Eric D. Green
- Sensory Systems top 0.2%
- Hearing, Cochlea, Tinnitus, Genetics 9
- Molecular Biology top 0.5%
- Genomics and Phylogenetic Studies 23
- RNA and protein synthesis mechanisms 19
- Genomics and Chromatin Dynamics 11
- Genetics top 0.2%
- Genomics and Rare Diseases 18
- BRCA gene mutations in cancer 12
- Genomic variations and chromosomal abnormalities 12
- Neurology top 1%
- Otorhinolaryngology top 1%
-
- Chromosomal and Genetic Variations 23
- Co-authors
- Mark S. GuyerFrancis S. CollinsAlan E. GuttmacherMark T. KeatingKatherine W. TimothyIgor SplawskiMark CurranGregory M. Cooper
- Journals
- Genome Research (15 papers)The American Journal of Human Genetics (9 papers)Proceedings of the National Academy of Sciences (6 papers)
- Partner nations
- United StatesUnited KingdomItaly
In The Last Decade
Eric D. Green
120 papers receiving 14.0k citations
Hit Papers
Peers
Comparison fields: 5 of 203
- Sensory Systems 1.3k
- Molecular Biology 9.3k
- Genetics 3.8k
- Neurology 767
- Otorhinolaryngology 396
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 2 | |
| 2 | 2023 | 5 | |
| 3 | 2022 | 3 | |
| 4 | 2019 | 10 | |
| 5 | 2011 | 18 | |
| 6 | 2009 | 105 | |
| 7 | 2005 | 76 | |
| 8 | Distribution and intensity of constraint in mammalian genomic sequencebreakdown → | 2005 | 912 |
| 9 | 2004 | 129 | |
| 10 | Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model | 2004 | 1 |
| 11 | Aligning Multiple Genomic Sequences With the Threaded Blockset Alignerbreakdown → | 2004 | 1045 |
| 12 | 2004 | 90 | |
| 13 | 2003 | 117 | |
| 14 | A vision for the future of genomics researchbreakdown → | 2003 | 1169 |
| 15 | LAGAN and Multi-LAGAN: Efficient Tools for Large-Scale Multiple Alignment of Genomic DNAbreakdown → | 2003 | 876 |
| 16 | 2002 | 60 | |
| 17 | 2002 | 56 | |
| 18 | Genome analysis : a laboratory manual | 1997 | 201 |
| 19 | 1997 | 76 | |
| 20 | A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromebreakdown → | 1995 | 1746 |
About Eric D. Green
Eric D. Green is a scholar working on Genetics, Sensory Systems, Molecular Biology, Health Informatics and Developmental Neuroscience, having authored 125 papers that have together received 14.4k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (23 papers), Genomics and Phylogenetic Studies (23 papers), RNA and protein synthesis mechanisms (19 papers), Genomics and Rare Diseases (18 papers), BRCA gene mutations in cancer (12 papers), Genomic variations and chromosomal abnormalities (12 papers), Genomics and Chromatin Dynamics (11 papers) and Hearing, Cochlea, Tinnitus, Genetics (9 papers). The work is most often cited by research in Sensory Systems (1.3k citations), Molecular Biology (9.3k citations), Genetics (3.8k citations), Neurology (767 citations) and Otorhinolaryngology (396 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, Mark Curran, Gregory M. Cooper, Serafim Batzoglou and Lorraine A. Everett. Their work appears in journals such as Genome Research, The American Journal of Human Genetics, Proceedings of the National Academy of Sciences, Nature and American Journal of Physiology-Renal Physiology.
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.