Amanda E. Links

425 total citations
2 papers, 87 citations indexed

About

Amanda E. Links is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Amanda E. Links has authored 2 papers receiving a total of 87 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Amanda E. Links's work include Genomics and Rare Diseases (2 papers), Biomedical Text Mining and Ontologies (1 paper) and Cancer Genomics and Diagnostics (1 paper). Amanda E. Links is often cited by papers focused on Genomics and Rare Diseases (2 papers), Biomedical Text Mining and Ontologies (1 paper) and Cancer Genomics and Diagnostics (1 paper). Amanda E. Links collaborates with scholars based in United States, Germany and Canada. Amanda E. Links's co-authors include William A. Gahl, Cornelius F. Boerkoel, David R. Adams, Peter N. Robinson, Tal Friedman, Marta Gîrdea, Bailey Gallinger, Taila Hartley, William P. Bone and Sergiu Dumitriu and has published in prestigious journals such as Human Mutation and Genetics in Medicine.

In The Last Decade

Amanda E. Links

2 papers receiving 86 citations

Peers

Amanda E. Links

GENET

MB

CR

PHEOH

PHARM

Elise D. Flynn United States

Daniel Perrett United Kingdom

Carol Smee United Kingdom

Anu Reigo Estonia

Ellen Adlem United Kingdom

David Bujold Canada

Mullai Murugan United States

Chi Gao United States

Dawn Muddyman United Kingdom

Elise D. Flynn United States

Amanda E. Links

45 ×0.6

GENET

114 ×2.6

MB

22 ×0.9

CR

3 ×0.3

PHEOH

9 ×1.0

PHARM

Citations per year, relative to Amanda E. Links Amanda E. Links (= 1×) peers Elise D. Flynn

Countries citing papers authored by Amanda E. Links

Since Specialization

Citations

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

Fields of papers citing papers by Amanda E. Links

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amanda E. Links. 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 E. Links. The network helps show where Amanda E. Links may publish in the future.

Co-authorship network of co-authors of Amanda E. Links

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

All Works

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2 of 2 papers shown

1.

Xu, Karen, Amanda E. Links, David R. Adams, et al.. (2016). Pharmacogenomic incidental findings in 308 families: The NIH Undiagnosed Diseases Program experience. Genetics in Medicine. 18(12). 1303–1307. 12 indexed citations

2.

Buske, Orion J., Marta Gîrdea, Sergiu Dumitriu, et al.. (2015). PhenomeCentral: A Portal for Phenotypic and Genotypic Matchmaking of Patients with Rare Genetic Diseases. Human Mutation. 36(10). 931–940. 75 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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