Seth Berger
Impact in
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- Computational Drug Discovery Methods
- Molecular Biology top 10%
- Bioinformatics and Genomic Networks
- Gene Regulatory Network Analysis
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
Papers in
- Genetics 29
- Genomics and Rare Diseases 18
- Genetics and Neurodevelopmental Disorders 11
- Genomic variations and chromosomal abnormalities 8
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- Hedgehog Signaling Pathway Studies 8
- Co-authors
- Ravi Iyengar (6 shared papers)Avi Ma’ayan (5 shared papers)Huilei Xu (1 shared paper)Amin R. Mazloom (1 shared paper)Alexander Lachmann (1 shared paper)Huda B. Al‐Kouatly (12 shared papers)Andrea Quinn (2 shared papers)Maximilian Muenke (7 shared papers)
- Journals
- Genetics in Medicine (8 papers)The American Journal of Human Genetics (8 papers)Prenatal Diagnosis (3 papers)Nature Communications (3 papers)Brain (3 papers)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Seth Berger
67 papers receiving 2.4k citations
Seth Berger's Hit Papers
Peers
Comparison fields: 5 of 126
- Computational Theory and Mathematics 350
- Molecular Biology 1.4k
- Pharmacology 149
- Genetics 380
- Cancer Research 171
Countries citing papers authored by Seth Berger
This map shows the geographic impact of Seth Berger'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 Seth Berger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Seth Berger more than expected).
Fields of papers citing papers by Seth Berger
This network shows the impact of papers produced by Seth Berger. 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 Seth Berger. The network helps show where Seth Berger may publish in the future.
Co-authors
The 25 scholars most cited alongside Seth Berger, 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 70 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experiments Hit paper breakdown → | 2010 | 773 |
| 2 | 2009 | 416 | |
| 3 | 2007 | 125 | |
| 4 | 2010 | 115 | |
| 5 | 2010 | 102 | |
| 6 | 2023 | 72 | |
| 7 | 2024 | 68 | |
| 8 | 2009 | 62 | |
| 9 | 2019 | 47 | |
| 10 | 2019 | 37 | |
| 11 | 2021 | 35 | |
| 12 | 2020 | 34 | |
| 13 | 2019 | 33 | |
| 14 | 2009 | 28 | |
| 15 | 2017 | 27 | |
| 16 | 2020 | 26 | |
| 17 | 2017 | 25 | |
| 18 | 2007 | 24 | |
| 19 | 2021 | 23 | |
| 20 | 2018 | 23 |
About Seth Berger
Seth Berger is a scholar working on Genetics, Molecular Biology, Hematology, Infectious Diseases and Physiology, having authored 70 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (18 papers), Genetics and Neurodevelopmental Disorders (11 papers), Genomic variations and chromosomal abnormalities (8 papers), Hedgehog Signaling Pathway Studies (8 papers), Parvovirus B19 Infection Studies (8 papers), Erythrocyte Function and Pathophysiology (7 papers), Blood groups and transfusion (6 papers) and Computational Drug Discovery Methods (5 papers). The work is most often cited by research in Computational Theory and Mathematics (350 citations), Molecular Biology (1.4k citations), Pharmacology (149 citations), Genetics (380 citations) and Cancer Research (171 citations). Seth Berger has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Ravi Iyengar, Avi Ma’ayan, Huilei Xu, Amin R. Mazloom, Alexander Lachmann, Huda B. Al‐Kouatly, Andrea Quinn, Maximilian Muenke, Ariel F. Martinez and Paul Stephen Kruszka. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Prenatal Diagnosis, Nature Communications and Brain.
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.