Eddie Ip

557 total citations
7 papers, 124 citations indexed

About

Eddie Ip is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Eddie Ip has authored 7 papers receiving a total of 124 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Epidemiology. Recurrent topics in Eddie Ip's work include Genomics and Rare Diseases (4 papers), Congenital heart defects research (3 papers) and Congenital Heart Disease Studies (3 papers). Eddie Ip is often cited by papers focused on Genomics and Rare Diseases (4 papers), Congenital heart defects research (3 papers) and Congenital Heart Disease Studies (3 papers). Eddie Ip collaborates with scholars based in Australia, United States and Netherlands. Eddie Ip's co-authors include Eleni Giannoulatou, Sally L. Dunwoodie, David S. Winlaw, Gary F. Sholler, Gillian M. Blue, Gavin Chapman, Joshua W. K. Ho, David T. Humphreys, Paul Leo and Robert M. Graham and has published in prestigious journals such as Bioinformatics, American Heart Journal and Frontiers in Genetics.

In The Last Decade

Eddie Ip

7 papers receiving 124 citations

Peers

Eddie Ip
Ismee Williams United States
Lisa D.S. Bloomer United Kingdom
K. Addison United Kingdom
David Davidson United States
Irum Atta Pakistan
Ismee Williams United States
Eddie Ip
Citations per year, relative to Eddie Ip Eddie Ip (= 1×) peers Ismee Williams

Countries citing papers authored by Eddie Ip

Since Specialization
Citations

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

Fields of papers citing papers by Eddie Ip

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eddie Ip

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

All Works

7 of 7 papers shown
1.
Ip, Eddie, Michael Troup, Colin Xu, et al.. (2022). Benchmarking the Effectiveness and Accuracy of Multiple Mitochondrial DNA Variant Callers: Practical Implications for Clinical Application. Frontiers in Genetics. 13. 692257–692257. 9 indexed citations
2.
Blue, Gillian M., Debjani Das, Michael Troup, et al.. (2021). Whole genome sequencing in transposition of the great arteries and associations with clinically relevant heart, brain and laterality genes. American Heart Journal. 244. 1–13. 12 indexed citations
3.
Ip, Eddie, et al.. (2020). dv-trio: a family-based variant calling pipeline using DeepVariant. Bioinformatics. 36(11). 3549–3551. 6 indexed citations
4.
Ip, Eddie, Gavin Chapman, David S. Winlaw, Sally L. Dunwoodie, & Eleni Giannoulatou. (2019). VPOT: A Customizable Variant Prioritization Ordering Tool for Annotated Variants. Genomics Proteomics & Bioinformatics. 17(5). 540–545. 9 indexed citations
5.
Troup, Michael, et al.. (2019). Spliceogen: an integrative, scalable tool for the discovery of splice-altering variants. Bioinformatics. 35(21). 4405–4407. 7 indexed citations
6.
Blue, Gillian M., Eddie Ip, Karen Walker, et al.. (2018). Genetic burden and associations with adverse neurodevelopment in neonates with congenital heart disease. American Heart Journal. 201. 33–39. 20 indexed citations
7.
Szot, Justin O., Hartmut Cuny, Gillian M. Blue, et al.. (2018). A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. Circulation Genomic and Precision Medicine. 11(3). e001978–e001978. 61 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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