Marcel Freund
Impact in
- Cancer Research top 5%
- Carcinogens and Genotoxicity Assessment
- Genetics top 2%
- BRCA gene mutations in cancer
Papers in
- Virology 4
- HIV Research and Treatment 4
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- DNA Repair Mechanisms 7
- RNA Research and Splicing 6
- RNA and protein synthesis mechanisms 3
- CRISPR and Genetic Engineering 2
- RNA Interference and Gene Delivery 2
- RNA modifications and cancer 2
- Co-authors
- Helmut Hanenberg (11 shared papers)Kornelia Neveling (4 shared papers)Arleen D. Auerbach (3 shared papers)Detlev Schindler (3 shared papers)Francis P. Lach (2 shared papers)Heiner Schaal (5 shared papers)Melanie Wurm (2 shared papers)Nazneen Rahman (2 shared papers)
- Journals
- Nature Genetics (3 papers)Nucleic Acids Research (2 papers)European Journal of Neuroscience (1 paper)Synlett (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Marcel Freund
22 papers receiving 2.4k citations
Marcel Freund's Hit Papers
Peers
Comparison fields: 5 of 89
- Cancer Research 470
- Genetics 918
- Virology 127
- Molecular Biology 1.7k
- Oncology 480
Countries citing papers authored by Marcel Freund
This map shows the geographic impact of Marcel Freund'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 Marcel Freund with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marcel Freund more than expected).
Fields of papers citing papers by Marcel Freund
This network shows the impact of papers produced by Marcel Freund. 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 Marcel Freund. The network helps show where Marcel Freund may publish in the future.
Co-authors
The 25 scholars most cited alongside Marcel Freund, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene Hit paper breakdown → | 2010 | 592 |
| 2 | 2006 | 521 | |
| 3 | 2010 | 335 | |
| 4 | 2007 | 241 | |
| 5 | 2013 | 109 | |
| 6 | 1987 | 86 | |
| 7 | 2003 | 78 | |
| 8 | 2004 | 77 | |
| 9 | 2001 | 75 | |
| 10 | Interaction of human immunodeficiency virus with human sperm in vitro. | 1988 | 60 |
| 11 | 2009 | 55 | |
| 12 | 2010 | 53 | |
| 13 | 2014 | 50 | |
| 14 | 2005 | 45 | |
| 15 | 2012 | 31 | |
| 16 | 2013 | 26 | |
| 17 | 2001 | 20 | |
| 18 | 2015 | 15 | |
| 19 | 2021 | 10 | |
| 20 | 2020 | 5 |
About Marcel Freund
Marcel Freund is a scholar working on Virology, Molecular Biology, Genetics, Pharmacology and Genetics, having authored 23 papers that have together received 2.5k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (7 papers), RNA Research and Splicing (6 papers), HIV Research and Treatment (4 papers), BRCA gene mutations in cancer (3 papers), RNA and protein synthesis mechanisms (3 papers), CRISPR and Genetic Engineering (2 papers), RNA Interference and Gene Delivery (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Cancer Research (470 citations), Genetics (918 citations), Virology (127 citations), Molecular Biology (1.7k citations) and Oncology (480 citations). Marcel Freund has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Helmut Hanenberg, Kornelia Neveling, Arleen D. Auerbach, Detlev Schindler, Francis P. Lach, Heiner Schaal, Melanie Wurm, Nazneen Rahman, Karen T. Barker and Christopher George Mathew. Their work appears in journals such as Nature Genetics, Nucleic Acids Research, European Journal of Neuroscience, Synlett and The American Journal of Human 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.