have together received 352 indexed citations. Recurring topics across this work include Wnt/β-catenin signaling in development and cancer (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Cancer-related gene regulation (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Rare Diseases (1 paper), Genetic Syndromes and Imprinting (1 paper), Liver physiology and pathology (1 paper) and Genetic and Kidney Cyst Diseases (1 paper). The work is most often cited by research in Molecular Biology (221 citations), Developmental Neuroscience (11 citations), Hepatology (17 citations), Genetics (65 citations) and Oncology (55 citations). Moritz Menzel has collaborated with scholars based in Germany, Finland and Saudi Arabia. Frequent co-authors include Michael Schwarz, Birgit Sauer, Claus Garbe, Tobias Sinnberg, Birgit Schittek, Saskia Biskup, Max Schubach, Dennis Döcker, Martin Schaller and Christiane Spaich. Their work appears in journals such as European Journal of Human Genetics, FEBS Journal, Journal of Translational Medicine, Zoomorphology and Cancer 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.