Eva M. Eicher
Impact in
- Reproductive Medicine top 0.5%
- Sperm and Testicular Function
- Genetics top 0.1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
Papers in
-
- Sexual Differentiation and Disorders 30
- Genomics and Chromatin Dynamics 19
- Genetics 87
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 52
- Animal Genetics and Reproduction 28
- Genetic Mapping and Diversity in Plants and Animals 13
- Genetic Syndromes and Imprinting 9
- Co-authors
- Linda L. Washburn (32 shared papers)K. Albrecht (12 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)Edwin D. Murphy (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 KingdomFrance
In The Last Decade
Eva M. Eicher
145 papers receiving 8.1k citations
Eva M. Eicher's Hit Papers
Peers
Comparison fields: 5 of 127
- Reproductive Medicine 1.4k
- Genetics 4.6k
- Molecular Biology 5.0k
- Aging 85
- Developmental Neuroscience 169
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 150 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Purkinje cell degeneration, a new neurological mutation in the mouse. Hit paper breakdown → | 1976 | 530 |
| 2 | 2001 | 315 | |
| 3 | 1992 | 312 | |
| 4 | 2002 | 298 | |
| 5 | 2000 | 282 | |
| 6 | 1982 | 265 | |
| 7 | 1984 | 255 | |
| 8 | 1986 | 236 | |
| 9 | 1990 | 229 | |
| 10 | 1976 | 218 | |
| 11 | 1980 | 217 | |
| 12 | 1999 | 172 | |
| 13 | 1992 | 159 | |
| 14 | 1977 | 151 | |
| 15 | 1981 | 145 | |
| 16 | 2001 | 142 | |
| 17 | 1995 | 138 | |
| 18 | 1978 | 136 | |
| 19 | 1999 | 116 | |
| 20 | 1970 | 109 |
About Eva M. Eicher
Eva M. Eicher is a scholar working on Molecular Biology, Genetics, Plant Science, Reproductive Medicine and Immunology, having authored 150 papers that have together received 8.5k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (52 papers), Sexual Differentiation and Disorders (30 papers), Animal Genetics and Reproduction (28 papers), Genomics and Chromatin Dynamics (19 papers), Chromosomal and Genetic Variations (17 papers), Sperm and Testicular Function (14 papers), Genetic Mapping and Diversity in Plants and Animals (13 papers) and Genetic Syndromes and Imprinting (9 papers). The work is most often cited by research in Reproductive Medicine (1.4k citations), Genetics (4.6k citations), Molecular Biology (5.0k citations), Aging (85 citations) and Developmental Neuroscience (169 citations). Eva M. Eicher has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Linda L. Washburn, K. Albrecht, Wesley G. Beamer, Richard J. Mullen, R. L. Sidman, Blanche Capel, David Coleman, Edwin D. Murphy, J B Roths 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.