Eva M. Eicher
Impact in
- Genetics top 0.5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Genomic variations and chromosomal abnormalities
- Reproductive Medicine top 1%
- Sperm and Testicular Function
Papers in
- Genetics 103
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 54
- Genetic Mapping and Diversity in Plants and Animals 36
- Genomic variations and chromosomal abnormalities 24
- Genetic Associations and Epidemiology 10
- Genetic diversity and population structure 6
- Animal Genetics and Reproduction 6
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- Chromosomal and Genetic Variations 27
- Co-authors
- Linda L. Washburn (31 shared papers)Kenneth H Albrecht (11 shared papers)Wesley G. Beamer (7 shared papers)Richard J. Mullen (1 shared paper)R. L. Sidman (1 shared paper)Blanche Capel (3 shared papers)David Coleman (1 shared paper)John B. Roths (1 shared paper)
- Journals
- Genetics (16 papers)Journal of Heredity (11 papers)Genomics (10 papers)Mammalian Genome (8 papers)Proceedings of the National Academy of Sciences (7 papers)
- Partner nations
- United StatesUnited KingdomAustralia
In The Last Decade
Eva M. Eicher
142 papers receiving 8.1k citations
Peers
Comparison fields: 5 of 105
- Genetics 4.1k
- Reproductive Medicine 688
- Developmental Neuroscience 162
- Molecular Biology 1.8k
- Rheumatology 384
Countries citing papers authored by Eva M. Eicher
This map shows the geographic impact of Eva M. Eicher'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 Eva M. Eicher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eva M. Eicher more than expected).
Fields of papers citing papers by Eva M. Eicher
This network shows the impact of papers produced by Eva M. Eicher. 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 Eva M. Eicher. The network helps show where Eva M. Eicher may publish in the future.
Co-authors
The 25 scholars most cited alongside Eva M. Eicher, 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 147 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1976 | 539 | |
| 2 | 2001 | 319 | |
| 3 | 1992 | 309 | |
| 4 | 2002 | 305 | |
| 5 | 2000 | 274 | |
| 6 | 1982 | 262 | |
| 7 | 1984 | 256 | |
| 8 | 1986 | 235 | |
| 9 | 1990 | 226 | |
| 10 | 1980 | 220 | |
| 11 | 1976 | 218 | |
| 12 | 1999 | 170 | |
| 13 | 2003 | 165 | |
| 14 | 1992 | 155 | |
| 15 | 1977 | 150 | |
| 16 | 2001 | 142 | |
| 17 | 1981 | 141 | |
| 18 | 1995 | 136 | |
| 19 | 1978 | 133 | |
| 20 | 1999 | 121 |
About Eva M. Eicher
Eva M. Eicher is a scholar working on Genetics, Plant Science, Immunology, Nephrology and Cell Biology, having authored 147 papers that have together received 8.7k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (54 papers), Genetic Mapping and Diversity in Plants and Animals (36 papers), Chromosomal and Genetic Variations (27 papers), Genomic variations and chromosomal abnormalities (24 papers), Genetic Associations and Epidemiology (10 papers), T-cell and B-cell Immunology (6 papers), Genetic diversity and population structure (6 papers) and Animal Genetics and Reproduction (6 papers). The work is most often cited by research in Genetics (4.1k citations), Reproductive Medicine (688 citations), Developmental Neuroscience (162 citations), Molecular Biology (1.8k citations) and Rheumatology (384 citations). Eva M. Eicher has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Linda L. Washburn, Kenneth H Albrecht, Wesley G. Beamer, Richard J. Mullen, R. L. Sidman, Blanche Capel, David Coleman, John B. Roths, Edwin D. Murphy and Barbara K. Lee. Their work appears in journals such as Genetics, Journal of Heredity, Genomics, Mammalian Genome and Proceedings of the National Academy of Sciences.
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.