Erin Thorpe

485 total citations
5 papers, 29 citations indexed

About

Erin Thorpe is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Erin Thorpe has authored 5 papers receiving a total of 29 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Erin Thorpe's work include Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Erin Thorpe is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Erin Thorpe collaborates with scholars based in United States, Mexico and Italy. Erin Thorpe's co-authors include MaryAnn Campion, Quinn Stein, Jiang Chen, Yun Stone Shi, Diane Masser‐Frye, Dan Wu, Carolyn M. Brown, Berardo Rinaldi, Allan Bayat and Bénédicte Gérard and has published in prestigious journals such as PLoS Genetics, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Erin Thorpe

5 papers receiving 29 citations

Peers

Erin Thorpe
Joe Gleeson United States
Elizabeth L. Fieg United States
Lisa Salz United States
Ayeshah Chaudhry Canada
Julie Hathaway Canada
Alyna Khan United States
Mattia Cordioli Finland
Somayeh Bakhtiari United States
Kirsten Boggs Australia
Tasnim Fadl Qatar
Joe Gleeson United States
Erin Thorpe
Citations per year, relative to Erin Thorpe Erin Thorpe (= 1×) peers Joe Gleeson

Countries citing papers authored by Erin Thorpe

Since Specialization
Citations

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

Fields of papers citing papers by Erin Thorpe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erin Thorpe. 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 Erin Thorpe. The network helps show where Erin Thorpe may publish in the future.

Co-authorship network of co-authors of Erin Thorpe

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

All Works

5 of 5 papers shown
1.
Brown, Carolyn M., Laura M. Amendola, Anjana Chandrasekhar, et al.. (2024). A framework for the evaluation and reporting of incidental findings in clinical genomic testing. European Journal of Human Genetics. 32(6). 665–672. 1 indexed citations
2.
Chandrasekhar, Anjana, Nora Urraca, Andrew M. Gross, et al.. (2023). Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes. American Journal of Medical Genetics Part A. 194(3). e63462–e63462. 2 indexed citations
3.
Taylor, Julie P., Alka Malhotra, Nicole Burns, et al.. (2022). A clinical laboratory's experience using GeneMatcher—Building stronger gene–disease relationships. Human Mutation. 43(6). 765–771. 2 indexed citations
4.
Sun, Jiahui, Jiang Chen, Carolyn M. Brown, et al.. (2021). X-linked neonatal-onset epileptic encephalopathy associated with a gain-of-function variant p.R660T in GRIA3. PLoS Genetics. 17(6). e1009608–e1009608. 12 indexed citations
5.
Stein, Quinn, et al.. (2017). Experiences of Genetic Counselors Practicing in Rural Areas. Journal of Genetic Counseling. 27(1). 140–154. 12 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