Máximo E. Drets
Impact in
- Cancer Research top 10%
- Carcinogens and Genotoxicity Assessment
- Plant Science top 10%
- Chromosomal and Genetic Variations
Papers in ⓘ
- Genetics 12
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Co-authors
- Margery W. Shaw (1 shared paper)Gustavo A. Folle (6 shared papers)David E. Comings (1 shared paper)Petra Pfeiffer (2 shared papers)John R. K. Savage (2 shared papers)Wolfgang Goedecke (2 shared papers)Christian Johannes (2 shared papers)Wilner Martínez‐López (2 shared papers)
- Journals
- Chromosoma (4 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (2 papers)Cytogenetic and Genome Research (2 papers)The Lancet (2 papers)Interciencia (1 paper)
- Partner nations
- UruguayUnited StatesAustralia
In The Last Decade
Máximo E. Drets
27 papers receiving 689 citations
Peers
Comparison fields: 5 of 94
- Cancer Research 178
- Plant Science 289
- Genetics 212
- Molecular Biology 451
- Chemical Health and Safety 3
Countries citing papers authored by Máximo E. Drets
This map shows the geographic impact of Máximo E. Drets'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 Máximo E. Drets with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Máximo E. Drets more than expected).
Fields of papers citing papers by Máximo E. Drets
This network shows the impact of papers produced by Máximo E. Drets. 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 Máximo E. Drets. The network helps show where Máximo E. Drets may publish in the future.
Co-authors
The 25 scholars most cited alongside Máximo E. Drets, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 234 | |
| 2 | 1971 | 189 | |
| 3 | 1977 | 81 | |
| 4 | 1976 | 50 | |
| 5 | 1974 | 42 | |
| 6 | 1970 | 36 | |
| 7 | 1983 | 33 | |
| 8 | 1978 | 13 | |
| 9 | 1974 | 11 | |
| 10 | 1970 | 10 | |
| 11 | 1998 | 8 | |
| 12 | 1982 | 8 | |
| 13 | Further analyses of subtelomeric and paracentric holes induced in human and Chinese hamster ovary cell chromosomes | 1995 | 6 |
| 14 | Una saga citogenética: El descubrimiento de los métodos de bandeo cromosómico. Significado y proyección bio-médica | 2002 | 4 |
| 15 | 2004 | 4 | |
| 16 | 2000 | 4 | |
| 17 | 1980 | 4 | |
| 18 | 1998 | 4 | |
| 19 | 1996 | 3 | |
| 20 | 1969 | 2 |
About Máximo E. Drets
Máximo E. Drets is a scholar working on Developmental Biology, Genetics, Plant Science, Molecular Biology and Cancer Research, having authored 28 papers that have together received 754 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (12 papers), Genomics and Chromatin Dynamics (6 papers), Genomic variations and chromosomal abnormalities (6 papers), DNA Repair Mechanisms (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), DNA and Nucleic Acid Chemistry (4 papers), CRISPR and Genetic Engineering (3 papers) and Telomeres, Telomerase, and Senescence (3 papers). The work is most often cited by research in Cancer Research (178 citations), Plant Science (289 citations), Genetics (212 citations), Molecular Biology (451 citations) and Chemical Health and Safety (3 citations). Máximo E. Drets has collaborated with scholars based in Uruguay, United States and Australia. Frequent co-authors include Margery W. Shaw, Gustavo A. Folle, David E. Comings, Petra Pfeiffer, John R. K. Savage, Wolfgang Goedecke, Christian Johannes, Wilner Martínez‐López, G. Obe and A.T. Natarajan. Their work appears in journals such as Chromosoma, Mutation research. Fundamental and molecular mechanisms of mutagenesis, Cytogenetic and Genome Research, The Lancet and Interciencia.
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.