Amy B. Wilfert
- Genetics top 10%
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- Genetic Associations and Epidemiology 1
-
- Epigenetics and DNA Methylation 2
- Single-cell and spatial transcriptomics 1
-
- Cancer Genomics and Diagnostics 2
- Cancer, Hypoxia, and Metabolism 1
- Co-authors
- Evan E. EichlerTychele N. TurnerBradley P. CoeArvis SulovariZhancheng ZhangRebecca I. ToreneRaphael BernierMicah Pepper
- Partner nations
- United StatesNetherlandsUnited Kingdom
In The Last Decade
Amy B. Wilfert
6 papers receiving 364 citations
Peers
Comparison fields: 5 of 57
- Genetics 197
- Developmental Neuroscience 22
- Molecular Biology 244
- Cognitive Neuroscience 54
- Cancer Research 33
Countries citing papers authored by Amy B. Wilfert
This map shows the geographic impact of Amy B. Wilfert'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 B. Wilfert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amy B. Wilfert more than expected).
Fields of papers citing papers by Amy B. Wilfert
This network shows the impact of papers produced by Amy B. Wilfert. 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 B. Wilfert. The network helps show where Amy B. Wilfert may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Amy B. Wilfert, 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 | 2025 | 1 | |
| 2 | 2021 | 153 | |
| 3 | 2021 | 8 | |
| 4 | 2019 | 87 | |
| 5 | 2017 | 91 | |
| 6 | 2016 | 25 |
About Amy B. Wilfert
Amy B. Wilfert is a scholar working on Genetics, Cancer Research and Cognitive Neuroscience, having authored 6 papers that have together received 365 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Cancer Genomics and Diagnostics (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Epigenetics and DNA Methylation (2 papers), Genetic Associations and Epidemiology (1 paper), Single-cell and spatial transcriptomics (1 paper) and Cancer, Hypoxia, and Metabolism (1 paper). The work is most often cited by research in Genetics (197 citations), Developmental Neuroscience (22 citations) and Molecular Biology (244 citations). Amy B. Wilfert has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Evan E. Eichler, Tychele N. Turner, Bradley P. Coe, Arvis Sulovari, Zhancheng Zhang, Rebecca I. Torene, Raphael Bernier, Micah Pepper, Kyle Retterer and Trygve E. Bakken. Their work appears in journals such as Nature, Nature Genetics and Cancer Research.
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.