Michael J. McEachern

3.8k total citations · 2 hit papers
52 papers, 3.2k citations indexed

About

Michael J. McEachern is a scholar working on Molecular Biology, Physiology and Aging. According to data from OpenAlex, Michael J. McEachern has authored 52 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 34 papers in Physiology and 14 papers in Aging. Recurrent topics in Michael J. McEachern's work include Telomeres, Telomerase, and Senescence (34 papers), DNA Repair Mechanisms (21 papers) and Genetics, Aging, and Longevity in Model Organisms (14 papers). Michael J. McEachern is often cited by papers focused on Telomeres, Telomerase, and Senescence (34 papers), DNA Repair Mechanisms (21 papers) and Genetics, Aging, and Longevity in Model Organisms (14 papers). Michael J. McEachern collaborates with scholars based in United States, Israel and Sweden. Michael J. McEachern's co-authors include Elizabeth H. Blackburn, Anat Krauskopf, James E. Haber, James Hicks, Donald R. Helinski, Marcin Filutowicz, Shilpa Iyer, Chanchal Sadhu, Sarit Smolikov and Martin Kupiec and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Michael J. McEachern

50 papers receiving 3.1k citations

Hit Papers

TELOMERES AND THEIR CONTROL 1995 2026 2005 2015 2000 1995 100 200 300 400 500

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Michael J. McEachern United States 27 2.5k 1.7k 631 512 472 52 3.2k
Guido Krupp Germany 27 1.5k 0.6× 299 0.2× 399 0.6× 64 0.1× 237 0.5× 62 2.1k
Sabine Strahl‐Bolsinger Germany 14 2.4k 1.0× 212 0.1× 582 0.9× 121 0.2× 179 0.4× 16 2.7k
Verena Pfeiffer Germany 17 1.4k 0.6× 277 0.2× 131 0.2× 40 0.1× 894 1.9× 28 2.0k
Lois M. Banta United States 19 2.1k 0.9× 190 0.1× 602 1.0× 18 0.0× 192 0.4× 22 3.0k
Antony P. Page United Kingdom 26 783 0.3× 84 0.0× 162 0.3× 505 1.0× 77 0.2× 56 1.8k
K Makino Japan 20 2.6k 1.0× 27 0.0× 388 0.6× 139 0.3× 1.1k 2.3× 22 3.0k
William Walter United States 32 3.7k 1.5× 48 0.0× 136 0.2× 50 0.1× 1.5k 3.2× 43 4.2k
Antonia P. Sagona United Kingdom 20 717 0.3× 128 0.1× 100 0.2× 63 0.1× 83 0.2× 36 1.4k
Marianna Feretzaki United States 17 750 0.3× 206 0.1× 424 0.7× 38 0.1× 62 0.1× 24 1.3k
Kris N. Lambert United States 30 878 0.4× 32 0.0× 1.7k 2.7× 64 0.1× 83 0.2× 61 2.6k

Countries citing papers authored by Michael J. McEachern

Since Specialization
Citations

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

Fields of papers citing papers by Michael J. McEachern

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael J. McEachern

This figure shows the co-authorship network connecting the top 25 collaborators of Michael J. McEachern. A scholar is included among the top collaborators of Michael J. McEachern based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Michael J. McEachern. Michael J. McEachern is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
McEachern, Michael J., et al.. (2018). Chromosome ends as adaptive beginnings: the potential role of dysfunctional telomeres in subtelomeric evolvability. Current Genetics. 64(5). 997–1000. 15 indexed citations
2.
McEachern, Michael J., et al.. (2017). Mild Telomere Dysfunction as a Force for Altering the Adaptive Potential of Subtelomeric Genes. Genetics. 208(2). 537–548. 11 indexed citations
4.
Xu, Jianing & Michael J. McEachern. (2012). Long Telomeres Produced by Telomerase-Resistant Recombination Are Established from a Single Source and Are Subject to Extreme Sequence Scrambling. PLoS Genetics. 8(11). e1003017–e1003017. 1 indexed citations
5.
Zhang, Dong, et al.. (2011). TRFolder: computational prediction of novel telomerase RNA structures in yeast genomes. International Journal of Bioinformatics Research and Applications. 7(1). 63–63. 2 indexed citations
6.
Basenko, Evelina Y., Anthony J. Cesare, Shilpa Iyer, Jack D. Griffith, & Michael J. McEachern. (2009). Telomeric circles are abundant in the stn1-M1 mutant that maintains its telomeres through recombination. Nucleic Acids Research. 38(1). 182–189. 18 indexed citations
8.
McEachern, Michael J. & James E. Haber. (2006). 8 Telomerase-independent Telomere Maintenance in Yeast. Cold Spring Harbor Monograph Archive. 45. 199–224. 7 indexed citations
9.
McEachern, Michael J., et al.. (2006). Screening for telomeric recombination in wild-typeKluyveromyces lactis. FEMS Yeast Research. 6(3). 442–448. 5 indexed citations
10.
Cesare, Anthony J., et al.. (2005). Recombination at Long Mutant Telomeres Produces Tiny Single- and Double-Stranded Telomeric Circles. Molecular and Cellular Biology. 25(11). 4406–4412. 42 indexed citations
11.
Askree, S. Hussain, Sarit Smolikov, Raya Gurevich, et al.. (2004). A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length. Proceedings of the National Academy of Sciences. 101(23). 8658–8663. 281 indexed citations
12.
McEachern, Michael J., et al.. (2004). Characterization of Kluyveromyces lactis subtelomeric sequences including a distal element with strong purine/pyrimidine strand bias. Yeast. 21(10). 813–830. 12 indexed citations
13.
Tomáška, Ľubomír, Michael J. McEachern, & Jozef Nosek. (2004). Alternatives to telomerase: keeping linear chromosomes via telomeric circles. FEBS Letters. 567(1). 142–146. 49 indexed citations
14.
Zinzen, Robert P., et al.. (2003). Template Requirements for Telomerase Translocation in Kluyveromyces lactis. Molecular and Cellular Biology. 24(2). 912–923. 12 indexed citations
15.
McEachern, Michael J., et al.. (2002). Recombinational Telomere Elongation Promoted by DNA Circles. Molecular and Cellular Biology. 22(13). 4512–4521. 98 indexed citations
16.
McEachern, Michael J. & Shilpa Iyer. (2001). Short Telomeres in Yeast Are Highly Recombinogenic. Molecular Cell. 7(4). 695–704. 68 indexed citations
17.
McEachern, Michael J., et al.. (2001). Totally Mutant Telomeres: Single-Step Mutagenesis of Tandem Repeat DNA Sequences. BioTechniques. 30(5). 934–938. 8 indexed citations
18.
Blackburn, Elizabeth H., Jen Chang, Tracy B. Fulton, et al.. (2000). Molecular Manifestations and Molecular Determinants of Telomere Capping. Cold Spring Harbor Symposia on Quantitative Biology. 65(0). 253–264. 56 indexed citations
19.
Cohn, Marita, Michael J. McEachern, & Elizabeth H. Blackburn. (1998). Telomeric sequence diversity within the genus Saccharomyces. Current Genetics. 33(2). 83–91. 61 indexed citations
20.
McEachern, Michael J. & Elizabeth H. Blackburn. (1995). Runaway telomere elongation caused by telomerase RNA gene mutations. Nature. 376(6539). 403–409. 299 indexed citations breakdown →

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026