Ellie Quinn

1.0k total citations
7 papers, 131 citations indexed

About

Ellie Quinn is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ellie Quinn has authored 7 papers receiving a total of 131 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cardiology and Cardiovascular Medicine, 2 papers in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Ellie Quinn's work include Cardiomyopathy and Myosin Studies (4 papers), Cardiovascular Function and Risk Factors (3 papers) and Congenital heart defects research (2 papers). Ellie Quinn is often cited by papers focused on Cardiomyopathy and Myosin Studies (4 papers), Cardiovascular Function and Risk Factors (3 papers) and Congenital heart defects research (2 papers). Ellie Quinn collaborates with scholars based in United Kingdom, United States and Netherlands. Ellie Quinn's co-authors include Perry Elliott, Luís R. Lopes, Juan Pablo Ochoa, Gabrielle Norrish, Ella Field, Marcos Cicerchia, Elena Cervi, Juan Pablo Kaski, Petros Syrris and Caroline Stanasiuk and has published in prestigious journals such as Circulation, Journal of the American Heart Association and European Journal of Human Genetics.

In The Last Decade

Ellie Quinn

6 papers receiving 129 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ellie Quinn United Kingdom	5	102	39	18	13	12	7	131
Emma S. Singer Australia	9	136 1.3×	100 2.6×	18 1.0×	18 1.4×	20 1.7×	12	194
Martín Ortiz-Genga Spain	9	195 1.9×	86 2.2×	21 1.2×	11 0.8×	8 0.7×	16	214
Freyja H.M. van Lint Netherlands	8	192 1.9×	31 0.8×	13 0.7×	26 2.0×	3 0.3×	11	252
María José Oliva‐Sandoval Spain	8	320 3.1×	62 1.6×	26 1.4×	13 1.0×	8 0.7×	9	330
Inmaculada Pérez-Sánchez Spain	7	193 1.9×	105 2.7×	38 2.1×	10 0.8×	3 0.3×	8	221
Marcos Cicerchia Spain	4	169 1.7×	62 1.6×	37 2.1×	9 0.7×	6 0.5×	11	178
Berglind Aðalsteinsdóttir Iceland	5	72 0.7×	66 1.7×	49 2.7×	11 0.8×	8 0.7×	6	142
Martín Ortiz Spain	7	267 2.6×	97 2.5×	12 0.7×	10 0.8×	3 0.3×	11	281
J.F. Hermans-van Ast Netherlands	5	366 3.6×	172 4.4×	15 0.8×	9 0.7×	12 1.0×	5	421
Jaap I. van Waning Netherlands	6	138 1.4×	90 2.3×	14 0.8×	6 0.5×	3 0.3×	8	153

Countries citing papers authored by Ellie Quinn

Since Specialization

Citations

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

Fields of papers citing papers by Ellie Quinn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ellie Quinn

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Quinn, Ellie, et al.. (2022). The experiences of UK-based genetic counsellors working in mainstream settings. European Journal of Human Genetics. 30(11). 1283–1287. 10 indexed citations

2.

Morris-Rosendahl, Déborah, Matthew S. Edwards, Andrew J. Fleming, et al.. (2022). 10 Disease penetrance in asymptomatic carriers of familial cardiomyopathy variants. A9.1–A9.

3.

Hughes, Rebecca, Claudia Camaioni, João B. Augusto, et al.. (2021). Myocardial Perfusion Defects in Hypertrophic Cardiomyopathy Mutation Carriers. Journal of the American Heart Association. 10(15). e020227–e020227. 31 indexed citations

4.

Ochoa, Juan Pablo, Luís R. Lopes, Ellie Quinn, et al.. (2020). Deletions of specific exons of FHOD3 detected by next‐generation sequencing are associated with hypertrophic cardiomyopathy. Clinical Genetics. 98(1). 86–90. 12 indexed citations

5.

Protonotarios, Alexandros, Andreas Brodehl, Angeliki Asimaki, et al.. (2020). The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy. Canadian Journal of Cardiology. 37(6). 857–866. 28 indexed citations

6.

Norrish, Gabrielle, Ella Field, Ellie Quinn, et al.. (2019). Yield of Clinical Screening for Hypertrophic Cardiomyopathy in Child First-Degree Relatives. Circulation. 140(3). 184–192. 48 indexed citations

7.

Lind, T., Michael J. Pitt, B. M. Groves, J. E. White, & Ellie Quinn. (1975). The abnormal left hilum.. Circulation. 51(1). 183–187. 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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