Amanda Gerard
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
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- Diversity and Career in Medicine
Papers in
- Genetics 6
- BRCA gene mutations in cancer 4
- Genomics and Rare Diseases 3
- Connective tissue disorders research 1
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- Chromatin Remodeling and Cancer 1
- Co-authors
- Haley Streff (3 shared papers)Rebecca O. Littlejohn (2 shared papers)Hadley Stevens Smith (2 shared papers)Andrew J. Bean (1 shared paper)Kimberly Nugent (1 shared paper)William Mattox (1 shared paper)Andrea M. Lewis (1 shared paper)Blair Stevens (1 shared paper)
- Journals
- Genetics in Medicine (3 papers)Human Genetics and Genomics Advances (1 paper)American Journal of Medical Genetics Part A (3 papers)Journal of Genetic Counseling (1 paper)
- Partner nations
- United StatesHong KongSaudi Arabia
In The Last Decade
Amanda Gerard
5 papers receiving 48 citations
Peers
Comparison fields: 5 of 25
- Genetics 37
- Gender Studies 6
- Pediatrics, Perinatology and Child Health 10
- Family Practice 1
- Cognitive Neuroscience 8
Countries citing papers authored by Amanda Gerard
This map shows the geographic impact of Amanda Gerard'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 Amanda Gerard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amanda Gerard more than expected).
Fields of papers citing papers by Amanda Gerard
This network shows the impact of papers produced by Amanda Gerard. 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 Amanda Gerard. The network helps show where Amanda Gerard may publish in the future.
Co-authors
The 25 scholars most cited alongside Amanda Gerard, 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 | 2021 | 19 | |
| 2 | 2021 | 13 | |
| 3 | 2018 | 12 | |
| 4 | 2022 | 4 | |
| 5 | 2024 | 1 | |
| 6 | 2024 | 0 | |
| 7 | 2022 | 0 | |
| 8 | 2022 | 0 |
About Amanda Gerard
Amanda Gerard is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Social Psychology and Neurology, having authored 8 papers that have together received 49 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (4 papers), Genomics and Rare Diseases (3 papers), interferon and immune responses (1 paper), Connective tissue disorders research (1 paper), Ethics and Legal Issues in Pediatric Healthcare (1 paper), Chromatin Remodeling and Cancer (1 paper), Neurofibromatosis and Schwannoma Cases (1 paper) and Diversity and Career in Medicine (1 paper). The work is most often cited by research in Genetics (37 citations), Gender Studies (6 citations), Pediatrics, Perinatology and Child Health (10 citations), Family Practice (1 citation) and Cognitive Neuroscience (8 citations). Amanda Gerard has collaborated with scholars based in United States, Hong Kong and Saudi Arabia. Frequent co-authors include Haley Streff, Rebecca O. Littlejohn, Hadley Stevens Smith, Andrew J. Bean, Kimberly Nugent, William Mattox, Andrea M. Lewis, Blair Stevens, Sarah Noblin and Katie Bergstrom. Their work appears in journals such as Genetics in Medicine, Human Genetics and Genomics Advances, American Journal of Medical Genetics Part A and Journal of Genetic Counseling.
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.