Michael A. Eberle

13.7k citations

49 papers · 4.6k indexed · 1 hit paper · h-index 27

Impact in

Genetics top 0.5%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genomics and Rare Diseases
- Genetic and phenotypic traits in livestock
- Genomic variations and chromosomal abnormalities
- Genetic diversity and population structure
Molecular Biology top 5%
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms

Papers in ⓘ

Genetics 22
- Genetic Associations and Epidemiology 13
- Genomics and Rare Diseases 8
- Genetic Mapping and Diversity in Plants and Animals 6
Geophysics 6
- Geological and Geochemical Analysis 6
- earthquake and tectonic studies 6
- High-pressure geophysics and materials 6

Co-authors: Leonid Kruglyak (13 shared papers)Deborah A. Nickerson (12 shared papers)Christopher S. Carlson (6 shared papers)Mark J. Rieder (7 shared papers)Yi Qian (3 shared papers)Joshua D. Smith (2 shared papers)Joshua M. Akey (2 shared papers)Mark D. Shriver (1 shared paper)
Journals: The American Journal of Human Genetics (8 papers)PLoS Genetics (4 papers)Bioinformatics (3 papers)Journal of Geophysical Research Atmospheres (3 papers)Genome Research (3 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

Michael A. Eberle

47 papers receiving 4.5k citations

Hit Papers

align trajectories log scale

Selecting a Maximally Informative Set of Single-Nucleotide Polymorphisms for Association Analyses Using Linkage Disequilibrium 2004 · 1.2k citations

Peers

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

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20 of 20 papers shown

Showing the 20 most-cited of 49 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 The American Journal of Human Genetics ·Christopher S. Carlson, Michael A. Eberle, Mark J. Rieder, Yi Qian, Leonid Kruglyak, Deborah A. Nickerson Hit paper breakdown →	2004	1221
2	Mapping complex disease loci in whole-genome association studies Nature ·Christopher S. Carlson, Michael A. Eberle, Leonid Kruglyak, Deborah A. Nickerson	2004	433
3	Population History and Natural Selection Shape Patterns of Genetic Variation in 132 Genes PLoS Biology ·Joshua M. Akey, Michael A. Eberle, Mark J. Rieder, Christopher S. Carlson, Mark D. Shriver, Deborah A. Nickerson, Leonid Kruglyak	2004	393
4	Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans Nature Genetics ·Christopher S. Carlson, Michael A. Eberle, Mark J. Rieder, Joshua D. Smith, Leonid Kruglyak, Deborah A. Nickerson	2003	257
5	Extensive and breed-specific linkage disequilibrium in Canis familiaris Genome Research ·Nathan B. Sutter, Michael A. Eberle, Heidi G. Parker, Barbara Pullar, Ewen F. Kirkness, Leonid Kruglyak, Elaine A. Ostrander	2004	238
6	A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree Genome Research ·Michael A. Eberle, Epameinondas Fritzilas, Peter Krusche, Morten Källberg, Benjamin L. Moore, Mitchell A. Bekritsky, Zamin Iqbal, Han‐Yu Chuang, Sean Humphray, Aaron L. Halpern, Semyon Kruglyak, Elliott H. Margulies, Gil McVean, David Bentley	2016	220
7	Genomic regions exhibiting positive selection identified from dense genotype data Genome Research ·Christopher S. Carlson, Daryl J. Thomas, Michael A. Eberle, Johanna Swanson, Robert Livingston, Mark J. Rieder, Deborah A. Nickerson	2005	214
8	Best practices for benchmarking germline small-variant calls in human genomes Nature Biotechnology ·(unknown), Peter Krusche, Len Trigg, Paul C. Boutros, Christopher E. Mason, Francisco M. De La Vega, Benjamin L. Moore, Mar Gonzàlez-Porta, Michael A. Eberle, Živana Težak, Samir Lababidi, Rebecca Truty, George Asimenos, Birgit Funke, Mark Fleharty, Brad Chapman, Marc Salit, Justin M. Zook	2019	182
9	Haplotype Diversity across 100 Candidate Genes for Inflammation, Lipid Metabolism, and Blood Pressure Regulation in Two Populations The American Journal of Human Genetics ·Dana C. Crawford, Christopher S. Carlson, Mark J. Rieder, Dana P. Carrington, Yi Qian, Joshua D. Smith, Michael A. Eberle, Leonid Kruglyak, Deborah A. Nickerson	2004	138
10	Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease The American Journal of Human Genetics ·Galen E.B. Wright, Jennifer A. Collins, Chris Kay, Cassandra McDonald, Egor Dolzhenko, Qingwen Xia, Kristina Bečanović, Britt I. Drögemöller, Alicia Semaka, Charlotte Nguyen, Brett Trost, Fiona Richards, Emilia K. Bijlsma, Ferdinando Squitieri, Colin J.D. Ross, Stephen W. Scherer, Michael A. Eberle, Ryan K. C. Yuen, Michael R. Hayden	2019	120
11	Paragraph: a graph-based structural variant genotyper for short-read sequence data Genome biology ·Sai Chen, Peter Krusche, Egor Dolzhenko, Rachel M. Sherman, Roman Petrovski, Felix Schlesinger, Melanie Kirsche, David Bentley, Michael C. Schatz, Fritz J. Sedlazeck, Michael A. Eberle	2019	100
12	A New Susceptibility Locus for Autosomal Dominant Pancreatic Cancer Maps to Chromosome 4q32-34 The American Journal of Human Genetics ·Michael A. Eberle, Roland H. Pfützer, Kay L. Pogue-Geile, Mary P. Bronner, David A. Crispin, Michael B. Kimmey, Richard H. Duerr, Leonid Kruglyak, David C. Whitcomb, Teresa A. Brentnall	2002	97
13	ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing data Genome biology ·Egor Dolzhenko, Mark F. Bennett, Phillip A. Richmond, Brett Trost, Sai Chen, Joke J.F.A. van Vugt, Charlotte Nguyen, Giuseppe Narzisi, Vladimir G. Gainullin, Andrew M. Gross, Bryan R. Lajoie, Ryan J. Taft, Wyeth W. Wasserman, Stephen W. Scherer, Jan H. Veldink, David Bentley, Ryan K. C. Yuen, Melanie Bahlo, Michael A. Eberle	2020	95
14	Lower-Than-Expected Linkage Disequilibrium between Tightly Linked Markers in Humans Suggests a Role for Gene Conversion The American Journal of Human Genetics ·Kristin Ardlie, Shau Neen Liu-Cordero, Michael A. Eberle, Mark J. Daly, Jeff Barrett, Ellen Winchester, Eric S. Lander, Leonid Kruglyak	2001	82
15	Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data Genetics in Medicine ·Xiao Chen, Alba Sanchis‐Juan, Courtney E. French, Andrew J. Connell, Isabelle Delon, Zoya Kingsbury, Aditi Chawla, Aaron L. Halpern, Ryan J. Taft, David Bentley, Matthew E.R. Butchbach, F. Lucy Raymond, Michael A. Eberle	2020	79
16	A numerical study of the interaction between the mantle wedge, subducting slab, and overriding plate Physics of The Earth and Planetary Interiors ·Michael A. Eberle, O. Grasset, C. Sotin	2002	76
17	Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels PLoS Genetics ·Michael A. Eberle, Pauline C. Ng, Kenneth Kuhn, Lixin Zhou, Daniel A. Peiffer, Luana Galver, Karine A. Viaud‐Martinez, Cindy Lawley, Kevin L. Gunderson, Richard Shen, Sarah S. Murray	2007	74
18	Allele Frequency Matching Between SNPs Reveals an Excess of Linkage Disequilibrium in Genic Regions of the Human Genome PLoS Genetics ·Michael A. Eberle, Mark J. Rieder, Leonid Kruglyak, Deborah A. Nickerson	2006	68
19	Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data The Pharmacogenomics Journal ·Xiao Chen, Fei Shen, Nina Gonzaludo, Alka Malhotra, Cande Rogert, Ryan J. Taft, David Bentley, Michael A. Eberle	2021	54
20	Whole-genome haplotyping by dilution, amplification, and sequencing Proceedings of the National Academy of Sciences ·Fiona Kaper, Sajani Swamy, Brandy Klotzle, Sarah Munchel, Joseph Cottrell, Marina Bibikova, Han‐Yu Chuang, Semyon Kruglyak, Mostafa Ronaghi, Michael A. Eberle, Jian‐Bing Fan	2013	50

About Michael A. Eberle

Michael A. Eberle is a scholar working on Genetics, Geophysics, Molecular Biology, Genetics and Cellular and Molecular Neuroscience, having authored 49 papers that have together received 4.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (13 papers), Genomics and Rare Diseases (8 papers), Genomics and Phylogenetic Studies (7 papers), Geological and Geochemical Analysis (6 papers), earthquake and tectonic studies (6 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers), High-pressure geophysics and materials (6 papers) and Genetic Neurodegenerative Diseases (5 papers). The work is most often cited by research in Genetics (2.4k citations), Molecular Biology (2.1k citations), Cancer Research (394 citations), Cellular and Molecular Neuroscience (298 citations) and Immunology (310 citations). Michael A. Eberle has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Leonid Kruglyak, Deborah A. Nickerson, Christopher S. Carlson, Mark J. Rieder, Yi Qian, Joshua D. Smith, Joshua M. Akey, Mark D. Shriver, David Bentley and Donald W. Forsyth. Their work appears in journals such as The American Journal of Human Genetics, PLoS Genetics, Bioinformatics, Journal of Geophysical Research Atmospheres and Genome Research.

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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