Carey-Anne Eddy

410 total citations
6 papers, 281 citations indexed

About

Carey-Anne Eddy is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Hematology. According to data from OpenAlex, Carey-Anne Eddy has authored 6 papers receiving a total of 281 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Cardiology and Cardiovascular Medicine and 1 paper in Hematology. Recurrent topics in Carey-Anne Eddy's work include Cardiac electrophysiology and arrhythmias (4 papers), Ion channel regulation and function (4 papers) and DNA Repair Mechanisms (2 papers). Carey-Anne Eddy is often cited by papers focused on Cardiac electrophysiology and arrhythmias (4 papers), Ion channel regulation and function (4 papers) and DNA Repair Mechanisms (2 papers). Carey-Anne Eddy collaborates with scholars based in United Kingdom, New Zealand and Australia. Carey-Anne Eddy's co-authors include Jackie Crawford, Andrew N. Shelling, Mark I. Rees, Judith MacCormick, Jonathan R. Skinner, J. French, Seo‐Kyung Chung, Hugh McAlister, Ian Crozier and Donald R. Love and has published in prestigious journals such as Leukemia, Journal of Medical Genetics and Annals of Emergency Medicine.

In The Last Decade

Carey-Anne Eddy

5 papers receiving 275 citations

Peers

Carey-Anne Eddy
Julie Curran United Kingdom
Koichi Kato Japan
Fabienne Prieur France
Yo Okizuka Japan
Yoshiaki Yamaguchi Japan
Marja Luodonpää Finland
B. Kerem Israel
Cherisse A. Marcou United States
Chris Newton-Cheh United States
Roselie Jongbloed Netherlands
Julie Curran United Kingdom
Carey-Anne Eddy
Citations per year, relative to Carey-Anne Eddy Carey-Anne Eddy (= 1×) peers Julie Curran

Countries citing papers authored by Carey-Anne Eddy

Since Specialization
Citations

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

Fields of papers citing papers by Carey-Anne Eddy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carey-Anne Eddy. 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 Carey-Anne Eddy. The network helps show where Carey-Anne Eddy may publish in the future.

Co-authorship network of co-authors of Carey-Anne Eddy

This figure shows the co-authorship network connecting the top 25 collaborators of Carey-Anne Eddy. A scholar is included among the top collaborators of Carey-Anne Eddy 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 Carey-Anne Eddy. Carey-Anne Eddy 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.
MacCormick, Judith, Hugh McAlister, Jackie Crawford, et al.. (2009). Misdiagnosis of Long QT Syndrome as Epilepsy at First Presentation. Annals of Emergency Medicine. 54(1). 26–32. 93 indexed citations
2.
Yang, Tao, Seo‐Kyung Chung, Wei Zhang, et al.. (2009). Biophysical Properties of 9 KCNQ1 Mutations Associated With Long-QT Syndrome. Circulation Arrhythmia and Electrophysiology. 2(4). 417–426. 34 indexed citations
3.
Eddy, Carey-Anne, Judith MacCormick, Seo‐Kyung Chung, et al.. (2008). Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome. Heart Rhythm. 5(9). 1275–1281. 62 indexed citations
4.
Chung, Seo‐Kyung, Judith MacCormick, Caroline McCulley, et al.. (2007). Long QT and Brugada syndrome gene mutations in New Zealand. Heart Rhythm. 4(10). 1306–1314. 31 indexed citations
5.
Tischkowitz, Marc, Neil V. Morgan, David Grimwade, et al.. (2004). Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia. Leukemia. 18(3). 420–425. 61 indexed citations
6.
Tischkowitz, Marc, Neil V. Morgan, S V Hodgson, et al.. (2001). Mutation analysis of the Fanconi Anaemia group A, C, E, F and G genes in sporadic acute myeloid leukaemia. Journal of Medical Genetics. 38.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Julie Curran Breakdown of academic impact, for papers by Koichi Kato Breakdown of academic impact, for papers by Fabienne Prieur Breakdown of academic impact, for papers by Yo Okizuka Breakdown of academic impact, for papers by Yoshiaki Yamaguchi Breakdown of academic impact, for papers by Marja Luodonpää Breakdown of academic impact, for papers by B. Kerem Breakdown of academic impact, for papers by Cherisse A. Marcou Breakdown of academic impact, for papers by Chris Newton-Cheh Breakdown of academic impact, for papers by Roselie Jongbloed
Rankless by CCL
2026