Michael A. Eberle

14.2k citations
72 papers · 7.9k · 5 hit papers · h-index 38

Impact in

  • Genetics top 0.5%
    • Genetic Associations and Epidemiology
    • Genomics and Rare Diseases
    • Genetic Mapping and Diversity in Plants and Animals
    • Genomic variations and chromosomal abnormalities
    • Genetic and phenotypic traits in livestock
    • Genetic Neurodegenerative Diseases

Papers in

Michael A. Eberle

69 papers receiving 7.7k citations

Michael A. Eberle's Hit Papers

Human de novo mutation rates from a four-generation pedigree reference 2025 · 31 citations
310+7+14Years since publication4008001.2k

Peers

Michael A. Eberle
Comparison fields: 5 of 162
  • Genetics 3.5k
  • Cellular and Molecular Neuroscience 942
  • Molecular Biology 3.2k
  • Cancer Research 518
  • Neurology 461
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Citations per field
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Citations per year

Countries citing papers authored by Michael A. Eberle

Since Specialization
Citations

This map shows the geographic impact of Michael A. Eberle'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 Michael A. Eberle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael A. Eberle more than expected).

Fields of papers citing papers by Michael A. Eberle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael A. Eberle. 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 Michael A. Eberle. The network helps show where Michael A. Eberle may publish in the future.

Co-authors

The 25 scholars most cited alongside Michael A. Eberle, 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 Michael A. Eberle Line = papers co-authored together Michael A. Eberle links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 72 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Selecting a Maximally Informative Set of Single-Nucleotide Polymorphisms for Association Analyses Using Linkage Disequilibrium
Hit paper breakdown →
20041359
2
A global reference for human genetic variation
Hit paper breakdown →
2015476
3 2004476
4
Demographic history and rare allele sharing among human populations
Hit paper breakdown →
2011475
5 2004424
6 2010416
7
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Hit paper breakdown →
2021337
8 2014321
9 2003267
10 2019248
11 2019241
12 2019189
13 2020153
14 2019153
15 2020146
16 2004143
17 2019128
18 2020127
19 2022121
20
Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study
2022106

About Michael A. Eberle

Michael A. Eberle is a scholar working on Genetics, Cellular and Molecular Neuroscience, Molecular Biology, Geophysics and Genetics, having authored 72 papers that have together received 7.9k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (17 papers), Genetic Neurodegenerative Diseases (13 papers), Genomics and Rare Diseases (11 papers), RNA and protein synthesis mechanisms (8 papers), Genomics and Phylogenetic Studies (7 papers), Genetic Mapping and Diversity in Plants and Animals (7 papers), earthquake and tectonic studies (6 papers) and Geological and Geochemical Analysis (6 papers). The work is most often cited by research in Genetics (3.5k citations), Cellular and Molecular Neuroscience (942 citations), Molecular Biology (3.2k citations), Cancer Research (518 citations) and Neurology (461 citations). Michael A. Eberle has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Leonid Kruglyak, Deborah A. Nickerson, Christopher S. Carlson, Mark J. Rieder, Yi Qian, Joshua M. Akey, Mark D. Shriver, Joshua D. Smith, Donald W. Forsyth and Egor Dolzhenko. Their work appears in journals such as The American Journal of Human Genetics, Nature, Nature Genetics, Bioinformatics and PLoS 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.

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