Lars Beckmann
Impact in
- Genetics top 5%
- Genetic Associations and Epidemiology
- BRCA gene mutations in cancer
- Genetic Mapping and Diversity in Plants and Animals
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 23
- Genetic Associations and Epidemiology 17
- Genetic Mapping and Diversity in Plants and Animals 8
- BRCA gene mutations in cancer 6
- Estrogen and related hormone effects 4
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Jenny C. Chang-Claude (18 shared papers)Dajun Qian (1 shared paper)Rebecca Hein (5 shared papers)Evelin Deeg (2 shared papers)Alexandra Nieters (1 shared paper)Nikolaus Becker (1 shared paper)André Scherag (2 shared papers)Heiner Schäfer (2 shared papers)
- Journals
- Genetic Epidemiology (4 papers)Cancer Epidemiology Biomarkers & Prevention (3 papers)Human Molecular Genetics (3 papers)Human Heredity (2 papers)Carcinogenesis (2 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Lars Beckmann
47 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 126
- Genetics 775
- Cancer Research 341
- Oncology 320
- Molecular Biology 730
- Pathology and Forensic Medicine 160
Countries citing papers authored by Lars Beckmann
This map shows the geographic impact of Lars Beckmann'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 Lars Beckmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lars Beckmann more than expected).
Fields of papers citing papers by Lars Beckmann
This network shows the impact of papers produced by Lars Beckmann. 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 Lars Beckmann. The network helps show where Lars Beckmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Lars Beckmann, 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 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 348 | |
| 2 | 2012 | 149 | |
| 3 | 2008 | 138 | |
| 4 | 2006 | 126 | |
| 5 | 2008 | 116 | |
| 6 | 2002 | 97 | |
| 7 | 2016 | 90 | |
| 8 | 2014 | 76 | |
| 9 | 2009 | 58 | |
| 10 | 2009 | 56 | |
| 11 | 2012 | 56 | |
| 12 | 2010 | 53 | |
| 13 | 2005 | 45 | |
| 14 | 2008 | 42 | |
| 15 | 2010 | 40 | |
| 16 | 2011 | 39 | |
| 17 | 2014 | 39 | |
| 18 | 2007 | 37 | |
| 19 | 2006 | 33 | |
| 20 | 2007 | 33 |
About Lars Beckmann
Lars Beckmann is a scholar working on Genetics, Cancer Research, Molecular Biology, Oncology and Finance, having authored 47 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (17 papers), Genetic Mapping and Diversity in Plants and Animals (8 papers), BRCA gene mutations in cancer (6 papers), Estrogen and related hormone effects (4 papers), Bioinformatics and Genomic Networks (4 papers), Genomics and Chromatin Dynamics (3 papers), Financial Markets and Investment Strategies (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (775 citations), Cancer Research (341 citations), Oncology (320 citations), Molecular Biology (730 citations) and Pathology and Forensic Medicine (160 citations). Lars Beckmann has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Jenny C. Chang-Claude, Dajun Qian, Rebecca Hein, Evelin Deeg, Alexandra Nieters, Nikolaus Becker, André Scherag, Heiner Schäfer, Astrid Dempfle and Christine Fischer. Their work appears in journals such as Genetic Epidemiology, Cancer Epidemiology Biomarkers & Prevention, Human Molecular Genetics, Human Heredity and Carcinogenesis.
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.