Andreas Weith
- Cancer Research top 5%
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 8
- 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
- Immunology top 5%
- Molecular Biology top 5%
- Genomics and Chromatin Dynamics 11
- Gene expression and cancer classification 9
- Molecular Biology Techniques and Applications 6
- Oncology top 5%
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- Chromosomal and Genetic Variations 12
- Co-authors
- Martin J.H. NicklinPeter SeitherWalther TrautDetlev MennerichMeinrad BusslingerZbyněk KozmíkCelina CziepluchManfred Schwab
- Cited by
- Cancer ResearchGeneticsImmunology
- Partner nations
- GermanyAustriaUnited Kingdom
In The Last Decade
Andreas Weith
58 papers receiving 3.0k citations
Peers
Comparison fields: 5 of 127
- Cancer Research 450
- Genetics 772
- Immunology 518
- Molecular Biology 1.7k
- Oncology 490
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 83 | |
| 2 | 2009 | 72 | |
| 3 | 2008 | 55 | |
| 4 | 2006 | 171 | |
| 5 | 2006 | 24 | |
| 6 | 2005 | 53 | |
| 7 | 2004 | 18 | |
| 8 | 1999 | 117 | |
| 9 | 1998 | 13 | |
| 10 | 1998 | 12 | |
| 11 | 1993 | 179 | |
| 12 | 1992 | 9 | |
| 13 | 1992 | 16 | |
| 14 | 1991 | 6 | |
| 15 | 1991 | 35 | |
| 16 | 1991 | 11 | |
| 17 | 1990 | 8 | |
| 18 | 1989 | 146 | |
| 19 | 1988 | 10 | |
| 20 | 1988 | 13 |
About Andreas Weith
Andreas Weith is a scholar working on Genetics, Molecular Biology, Cancer Research, Neurology and Plant Science, having authored 59 papers that have together received 3.0k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (12 papers), Genomics and Chromatin Dynamics (11 papers), Gene expression and cancer classification (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), Molecular Biology Techniques and Applications (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 (450 citations), Genetics (772 citations), Immunology (518 citations), Molecular Biology (1.7k citations) and Oncology (490 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, Meinrad Busslinger, Zbyněk Kozmík, Celina Cziepluch, Manfred Schwab, Thomas Waerner and Wilfried Ellmeier. Their work appears in journals such as Genomics, Chromosoma, Cytogenetic and Genome Research, Genes Chromosomes and Cancer and Nucleic Acids 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.