Jonathan Rodgers

494 total citations
5 papers, 14 citations indexed

About

Jonathan Rodgers is a scholar working on Genetics, Physiology and Surgery. According to data from OpenAlex, Jonathan Rodgers has authored 5 papers receiving a total of 14 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Physiology and 1 paper in Surgery. Recurrent topics in Jonathan Rodgers's work include Genomics and Rare Diseases (3 papers), Telomeres, Telomerase, and Senescence (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Jonathan Rodgers is often cited by papers focused on Genomics and Rare Diseases (3 papers), Telomeres, Telomerase, and Senescence (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Jonathan Rodgers collaborates with scholars based in Australia. Jonathan Rodgers's co-authors include Cheryl Shoubridge, Sophie Calvert, Julie McGaughran, Christopher M. Richmond, Piers Blombery, Jessica K. Holien, Julie Curtin, Raja S. Vasireddy, Ian A. Yang and Pasquale Barbaro and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Clinical Medicine and American Journal of Medical Genetics Part A.

In The Last Decade

Jonathan Rodgers

5 papers receiving 14 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jonathan Rodgers Australia	3	6	6	4	3	3	5	14
Courtney Kiss Canada	3	5 0.8×	5 0.8×	3 0.8×	2 0.7×		3	10
Jazib Hussain Denmark	3	6 1.0×	2 0.3×	2 0.5×	4 1.3×	5 1.7×	5	15
Nebal Waill Saadi Iraq	3	13 2.2×	5 0.8×	2 0.5×	6 2.0×	6 2.0×	6	25
Svetlana Stoma United Kingdom	3	7 1.2×	10 1.7×	10 2.5×	5 1.7×	1 0.3×	6	32
Shawn Leonard United States	3	4 0.7×	6 1.0×	6 1.5×			3	17
Nandini Badarinarayan United Kingdom	2	5 0.8×	4 0.7×	4 1.0×	1 0.3×		2	11
Olesya Yur'evna Shabel'nikova Russia	3	5 0.8×	10 1.7×	4 1.0×	1 0.3×		6	20
Attila Jones United States	2	4 0.7×	5 0.8×	3 0.8×	1 0.3×		3	10
A. Lee United States	1	6 1.0×	4 0.7×	2 0.5×			2	8

Countries citing papers authored by Jonathan Rodgers

Since Specialization

Citations

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

Fields of papers citing papers by Jonathan Rodgers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan Rodgers

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

All Works

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5 of 5 papers shown

1.

Vasireddy, Raja S., et al.. (2023). Telomere biology disorder presenting acutely with pulmonary fibrosis and hepatopulmonary syndrome in a young adult male. SHILAP Revista de lepidopterología. 11(8). e01182–e01182. 3 indexed citations

2.

Fox, Lucy C., Piers Blombery, Raja S. Vasireddy, et al.. (2022). Functional interaction between compound heterozygous TERT mutations causes severe telomere biology disorder. Blood Advances. 6(12). 3779–3791. 2 indexed citations

3.

Rodgers, Jonathan, Christopher M. Richmond, & Julie McGaughran. (2022). Delineating the CCDC22‐related Ritscher–Schinzel syndrome phenotype in the original family. American Journal of Medical Genetics Part A. 188(11). 3324–3330. 2 indexed citations

4.

Vadlamudi, Lata, Ben Lundie, Hnin Hnin Aung, et al.. (2022). A Multi-Disciplinary Team Approach to Genomic Testing for Drug-Resistant Epilepsy Patients—The GENIE Study. Journal of Clinical Medicine. 11(14). 4238–4238. 5 indexed citations

5.

Rodgers, Jonathan, Sophie Calvert, Cheryl Shoubridge, & Julie McGaughran. (2021). A novel ARX loss of function variant in female monozygotic twins is associated with chorea. European Journal of Medical Genetics. 64(11). 104315–104315. 2 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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