Asaf Hellman
Impact in
- Molecular Biology top 5%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Cancer-related gene regulation
- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Papers in
- Genetics 7
- Genetic Syndromes and Imprinting 3
- Genomic variations and chromosomal abnormalities 2
- Genetics and Neurodevelopmental Disorders 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
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- Epigenetics and DNA Methylation 12
- RNA modifications and cancer 3
- Genomics and Chromatin Dynamics 2
- Cancer-related gene regulation 2
- Co-authors
- Andrew J. Chess (3 shared papers)Dvir Aran (10 shared papers)Sivan Sabato (1 shared paper)Michael H. Rosenberg (2 shared papers)Batsheva Kerem (2 shared papers)Stephen W. Scherer (2 shared papers)Joseph Cheung (1 shared paper)Jeremy D. Kark (2 shared papers)
- Journals
- Genome biology (3 papers)Epigenetics & Chromatin (2 papers)Human Molecular Genetics (2 papers)Clinical Epigenetics (1 paper)Cell (1 paper)
- Partner nations
- IsraelUnited StatesGermany
In The Last Decade
Asaf Hellman
19 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 102
- Molecular Biology 1.7k
- Genetics 675
- Cancer Research 263
- Pediatrics, Perinatology and Child Health 166
- Aging 16
Countries citing papers authored by Asaf Hellman
This map shows the geographic impact of Asaf Hellman'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 Asaf Hellman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Asaf Hellman more than expected).
Fields of papers citing papers by Asaf Hellman
This network shows the impact of papers produced by Asaf Hellman. 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 Asaf Hellman. The network helps show where Asaf Hellman may publish in the future.
Co-authors
The 25 scholars most cited alongside Asaf Hellman, 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 | 2007 | 572 | |
| 2 | 2011 | 285 | |
| 3 | 2013 | 265 | |
| 4 | 2002 | 241 | |
| 5 | 2010 | 233 | |
| 6 | 2013 | 127 | |
| 7 | 2000 | 100 | |
| 8 | 2010 | 86 | |
| 9 | 2013 | 82 | |
| 10 | 2016 | 75 | |
| 11 | 2015 | 65 | |
| 12 | 2015 | 34 | |
| 13 | 2003 | 21 | |
| 14 | 2013 | 11 | |
| 15 | 2002 | 8 | |
| 16 | 2023 | 7 | |
| 17 | 2016 | 6 | |
| 18 | Type C retrovirus activation and possible functions in the normal and tumor-bearing host. | 1979 | 5 |
| 19 | 2014 | 1 |
About Asaf Hellman
Asaf Hellman is a scholar working on Genetics, Molecular Biology, Sensory Systems, Animal Science and Zoology and Cancer Research, having authored 19 papers that have together received 2.2k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (12 papers), RNA modifications and cancer (3 papers), Genetic Syndromes and Imprinting (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Chromatin Dynamics (2 papers), Cancer-related gene regulation (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Molecular Biology (1.7k citations), Genetics (675 citations), Cancer Research (263 citations), Pediatrics, Perinatology and Child Health (166 citations) and Aging (16 citations). Asaf Hellman has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Andrew J. Chess, Dvir Aran, Sivan Sabato, Michael H. Rosenberg, Batsheva Kerem, Stephen W. Scherer, Joseph Cheung, Jeremy D. Kark, Benjamin Gläser and John B. Vincent. Their work appears in journals such as Genome biology, Epigenetics & Chromatin, Human Molecular Genetics, Clinical Epigenetics and Cell.
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.