Amy Brower
Impact in
- Pharmacology top 1%
- Pharmacogenetics and Drug Metabolism
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
- Genetics 19
- Genomics and Rare Diseases 16
- Neurogenetic and Muscular Disorders Research 3
- Genetics and Neurodevelopmental Disorders 3
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- Metabolism and Genetic Disorders 13
- Co-authors
- Stacey S. Cherny (1 shared paper)David W. Fulker (1 shared paper)Bruce F. Pennington (1 shared paper)Lon R. Cardon (1 shared paper)Javier Gayán (2 shared papers)Shelley D. Smith (2 shared papers)John C. DeFries (1 shared paper)Richard K. Olson (2 shared papers)
- Journals
- International Journal of Neonatal Screening (7 papers)Genetics in Medicine (4 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (4 papers)Frontiers in Genetics (2 papers)Journal of Learning Disabilities (1 paper)
- Partner nations
- United StatesUnited KingdomFrance
In The Last Decade
Amy Brower
28 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 91
- Pharmacology 340
- Sensory Systems 83
- Biochemistry 99
- Developmental and Educational Psychology 167
- Statistics and Probability 90
Countries citing papers authored by Amy Brower
This map shows the geographic impact of Amy Brower'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 Amy Brower with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amy Brower more than expected).
Fields of papers citing papers by Amy Brower
This network shows the impact of papers produced by Amy Brower. 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 Amy Brower. The network helps show where Amy Brower may publish in the future.
Co-authors
The 25 scholars most cited alongside Amy Brower, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 390 | |
| 2 | 1999 | 204 | |
| 3 | 1992 | 125 | |
| 4 | 1999 | 77 | |
| 5 | 1988 | 36 | |
| 6 | Molecular approaches to the genetic analysis of specific reading disability. | 1998 | 27 |
| 7 | 2010 | 21 | |
| 8 | 2007 | 21 | |
| 9 | 2018 | 19 | |
| 10 | 2016 | 17 | |
| 11 | 2018 | 16 | |
| 12 | 2021 | 15 | |
| 13 | 2022 | 14 | |
| 14 | 2022 | 12 | |
| 15 | 2007 | 9 | |
| 16 | 2023 | 7 | |
| 17 | 2023 | 6 | |
| 18 | 2019 | 6 | |
| 19 | 2023 | 5 | |
| 20 | 2018 | 5 |
About Amy Brower
Amy Brower is a scholar working on Genetics, Clinical Biochemistry, Molecular Biology, Pediatrics, Perinatology and Child Health and Physiology, having authored 34 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (16 papers), Metabolism and Genetic Disorders (13 papers), Prenatal Screening and Diagnostics (4 papers), Muscle Physiology and Disorders (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Telomeres, Telomerase, and Senescence (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Ethics and Legal Issues in Pediatric Healthcare (2 papers). The work is most often cited by research in Pharmacology (340 citations), Sensory Systems (83 citations), Biochemistry (99 citations), Developmental and Educational Psychology (167 citations) and Statistics and Probability (90 citations). Amy Brower has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Stacey S. Cherny, David W. Fulker, Bruce F. Pennington, Lon R. Cardon, Javier Gayán, Shelley D. Smith, John C. DeFries, Richard K. Olson, Tarif Awad and Charles Eby. Their work appears in journals such as International Journal of Neonatal Screening, Genetics in Medicine, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Frontiers in Genetics and Journal of Learning Disabilities.
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.