Elizabeth A. Worthey

10.0k total citations
58 papers, 2.0k citations indexed

About

Elizabeth A. Worthey is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Elizabeth A. Worthey has authored 58 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 15 papers in Genetics and 11 papers in Cancer Research. Recurrent topics in Elizabeth A. Worthey's work include Genomics and Rare Diseases (11 papers), Cancer Genomics and Diagnostics (9 papers) and Bioinformatics and Genomic Networks (9 papers). Elizabeth A. Worthey is often cited by papers focused on Genomics and Rare Diseases (11 papers), Cancer Genomics and Diagnostics (9 papers) and Bioinformatics and Genomic Networks (9 papers). Elizabeth A. Worthey collaborates with scholars based in United States, United Kingdom and Canada. Elizabeth A. Worthey's co-authors include Jeremy C. Mottram, Marilyn Parsons, Howard J. Jacob, Peter J. Myler, Melinda R. Dwinell, Jennifer R. Smith, Stanley J. F. Laulederkind, Allan McI. Mowat, Margaret Steel and Paul Garside and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and The Journal of Immunology.

In The Last Decade

Elizabeth A. Worthey

55 papers receiving 2.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Elizabeth A. Worthey United States 24 1.1k 499 446 395 266 58 2.0k
Ana M. Aransay Spain 32 1.5k 1.4× 560 1.1× 549 1.2× 282 0.7× 375 1.4× 106 3.0k
Katherine J. Martin United States 30 1.4k 1.3× 235 0.5× 392 0.9× 399 1.0× 235 0.9× 66 2.7k
Heuiran Lee South Korea 26 1.0k 1.0× 1.1k 2.2× 209 0.5× 363 0.9× 341 1.3× 108 2.7k
Isabelle Beau France 32 1.7k 1.6× 1.4k 2.8× 1.0k 2.3× 809 2.0× 310 1.2× 60 3.9k
Richard Coulson United Kingdom 23 1.4k 1.3× 307 0.6× 382 0.9× 234 0.6× 333 1.3× 30 2.3k
Susana de la Luna Spain 39 2.3k 2.1× 981 2.0× 592 1.3× 651 1.6× 528 2.0× 68 3.6k
Martyn K. White United States 32 1.1k 1.0× 331 0.7× 163 0.4× 265 0.7× 196 0.7× 99 3.1k
Daniel Hicks United Kingdom 20 808 0.7× 321 0.6× 153 0.3× 315 0.8× 184 0.7× 45 2.0k
Begoña Aguado Spain 19 543 0.5× 367 0.7× 307 0.7× 103 0.3× 161 0.6× 53 1.2k
Vincent A. Blomen Netherlands 24 2.5k 2.3× 295 0.6× 159 0.4× 420 1.1× 265 1.0× 31 3.4k

Countries citing papers authored by Elizabeth A. Worthey

Since Specialization
Citations

This map shows the geographic impact of Elizabeth A. Worthey'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 Elizabeth A. Worthey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elizabeth A. Worthey more than expected).

Fields of papers citing papers by Elizabeth A. Worthey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth A. Worthey. 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 Elizabeth A. Worthey. The network helps show where Elizabeth A. Worthey may publish in the future.

Co-authorship network of co-authors of Elizabeth A. Worthey

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth A. Worthey. A scholar is included among the top collaborators of Elizabeth A. Worthey 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 Elizabeth A. Worthey. Elizabeth A. Worthey is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Lai, HuiChuan J., Katryn N. Furuya, Nicholas Antos, et al.. (2025). The Frequency and Potential Implications of HFE Genetic Variants in Children With Cystic Fibrosis. Pediatric Pulmonology. 60(3). e71042–e71042.
2.
Schmidt, Ryan J., Larissa V. Furtado, Matthew S. Lebo, et al.. (2025). Clinical Bioinformatician Body of Knowledge—Clinical Laboratory Regulation and Data Security Core. Journal of Molecular Diagnostics. 27(7). 583–601. 2 indexed citations
3.
Bar-Peled, Yael, et al.. (2024). Pharmacogenomics for Prader-Willi syndrome: caregiver interest and planned utilization. Pharmacogenomics. 25(4). 207–216.
4.
Wilk, Brandon, et al.. (2023). Ten simple rules for using public biological data for your research. PLoS Computational Biology. 19(1). e1010749–e1010749. 2 indexed citations
5.
Worthey, Elizabeth A., et al.. (2023). O48: DITTO4NF: In silico classification and prioritization of likely pathogenic variants for NF1 using explainable machine learning. SHILAP Revista de lepidopterología. 1(1). 100701–100701. 1 indexed citations
6.
Samani, Adrienne, Michael A. Lopez, Camille L. Birch, et al.. (2022). DOCKopathies: A systematic review of the clinical pathologies associated with human DOCK pathogenic variants. Human Mutation. 43(9). 1149–1161. 7 indexed citations
7.
Marshall, Christian R., Shimul Chowdhury, Ryan J. Taft, et al.. (2020). Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease. npj Genomic Medicine. 5(1). 47–47. 85 indexed citations
8.
Wilk, Melissa A., Andrew T. Braun, Philip M. Farrell, et al.. (2020). Applying whole-genome sequencing in relation to phenotype and outcomes in siblings with cystic fibrosis. Molecular Case Studies. 6(1). a004531–a004531. 9 indexed citations
9.
McKinley, Emily, J. Nicholas Cochran, Michelle D. Amaral, et al.. (2019). Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles. Molecular Case Studies. 5(6). a003491–a003491. 22 indexed citations
10.
Zastrow, Diane B., Jennefer N. Kohler, Devon Bonner, et al.. (2019). A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing. Journal of Genetic Counseling. 28(2). 213–228. 5 indexed citations
11.
Cumming, Sarah A., Mark Hamilton, Helen Gregory, et al.. (2018). De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1. European Journal of Human Genetics. 26(11). 1635–1647. 69 indexed citations
12.
Prokop, Jeremy W., Thomas May, Stephanie M. Bilinovich, et al.. (2018). Genome sequencing in the clinic: the past, present, and future of genomic medicine. Physiological Genomics. 50(8). 563–579. 58 indexed citations
13.
Shimoyama, Mary, Jeff De Pons, G. Thomas Hayman, et al.. (2014). The Rat Genome Database 2015: genomic, phenotypic and environmental variations and disease. Nucleic Acids Research. 43(D1). D743–D750. 164 indexed citations
14.
15.
Laulederkind, Stanley J. F., G. Thomas Hayman, Shuu‐Jiun Wang, et al.. (2013). The Rat Genome Database 2013--data, tools and users. Briefings in Bioinformatics. 14(4). 520–526. 55 indexed citations
16.
Worthey, Elizabeth A., Gordana Raca, Jennifer Laffin, et al.. (2013). Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech. Journal of Neurodevelopmental Disorders. 5(1). 29–29. 62 indexed citations
17.
Nigam, Rajni, Diane H. Munzenmaier, Elizabeth A. Worthey, et al.. (2013). Rat Strain Ontology: structured controlled vocabulary designed to facilitate access to strain data at RGD. Journal of Biomedical Semantics. 4(1). 36–36. 11 indexed citations
18.
Worthey, Elizabeth A.. (2003). Leishmania major chromosome 3 contains two long convergent polycistronic gene clusters separated by a tRNA gene. Nucleic Acids Research. 31(14). 4201–4210. 61 indexed citations
19.
Worthey, Elizabeth A.. (2003). Comparative analysis of editosome proteins in trypanosomatids. Nucleic Acids Research. 31(22). 6392–6408. 75 indexed citations
20.
Mowat, Allan McI., Margaret Steel, Elizabeth A. Worthey, Peter Kewin, & Paul Garside. (1996). Inactivation of Th1 and Th2 Cells by Feeding Ovalbumina. Annals of the New York Academy of Sciences. 778(1). 122–132. 36 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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