Amanda Gerard
Impact in
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- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Diversity and Career in Medicine
Papers in
- Genetics 5
- BRCA gene mutations in cancer 3
- Genomics and Rare Diseases 2
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- Chromatin Remodeling and Cancer 1
- Co-authors
- Hadley Stevens Smith (2 shared papers)Kimberly Nugent (1 shared paper)Rebecca O. Littlejohn (2 shared papers)Haley Streff (3 shared papers)Andrea M. Lewis (1 shared paper)Blair Stevens (1 shared paper)Sarah Noblin (1 shared paper)William Mattox (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
6 papers receiving 52 citations
Peers
Comparison fields: 5 of 24
- Genetics 36
- Gender Studies 6
- Family Practice 1
- Cognitive Neuroscience 8
- Pediatrics, Perinatology and Child Health 5
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 | 20 | |
| 2 | 2021 | 14 | |
| 3 | 2018 | 12 | |
| 4 | 2022 | 4 | |
| 5 | 2024 | 2 | |
| 6 | 2022 | 1 | |
| 7 | 2024 | 0 | |
| 8 | 2022 | 0 |
About Amanda Gerard
Amanda Gerard is a scholar working on Genetics, Molecular Biology, Social Psychology, Neurology and Oncology, having authored 8 papers that have together received 53 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (3 papers), Genomics and Rare Diseases (2 papers), Neurofibromatosis and Schwannoma Cases (1 paper), Neuroendocrine Tumor Research Advances (1 paper), Counseling Practices and Supervision (1 paper), Peptidase Inhibition and Analysis (1 paper), Biomedical Ethics and Regulation (1 paper) and Chromatin Remodeling and Cancer (1 paper). The work is most often cited by research in Genetics (36 citations), Gender Studies (6 citations), Family Practice (1 citation), Cognitive Neuroscience (8 citations) and Pediatrics, Perinatology and Child Health (5 citations). Amanda Gerard has collaborated with scholars based in United States, Hong Kong and Saudi Arabia. Frequent co-authors include Hadley Stevens Smith, Kimberly Nugent, Rebecca O. Littlejohn, Haley Streff, Andrea M. Lewis, Blair Stevens, Sarah Noblin, William Mattox, S. Shahrukh Hashmi and Andrew J. Bean. 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.