Michael McClellan
Impact in
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- Cancer Genomics and Diagnostics
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- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- RNA modifications and cancer
- RNA Research and Splicing
- CRISPR and Genetic Engineering
- DNA Repair Mechanisms
Papers in
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- Epigenetics and DNA Methylation 2
- RNA modifications and cancer 2
- DNA Repair Mechanisms 1
- Genomics and Chromatin Dynamics 1
- Genetics 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Co-authors
- Skirmantas Kriaučionis (4 shared papers)Benjamin Schuster‐Böckler (2 shared papers)Markéta Tomková (2 shared papers)Tatyana B. Nesterova (1 shared paper)Édith Heard (1 shared paper)Wolf Reik (1 shared paper)Greta Pintacuda (1 shared paper)Job Dekker (1 shared paper)
- Journals
- Nature Communications (1 paper)Clinical Genetics (1 paper)The Journal of Maternal-Fetal & Neonatal Medicine (1 paper)British Journal of Cancer (1 paper)DNA repair (1 paper)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Michael McClellan
6 papers receiving 170 citations
Peers
Comparison fields: 5 of 36
- Cancer Research 32
- Molecular Biology 131
- Genetics 49
- Aging 3
- Pediatrics, Perinatology and Child Health 17
Countries citing papers authored by Michael McClellan
This map shows the geographic impact of Michael McClellan'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 McClellan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael McClellan more than expected).
Fields of papers citing papers by Michael McClellan
This network shows the impact of papers produced by Michael McClellan. 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 McClellan. The network helps show where Michael McClellan may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael McClellan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 80 | |
| 2 | 2016 | 34 | |
| 3 | 2017 | 33 | |
| 4 | 2013 | 15 | |
| 5 | 2018 | 9 | |
| 6 | 1994 | 2 |
About Michael McClellan
Michael McClellan is a scholar working on Molecular Biology, Genetics, Cancer Research, Pediatrics, Perinatology and Child Health and Physiology, having authored 6 papers that have together received 173 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (2 papers), Cancer Genomics and Diagnostics (2 papers), RNA modifications and cancer (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), DNA Repair Mechanisms (1 paper), Genomics and Chromatin Dynamics (1 paper), Telomeres, Telomerase, and Senescence (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Cancer Research (32 citations), Molecular Biology (131 citations), Genetics (49 citations), Aging (3 citations) and Pediatrics, Perinatology and Child Health (17 citations). Michael McClellan has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Skirmantas Kriaučionis, Benjamin Schuster‐Böckler, Markéta Tomková, Tatyana B. Nesterova, Édith Heard, Wolf Reik, Greta Pintacuda, Job Dekker, Michał R. Gdula and Neil Brockdorff. Their work appears in journals such as Nature Communications, Clinical Genetics, The Journal of Maternal-Fetal & Neonatal Medicine, British Journal of Cancer and DNA repair.
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.