Bethany Friedman
Impact in
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Monoclonal and Polyclonal Antibodies Research
Papers in
- Genetics 6
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- BRCA gene mutations in cancer 2
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- Biochemical and Structural Characterization 1
- Protein purification and stability 1
- Co-authors
- Jane Juusola (5 shared papers)Kyle Retterer (4 shared papers)Julie Scuffins (2 shared papers)Gabriele Richard (1 shared paper)Kristin G. Monaghan (1 shared paper)P. Ann Boriack‐Sjodin (1 shared paper)Stephan Miller (1 shared paper)Woody Sherman (1 shared paper)
- Journals
- Genetics in Medicine (3 papers)Molecular Case Studies (1 paper)American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)Neuromuscular Disorders (1 paper)Protein Science (1 paper)
- Partner nations
- United StatesPolandIran
In The Last Decade
Bethany Friedman
11 papers receiving 397 citations
Peers
Comparison fields: 5 of 56
- Genetics 175
- Radiology, Nuclear Medicine and Imaging 104
- Pediatrics, Perinatology and Child Health 84
- Molecular Biology 229
- 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-authors
The 25 scholars most cited alongside Bethany Friedman, 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 | 2006 | 136 | |
| 2 | 2017 | 112 | |
| 3 | 2016 | 42 | |
| 4 | 2020 | 39 | |
| 5 | 2015 | 25 | |
| 6 | 2018 | 16 | |
| 7 | 2018 | 14 | |
| 8 | 2013 | 11 | |
| 9 | 2020 | 6 | |
| 10 | 2013 | 3 | |
| 11 | Treatment of Working Memory in a Patient with Moderate Aphasia | 2012 | 1 |
About Bethany Friedman
Bethany Friedman is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Neurology and Cardiology and Cardiovascular Medicine, 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), Genetics and Neurodevelopmental Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers), BRCA gene mutations in cancer (2 papers), Biochemical and Structural Characterization (1 paper), Vascular Malformations Diagnosis and Treatment (1 paper) and Protein purification and stability (1 paper). The work is most often cited by research in Genetics (175 citations), Radiology, Nuclear Medicine and Imaging (104 citations), Pediatrics, Perinatology and Child Health (84 citations), Molecular Biology (229 citations) and Immunology (38 citations). Bethany Friedman has collaborated with scholars based in United States, Poland and Iran. Frequent co-authors include Jane Juusola, Kyle Retterer, Julie Scuffins, Gabriele Richard, Kristin G. Monaghan, P. Ann Boriack‐Sjodin, Stephan Miller, Woody Sherman, Herman van Vlijmen and Louis A. Clark. Their work appears in journals such as Genetics in Medicine, Molecular Case Studies, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Neuromuscular Disorders and Protein Science.
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.