Eriskay Liston

1.4k total citations
7 papers, 268 citations indexed

About

Eriskay Liston is a scholar working on Genetics, Molecular Biology and Pharmacology. According to data from OpenAlex, Eriskay Liston has authored 7 papers receiving a total of 268 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Pharmacology. Recurrent topics in Eriskay Liston's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (2 papers) and Ethics in Clinical Research (1 paper). Eriskay Liston is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (2 papers) and Ethics in Clinical Research (1 paper). Eriskay Liston collaborates with scholars based in Canada, United States and Netherlands. Eriskay Liston's co-authors include Rebekah Jobling, Raymond H. Kim, Melanie Care, Michael H. Gollob, Gregory Costain, Chantal F. Morel, Arthur A.M. Wilde, Seema M. Jamal, S. Mohsen Hosseini and John Garcia and has published in prestigious journals such as Circulation, Human Genetics and JAMA Network Open.

In The Last Decade

Eriskay Liston

6 papers receiving 262 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eriskay Liston Canada	4	180	140	65	28	17	7	268
Tanya Stubblefield United States	9	539 3.0×	187 1.3×	32 0.5×	3 0.1×	10 0.6×	13	593
Gayle Kucera United States	7	469 2.6×	176 1.3×	27 0.4×	3 0.1×	9 0.5×	11	519
Nathalie Chami United States	6	46 0.3×	86 0.6×	71 1.1×	8 0.3×		7	202
Jaakko T. Leinonen Finland	6	77 0.4×	77 0.6×	23 0.4×	7 0.3×		14	146
Ragan Hart United States	6	16 0.1×	12 0.1×	89 1.4×	29 1.0×	15 0.9×	7	138
Rita Menassa France	8	9 0.1×	181 1.3×	71 1.1×	32 1.1×	6 0.4×	14	234
Burak Hacıhanefioğlu Türkiye	7	29 0.2×	79 0.6×	24 0.4×	16 0.6×	5 0.3×	7	320
Peeter Juhanson Estonia	7	11 0.1×	49 0.3×	29 0.4×	12 0.4×	2 0.1×	7	118
Jennifer Arroyo United States	6	21 0.1×	75 0.5×	59 0.9×	14 0.5×		9	129
Tamás Oroszlán Hungary	6	29 0.2×	49 0.3×	99 1.5×	5 0.2×	2 0.1×	9	213

Countries citing papers authored by Eriskay Liston

Since Specialization

Citations

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

Fields of papers citing papers by Eriskay Liston

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eriskay Liston

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

All Works

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7 of 7 papers shown

1.

Ding, Qiliang, Roozbeh Manshaei, Brett Trost, et al.. (2022). SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing. Human Genetics. 142(2). 201–216. 3 indexed citations

2.

Tsiplova, Kate, Robin Z. Hayeems, Christian R. Marshall, et al.. (2022). Trio genome sequencing for developmental delay and pediatric heart conditions: A comparative microcost analysis. Genetics in Medicine. 24(5). 1027–1036. 9 indexed citations

3.

Liston, Eriskay, Rajiv Chaturvedi, Iris Cohn, et al.. (2022). A Model for the Integration of Genome Sequencing Into a Pediatric Cardiology Clinic. Canadian Journal of Cardiology. 38(9). 1454–1457.

4.

Cohn, Iris, Roozbeh Manshaei, Eriskay Liston, et al.. (2021). Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting. JAMA Network Open. 4(5). e2110446–e2110446. 24 indexed citations

5.

Curtis, Meredith, Danielle Baribeau, Susan Walker, et al.. (2020). A novel intronic variant in UBE3A identified by genome sequencing in a patient with an atypical presentation of Angelman syndrome. American Journal of Medical Genetics Part A. 182(9). 2145–2151. 3 indexed citations

6.

Liston, Eriskay, Laura Zahavich, Dimitri J. Stavropoulos, et al.. (2019). Return of genetic and genomic research findings: experience of a pediatric biorepository. BMC Medical Genomics. 12(1). 173–173. 19 indexed citations

7.

Hosseini, S. Mohsen, Raymond H. Kim, Sharmila Udupa, et al.. (2018). Reappraisal of Reported Genes for Sudden Arrhythmic Death. Circulation. 138(12). 1195–1205. 210 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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