Paz P Polak
Impact in
- Cancer Research top 0.05%
- Cancer Genomics and Diagnostics
- Molecular Biology top 0.2%
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- RNA modifications and cancer
- DNA Repair Mechanisms
Papers in
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- Cancer Genomics and Diagnostics 46
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- Genetic factors in colorectal cancer 21
- Co-authors
- Gad A. Getz (9 shared papers)Amnon Koren (6 shared papers)Michael S. Lawrence (6 shared papers)Eytan Domany (1 shared paper)Jaegil Kim (6 shared papers)Atanas Kamburov (5 shared papers)Shamil R. Sunyaev (4 shared papers)Nicholas J. Haradhvala (5 shared papers)
- Journals
- Nature Communications (16 papers)Nature (12 papers)Nature Genetics (11 papers)Cell (3 papers)Nature Biotechnology (3 papers)
- Partner nations
- United StatesCanadaGermany
In The Last Decade
Paz P Polak
86 papers receiving 26.9k citations
Paz P Polak's Hit Papers
Peers
Comparison fields: 5 of 199
- Cancer Research 9.0k
- Molecular Biology 14.4k
- Genetics 5.6k
- Oncology 5.0k
- Pathology and Forensic Medicine 2.4k
Countries citing papers authored by Paz P Polak
This map shows the geographic impact of Paz P Polak'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 Paz P Polak with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paz P Polak more than expected).
Fields of papers citing papers by Paz P Polak
This network shows the impact of papers produced by Paz P Polak. 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 Paz P Polak. The network helps show where Paz P Polak may publish in the future.
Co-authors
The 25 scholars most cited alongside Paz P Polak, 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 88 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Integrative analysis of 111 reference human epigenomes Hit paper breakdown → | 2015 | 4564 |
| 2 | Mutational heterogeneity in cancer and the search for new cancer-associated genes Hit paper breakdown → | 2013 | 4266 |
| 3 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2339 |
| 4 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 5 | Patterns and rates of exonic de novo mutations in autism spectrum disorders Hit paper breakdown → | 2012 | 1378 |
| 6 | Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors Hit paper breakdown → | 2017 | 735 |
| 7 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 705 |
| 8 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 550 |
| 9 | Whole-genome sequence variation, population structure and demographic history of the Dutch population Hit paper breakdown → | 2014 | 521 |
| 10 | 2006 | 520 | |
| 11 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 476 |
| 12 | 2011 | 473 | |
| 13 | Genomic correlates of response to immune checkpoint blockade in microsatellite-stable solid tumors Hit paper breakdown → | 2018 | 452 |
| 14 | Analyses of non-coding somatic drivers in 2,658 cancer whole genomes Hit paper breakdown → | 2020 | 419 |
| 15 | 2015 | 407 | |
| 16 | An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Hit paper breakdown → | 2014 | 406 |
| 17 | A mutational signature reveals alterations underlying deficient homologous recombination repair in breast cancer Hit paper breakdown → | 2017 | 382 |
| 18 | RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues Hit paper breakdown → | 2019 | 368 |
| 19 | 2020 | 317 | |
| 20 | 2016 | 309 |
About Paz P Polak
Paz P Polak is a scholar working on Cancer Research, Pathology and Forensic Medicine, Genetics, Molecular Biology and Oncology, having authored 88 papers that have together received 27.2k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (46 papers), Genetic factors in colorectal cancer (21 papers), Genomics and Chromatin Dynamics (10 papers), Genomics and Rare Diseases (10 papers), DNA Repair Mechanisms (10 papers), Evolution and Genetic Dynamics (6 papers), Genomics and Phylogenetic Studies (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Cancer Research (9.0k citations), Molecular Biology (14.4k citations), Genetics (5.6k citations), Oncology (5.0k citations) and Pathology and Forensic Medicine (2.4k citations). Paz P Polak has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Gad A. Getz, Amnon Koren, Michael S. Lawrence, Eytan Domany, Jaegil Kim, Atanas Kamburov, Shamil R. Sunyaev, Nicholas J. Haradhvala, Rosa Karlić and John A. Stamatoyannopoulos. Their work appears in journals such as Nature Communications, Nature, Nature Genetics, Cell and Nature Biotechnology.
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.