Catherine McWilliam

1.9k total citations
9 papers, 135 citations indexed

About

Catherine McWilliam is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Catherine McWilliam has authored 9 papers receiving a total of 135 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Catherine McWilliam's work include Genetic Neurodegenerative Diseases (3 papers), Aortic Disease and Treatment Approaches (2 papers) and Mitochondrial Function and Pathology (2 papers). Catherine McWilliam is often cited by papers focused on Genetic Neurodegenerative Diseases (3 papers), Aortic Disease and Treatment Approaches (2 papers) and Mitochondrial Function and Pathology (2 papers). Catherine McWilliam collaborates with scholars based in United Kingdom, Singapore and Netherlands. Catherine McWilliam's co-authors include Cheryl Longman, Richard Petty, Mark Hamilton, Maria Elena Farrugia, Helen Gregory, Sarah A. Cumming, Anneli Cooper, Berit Adam, Darren G. Monckton and Elizabeth A. Worthey and has published in prestigious journals such as PLoS ONE, Scientific Reports and European Heart Journal.

In The Last Decade

Catherine McWilliam

9 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
Catherine McWilliam United Kingdom 4 87 66 37 27 7 9 135
Eugenia Borgione Italy 8 81 0.9× 27 0.4× 31 0.8× 22 0.8× 3 0.4× 19 125
Max van Min Netherlands 5 152 1.7× 27 0.4× 66 1.8× 15 0.6× 3 0.4× 7 217
Andrew B. Singleton United States 4 78 0.9× 77 1.2× 38 1.0× 32 1.2× 3 0.4× 4 127
Michelle M. Axford Canada 6 180 2.1× 130 2.0× 61 1.6× 29 1.1× 5 0.7× 9 223
Sanjog R. Chintalaphani Australia 3 81 0.9× 66 1.0× 38 1.0× 19 0.7× 2 0.3× 5 113
Christina DiVincenzo United States 2 47 0.5× 121 1.8× 26 0.7× 37 1.4× 4 0.6× 2 162
Rakshita A. Charan United States 7 145 1.7× 30 0.5× 64 1.7× 75 2.8× 14 2.0× 7 237
Sydney E. Cason United States 6 116 1.3× 44 0.7× 17 0.5× 26 1.0× 9 240
Shubham Saini United States 5 166 1.9× 71 1.1× 151 4.1× 13 0.5× 4 0.6× 6 252
Elżbieta Zdzienicka Poland 6 61 0.7× 68 1.0× 48 1.3× 24 0.9× 2 0.3× 16 114

Countries citing papers authored by Catherine McWilliam

Since Specialization
Citations

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

Fields of papers citing papers by Catherine McWilliam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine McWilliam

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

All Works

9 of 9 papers shown
1.
Rendtorff, Nanna Dahl, Marianne Lodahl, John Tolmie, et al.. (2022). Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients. Scientific Reports. 12(1). 14959–14959. 3 indexed citations
2.
Gillingwater, Thomas H., Catherine McWilliam, Iain Horrocks, et al.. (2022). A call to introduce newborn screening for spinal muscular atrophy (SMA) in Scotland. Scottish Medical Journal. 67(1). 46–47. 2 indexed citations
3.
Petty, Richard, Maria Eugenicos, Mark Hamilton, et al.. (2019). The prevalence of faecal incontinence in myotonic dystrophy type 1. Neuromuscular Disorders. 29(7). 562–566. 10 indexed citations
4.
Huang, Jeffrey, Ify Mordi, Calvin Chin, et al.. (2019). P6505Urinary desmosine, an elastin-specific degradation product is associated with maximum aortic root size and aortic z-scores in patients with bicuspid aortic valve. European Heart Journal. 40(Supplement_1). 1 indexed citations
5.
Huang, Jeffrey, Calvin Chin, Ify Mordi, et al.. (2019). 126 Urinary desmosine, a biomarker of elastin degradation is significantly elevated and associated with maximum aortic root size and aortic Z-scores in patients with bicuspid aortic valve. Discovery Research Portal (University of Dundee). A103–A104. 1 indexed citations
6.
Cumming, Sarah A., Mark Hamilton, Helen Gregory, et al.. (2018). De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1. European Journal of Human Genetics. 26(11). 1635–1647. 69 indexed citations
7.
Hamilton, Mark, Sarah A. Cumming, Helen Gregory, et al.. (2017). Elevated plasma levels of cardiac troponin-I predict left ventricular systolic dysfunction in patients with myotonic dystrophy type 1: A multicentre cohort follow-up study. PLoS ONE. 12(3). e0174166–e0174166. 29 indexed citations
8.
Laskowski, Roman A., Nidhi Tyagi, Diana Johnson, et al.. (2016). Integrating population variation and protein structural analysis to improve clinical interpretation of missense variation: application to the WD40 domain. Human Molecular Genetics. 25(5). 927–935. 19 indexed citations
9.
McWilliam, Catherine, Andrew Cooke, Daniela Lobo, et al.. (2009). Semi-dominant X-chromosome linked learning disability with progressive ataxia, spasticity and dystonia associated with the novel MECP2 variant p.V122A: Akin to the new MECP2 duplication syndrome?. European Journal of Paediatric Neurology. 14(3). 267–269. 1 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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2026