Bethany Friedman
- Molecular Biology
- Genetics
- Radiology, Nuclear Medicine and Imaging
- Pediatrics, Perinatology and Child Health
- Immunology
- Co-authors
- Jane JuusolaKyle RettererJulie ScuffinsGabriele RichardKristin G. MonaghanMia RusheStephan MillerJohn Eldredge
- Topics
- Genomics and Rare Diseases (5 papers)Genomic variations and chromosomal abnormalities (3 papers)BRCA gene mutations in cancer (2 papers)
- Partner nations
- United StatesPolandCanada
In The Last Decade
Bethany Friedman
11 papers receiving 397 citations
Peers
Comparison fields: 5 of 56
- Molecular Biology 229
- Genetics 175
- Radiology, Nuclear Medicine and Imaging 104
- Pediatrics, Perinatology and Child Health 84
- Immunology 38
Countries citing papers authored by Bethany Friedman
This map shows the geographic impact of Bethany Friedman'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 Bethany Friedman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bethany Friedman more than expected).
Fields of papers citing papers by Bethany Friedman
This network shows the impact of papers produced by Bethany Friedman. 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 Bethany Friedman. The network helps show where Bethany Friedman may publish in the future.
Co-authorship network of co-authors of Bethany Friedman
This figure shows the co-authorship network connecting the top 25 collaborators of Bethany Friedman. A scholar is included among the top collaborators of Bethany Friedman 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 Bethany Friedman. Bethany Friedman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 39 | |
| 2 | 6 | |
| 3 | 14 | |
| 4 | 16 | |
| 5 | 112 | |
| 6 | 42 | |
| 7 | 25 | |
| 8 | 3 | |
| 9 | 11 | |
| 10 | Treatment of Working Memory in a Patient with Moderate Aphasia | 1 |
| 11 | 136 |
About Bethany Friedman
Bethany Friedman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Neurology, having authored 11 papers that have together received 405 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (3 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Genetics (175 citations), Radiology, Nuclear Medicine and Imaging (104 citations) and Pediatrics, Perinatology and Child Health (84 citations). Bethany Friedman has collaborated with scholars based in United States, Poland and Canada. Frequent co-authors include Jane Juusola, Kyle Retterer, Julie Scuffins, Gabriele Richard, Kristin G. Monaghan, Mia Rushe, Stephan Miller, John Eldredge, Matthew Jarpe and Kenneth J. Simon. Their work appears in journals such as Protein Science, Journal of the Neurological Sciences 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.