Emma S. Singer

466 total citations
12 papers, 194 citations indexed

About

Emma S. Singer is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Emma S. Singer has authored 12 papers receiving a total of 194 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cardiology and Cardiovascular Medicine, 9 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Emma S. Singer's work include Cardiomyopathy and Myosin Studies (7 papers), Cardiac electrophysiology and arrhythmias (4 papers) and Congenital heart defects research (4 papers). Emma S. Singer is often cited by papers focused on Cardiomyopathy and Myosin Studies (7 papers), Cardiac electrophysiology and arrhythmias (4 papers) and Congenital heart defects research (4 papers). Emma S. Singer collaborates with scholars based in Australia, Canada and Denmark. Emma S. Singer's co-authors include Richard D. Bagnall, Jodie Ingles, Christopher Semsarian, Samantha Barratt Ross, Raymond W. Sy, Laura Yeates, Jacob Tfelt‐Hansen, Robert G. Weintraub, Marc R. Wilkins and John Common and has published in prestigious journals such as Journal of the American College of Cardiology, Cell Death and Disease and Genetics in Medicine.

In The Last Decade

Emma S. Singer

11 papers receiving 193 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emma S. Singer Australia 9 136 100 20 18 18 12 194
Martín Ortiz-Genga Spain 9 195 1.4× 86 0.9× 8 0.4× 21 1.2× 11 0.6× 16 214
Ellie Quinn United Kingdom 5 102 0.8× 39 0.4× 12 0.6× 18 1.0× 13 0.7× 7 131
Angela C. Tai United States 4 138 1.0× 118 1.2× 9 0.5× 30 1.7× 21 1.2× 7 198
J.F. Hermans-van Ast Netherlands 5 366 2.7× 172 1.7× 12 0.6× 15 0.8× 9 0.5× 5 421
Marcos Cicerchia Spain 4 169 1.2× 62 0.6× 6 0.3× 37 2.1× 9 0.5× 11 178
Akihiko Hodatsu Japan 12 246 1.8× 83 0.8× 8 0.4× 23 1.3× 10 0.6× 15 281
Martín Ortiz Spain 7 267 2.0× 97 1.0× 3 0.1× 12 0.7× 10 0.6× 11 281
Berglind Aðalsteinsdóttir Iceland 5 72 0.5× 66 0.7× 8 0.4× 49 2.7× 11 0.6× 6 142
Karen Livesey United Kingdom 4 185 1.4× 128 1.3× 11 0.6× 23 1.3× 11 0.6× 7 259
Corinna Armentano Italy 3 484 3.6× 203 2.0× 8 0.4× 86 4.8× 16 0.9× 4 500

Countries citing papers authored by Emma S. Singer

Since Specialization
Citations

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

Fields of papers citing papers by Emma S. Singer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emma S. Singer. 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 Emma S. Singer. The network helps show where Emma S. Singer may publish in the future.

Co-authorship network of co-authors of Emma S. Singer

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

All Works

12 of 12 papers shown
1.
2.
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
3.
4.
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
5.
Yeates, Laura, Emma S. Singer, Raymond W. Sy, et al.. (2022). Concealed Cardiomyopathy in Autopsy-Inconclusive Cases of Sudden Cardiac Death and Implications for Families. Journal of the American College of Cardiology. 80(22). 2057–2068. 30 indexed citations
6.
Richardson, Ebony, Charlotte Burns, Belinda Gray, et al.. (2022). The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic. Genome Medicine. 14(1). 145–145. 10 indexed citations
7.
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
8.
Singer, Emma S., Samantha Barratt Ross, Jonathan R. Skinner, et al.. (2020). Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death. Genetics in Medicine. 23(1). 86–93. 20 indexed citations
9.
Ross, Samantha Barratt, Emma S. Singer, Laura Yeates, et al.. (2020). Genetic architecture of left ventricular noncompaction in adults. Human Genome Variation. 7(1). 33–33. 25 indexed citations
10.
Bagnall, Richard D., Emma S. Singer, & Jacob Tfelt‐Hansen. (2019). Sudden Cardiac Death in the Young. Heart Lung and Circulation. 29(4). 498–504. 15 indexed citations
11.
Singer, Emma S., Jodie Ingles, Christopher Semsarian, & Richard D. Bagnall. (2019). Key Value of RNA Analysis of MYBPC3 Splice-Site Variants in Hypertrophic Cardiomyopathy. Circulation Genomic and Precision Medicine. 12(1). e002368–e002368. 23 indexed citations
12.
Corley, Susan, Nichole Giles, Emma S. Singer, et al.. (2018). Plau and Tgfbr3 are YAP-regulated genes that promote keratinocyte proliferation. Cell Death and Disease. 9(11). 1106–1106. 27 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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