Amanda Mitchell
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Plant Science top 5%
- Chromosomal and Genetic Variations
Papers in
-
- Chromosomal and Genetic Variations 20
- Genetics 15
- Genomic variations and chromosomal abnormalities 13
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Co-authors
- John R. Gosden (9 shared papers)Christopher J. Bostock (3 shared papers)Richard A. Buckland (4 shared papers)H. John Evans (3 shared papers)D.A. Miller (3 shared papers)E.M. Southern (1 shared paper)O. J. Miller (1 shared paper)J.R. Gosden (4 shared papers)
- Journals
- Chromosoma (5 papers)Experimental Cell Research (4 papers)Human Genetics (3 papers)Journal of Medical Genetics (2 papers)Nature (2 papers)
- Partner nations
- United KingdomUnited StatesAustria
In The Last Decade
Amanda Mitchell
27 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 46
- Genetics 533
- Plant Science 677
- Molecular Biology 379
- Cancer Research 42
- Cell Biology 40
Countries citing papers authored by Amanda Mitchell
This map shows the geographic impact of Amanda Mitchell'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 Amanda Mitchell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amanda Mitchell more than expected).
Fields of papers citing papers by Amanda Mitchell
This network shows the impact of papers produced by Amanda Mitchell. 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 Amanda Mitchell. The network helps show where Amanda Mitchell may publish in the future.
Co-authors
The 25 scholars most cited alongside Amanda Mitchell, 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 | 1975 | 227 | |
| 2 | 1985 | 141 | |
| 3 | 1978 | 118 | |
| 4 | 1989 | 96 | |
| 5 | 1979 | 82 | |
| 6 | 1971 | 73 | |
| 7 | 1979 | 64 | |
| 8 | 1974 | 55 | |
| 9 | 1977 | 40 | |
| 10 | 1986 | 37 | |
| 11 | 1987 | 31 | |
| 12 | A dicentric recombinant 9 derived from a paracentric inversion: phenotype, cytogenetics, and molecular analysis of centromeres. | 1989 | 25 |
| 13 | 1991 | 25 | |
| 14 | 2000 | 25 | |
| 15 | 1978 | 24 | |
| 16 | 1977 | 23 | |
| 17 | 1981 | 20 | |
| 18 | 1986 | 20 | |
| 19 | 1998 | 16 | |
| 20 | 1975 | 14 |
About Amanda Mitchell
Amanda Mitchell is a scholar working on Plant Science, Genetics, Molecular Biology, Reproductive Medicine and Spectroscopy, having authored 28 papers that have together received 1.2k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (20 papers), Genomic variations and chromosomal abnormalities (13 papers), Genomics and Chromatin Dynamics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Down syndrome and intellectual disability research (1 paper), Epigenetics and DNA Methylation (1 paper), Telomeres, Telomerase, and Senescence (1 paper) and Nuclear Structure and Function (1 paper). The work is most often cited by research in Genetics (533 citations), Plant Science (677 citations), Molecular Biology (379 citations), Cancer Research (42 citations) and Cell Biology (40 citations). Amanda Mitchell has collaborated with scholars based in United Kingdom, United States and Austria. Frequent co-authors include John R. Gosden, Christopher J. Bostock, Richard A. Buckland, H. John Evans, D.A. Miller, E.M. Southern, O. J. Miller, J.R. Gosden, Christine M Gosden and Hector Nicolas Seuánez. Their work appears in journals such as Chromosoma, Experimental Cell Research, Human Genetics, Journal of Medical Genetics and Nature.
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.