Lisa Ewans

1.5k total citations
11 papers, 145 citations indexed

About

Lisa Ewans is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Lisa Ewans has authored 11 papers receiving a total of 145 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Lisa Ewans's work include Genomics and Rare Diseases (4 papers), Genetic Syndromes and Imprinting (2 papers) and Connective tissue disorders research (2 papers). Lisa Ewans is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetic Syndromes and Imprinting (2 papers) and Connective tissue disorders research (2 papers). Lisa Ewans collaborates with scholars based in Australia, United Kingdom and United States. Lisa Ewans's co-authors include Richard Reynolds, Danielle Pham-Dinh, Dimitrios Papadopoulos, Matthew Law, Leslie Burnett, Tri Giang Phan, Julie McGaughran, Michael F. Buckley, Mark J. Cowley and Tony Roscioli and has published in prestigious journals such as American Journal of Neuroradiology, Journal of Medical Genetics and Molecular and Cellular Neuroscience.

In The Last Decade

Lisa Ewans

10 papers receiving 134 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lisa Ewans Australia 6 84 48 33 20 17 11 145
Jelena Pozojevic Germany 8 55 0.7× 111 2.3× 23 0.7× 12 0.6× 13 0.8× 17 167
Wendy Alcaraz United States 8 140 1.7× 144 3.0× 14 0.4× 19 0.9× 25 1.5× 14 264
Erika Della Mina Italy 8 167 2.0× 124 2.6× 25 0.8× 17 0.8× 20 1.2× 16 263
Agostino Seresini Italy 6 35 0.4× 96 2.0× 23 0.7× 13 0.7× 16 0.9× 8 160
Sameera Sogaty Saudi Arabia 8 105 1.3× 179 3.7× 12 0.4× 8 0.4× 20 1.2× 8 255
Bekir Ergüner Türkiye 7 68 0.8× 78 1.6× 6 0.2× 7 0.3× 13 0.8× 14 162
Melanie Leffler Australia 4 46 0.5× 58 1.2× 5 0.2× 11 0.6× 12 0.7× 9 161
Elham Alehabib Iran 9 51 0.6× 114 2.4× 11 0.3× 10 0.5× 11 0.6× 24 181
Kelly Radtke United States 5 133 1.6× 71 1.5× 20 0.6× 25 1.3× 21 1.2× 8 191

Countries citing papers authored by Lisa Ewans

Since Specialization
Citations

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

Fields of papers citing papers by Lisa Ewans

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisa Ewans

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

All Works

11 of 11 papers shown
1.
Ewans, Lisa, Fulya Taylan, Lorenzo D. Botto, et al.. (2023). International Undiagnosed Diseases Programs (UDPs): components and outcomes. Orphanet Journal of Rare Diseases. 18(1). 348–348. 3 indexed citations
3.
Baynam, Gareth, Lisa Ewans, Lynn Greenhalgh, et al.. (2022). Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim Syndrome. American Journal of Neuroradiology. 43(11). 1660–1666. 1 indexed citations
4.
Cornish, Elisa E., Sulekha Rajagopalan, Lisa Ewans, et al.. (2021). MERTK retinopathy: biomarkers assessing vision loss. Ophthalmic Genetics. 42(6). 706–716. 5 indexed citations
5.
Ewans, Lisa, Alison Colley, Carles Gaston‐Massuet, et al.. (2019). Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complications. Journal of Medical Genetics. 56(9). 629–638. 24 indexed citations
6.
Azmanov, Dimitar N., John Beilby, Lisa Ewans, et al.. (2018). Silver Russel syndrome in an aboriginal patient from Australia. American Journal of Medical Genetics Part A. 176(12). 2561–2563. 14 indexed citations
7.
Ewans, Lisa, Michael Field, Ying Zhu, et al.. (2017). Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsy. European Journal of Human Genetics. 25(6). 763–767. 14 indexed citations
8.
Ewans, Lisa, Thomas Ohnesorg, Katie Ayers, et al.. (2017). Painful ovulation in a 46,XX SRY −ve adult male with SOX9 duplication. Endocrinology Diabetes and Metabolism Case Reports. 2017. 5 indexed citations
9.
Jedraszak, Guillaume, Bénédicte Demeer, Michèle Mathieu‐Dramard, et al.. (2015). Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: Six new patients. American Journal of Medical Genetics Part A. 167(3). 504–511. 17 indexed citations
10.
Ewans, Lisa, et al.. (2015). Losartan therapy for cardiac disease in paediatric Marfan syndrome. Journal of Paediatrics and Child Health. 51(9). 927–931.
11.
Papadopoulos, Dimitrios, et al.. (2006). Upregulation of α-synuclein in neurons and glia in inflammatory demyelinating disease. Molecular and Cellular Neuroscience. 31(4). 597–612. 38 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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