Jodie Ingles

15.4k total citations · 1 hit paper
152 papers, 4.5k citations indexed

About

Jodie Ingles is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Epidemiology. According to data from OpenAlex, Jodie Ingles has authored 152 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 140 papers in Cardiology and Cardiovascular Medicine, 26 papers in Molecular Biology and 19 papers in Epidemiology. Recurrent topics in Jodie Ingles's work include Cardiomyopathy and Myosin Studies (99 papers), Cardiovascular Effects of Exercise (64 papers) and Cardiac electrophysiology and arrhythmias (47 papers). Jodie Ingles is often cited by papers focused on Cardiomyopathy and Myosin Studies (99 papers), Cardiovascular Effects of Exercise (64 papers) and Cardiac electrophysiology and arrhythmias (47 papers). Jodie Ingles collaborates with scholars based in Australia, United States and United Kingdom. Jodie Ingles's co-authors include Christopher Semsarian, Martin S. Maron, Barry J. Maron, Laura Yeates, Richard D. Bagnall, Charlotte Burns, J. Atherton, Arthur A.M. Wilde, Julie McGaughran and Joanne M. Lind and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and SHILAP Revista de lepidopterología.

In The Last Decade

Jodie Ingles

142 papers receiving 4.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

New Perspectives on the Prevalence of Hypertrophic Cardiomyopathy

2015 889 citations Christopher Semsarian, Jodie Ingles et al. profile →

Peers

Jodie Ingles

CCM

EPIDE

GENET

Savina Mannarino Italy

Jens Jakob Thune Denmark

Gregory C. Allen United States

Giuliano Bosi Italy

Amparo L. Figueroa United States

C.‐H. Bergh Sweden

Teresa Caulin‐Glaser United States

Toshihiro Takenaka Japan

Carol Marshall United States

Russell E. Brown United States

Savina Mannarino Italy

Jodie Ingles

849 ×0.2

CCM

528 ×0.4

210 ×0.4

EPIDE

120 ×0.3

GENET

10 ×0.0

Citations per year, relative to Jodie Ingles Jodie Ingles (= 1×) peers Savina Mannarino

Countries citing papers authored by Jodie Ingles

Since Specialization

Citations

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

Fields of papers citing papers by Jodie Ingles

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jodie Ingles

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

All Works

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20 of 20 papers shown

Gray, Belinda, et al.. (2024). The role of genetic testing in management and prognosis of individuals with inherited cardiomyopathies. Trends in Cardiovascular Medicine. 35(1). 34–44. 2 indexed citations

O’Neill, Matthew J., Ebony Richardson, Kate Thomson, et al.. (2024). Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome–Associated Variants. Circulation Genomic and Precision Medicine. 17(4). e004569–e004569. 3 indexed citations

Macintosh, Rebecca, Joanna Sweeting, Jodie Ingles, et al.. (2024). A mixed-methods assessment of the Australasian Society of Genetic Counselors (ASGC) Mentor Program. SHILAP Revista de lepidopterología. 2(Suppl 2). 101865–101865.

Leslie, Felicity, Suzanne Avis, Richard D. Bagnall, et al.. (2023). The New South Wales Sudden Cardiac Arrest Registry: A Data Linkage Cohort Study. Heart Lung and Circulation. 32(9). 1069–1075. 1 indexed citations

Singer, Emma S., Mira Holliday, Sean Lal, et al.. (2023). The burden of splice-disrupting variants in inherited heart disease and unexplained sudden cardiac death. npj Genomic Medicine. 8(1). 29–29. 5 indexed citations

Paratz, E., Dominica Zentner, Natalie Morgan, et al.. (2023). Sudden Cardiac Death in People With Schizophrenia. JACC. Clinical electrophysiology. 9(8). 1310–1318. 4 indexed citations

Yeates, Laura, et al.. (2022). Using codesign focus groups to develop an online COmmunity suPporting familiEs after Sudden Cardiac Death (COPE-SCD) in the young. BMJ Open. 12(8). e053785–e053785. 5 indexed citations

Castelletti, Silvia, Belinda Gray, Cristina Basso, et al.. (2022). Indications and utility of cardiac genetic testing in athletes. European Journal of Preventive Cardiology. 29(12). 1582–1591. 18 indexed citations

Bagnall, Richard D., Emma S. Singer, Julie Wacker, et al.. (2022). Genetic Basis of Childhood Cardiomyopathy. Circulation Genomic and Precision Medicine. 15(6). e003686–e003686. 18 indexed citations

10.

Paratz, E., Dominica Zentner, Natalie Morgan, et al.. (2022). Causes, circumstances, and potential preventability of cardiac arrest in the young: insights from a state-wide clinical and forensic registry. EP Europace. 24(12). 1933–1941. 23 indexed citations

11.

Paratz, E., Jocasta Ball, Karen Smith, et al.. (2022). Inconsistent discharge diagnoses for young cardiac arrest episodes: insights from a statewide registry. Internal Medicine Journal. 53(10). 1776–1782. 1 indexed citations

12.

Holliday, Mira, Emma S. Singer, Samantha Barratt Ross, et al.. (2021). Transcriptome Sequencing of Patients With Hypertrophic Cardiomyopathy Reveals Novel Splice-Altering Variants in MYBPC3. Circulation Genomic and Precision Medicine. 14(2). e003202–e003202. 18 indexed citations

13.

Repetti, Giuliana G., Yuri Kim, Alexandre C. Pereira, et al.. (2021). Discordant clinical features of identical hypertrophic cardiomyopathy twins. Proceedings of the National Academy of Sciences. 118(10). 27 indexed citations

14.

Bagnall, Richard D., et al.. (2021). Clinical Profile and Health Disparities in a Multiethnic Cohort of Patients With Hypertrophic Cardiomyopathy. Circulation Heart Failure. 14(3). e007537–e007537. 10 indexed citations

15.

Arnott, Clare, et al.. (2021). Sex Disparities in Sudden Cardiac Death. Circulation Arrhythmia and Electrophysiology. 14(8). e009834–e009834. 22 indexed citations

16.

Sharpe, Louise, et al.. (2020). Needs analysis of parents following sudden cardiac death in the young. Open Heart. 7(2). e001120–e001120. 10 indexed citations

17.

Gray, Belinda, Can Hasdemir, Jodie Ingles, et al.. (2018). Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants. Heart Rhythm. 15(7). 1051–1057. 14 indexed citations

18.

Bagnall, Richard D., Jodie Ingles, Laura Yeates, Samuel F. Berkovic, & Christopher Semsarian. (2017). Exome sequencing–based molecular autopsy of formalin-fixed paraffin-embedded tissue after sudden death. Genetics in Medicine. 19(10). 1127–1133. 30 indexed citations

19.

Ingles, Jodie, Charlotte Burns, Richard D. Bagnall, et al.. (2017). Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications.. PubMed. 10(2). 109 indexed citations

20.

Burns, Charlotte, Julie McGaughran, Andrew M. Davis, Christopher Semsarian, & Jodie Ingles. (2015). Factors influencing uptake of familial long QT syndrome genetic testing. American Journal of Medical Genetics Part A. 170(2). 418–425. 37 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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