Pauline Hensman

439 total citations
9 papers, 124 citations indexed

About

Pauline Hensman is a scholar working on Physiology, Rheumatology and Organic Chemistry. According to data from OpenAlex, Pauline Hensman has authored 9 papers receiving a total of 124 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Physiology, 4 papers in Rheumatology and 2 papers in Organic Chemistry. Recurrent topics in Pauline Hensman's work include Lysosomal Storage Disorders Research (8 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Carbohydrate Chemistry and Synthesis (2 papers). Pauline Hensman is often cited by papers focused on Lysosomal Storage Disorders Research (8 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Carbohydrate Chemistry and Synthesis (2 papers). Pauline Hensman collaborates with scholars based in United Kingdom, United States and Spain. Pauline Hensman's co-authors include Simon Jones, Elisabeth Jameson, Jean Mercer, Alexander Broomfield, Jane Ashworth, Julija Pavaine, Helen Prunty, Ronnie Wright, Anupam Chakrapani and James Davison and has published in prestigious journals such as The Journal of Pediatrics, Orphanet Journal of Rare Diseases and Molecular Genetics and Metabolism.

In The Last Decade

Pauline Hensman

8 papers receiving 124 citations

Peers

Pauline Hensman
Pauline Hensman
Citations per year, relative to Pauline Hensman Pauline Hensman (= 1×) peers Louise L. C. Pinto

Countries citing papers authored by Pauline Hensman

Since Specialization
Citations

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

Fields of papers citing papers by Pauline Hensman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pauline Hensman

This figure shows the co-authorship network connecting the top 25 collaborators of Pauline Hensman. A scholar is included among the top collaborators of Pauline Hensman 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 Pauline Hensman. Pauline Hensman 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.
Jones, Simon, et al.. (2021). Open-label phase 1/2 study of vestronidase alfa for mucopolysaccharidosis VII. Molecular Genetics and Metabolism Reports. 28. 100774–100774. 2 indexed citations
2.
Broomfield, Alexander, Jason Sims, Jean Mercer, et al.. (2020). The evolution of pulmonary function in childhood onset Mucopolysaccharidosis type I. Molecular Genetics and Metabolism. 132(2). 94–99. 5 indexed citations
4.
Broomfield, Alexander, James Davison, Joseph Roberts, et al.. (2019). Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in England. Molecular Genetics and Metabolism. 129(2). 98–105. 36 indexed citations
5.
Broomfield, Alexander, Jean Mercer, Pauline Hensman, et al.. (2018). Outcomes from 18 years of cervical spine surgery in MPS IVA: a single centre’s experience. Child s Nervous System. 34(9). 1705–1716. 9 indexed citations
6.
Broomfield, Alexander, Pauline Hensman, Ronnie Wright, et al.. (2017). Rapidly Progressive White Matter Involvement in Early Childhood: The Expanding Phenotype of Infantile Onset Pompe?. JIMD Reports. 39. 55–62. 23 indexed citations
7.
Mercer, Jean, et al.. (2016). Outcomes of Long-Term Treatment with Laronidase in Patients with Mucopolysaccharidosis Type I. The Journal of Pediatrics. 178. 219–226.e1. 38 indexed citations
8.
Broomfield, Alexander, James Davison, Michelle Wood, et al.. (2015). The UK experience of enzyme replacement therapy in patients with infantile onset Pompe disease. Molecular Genetics and Metabolism. 114(2). S24–S25. 1 indexed citations
9.
Sen, Ethan S, et al.. (2014). Assessment of musculoskeletal abnormalities in children with mucopolysaccharidoses using pGALS. Pediatric Rheumatology. 12(1). 32–32. 10 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