Andreas Weith
Impact in
- Cancer Research top 5%
- Genetics top 5%
Papers in
- Genetics 25
- Genomic variations and chromosomal abnormalities 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Animal Genetics and Reproduction 6
- Genetic Mapping and Diversity in Plants and Animals 5
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- Genomics and Chromatin Dynamics 11
- Gene expression and cancer classification 8
- Co-authors
- Martin J.H. Nicklin (1 shared paper)Peter Seither (4 shared papers)Walther Traut (8 shared papers)Detlev Mennerich (7 shared papers)Zbyněk Kozmík (3 shared papers)Meinrad Busslinger (3 shared papers)Celina Cziepluch (4 shared papers)Manfred Schwab (4 shared papers)
- Journals
- Genomics (10 papers)Chromosoma (5 papers)Genes Chromosomes and Cancer (3 papers)Nucleic Acids Research (2 papers)BMC Genomics (2 papers)
- Partner nations
- GermanyAustriaUnited Kingdom
In The Last Decade
Andreas Weith
60 papers receiving 3.0k citations
Peers
Comparison fields: 5 of 126
- Cancer Research 409
- Genetics 711
- Molecular Biology 1.6k
- Immunology 453
- Oncology 466
Countries citing papers authored by Andreas Weith
This map shows the geographic impact of Andreas Weith'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 Weith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Weith more than expected).
Fields of papers citing papers by Andreas Weith
This network shows the impact of papers produced by Andreas Weith. 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 Weith. The network helps show where Andreas Weith may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Weith, 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 62 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 291 | |
| 2 | 2003 | 247 | |
| 3 | 1993 | 191 | |
| 4 | 2006 | 180 | |
| 5 | 1989 | 158 | |
| 6 | 2005 | 149 | |
| 7 | Human colorectal cancer: high frequency of deletions at chromosome 1p35. | 1990 | 125 |
| 8 | 2005 | 121 | |
| 9 | 1999 | 121 | |
| 10 | Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas. | 1991 | 118 |
| 11 | 1995 | 98 | |
| 12 | 1992 | 97 | |
| 13 | 2010 | 89 | |
| 14 | 2010 | 76 | |
| 15 | 2009 | 75 | |
| 16 | 2011 | 73 | |
| 17 | 1988 | 64 | |
| 18 | 2008 | 61 | |
| 19 | 1980 | 60 | |
| 20 | 1989 | 58 |
About Andreas Weith
Andreas Weith is a scholar working on Genetics, Molecular Biology, Cancer Research, Plant Science and Neurology, having authored 62 papers that have together received 3.1k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (12 papers), Genomics and Chromatin Dynamics (11 papers), Genomic variations and chromosomal abnormalities (9 papers), Gene expression and cancer classification (8 papers), Neuroblastoma Research and Treatments (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Animal Genetics and Reproduction (6 papers) and Genetic Mapping and Diversity in Plants and Animals (5 papers). The work is most often cited by research in Cancer Research (409 citations), Genetics (711 citations), Molecular Biology (1.6k citations), Immunology (453 citations) and Oncology (466 citations). Andreas Weith has collaborated with scholars based in Germany, Austria and United Kingdom. Frequent co-authors include Martin J.H. Nicklin, Peter Seither, Walther Traut, Detlev Mennerich, Zbyněk Kozmík, Meinrad Busslinger, Celina Cziepluch, Manfred Schwab, Thomas Waerner and Wilfried Ellmeier. Their work appears in journals such as Genomics, Chromosoma, Genes Chromosomes and Cancer, Nucleic Acids Research and BMC Genomics.
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.