Scott McLean
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- Plant tissue culture and regeneration
Papers in
- Genetics 15
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
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- Genetics and Plant Breeding 6
- Chromosomal and Genetic Variations 4
- Co-authors
- David A. Hoisington (6 shared papers)R. M. Brito (5 shared papers)Alessandro Pellegrineschi (4 shared papers)Natasha Bohorova (4 shared papers)María Pacheco (3 shared papers)William John Rogers (1 shared paper)Christopher Graham Fenton (1 shared paper)Frederick V. Schaefer (1 shared paper)
- Journals
- The American Journal of Human Genetics (4 papers)Crop Science (4 papers)Genetics in Medicine (3 papers)Euphytica (2 papers)Theoretical and Applied Genetics (2 papers)
- Partner nations
- United StatesMexicoFrance
In The Last Decade
Scott McLean
35 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 105
- Genetics 515
- Molecular Biology 658
- Cancer Research 96
- Plant Science 262
- Biotechnology 52
Countries citing papers authored by Scott McLean
This map shows the geographic impact of Scott McLean'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 Scott McLean with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Scott McLean more than expected).
Fields of papers citing papers by Scott McLean
This network shows the impact of papers produced by Scott McLean. 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 Scott McLean. The network helps show where Scott McLean may publish in the future.
Co-authors
The 25 scholars most cited alongside Scott McLean, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 349 | |
| 2 | 2017 | 130 | |
| 3 | 2017 | 86 | |
| 4 | 2009 | 76 | |
| 5 | 2017 | 58 | |
| 6 | 2001 | 46 | |
| 7 | 2016 | 45 | |
| 8 | 1999 | 41 | |
| 9 | 2011 | 36 | |
| 10 | 2019 | 34 | |
| 11 | 2018 | 33 | |
| 12 | 2006 | 33 | |
| 13 | 2023 | 27 | |
| 14 | 2002 | 22 | |
| 15 | 2019 | 22 | |
| 16 | 1992 | 21 | |
| 17 | 2004 | 17 | |
| 18 | 2020 | 17 | |
| 19 | 2001 | 14 | |
| 20 | 2021 | 14 |
About Scott McLean
Scott McLean is a scholar working on Genetics, Plant Science, Molecular Biology, Agronomy and Crop Science and Biotechnology, having authored 41 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetics and Plant Breeding (6 papers), Plant tissue culture and regeneration (6 papers), Genomics and Rare Diseases (5 papers), Chromosomal and Genetic Variations (4 papers), Crop Yield and Soil Fertility (3 papers), Transgenic Plants and Applications (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (515 citations), Molecular Biology (658 citations), Cancer Research (96 citations), Plant Science (262 citations) and Biotechnology (52 citations). Scott McLean has collaborated with scholars based in United States, Mexico and France. Frequent co-authors include David A. Hoisington, R. M. Brito, Alessandro Pellegrineschi, Natasha Bohorova, María Pacheco, William John Rogers, Christopher Graham Fenton, Frederick V. Schaefer, Jordan E. Pinsker and Maristela Marques Salgado. Their work appears in journals such as The American Journal of Human Genetics, Crop Science, Genetics in Medicine, Euphytica and Theoretical and Applied Genetics.
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.