Ruth Y. Eberhardt
Impact in
- Molecular Biology top 0.5%
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
- Plant Gene Expression Analysis
- Photosynthetic Processes and Mechanisms
- Endocrinology top 0.5%
Papers in
-
- Genomics and Phylogenetic Studies 10
- Machine Learning in Bioinformatics 5
- RNA and protein synthesis mechanisms 5
- Genetics 12
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Alex Bateman (12 shared papers)John Tate (6 shared papers)Sean R. Eddy (5 shared papers)ROBERT FINN (7 shared papers)Marco Punta (9 shared papers)Jaina Mistry (5 shared papers)Penelope Coggill (5 shared papers)Jody Clements (2 shared papers)
- Journals
- BMC Bioinformatics (6 papers)Nucleic Acids Research (5 papers)Database (3 papers)Ultrasound in Obstetrics and Gynecology (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
Ruth Y. Eberhardt
27 papers receiving 13.6k citations
Ruth Y. Eberhardt's Hit Papers
Peers
Comparison fields: 5 of 163
- Molecular Biology 9.3k
- Endocrinology 541
- Plant Science 3.9k
- Ecology 2.0k
- Biotechnology 626
Countries citing papers authored by Ruth Y. Eberhardt
This map shows the geographic impact of Ruth Y. Eberhardt'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 Ruth Y. Eberhardt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruth Y. Eberhardt more than expected).
Fields of papers citing papers by Ruth Y. Eberhardt
This network shows the impact of papers produced by Ruth Y. Eberhardt. 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 Ruth Y. Eberhardt. The network helps show where Ruth Y. Eberhardt may publish in the future.
Co-authors
The 25 scholars most cited alongside Ruth Y. Eberhardt, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Pfam: the protein families database Hit paper breakdown → | 2013 | 4740 |
| 2 | The Pfam protein families database: towards a more sustainable future Hit paper breakdown → | 2015 | 4051 |
| 3 | The Pfam protein families database Hit paper breakdown → | 2011 | 3003 |
| 4 | Rfam 12.0: updates to the RNA families database Hit paper breakdown → | 2014 | 805 |
| 5 | Rfam 11.0: 10 years of RNA families Hit paper breakdown → | 2012 | 615 |
| 6 | 2014 | 59 | |
| 7 | 2020 | 51 | |
| 8 | 2013 | 50 | |
| 9 | 2001 | 44 | |
| 10 | 2018 | 41 | |
| 11 | 2000 | 37 | |
| 12 | 2021 | 34 | |
| 13 | 2014 | 33 | |
| 14 | 2012 | 33 | |
| 15 | 2000 | 29 | |
| 16 | 2022 | 27 | |
| 17 | 2013 | 23 | |
| 18 | 2014 | 12 | |
| 19 | 2013 | 12 | |
| 20 | 2021 | 11 |
About Ruth Y. Eberhardt
Ruth Y. Eberhardt is a scholar working on Molecular Biology, Genetics, Spectroscopy, Materials Chemistry and Pediatrics, Perinatology and Child Health, having authored 28 papers that have together received 13.7k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (10 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Machine Learning in Bioinformatics (5 papers), RNA and protein synthesis mechanisms (5 papers), Advanced Proteomics Techniques and Applications (5 papers), Prenatal Screening and Diagnostics (4 papers) and Enzyme Structure and Function (4 papers). The work is most often cited by research in Molecular Biology (9.3k citations), Endocrinology (541 citations), Plant Science (3.9k citations), Ecology (2.0k citations) and Biotechnology (626 citations). Ruth Y. Eberhardt has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Alex Bateman, John Tate, Sean R. Eddy, ROBERT FINN, Marco Punta, Jaina Mistry, Penelope Coggill, Jody Clements, Liisa Holm and Erik L. L. Sonnhammer. Their work appears in journals such as BMC Bioinformatics, Nucleic Acids Research, Database, Ultrasound in Obstetrics and Gynecology and Genetics in Medicine.
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.