Amy B. Wilfert

2.0k total citations
6 papers, 365 citations indexed

About

Amy B. Wilfert is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Amy B. Wilfert has authored 6 papers receiving a total of 365 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Cancer Research. Recurrent topics in Amy B. Wilfert's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cancer Genomics and Diagnostics (2 papers). Amy B. Wilfert is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cancer Genomics and Diagnostics (2 papers). Amy B. Wilfert collaborates with scholars based in United States, Netherlands and United Kingdom. Amy B. Wilfert's 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 and has published in prestigious journals such as Nature, Nature Genetics and Cancer Research.

In The Last Decade

Amy B. Wilfert

6 papers receiving 364 citations

Peers

Amy B. Wilfert
Clemer Abad United States
Dan Vershkov Israel
Danielle S. Rudd United States
Gavin J Sutton Australia
Jayon Lihm United States
Marty G. Yang United States
Lynne M. Overman United States
Ábel Vértesy Austria
Poornima Manavalan United States
Ariele Spanhol-Rosseto Italy
Clemer Abad United States
Amy B. Wilfert
Citations per year, relative to Amy B. Wilfert Amy B. Wilfert (= 1×) peers Clemer Abad

Countries citing papers authored by Amy B. Wilfert

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Amy B. Wilfert

This figure shows the co-authorship network connecting the top 25 collaborators of Amy B. Wilfert. A scholar is included among the top collaborators of Amy B. Wilfert based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Amy B. Wilfert. Amy B. Wilfert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

6 of 6 papers shown
1.
Quinn, Katie, Amy B. Wilfert, Sai Chen, et al.. (2025). Abstract 692: Analytical validation of a tissue-free epigenomic assay for circulating tumor DNA (ctDNA)-based molecular residual disease (MRD) detection in early-stage cancer. Cancer Research. 85(8_Supplement_1). 692–692. 1 indexed citations
2.
Ziffra, Ryan, Chang N. Kim, Jayden Ross, et al.. (2021). Single-cell epigenomics reveals mechanisms of human cortical development. Nature. 598(7879). 205–213. 153 indexed citations
3.
Goldmann, Jakob M., Wendy S.W. Wong, Amy B. Wilfert, et al.. (2021). Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticity. Genome Research. 31(9). 1513–1518. 8 indexed citations
4.
Turner, Tychele N., Amy B. Wilfert, Trygve E. Bakken, et al.. (2019). Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders. The American Journal of Human Genetics. 105(6). 1274–1285. 87 indexed citations
5.
Wilfert, Amy B., Arvis Sulovari, Tychele N. Turner, Bradley P. Coe, & Evan E. Eichler. (2017). Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications. Genome Medicine. 9(1). 101–101. 91 indexed citations
6.
Wilfert, Amy B., Katherine R. Chao, Madhurima Kaushal, et al.. (2016). Genome-wide significance testing of variation from single case exomes. Nature Genetics. 48(12). 1455–1461. 25 indexed citations

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.

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2026