Alison Meynert

9.5k total citations
28 papers, 770 citations indexed

About

Alison Meynert is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Alison Meynert has authored 28 papers receiving a total of 770 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Reproductive Medicine. Recurrent topics in Alison Meynert's work include Ovarian cancer diagnosis and treatment (8 papers), Genomics and Rare Diseases (5 papers) and RNA modifications and cancer (5 papers). Alison Meynert is often cited by papers focused on Ovarian cancer diagnosis and treatment (8 papers), Genomics and Rare Diseases (5 papers) and RNA modifications and cancer (5 papers). Alison Meynert collaborates with scholars based in United Kingdom, Canada and France. Alison Meynert's co-authors include Martin S. Taylor, David Fitzpatrick, Morad Ansari, Wendy Myrvold, Brendan D. McKay, Matthew E. Hurles, Colin A. Semple, Robert L. Hollis, Charlie Gourley and Michael Churchman and has published in prestigious journals such as Cell, Nature Communications and Cancer Research.

In The Last Decade

Alison Meynert

28 papers receiving 750 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alison Meynert United Kingdom 15 403 225 114 110 77 28 770
Silke Sperling Germany 23 1.3k 3.2× 240 1.1× 10 0.1× 124 1.1× 18 0.2× 58 1.7k
Sami Kilpinen Finland 20 1.4k 3.5× 190 0.8× 23 0.2× 465 4.2× 17 0.2× 39 2.0k
Anna Vähärautio Finland 12 950 2.4× 115 0.5× 224 2.0× 368 3.3× 6 0.1× 18 1.5k
Lei Song United States 14 466 1.2× 119 0.5× 82 0.7× 288 2.6× 3 0.0× 41 849
Shibo Li United States 22 961 2.4× 594 2.6× 92 0.8× 141 1.3× 3 0.0× 87 1.4k
Daisuke Matsubara Japan 22 721 1.8× 47 0.2× 10 0.1× 194 1.8× 23 0.3× 92 1.4k
Inês de Santiago United Kingdom 13 1.3k 3.2× 188 0.8× 60 0.5× 254 2.3× 4 0.1× 16 1.5k
Mary A. Allen United States 15 917 2.3× 82 0.4× 45 0.4× 198 1.8× 11 0.1× 36 1.3k
Xiuhui Chen China 15 532 1.3× 32 0.1× 23 0.2× 298 2.7× 8 0.1× 35 914
G Brugal France 17 422 1.0× 94 0.4× 27 0.2× 230 2.1× 4 0.1× 54 1.0k

Countries citing papers authored by Alison Meynert

Since Specialization
Citations

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

Fields of papers citing papers by Alison Meynert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alison Meynert

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

All Works

20 of 20 papers shown
1.
Procé, Sophie Marion de, José Luis Campos, Alison Meynert, et al.. (2024). Whole genome sequencing enhances molecular diagnosis of primary ciliary dyskinesia. Pediatric Pulmonology. 59(12). 3322–3332. 3 indexed citations
2.
Dudnakova, Tatiana, Julie Rodor, Anita C. Thomas, et al.. (2024). Control of endothelial cell function and arteriogenesis by MEG3:EZH2 epigenetic regulation of integrin expression. Molecular Therapy — Nucleic Acids. 35(2). 102173–102173. 5 indexed citations
3.
Jiménez-Castellanos, Juan-Carlos, Bartłomiej Waclaw, Alison Meynert, Sean P. McAteer, & Thamarai Schneiders. (2024). Rapid evolution of colistin resistance in a bioreactor model of infection of Klebsiella pneumoniae. Communications Biology. 7(1). 794–794. 2 indexed citations
4.
Halachev, Mihail, Viktoria‐Eleni Gountouna, Alison Meynert, et al.. (2024). Regionally enriched rare deleterious exonic variants in the UK and Ireland. Nature Communications. 15(1). 8454–8454. 2 indexed citations
5.
Thomson, John P., Robert L. Hollis, Michael Churchman, et al.. (2023). Whole exome sequencing of low grade serous ovarian carcinoma identifies genomic events associated with clinical outcome. Gynecologic Oncology. 174. 157–166. 8 indexed citations
6.
Vandersteen, Anthony M., Ruwan Weerakkody, David Parry, et al.. (2023). Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome. Journal of Medical Genetics. 61(3). 232–238. 7 indexed citations
7.
Parry, David, Mihail Halachev, Kathleen A. Williamson, et al.. (2023). Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia. Journal of Medical Genetics. 61(3). 250–261. 4 indexed citations
8.
Jarman, Edward J., Alison Meynert, Graeme R. Grimes, et al.. (2022). In Vivo Modeling of Patient Genetic Heterogeneity Identifies New Ways to Target Cholangiocarcinoma. Cancer Research. 82(8). 1548–1559. 7 indexed citations
9.
Azfer, Asim, Alison Meynert, Donald M. Salter, et al.. (2022). Gorham-Stout case report: a multi-omic analysis reveals recurrent fusions as new potential drivers of the disease. BMC Medical Genomics. 15(1). 128–128. 4 indexed citations
10.
Hollis, Robert L., Bárbara Stanley, John P. Thomson, et al.. (2021). Integrated molecular characterisation of endometrioid ovarian carcinoma identifies opportunities for stratification. npj Precision Oncology. 5(1). 47–47. 16 indexed citations
11.
Hollis, Robert L., John P. Thomson, Bárbara Stanley, et al.. (2020). Molecular stratification of endometrioid ovarian carcinoma predicts clinical outcome. Nature Communications. 11(1). 4995–4995. 83 indexed citations
12.
Halachev, Mihail, Alison Meynert, Martin S. Taylor, et al.. (2019). Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions. PLoS Genetics. 15(11). e1008480–e1008480. 14 indexed citations
13.
Kerr, Shona M., Lucija Klarić, Mihail Halachev, et al.. (2019). An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. Scientific Reports. 9(1). 10964–10964. 16 indexed citations
14.
Hollis, Robert L., Juliet Carmichael, Alison Meynert, et al.. (2019). Clinical and molecular characterization of ovarian carcinoma displaying isolated lymph node relapse. American Journal of Obstetrics and Gynecology. 221(3). 245.e1–245.e15. 20 indexed citations
15.
Hollis, Robert L., Alison Meynert, Michael Churchman, et al.. (2018). Enhanced response rate to pegylated liposomal doxorubicin in high grade serous ovarian carcinomas harbouring BRCA1 and BRCA2 aberrations. BMC Cancer. 18(1). 16–16. 16 indexed citations
16.
Taylor, Rachel L., Mark T. Handley, Sarah Waller, et al.. (2017). Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature. Investigative Ophthalmology & Visual Science. 58(1). 594–594. 24 indexed citations
17.
Meynert, Alison, Morad Ansari, David Fitzpatrick, & Martin S. Taylor. (2014). Variant detection sensitivity and biases in whole genome and exome sequencing. BMC Bioinformatics. 15(1). 247–247. 138 indexed citations
18.
Meynert, Alison, Louise S. Bicknell, Matthew E. Hurles, Andrew P. Jackson, & Martin S. Taylor. (2013). Quantifying single nucleotide variant detection sensitivity in exome sequencing. BMC Bioinformatics. 14(1). 195–195. 57 indexed citations
19.
Butland, Stefanie, Rebecca S. Devon, Yong Huang, et al.. (2007). CAG-encoded polyglutamine length polymorphism in the human genome. BMC Genomics. 8(1). 126–126. 65 indexed citations
20.
Meynert, Alison & Ewan Birney. (2006). Picking Pyknons out of the Human Genome. Cell. 125(5). 836–838. 7 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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