Eva M. Eicher

9.8k citations
141 papers · 7.9k indexed · 1 hit paper · h-index 51
  • Genetics top 0.2%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 49
    • Animal Genetics and Reproduction 26
    • Genetic Mapping and Diversity in Plants and Animals 13
    • Genetic Syndromes and Imprinting 8
    • Sperm and Testicular Function 13
    • Sexual Differentiation and Disorders 28
    • Genomics and Chromatin Dynamics 18
  • Aging top 5%
    • Chromosomal and Genetic Variations 17

Eva M. Eicher

139 papers receiving 7.6k citations

Hit Papers

Purkinje cell degeneration, a new neurological mutation i...4891976202619922009100200300400

Peers

Eva M. Eicher
Comparison fields: 5 of 122
  • Genetics 4.2k
  • Reproductive Medicine 1.2k
  • Molecular Biology 4.7k
  • Aging 80
  • Developmental Neuroscience 155
Replace Mary F. Lyon with:
Mary F. Lyon United Kingdom
Wolfgang Engel Germany
B.M. Cattanach United Kingdom
Liane B. Russell United States
Christine M. Distèche United States
Orsetta Zuffardi Italy
Kuniya Abe Japan
Sally A. Camper United States
Miles Wilkinson United States
P. Pearson Netherlands
Eva M. Eicher relative to Mary F. Lyon United Kingdom Mary F. Lyon's profile →
Citations per field
00.5×1.5×
Mary F. Lyon · 1×
Citations per year

Countries citing papers authored by Eva M. Eicher

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with Eva M. Eicher Line = papers co-authored together Eva M. Eicher links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20233
2 200651
3 200456
4 200368
5 1999155
6 199915
7 19944
8 199418
9 199420
10
Abrupt cline for sex chromosomes in a hybrid zone between two species of mice.
19921
11
SHORT COMMUNICATION Localization of Insulin-2 (Ins-2) and the Obesity Mutant Tubby (tub) to Distinct Regions of Mouse Chromosome 7
19920
12 1992298
13 199211
14 199059
15 198811
16 19872
17 1984242
18
The use of molecular probes and chromosomal rearrangements to partition the mouse Y chromosome into functional regions.
19831
19 19835
20 197916

About Eva M. Eicher

Eva M. Eicher is a scholar working on Genetics, Reproductive Medicine and Molecular Biology, having authored 141 papers that have together received 7.9k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (49 papers), Sexual Differentiation and Disorders (28 papers), Animal Genetics and Reproduction (26 papers), Genomics and Chromatin Dynamics (18 papers), Chromosomal and Genetic Variations (17 papers), Sperm and Testicular Function (13 papers), Genetic Mapping and Diversity in Plants and Animals (13 papers) and Genetic Syndromes and Imprinting (8 papers). The work is most often cited by research in Genetics (4.2k citations), Reproductive Medicine (1.2k citations) and Molecular Biology (4.7k citations). Eva M. Eicher has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Linda L. Washburn, K. Albrecht, Wesley G. Beamer, Richard J. Mullen, R. L. Sidman, David Coleman, Blanche Capel, Priscilla K. Tucker, Edwin D. Murphy and J B Roths. Their work appears in journals such as Genetics, Journal of Heredity, Genomics, Proceedings of the National Academy of Sciences 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.

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