Werner Schmid
Impact in
- Cancer Research top 0.2%
- Carcinogens and Genotoxicity Assessment
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Forensic and Genetic Research
Papers in
- Genetics 38
- Genomic variations and chromosomal abnormalities 25
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Forensic and Genetic Research 2
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- Carcinogens and Genotoxicity Assessment 17
- Co-authors
- Albert Schinzel (23 shared papers)Bernhard E. Matter (1 shared paper)P. Maier (2 shared papers)Kensuke Hayashi (6 shared papers)Klaus Böller (1 shared paper)Marco Mächler (6 shared papers)W. Bär (2 shared papers)Adelgunde Kratzer (1 shared paper)
- Journals
- Human Genetics (25 papers)Cytogenetic and Genome Research (6 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (5 papers)Prenatal Diagnosis (3 papers)The Lancet (2 papers)
- Partner nations
- SwitzerlandUnited StatesGermany
In The Last Decade
Werner Schmid
97 papers receiving 5.5k citations
Werner Schmid's Hit Papers
Peers
Comparison fields: 5 of 92
- Cancer Research 2.8k
- Genetics 1.0k
- Pediatrics, Perinatology and Child Health 216
- Radiology, Nuclear Medicine and Imaging 288
- Health, Toxicology and Mutagenesis 164
Countries citing papers authored by Werner Schmid
This map shows the geographic impact of Werner Schmid'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 Werner Schmid with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Werner Schmid more than expected).
Fields of papers citing papers by Werner Schmid
This network shows the impact of papers produced by Werner Schmid. 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 Werner Schmid. The network helps show where Werner Schmid may publish in the future.
Co-authors
The 25 scholars most cited alongside Werner Schmid, 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 101 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The micronucleus test Hit paper breakdown → | 1975 | 2077 |
| 2 | The Micronucleus Test for Cytogenetic Analysis Hit paper breakdown → | 1976 | 567 |
| 3 | 1963 | 334 | |
| 4 | 1973 | 242 | |
| 5 | 1971 | 213 | |
| 6 | 1973 | 204 | |
| 7 | 1976 | 190 | |
| 8 | 1981 | 170 | |
| 9 | 1988 | 169 | |
| 10 | 1965 | 118 | |
| 11 | 1970 | 107 | |
| 12 | 1971 | 96 | |
| 13 | 1969 | 82 | |
| 14 | 1976 | 80 | |
| 15 | 1981 | 80 | |
| 16 | Heterochromatin in mammals. | 1967 | 79 |
| 17 | 1962 | 66 | |
| 18 | 1980 | 65 | |
| 19 | 1962 | 61 | |
| 20 | 1975 | 58 |
About Werner Schmid
Werner Schmid is a scholar working on Genetics, Cancer Research, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health and Neurology, having authored 101 papers that have together received 6.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (25 papers), Carcinogens and Genotoxicity Assessment (17 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Genetic Neurodegenerative Diseases (6 papers), Prenatal Screening and Diagnostics (4 papers), Down syndrome and intellectual disability research (2 papers), Genomics and Chromatin Dynamics (2 papers) and Forensic and Genetic Research (2 papers). The work is most often cited by research in Cancer Research (2.8k citations), Genetics (1.0k citations), Pediatrics, Perinatology and Child Health (216 citations), Radiology, Nuclear Medicine and Imaging (288 citations) and Health, Toxicology and Mutagenesis (164 citations). Werner Schmid has collaborated with scholars based in Switzerland, United States and Germany. Frequent co-authors include Albert Schinzel, Bernhard E. Matter, P. Maier, Kensuke Hayashi, Klaus Böller, Marco Mächler, W. Bär, Adelgunde Kratzer, David T. Arakaki and Franz Binkert. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Mutation research. Fundamental and molecular mechanisms of mutagenesis, Prenatal Diagnosis and The Lancet.
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.