Maggie Williams

2.4k total citations
52 papers, 1.1k citations indexed

About

Maggie Williams is a scholar working on Molecular Biology, General Health Professions and Surgery. According to data from OpenAlex, Maggie Williams has authored 52 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in General Health Professions and 6 papers in Surgery. Recurrent topics in Maggie Williams's work include Lipoproteins and Cardiovascular Health (5 papers), Muscle Physiology and Disorders (4 papers) and Mitochondrial Function and Pathology (3 papers). Maggie Williams is often cited by papers focused on Lipoproteins and Cardiovascular Health (5 papers), Muscle Physiology and Disorders (4 papers) and Mitochondrial Function and Pathology (3 papers). Maggie Williams collaborates with scholars based in United Kingdom, South Africa and United States. Maggie Williams's co-authors include Steve E. Humphries, Marta Futema, Richard Caswell, Thalia Antoniadi, Konrad Paszkiewicz, Lynn Greenhalgh, Sian Ellard, Alison Taylor‐Beadling, Weijia Xie and Ruth Newbury‐Ecob and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Annals of the New York Academy of Sciences.

In The Last Decade

Maggie Williams

47 papers receiving 1.0k citations

Peers

Maggie Williams
Angelika Meyer Switzerland
Manfred Stuhrmann Germany
Anthony Carter Canada
Ivailo Tournev Bulgaria
Ana Cabello Spain
Duangrurdee Wattanasirichaigoon Thailand
Aida M. Bertoli‐Avella Netherlands
Miklós Góth Hungary
Hui Xiong China
Keith Nykamp United States
Angelika Meyer Switzerland
Maggie Williams
Citations per year, relative to Maggie Williams Maggie Williams (= 1×) peers Angelika Meyer

Countries citing papers authored by Maggie Williams

Since Specialization
Citations

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

Fields of papers citing papers by Maggie Williams

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maggie Williams

This figure shows the co-authorship network connecting the top 25 collaborators of Maggie Williams. A scholar is included among the top collaborators of Maggie Williams 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 Maggie Williams. Maggie Williams 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
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Ricks, Esmeralda, et al.. (2024). Experiences of patients living with HIV and AIDS on antiretroviral therapy in Accra, Ghana. Curationis. 47(1). e1–e7.
3.
Ricks, Esmeralda, et al.. (2022). Integrative literature review of evidence‐based guidelines on antiretroviral therapy adherence among adult persons living with HIV. Journal of Advanced Nursing. 78(7). 1909–1918. 1 indexed citations
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Nyoni, Champion N., et al.. (2022). Preceptor support during the COVID-19 pandemic: Recommendations for continuing development. Curationis. 45(1). e1–e10.
6.
Naylor, Richard W., Samantha Williamson, Bernard Davenport, et al.. (2022). Basement membrane defects in CD151-associated glomerular disease. Pediatric Nephrology. 37(12). 3105–3115. 8 indexed citations
7.
Barnicoat, Angela, Amaka C Offiah, Alistair Calder, et al.. (2021). AIFM1‐associated X‐linked spondylometaphyseal dysplasia with cerebral hypomyelination. American Journal of Medical Genetics Part A. 185(4). 1228–1235. 4 indexed citations
8.
Futema, Marta, Alison Taylor‐Beadling, Maggie Williams, & Steve E. Humphries. (2021). Genetic testing for familial hypercholesterolemia—past, present, and future. Journal of Lipid Research. 62. 100139–100139. 31 indexed citations
9.
Williams, Maggie, et al.. (2020). SAKHA ESETHU: nurturing value-centered group work for a community-based parent support Programme in the Eastern Cape, South Africa. Social Work With Groups. 44(4). 364–380. 3 indexed citations
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Willemse, Martijn, et al.. (2019). Radiographers’ experiences of the management of quality assurance programmes in public hospitals, South Africa. Radiography. 26(1). e1–e6. 6 indexed citations
12.
Williams, Maggie, Dalena van Rooyen, & Esmeralda Ricks. (2018). Provision of antiretroviral therapy for children in Nelson Mandela Bay: Health care professionals’ challenges. African Journal of Primary Health Care & Family Medicine. 10(1). e1–e10. 3 indexed citations
13.
Hancox, Jules C., Graham Stuart, Maggie Williams, et al.. (2018). A unique triadin exon deletion causing a null phenotype. HeartRhythm Case Reports. 4(11). 514–518. 12 indexed citations
14.
Williams, Maggie, et al.. (2018). Toward interprofessional service-learning and social accountability in health: One South African University’s process-oriented-participatory journey. Journal of Interprofessional Care. 33(3). 291–294. 3 indexed citations
15.
Rajatileka, Shavanthi, David Odd, Matthew T. Robinson, et al.. (2017). Variants of the EAAT2 Glutamate Transporter Gene Promoter Are Associated with Cerebral Palsy in Preterm Infants. Molecular Neurobiology. 55(3). 2013–2024. 16 indexed citations
16.
Wood, Libby, Chiara Marini‐Bettolo, Michela Guglieri, et al.. (2017). Respiratory involvement in ambulant and non-ambulant patients with facioscapulohumeral muscular dystrophy. Journal of Neurology. 264(6). 1271–1280. 29 indexed citations
17.
Sen, Ethan S, Agnieszka Bierżyńska, Geoff Woodward, et al.. (2017). Clinical genetic testing using a custom-designed steroid-resistant nephrotic syndrome gene panel: analysis and recommendations. Journal of Medical Genetics. 54(12). 795–804. 48 indexed citations
18.
Evangelista, Teresinha, Libby Wood, Roberto Fernández‐Torrón, et al.. (2016). Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry. Journal of Neurology. 263(7). 1401–1408. 25 indexed citations
19.
Faulkner, Claire, Hayley Ellis, Abigail Shaw, et al.. (2015). BRAF Fusion Analysis in Pilocytic Astrocytomas: KIAA1549-BRAF 15-9 Fusions Are More Frequent in the Midline Than Within the Cerebellum. Journal of Neuropathology & Experimental Neurology. 74(9). 867–872. 43 indexed citations
20.
Weedon, Michael N., Robert Hastings, Richard Caswell, et al.. (2011). Exome Sequencing Identifies a DYNC1H1 Mutation in a Large Pedigree with Dominant Axonal Charcot-Marie-Tooth Disease. The American Journal of Human Genetics. 89(2). 308–312. 200 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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