Asaf Hellman
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Molecular Biology top 5%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Cancer-related gene regulation
- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms
Papers in
-
- Epigenetics and DNA Methylation 11
- Cancer-related gene regulation 2
- RNA modifications and cancer 2
- DNA Repair Mechanisms 1
- Genetics 7
- Genetic Syndromes and Imprinting 3
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Co-authors
- Andrew Chess (3 shared papers)Dvir Aran (9 shared papers)Sivan Sabato (1 shared paper)Michael Rosenberg (2 shared papers)Batsheva Kerem (2 shared papers)Stephen W. Scherer (2 shared papers)Eitan Zlotorynski (1 shared paper)John B. Vincent (1 shared paper)
- Journals
- Genome biology (3 papers)Human Molecular Genetics (2 papers)Epigenetics & Chromatin (2 papers)Cell Death and Differentiation (1 paper)Cytokine (1 paper)
- Partner nations
- IsraelUnited StatesGermany
In The Last Decade
Asaf Hellman
18 papers receiving 2.0k citations
Asaf Hellman's Hit Papers
Peers
Comparison fields: 5 of 102
- Genetics 653
- Molecular Biology 1.6k
- Cancer Research 235
- Pediatrics, Perinatology and Child Health 163
- 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 | Gene Body-Specific Methylation on the Active X Chromosome Hit paper breakdown → | 2007 | 571 |
| 2 | 2011 | 274 | |
| 3 | 2013 | 261 | |
| 4 | 2002 | 246 | |
| 5 | 2010 | 228 | |
| 6 | 2000 | 104 | |
| 7 | 2010 | 84 | |
| 8 | 2013 | 78 | |
| 9 | 2016 | 69 | |
| 10 | 2015 | 63 | |
| 11 | 2015 | 33 | |
| 12 | 2003 | 21 | |
| 13 | 2013 | 11 | |
| 14 | 2002 | 8 | |
| 15 | 2016 | 6 | |
| 16 | Type C retrovirus activation and possible functions in the normal and tumor-bearing host. | 1979 | 5 |
| 17 | 2023 | 4 | |
| 18 | 2014 | 1 |
About Asaf Hellman
Asaf Hellman is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Animal Science and Zoology and Epidemiology, having authored 18 papers that have together received 2.1k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (11 papers), Genetic Syndromes and Imprinting (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Cancer-related gene regulation (2 papers), Genomic variations and chromosomal abnormalities (2 papers), RNA modifications and cancer (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Genetics (653 citations), Molecular Biology (1.6k citations), Cancer Research (235 citations), Pediatrics, Perinatology and Child Health (163 citations) and Aging (16 citations). Asaf Hellman has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Andrew Chess, Dvir Aran, Sivan Sabato, Michael Rosenberg, Batsheva Kerem, Stephen W. Scherer, Eitan Zlotorynski, John B. Vincent, Luba Trakhtenbrot and Joseph Cheung. Their work appears in journals such as Genome biology, Human Molecular Genetics, Epigenetics & Chromatin, Cell Death and Differentiation and Cytokine.
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.