Gill Bejerano
Impact in
- Molecular Biology top 0.5%
- Genomics and Chromatin Dynamics
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
- RNA Research and Splicing
- RNA modifications and cancer
- Epigenetics and DNA Methylation
- Genetics top 0.5%
- Genomics and Rare Diseases
Papers in
- Genetics 41
- Genomics and Rare Diseases 22
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- Genomics and Phylogenetic Studies 20
- RNA and protein synthesis mechanisms 20
- Genomics and Chromatin Dynamics 17
- RNA Research and Splicing 15
- RNA modifications and cancer 8
- Co-authors
- Aaron M. Wenger (17 shared papers)Craig B. Lowe (4 shared papers)Bruce T. Schaar (6 shared papers)Michael Hiller (4 shared papers)Cory Y. McLean (3 shared papers)David H. Haussler (13 shared papers)Shoa L. Clarke (5 shared papers)W. James Kent (3 shared papers)
- Journals
- Genetics in Medicine (19 papers)The American Journal of Human Genetics (11 papers)Nucleic Acids Research (6 papers)Bioinformatics (5 papers)Proceedings of the National Academy of Sciences (5 papers)
- Partner nations
- United StatesUnited KingdomIsrael
In The Last Decade
Gill Bejerano
128 papers receiving 12.0k citations
Gill Bejerano's Hit Papers
Peers
Comparison fields: 5 of 176
- Molecular Biology 8.1k
- Genetics 3.2k
- Cancer Research 1.4k
- Aging 79
- Immunology 676
Countries citing papers authored by Gill Bejerano
This map shows the geographic impact of Gill Bejerano'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 Gill Bejerano with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gill Bejerano more than expected).
Fields of papers citing papers by Gill Bejerano
This network shows the impact of papers produced by Gill Bejerano. 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 Gill Bejerano. The network helps show where Gill Bejerano may publish in the future.
Co-authors
The 25 scholars most cited alongside Gill Bejerano, 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 129 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | GREAT improves functional interpretation of cis-regulatory regions Hit paper breakdown → | 2010 | 3261 |
| 2 | Ultraconserved Elements in the Human Genome Hit paper breakdown → | 2004 | 1348 |
| 3 | M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity Hit paper breakdown → | 2016 | 627 |
| 4 | 2001 | 620 | |
| 5 | Enhancers: five essential questions Hit paper breakdown → | 2013 | 421 |
| 6 | 2006 | 397 | |
| 7 | 2006 | 385 | |
| 8 | 2011 | 370 | |
| 9 | 2006 | 354 | |
| 10 | 2016 | 255 | |
| 11 | 2019 | 240 | |
| 12 | 2006 | 227 | |
| 13 | 2007 | 196 | |
| 14 | 2007 | 186 | |
| 15 | 2019 | 157 | |
| 16 | 2001 | 120 | |
| 17 | 2013 | 118 | |
| 18 | 2012 | 108 | |
| 19 | 2017 | 102 | |
| 20 | 2017 | 100 |
About Gill Bejerano
Gill Bejerano is a scholar working on Genetics, Molecular Biology, Cancer Research, Artificial Intelligence and Cell Biology, having authored 129 papers that have together received 12.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (22 papers), Genomics and Phylogenetic Studies (20 papers), RNA and protein synthesis mechanisms (20 papers), Genomics and Chromatin Dynamics (17 papers), RNA Research and Splicing (15 papers), Algorithms and Data Compression (10 papers), Chromosomal and Genetic Variations (10 papers) and RNA modifications and cancer (8 papers). The work is most often cited by research in Molecular Biology (8.1k citations), Genetics (3.2k citations), Cancer Research (1.4k citations), Aging (79 citations) and Immunology (676 citations). Gill Bejerano has collaborated with scholars based in United States, United Kingdom and Israel. Frequent co-authors include Aaron M. Wenger, Craig B. Lowe, Bruce T. Schaar, Michael Hiller, Cory Y. McLean, David H. Haussler, Shoa L. Clarke, W. James Kent, Michael Pheasant and Igor V. Makunin. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Nucleic Acids Research, Bioinformatics and Proceedings of the National Academy of Sciences.
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.