Amanda McGovern

1.1k total citations
16 papers, 759 citations indexed

About

Amanda McGovern is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Amanda McGovern has authored 16 papers receiving a total of 759 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Cancer Research and 6 papers in Genetics. Recurrent topics in Amanda McGovern's work include Connective tissue disorders research (4 papers), T-cell and B-cell Immunology (4 papers) and Protease and Inhibitor Mechanisms (3 papers). Amanda McGovern is often cited by papers focused on Connective tissue disorders research (4 papers), T-cell and B-cell Immunology (4 papers) and Protease and Inhibitor Mechanisms (3 papers). Amanda McGovern collaborates with scholars based in United Kingdom, Switzerland and United States. Amanda McGovern's co-authors include Cay M. Kielty, Clair Baldock, Andrew K. Baldwin, Shazia S. Chaudhry, C. Adrian Shuttleworth, Paul Martin, Stephen Eyre, Kate Duffus, Gisela Orozco and Rawshan Choudhury and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and PLoS ONE.

In The Last Decade

Amanda McGovern

16 papers receiving 754 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amanda McGovern United Kingdom 13 366 323 168 127 111 16 759
Shelley N.-M. Thai United States 8 279 0.8× 84 0.3× 240 1.4× 60 0.5× 63 0.6× 8 598
Chandramouli Chillakuri United Kingdom 9 313 0.9× 130 0.4× 87 0.5× 58 0.5× 21 0.2× 10 553
Marie‐Hélène Laprise Canada 7 486 1.3× 82 0.3× 174 1.0× 91 0.7× 37 0.3× 7 783
Shu-Fang Jia United States 15 532 1.5× 147 0.5× 175 1.0× 127 1.0× 49 0.4× 19 845
Ali Nawshad United States 18 946 2.6× 505 1.6× 185 1.1× 61 0.5× 36 0.3× 25 1.4k
Wouter de Wet United States 11 475 1.3× 417 1.3× 109 0.6× 50 0.4× 180 1.6× 12 964
Pascale Jackers Belgium 12 608 1.7× 95 0.3× 105 0.6× 380 3.0× 45 0.4× 17 1.0k
Roger Lucas United States 6 711 1.9× 102 0.3× 123 0.7× 64 0.5× 73 0.7× 6 972
Timo Väisänen Finland 13 245 0.7× 76 0.2× 117 0.7× 70 0.6× 27 0.2× 20 630
Caroline M. Cardy United Kingdom 4 218 0.6× 300 0.9× 189 1.1× 35 0.3× 41 0.4× 9 534

Countries citing papers authored by Amanda McGovern

Since Specialization
Citations

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

Fields of papers citing papers by Amanda McGovern

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda McGovern

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

All Works

16 of 16 papers shown
1.
Kerick, Martin, Jenny Hankinson, James Ding, et al.. (2023). P152 Allele-associated chromatin interactions in primary immune cells uncover mechanisms of gene regulation. Lara D. Veeken. 62(Supplement_2). 1 indexed citations
2.
Kerick, Martin, Jenny Hankinson, James Ding, et al.. (2022). Identification of Mechanisms by Which Genetic Susceptibility Loci Influence Systemic Sclerosis Risk Using Functional Genomics in Primary T Cells and Monocytes. Arthritis & Rheumatology. 75(6). 1007–1020. 7 indexed citations
3.
Ray-Jones, Helen, James Ding, Kate Duffus, et al.. (2021). Chromatin Looping Links Target Genes with Genetic Risk Loci for Dermatological Traits. Journal of Investigative Dermatology. 141(8). 1975–1984. 18 indexed citations
4.
Ge, Xiangyu, Mojca Frank‐Bertoncelj, Kerstin Klein, et al.. (2021). Functional genomics atlas of synovial fibroblasts defining rheumatoid arthritis heritability. Genome biology. 22(1). 247–247. 35 indexed citations
5.
Ge, Xiangyu, Amanda McGovern, Kerstin Klein, et al.. (2021). OP0016 IDENTIFICATION OF FUNCTIONAL VARIANTS IN THE RHEUMATOID ARTHRITIS ASSOCIATED JAZF1 LOCUS IN SYNOVIAL FIBROBLASTS. Annals of the Rheumatic Diseases. 80. 9–9. 2 indexed citations
6.
Ray-Jones, Helen, Kate Duffus, Amanda McGovern, et al.. (2020). Mapping DNA interaction landscapes in psoriasis susceptibility loci highlights KLF4 as a target gene in 9q31. BMC Biology. 18(1). 47–47. 19 indexed citations
7.
Yang, Jing, Amanda McGovern, Paul Martin, et al.. (2020). Analysis of chromatin organization and gene expression in T cells identifies functional genes for rheumatoid arthritis. Nature Communications. 11(1). 4402–4402. 38 indexed citations
8.
Martin, Paul, James Ding, Kate Duffus, et al.. (2019). Chromatin interactions reveal novel gene targets for drug repositioning in rheumatic diseases. Annals of the Rheumatic Diseases. 78(8). 1127–1134. 18 indexed citations
9.
Martin, Paul, Amanda McGovern, Jonathan Massey, et al.. (2016). Identifying Causal Genes at the Multiple Sclerosis Associated Region 6q23 Using Capture Hi-C. PLoS ONE. 11(11). e0166923–e0166923. 24 indexed citations
10.
McGovern, Amanda, Stefan Schoenfelder, Paul Martin, et al.. (2016). Capture Hi-C identifies a novel causal gene, IL20RA, in the pan-autoimmune genetic susceptibility region 6q23. Genome biology. 17(1). 212–212. 66 indexed citations
11.
Martin, Paul, Amanda McGovern, Gisela Orozco, et al.. (2015). Capture Hi-C reveals novel candidate genes and complex long-range interactions with related autoimmune risk loci. Nature Communications. 6(1). 10069–10069. 118 indexed citations
12.
Cain, Stuart A., Amanda McGovern, Andrew K. Baldwin, Clair Baldock, & Cay M. Kielty. (2012). Fibrillin-1 Mutations Causing Weill-Marchesani Syndrome and Acromicric and Geleophysic Dysplasias Disrupt Heparan Sulfate Interactions. PLoS ONE. 7(11). e48634–e48634. 53 indexed citations
13.
Choudhury, Rawshan, Shazia S. Chaudhry, Andrew K. Baldwin, et al.. (2010). Assembly of fibrillin microfibrils governs extracellular deposition of latent TGFβ. Journal of Cell Science. 123(17). 3006–3018. 133 indexed citations
14.
Choudhury, Rawshan, Amanda McGovern, Caroline Ridley, et al.. (2009). Differential Regulation of Elastic Fiber Formation by Fibulin-4 and -5. Journal of Biological Chemistry. 284(36). 24553–24567. 90 indexed citations
15.
Cain, Stuart A., et al.. (2009). Defining Elastic Fiber Interactions by Molecular Fishing. Molecular & Cellular Proteomics. 8(12). 2715–2732. 24 indexed citations
16.
Williamson, Matthew R., Shazia S. Chaudhry, Kieran T. Mellody, et al.. (2008). Fibrillin-1 microfibril deposition is dependent on fibronectin assembly. Journal of Cell Science. 121(16). 2696–2704. 113 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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