Eric D. Green
Impact in
- Genetics top 0.2%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Molecular Biology top 0.1%
- Genomics and Chromatin Dynamics
- Genomics and Phylogenetic Studies
- Epigenetics and DNA Methylation
Papers in
- Genetics 53
- Genomics and Rare Diseases 24
- Genetic Associations and Epidemiology 14
- Genomic variations and chromosomal abnormalities 12
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- Genomics and Phylogenetic Studies 26
- Ion Transport and Channel Regulation 8
- Co-authors
- Mark S. Guyer (4 shared papers)Francis S. Collins (4 shared papers)Alan E. Guttmacher (2 shared papers)Mark T. Keating (1 shared paper)Katherine W. Timothy (1 shared paper)Igor Splawski (1 shared paper)G. Michael Vincent (1 shared paper)Mark E. Curran (1 shared paper)
- Journals
- Nature (12 papers)The American Journal of Human Genetics (11 papers)Proceedings of the National Academy of Sciences (7 papers)American Journal of Physiology-Renal Physiology (5 papers)Nature Genetics (5 papers)
- Partner nations
- United StatesUnited KingdomItaly
In The Last Decade
Eric D. Green
127 papers receiving 33.7k citations
Eric D. Green's Hit Papers
Peers
Comparison fields: 5 of 198
- Genetics 7.4k
- Molecular Biology 15.9k
- Sensory Systems 1.2k
- Cancer Research 2.7k
- Health Informatics 214
Countries citing papers authored by Eric D. Green
This map shows the geographic impact of Eric D. Green'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 Eric D. Green with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric D. Green more than expected).
Fields of papers citing papers by Eric D. Green
This network shows the impact of papers produced by Eric D. Green. 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 Eric D. Green. The network helps show where Eric D. Green may publish in the future.
Co-authors
The 25 scholars most cited alongside Eric D. Green, 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 131 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | An integrated encyclopedia of DNA elements in the human genome Hit paper breakdown → | 2012 | 13503 |
| 2 | Initial sequencing and comparative analysis of the mouse genome Hit paper breakdown → | 2002 | 5353 |
| 3 | A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome Hit paper breakdown → | 1995 | 1907 |
| 4 | A vision for the future of genomics research Hit paper breakdown → | 2003 | 1310 |
| 5 | Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS) Hit paper breakdown → | 1997 | 952 |
| 6 | A high-resolution map of human evolutionary constraint using 29 mammals Hit paper breakdown → | 2011 | 834 |
| 7 | Charting a course for genomic medicine from base pairs to bedside Hit paper breakdown → | 2011 | 702 |
| 8 | 2001 | 655 | |
| 9 | Defining functional DNA elements in the human genome Hit paper breakdown → | 2014 | 524 |
| 10 | 2001 | 468 | |
| 11 | Implementing genomic medicine in the clinic: the future is here Hit paper breakdown → | 2013 | 443 |
| 12 | Genomic basis for RNA alterations in cancer Hit paper breakdown → | 2020 | 310 |
| 13 | Prioritizing diversity in human genomics research Hit paper breakdown → | 2017 | 292 |
| 14 | 1990 | 278 | |
| 15 | 2008 | 260 | |
| 16 | Strategic vision for improving human health at The Forefront of Genomics Hit paper breakdown → | 2020 | 240 |
| 17 | 2003 | 229 | |
| 18 | 2004 | 229 | |
| 19 | 2014 | 224 | |
| 20 | 2013 | 223 |
About Eric D. Green
Eric D. Green is a scholar working on Genetics, Molecular Biology, Reproductive Medicine, Sensory Systems and Health Informatics, having authored 131 papers that have together received 34.7k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (26 papers), Genomics and Rare Diseases (24 papers), Genetic Associations and Epidemiology (14 papers), Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (11 papers), Science, Research, and Medicine (9 papers), Ion Transport and Channel Regulation (8 papers) and Hearing, Cochlea, Tinnitus, Genetics (7 papers). The work is most often cited by research in Genetics (7.4k citations), Molecular Biology (15.9k citations), Sensory Systems (1.2k citations), Cancer Research (2.7k citations) and Health Informatics (214 citations). Eric D. Green has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Mark S. Guyer, Francis S. Collins, Alan E. Guttmacher, Mark T. Keating, Katherine W. Timothy, Igor Splawski, G. Michael Vincent, Mark E. Curran, Lorraine A. Everett and Anthony Antonellis. Their work appears in journals such as Nature, The American Journal of Human Genetics, Proceedings of the National Academy of Sciences, American Journal of Physiology-Renal Physiology and Nature Genetics.
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.