Máximo E. Drets
Impact in
- Cancer Research top 10%
- Carcinogens and Genotoxicity Assessment
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
Papers in
-
- DNA Repair Mechanisms 6
- Genomics and Chromatin Dynamics 6
- DNA and Nucleic Acid Chemistry 4
-
- Chromosomal and Genetic Variations 13
- Co-authors
- Margery W. Shaw (1 shared paper)Gustavo A. Folle (7 shared papers)David E. Comings (1 shared paper)Wilner Martínez‐López (2 shared papers)G. Obe (1 shared paper)Wolfgang Goedecke (2 shared papers)A.T. Natarajan (1 shared paper)John R. K. Savage (2 shared papers)
- Journals
- Chromosoma (4 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (2 papers)The Lancet (2 papers)Cytogenetic and Genome Research (1 paper)Heredity (1 paper)
- Partner nations
- UruguayUnited StatesAustralia
In The Last Decade
Máximo E. Drets
30 papers receiving 760 citations
Peers
Comparison fields: 5 of 100
- Cancer Research 200
- Genetics 253
- Plant Science 336
- Molecular Biology 508
- Medical Terminology 1
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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 251 | |
| 2 | 1971 | 236 | |
| 3 | 1977 | 89 | |
| 4 | 1976 | 56 | |
| 5 | 1974 | 44 | |
| 6 | 1970 | 41 | |
| 7 | 1983 | 33 | |
| 8 | 1978 | 19 | |
| 9 | 1974 | 14 | |
| 10 | 1982 | 10 | |
| 11 | 1998 | 8 | |
| 12 | 1964 | 7 | |
| 13 | 1987 | 7 | |
| 14 | Further analyses of subtelomeric and paracentric holes induced in human and Chinese hamster ovary cell chromosomes | 1995 | 6 |
| 15 | 1994 | 6 | |
| 16 | 1990 | 5 | |
| 17 | Una saga citogenética: El descubrimiento de los métodos de bandeo cromosómico. Significado y proyección bio-médica | 2002 | 4 |
| 18 | 2004 | 4 | |
| 19 | 1998 | 4 | |
| 20 | 1980 | 4 |
About Máximo E. Drets
Máximo E. Drets is a scholar working on Molecular Biology, Plant Science, Genetics, Cancer Research and Physiology, having authored 32 papers that have together received 870 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (13 papers), DNA Repair Mechanisms (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (6 papers), Carcinogens and Genotoxicity Assessment (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), DNA and Nucleic Acid Chemistry (4 papers) and Telomeres, Telomerase, and Senescence (3 papers). The work is most often cited by research in Cancer Research (200 citations), Genetics (253 citations), Plant Science (336 citations), Molecular Biology (508 citations) and Medical Terminology (1 citation). 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, Wilner Martínez‐López, G. Obe, Wolfgang Goedecke, A.T. Natarajan, John R. K. Savage, Christian Johannes and Peter Jeppesen. Their work appears in journals such as Chromosoma, Mutation research. Fundamental and molecular mechanisms of mutagenesis, The Lancet, Cytogenetic and Genome Research and Heredity.
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.