Kelly D. Farwell
- Molecular Biology
- Genetics top 10%
- Clinical Psychology
- Cellular and Molecular Neuroscience
- Psychiatry and Mental health
- Co-authors
- Elizabeth ChaoDonn MuhlemanHezekiah BlakeGeorge DietzShijuan WuSha TangHsiao‐Mei LuLayla Shahmirzadi
- Topics
- Genomics and Rare Diseases (3 papers)Genomic variations and chromosomal abnormalities (3 papers)Genetics and Neurodevelopmental Disorders (2 papers)
- Journals
- PLoS ONEMutation research. Fundamental and molecular mechanisms of mutagenesisHuman Mutation
- Partner nations
- United StatesItalyCanada
In The Last Decade
Kelly D. Farwell
11 papers receiving 575 citations
Peers
Comparison fields: 5 of 84
- Molecular Biology 215
- Genetics 178
- Clinical Psychology 102
- Cellular and Molecular Neuroscience 93
- Psychiatry and Mental health 87
Countries citing papers authored by Kelly D. Farwell
This map shows the geographic impact of Kelly D. Farwell'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 Kelly D. Farwell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kelly D. Farwell more than expected).
Fields of papers citing papers by Kelly D. Farwell
This network shows the impact of papers produced by Kelly D. Farwell. 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 Kelly D. Farwell. The network helps show where Kelly D. Farwell may publish in the future.
Co-authorship network of co-authors of Kelly D. Farwell
This figure shows the co-authorship network connecting the top 25 collaborators of Kelly D. Farwell. A scholar is included among the top collaborators of Kelly D. Farwell based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kelly D. Farwell. Kelly D. Farwell is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 79 | |
| 2 | 7 | |
| 3 | 58 | |
| 4 | 33 | |
| 5 | 68 | |
| 6 | 49 | |
| 7 | 22 | |
| 8 | 23 | |
| 9 | 14 | |
| 10 | 126 | |
| 11 | 112 |
About Kelly D. Farwell
Kelly D. Farwell is a scholar working on Genetics, Genetics and Immunology and Allergy, having authored 11 papers that have together received 591 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (178 citations), Psychiatry and Mental health (87 citations) and Cellular and Molecular Neuroscience (93 citations). Kelly D. Farwell has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Elizabeth Chao, Donn Muhleman, Hezekiah Blake, George Dietz, Shijuan Wu, Sha Tang, Hsiao‐Mei Lu, Layla Shahmirzadi, Kathleen A. Hill and Steve S. Sommer. Their work appears in journals such as PLoS ONE, Mutation research. Fundamental and molecular mechanisms of mutagenesis and Human Mutation.
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.