R. Michael Liskay

12.3k total citations · 3 hit papers
97 papers, 10.2k citations indexed

About

R. Michael Liskay is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, R. Michael Liskay has authored 97 papers receiving a total of 10.2k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Molecular Biology, 52 papers in Pathology and Forensic Medicine and 22 papers in Genetics. Recurrent topics in R. Michael Liskay's work include DNA Repair Mechanisms (56 papers), Genetic factors in colorectal cancer (52 papers) and CRISPR and Genetic Engineering (20 papers). R. Michael Liskay is often cited by papers focused on DNA Repair Mechanisms (56 papers), Genetic factors in colorectal cancer (52 papers) and CRISPR and Genetic Engineering (20 papers). R. Michael Liskay collaborates with scholars based in United States, Canada and United Kingdom. R. Michael Liskay's co-authors include Tomas A. Prolla, Sean M. Baker, Thomas D. Petes, Micheline K. Strand, Alan S. Waldman, Andrew B. Buermeyer, Christian Bronner, Janet L. Stachelek, Phuoc T. Tran and Roni J. Bollag and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

R. Michael Liskay

97 papers receiving 9.9k citations

Hit Papers

Mutation in the DNA mismatch repair gene homologue hMLH 1... 1993 2026 2004 2015 1994 1993 1996 500 1000 1.5k

Peers

R. Michael Liskay
Hein te Riele Netherlands
C M Croce United States
Anthony N. Imbalzano United States
Dmitry A. Gordenin United States
Alex J. van der Eb Netherlands
Jeffrey A. Simon United States
Phang‐Lang Chen United States
William Warren United States
Hein te Riele Netherlands
R. Michael Liskay
Citations per year, relative to R. Michael Liskay R. Michael Liskay (= 1×) peers Hein te Riele

Countries citing papers authored by R. Michael Liskay

Since Specialization
Citations

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

Fields of papers citing papers by R. Michael Liskay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Michael Liskay

This figure shows the co-authorship network connecting the top 25 collaborators of R. Michael Liskay. A scholar is included among the top collaborators of R. Michael Liskay 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 R. Michael Liskay. R. Michael Liskay 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.
Fischer, Jared M., Peter Calabrese, Ashleigh Miller, et al.. (2016). Single cell lineage tracing reveals a role for TgfβR2 in intestinal stem cell dynamics and differentiation. Proceedings of the National Academy of Sciences. 113(43). 12192–12197. 18 indexed citations
2.
Fischer, Jared M., Sandra Dudley, Ashleigh Miller, & R. Michael Liskay. (2015). An intact Pms2 ATPase domain is not essential for male fertility. DNA repair. 39. 46–51. 6 indexed citations
3.
Johnson, Jennifer, et al.. (2010). Conservation of functional asymmetry in the mammalian MutLα ATPase. DNA repair. 9(11). 1209–1213. 10 indexed citations
4.
Vrugt, Henri J. van de, et al.. (2009). Embryonic Lethality after Combined Inactivation of Fancd2 and Mlh1 in Mice. Cancer Research. 69(24). 9431–9438. 6 indexed citations
5.
Liskay, R. Michael, Linda J. Wheeler, Christopher K. Mathews, & Naz Erdeniz. (2007). Involvement of deoxycytidylate deaminase in the response to Sn1-type methylation DNA damage in budding yeast. Current Biology. 17(17). R755–R757. 3 indexed citations
6.
Erdeniz, Naz, et al.. (2007). Mutations affecting a putative MutLα endonuclease motif impact multiple mismatch repair functions. DNA repair. 6(10). 1463–1470. 41 indexed citations
7.
Hegan, Denise C., Latha Narayanan, Frank R. Jirik, et al.. (2006). Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6. Carcinogenesis. 27(12). 2402–2408. 62 indexed citations
8.
Gibson, Shannon L., Latha Narayanan, Denise C. Hegan, et al.. (2006). Overexpression of the DNA mismatch repair factor, PMS2, confers hypermutability and DNA damage tolerance. Cancer Letters. 244(2). 195–202. 33 indexed citations
9.
Chen, Peng‐Chieh, Sandra Dudley, Diana Dizon, et al.. (2005). Contributions by MutL Homologues Mlh3 and Pms2 to DNA Mismatch Repair and Tumor Suppression in the Mouse. Cancer Research. 65(19). 8662–8670. 77 indexed citations
10.
11.
Tomer, Guy, et al.. (2002). Contribution of Human Mlh1 and Pms2 ATPase Activities to DNA Mismatch Repair. Journal of Biological Chemistry. 277(24). 21801–21809. 49 indexed citations
12.
Bowers, Jayson, et al.. (2001). MSH-MLH complexes formed at a DNA mismatch are disrupted by the PCNA sliding clamp. Journal of Molecular Biology. 306(5). 957–968. 68 indexed citations
13.
Tran, Phuoc T. & R. Michael Liskay. (2000). Functional Studies on the Candidate ATPase Domains of Saccharomyces cerevisiae MutLα. Molecular and Cellular Biology. 20(17). 6390–6398. 76 indexed citations
14.
Bronner, Christian, Sean M. Baker, Paul T. Morrison, et al.. (1994). Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer. Nature. 368(6468). 258–261. 1605 indexed citations breakdown →
15.
Farber, Rosann A., et al.. (1994). Instability of simple sequence repeats in a mammalian cell line. Human Molecular Genetics. 3(2). 253–256. 49 indexed citations
16.
Strand, Micheline K., Tomas A. Prolla, R. Michael Liskay, & Thomas D. Petes. (1993). Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair. Nature. 365(6443). 274–276. 878 indexed citations breakdown →
17.
Bollag, Roni J., et al.. (1992). Formation of Heteroduplex DNA during Mammalian Intrachromosomal Gene Conversion. Molecular and Cellular Biology. 12(4). 1546–1552. 11 indexed citations
18.
Bollag, Roni J. & R. Michael Liskay. (1988). Conservative intrachromosomal recombination between inverted repeats in mouse cells: association between reciprocal exchange and gene conversion.. Genetics. 119(1). 161–169. 54 indexed citations
19.
Stachelek, Janet L. & R. Michael Liskay. (1988). Accuracy of intrachromosomal gene conversion in mouse cells. Nucleic Acids Research. 16(9). 4069–4076. 9 indexed citations
20.
Liskay, R. Michael & David Patterson. (1979). A selective medium (GAMA) for the isolation of somatic cell hybrids from HPRT<sup>–</sup> and APRT<sup>–</sup> mutant cells. Cytogenetic and Genome Research. 23(1-2). 61–69. 5 indexed citations

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