Ivan P. Gorlov
Impact in
- Genetics top 2%
- Genetic Associations and Epidemiology
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 33
- Genetic Associations and Epidemiology 16
- Genetic Mapping and Diversity in Plants and Animals 7
-
- RNA modifications and cancer 11
- Genomics and Chromatin Dynamics 8
- RNA Research and Splicing 6
- RNA and protein synthesis mechanisms 6
- Epigenetics and DNA Methylation 6
- Co-authors
- Christopher Ian Amos (31 shared papers)Olga Y. Gorlova (26 shared papers)Margaret R. Spitz (12 shared papers)Xifeng Wu (8 shared papers)Qiong Dong (4 shared papers)Gordon Brent Mills (2 shared papers)Shamil R. Sunyaev (1 shared paper)Jayaram Vijayakrishnan (1 shared paper)
- Journals
- Heredity (4 papers)PLoS ONE (4 papers)Cancer Epidemiology Biomarkers & Prevention (3 papers)BMC Genomics (3 papers)Nature Genetics (3 papers)
- Partner nations
- United StatesSpainRussia
In The Last Decade
Ivan P. Gorlov
89 papers receiving 3.4k citations
Ivan P. Gorlov's Hit Papers
Peers
Comparison fields: 5 of 131
- Genetics 910
- Cancer Research 404
- Molecular Biology 1.5k
- Hepatology 157
- Pulmonary and Respiratory Medicine 419
Countries citing papers authored by Ivan P. Gorlov
This map shows the geographic impact of Ivan P. Gorlov'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 Ivan P. Gorlov with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ivan P. Gorlov more than expected).
Fields of papers citing papers by Ivan P. Gorlov
This network shows the impact of papers produced by Ivan P. Gorlov. 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 Ivan P. Gorlov. The network helps show where Ivan P. Gorlov may publish in the future.
Co-authors
The 25 scholars most cited alongside Ivan P. Gorlov, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 89 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1 Hit paper breakdown → | 2008 | 1074 |
| 2 | 2008 | 274 | |
| 3 | 2001 | 203 | |
| 4 | 2010 | 189 | |
| 5 | 2015 | 73 | |
| 6 | 2014 | 69 | |
| 7 | 2018 | 67 | |
| 8 | 2002 | 66 | |
| 9 | 2022 | 65 | |
| 10 | 2011 | 61 | |
| 11 | 2010 | 59 | |
| 12 | 2012 | 59 | |
| 13 | 2010 | 55 | |
| 14 | 2003 | 49 | |
| 15 | 2023 | 49 | |
| 16 | 2009 | 43 | |
| 17 | 2016 | 41 | |
| 18 | 2017 | 40 | |
| 19 | 2020 | 38 | |
| 20 | 2012 | 37 |
About Ivan P. Gorlov
Ivan P. Gorlov is a scholar working on Genetics, Molecular Biology, Cancer Research, Plant Science and Pulmonary and Respiratory Medicine, having authored 89 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (16 papers), RNA modifications and cancer (11 papers), Chromosomal and Genetic Variations (11 papers), Genomics and Chromatin Dynamics (8 papers), Genetic Mapping and Diversity in Plants and Animals (7 papers), RNA Research and Splicing (6 papers), RNA and protein synthesis mechanisms (6 papers) and Epigenetics and DNA Methylation (6 papers). The work is most often cited by research in Genetics (910 citations), Cancer Research (404 citations), Molecular Biology (1.5k citations), Hepatology (157 citations) and Pulmonary and Respiratory Medicine (419 citations). Ivan P. Gorlov has collaborated with scholars based in United States, Spain and Russia. Frequent co-authors include Christopher Ian Amos, Olga Y. Gorlova, Margaret R. Spitz, Xifeng Wu, Qiong Dong, Gordon Brent Mills, Shamil R. Sunyaev, Jayaram Vijayakrishnan, Peter Broderick and Timothy Eisen. Their work appears in journals such as Heredity, PLoS ONE, Cancer Epidemiology Biomarkers & Prevention, BMC Genomics 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.