Peter Romanienko
Impact in
- Molecular Biology top 2%
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
- Aging top 5%
Papers in
-
- DNA Repair Mechanisms 15
- CRISPR and Genetic Engineering 9
- Genomics and Chromatin Dynamics 6
- Mitochondrial Function and Pathology 4
- Epigenetics and DNA Methylation 2
- Genetics 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Co-authors
- R. Daniel Camerini‐OteroMaria JasinFeng‐Xia LiangÓscar Fernández-CapetilloWilliam M. BonnerArkady CelesteN. A. SmirnovaPavel P. Khil
- Journals
- Proceedings of the National Academy of Sciences (2 papers)Developmental Cell (2 papers)Nucleic Acids Research (2 papers)Differentiation (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesCanadaTaiwan
In The Last Decade
Peter Romanienko
28 papers receiving 3.8k citations
Hit Papers
Peers
Comparison fields: 5 of 97
- Molecular Biology 3.4k
- Aging 67
- Cancer Research 546
- Genetics 917
- Reproductive Medicine 254
Countries citing papers authored by Peter Romanienko
This map shows the geographic impact of Peter Romanienko'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 Peter Romanienko with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Romanienko more than expected).
Fields of papers citing papers by Peter Romanienko
This network shows the impact of papers produced by Peter Romanienko. 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 Peter Romanienko. The network helps show where Peter Romanienko may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Romanienko, 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 | 2025 | 0 | |
| 2 | 2024 | 2 | |
| 3 | 2024 | 1 | |
| 4 | 2023 | 7 | |
| 5 | 2023 | 2 | |
| 6 | 2022 | 8 | |
| 7 | 2022 | 10 | |
| 8 | 2022 | 9 | |
| 9 | 2021 | 6 | |
| 10 | 2018 | 5 | |
| 11 | 2018 | 45 | |
| 12 | 2016 | 13 | |
| 13 | 2009 | 27 | |
| 14 | 2004 | 246 | |
| 15 | 2003 | 142 | |
| 16 | DNA damage-induced G2–M checkpoint activation by histone H2AX and 53BP1 Hit paper breakdown → | 2002 | 562 |
| 17 | The Mouse Spo11 Gene Is Required for Meiotic Chromosome Synapsis Hit paper breakdown → | 2000 | 633 |
| 18 | 1999 | 131 | |
| 19 | 1997 | 143 | |
| 20 | 1995 | 170 |
About Peter Romanienko
Peter Romanienko is a scholar working on Molecular Biology, Genetics, Cell Biology, Oncology and Cellular and Molecular Neuroscience, having authored 29 papers that have together received 3.9k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (15 papers), CRISPR and Genetic Engineering (9 papers), Genomics and Chromatin Dynamics (6 papers), Mitochondrial Function and Pathology (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), SARS-CoV-2 and COVID-19 Research (2 papers), Carcinogens and Genotoxicity Assessment (2 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Molecular Biology (3.4k citations), Aging (67 citations), Cancer Research (546 citations), Genetics (917 citations) and Reproductive Medicine (254 citations). Peter Romanienko has collaborated with scholars based in United States, Canada and Taiwan. Frequent co-authors include R. Daniel Camerini‐Otero, Maria Jasin, Feng‐Xia Liang, Óscar Fernández-Capetillo, William M. Bonner, Arkady Celeste, N. A. Smirnova, Pavel P. Khil, Katia Manova and Paul S. Burgoyne. Their work appears in journals such as Proceedings of the National Academy of Sciences, Developmental Cell, Nucleic Acids Research, Differentiation and Nature 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.