Clare Beesley

1.8k total citations
29 papers, 980 citations indexed

About

Clare Beesley is a scholar working on Physiology, Epidemiology and Molecular Biology. According to data from OpenAlex, Clare Beesley has authored 29 papers receiving a total of 980 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Physiology, 13 papers in Epidemiology and 10 papers in Molecular Biology. Recurrent topics in Clare Beesley's work include Lysosomal Storage Disorders Research (18 papers), Trypanosoma species research and implications (11 papers) and Carbohydrate Chemistry and Synthesis (8 papers). Clare Beesley is often cited by papers focused on Lysosomal Storage Disorders Research (18 papers), Trypanosoma species research and implications (11 papers) and Carbohydrate Chemistry and Synthesis (8 papers). Clare Beesley collaborates with scholars based in United Kingdom, Greece and United States. Clare Beesley's co-authors include Bryan Winchester, Ashok Vellodi, Elisabeth Young, Peter T. Clayton, Philippa B. Mills, Neil Dalton, Johannes Zschocke, Robert Surtees, Peter Scambler and Georg F. Hoffmann and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Human Molecular Genetics.

In The Last Decade

Clare Beesley

29 papers receiving 961 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Clare Beesley United Kingdom 17 607 288 262 241 240 29 980
Ai-Chu Huang Taiwan 11 608 1.0× 290 1.0× 195 0.7× 337 1.4× 179 0.7× 15 940
María Josep Coll Spain 19 703 1.2× 370 1.3× 228 0.9× 180 0.7× 218 0.9× 37 1.1k
N. U. Bosshard Switzerland 18 446 0.7× 338 1.2× 128 0.5× 323 1.3× 223 0.9× 27 972
Laura Gort Spain 24 758 1.2× 629 2.2× 221 0.8× 226 0.9× 275 1.1× 67 1.3k
Giulia Polo Italy 17 589 1.0× 248 0.9× 200 0.8× 132 0.5× 165 0.7× 29 871
I Maire France 17 785 1.3× 341 1.2× 279 1.1× 287 1.2× 228 0.9× 85 1.2k
Jakub Sikora Czechia 20 487 0.8× 507 1.8× 182 0.7× 150 0.6× 137 0.6× 48 1.1k
Ana Marcão Portugal 12 402 0.7× 188 0.7× 169 0.6× 160 0.7× 128 0.5× 22 616
Rosanna Gatti Italy 17 422 0.7× 298 1.0× 141 0.5× 195 0.8× 151 0.6× 35 808
Esmée Oussoren Netherlands 15 383 0.6× 245 0.9× 169 0.6× 166 0.7× 67 0.3× 32 768

Countries citing papers authored by Clare Beesley

Since Specialization
Citations

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

Fields of papers citing papers by Clare Beesley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clare Beesley

This figure shows the co-authorship network connecting the top 25 collaborators of Clare Beesley. A scholar is included among the top collaborators of Clare Beesley 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 Clare Beesley. Clare Beesley 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.
Wakeling, Emma, Meriel McEntagart, Charles Shaw‐Smith, et al.. (2020). Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome. SHILAP Revista de lepidopterología. 2(1). 100015–100015. 11 indexed citations
2.
Browning, Andrew C., Oliver Baylis, Clare Beesley, et al.. (2019). A case of ocular cystinosis associated with two potentially severeCTNSmutations. Ophthalmic Genetics. 40(2). 157–160. 1 indexed citations
3.
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
4.
Reid, Emma, Apostolos Papandreou, Suzanne Drury, et al.. (2016). Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. Brain. 139(11). 2844–2854. 27 indexed citations
5.
Beesley, Clare, Linda Berná, Hana Vlášková, et al.. (2009). Mucopolysaccharidosis type I in 21 Czech and Slovak patients: Mutation analysis suggests a functional importance of C‐terminus of the IDUA protein. American Journal of Medical Genetics Part A. 149A(5). 965–974. 29 indexed citations
6.
Beesley, Clare, Elisabeth Young, Marie Jackson, et al.. (2009). Discovery of a new biomarker for the mucopolysaccharidoses (MPS), dipeptidyl peptidase IV (DPP-IV; CD26), by SELDI-TOF mass spectrometry. Molecular Genetics and Metabolism. 96(4). 218–224. 21 indexed citations
7.
Beesley, Clare, Daniela Concolino, Mirella Filocamo, Bryan Winchester, & Pietro Strisciuglio. (2006). Identification and characterisation of an 8.7kb deletion and a novel nonsense mutation in two Italian families with Sanfilippo syndrome type D (mucopolysaccharidosis IIID). Molecular Genetics and Metabolism. 90(1). 77–80. 10 indexed citations
8.
Mills, Kevin, Philippa B. Mills, Marie Jackson, et al.. (2006). Diagnosis of congenital disorders of glycosylation type‐I using protein chip technology. PROTEOMICS. 6(7). 2295–2304. 25 indexed citations
9.
Holton, Janice L., Clare Beesley, Marie Jackson, et al.. (2006). Autophagic vacuolar myopathy in twin girls. Neuropathology and Applied Neurobiology. 32(3). 253–259. 14 indexed citations
10.
Beesley, Clare, Marie Jackson, Elisabeth Young, Ashok Vellodi, & Bryan Winchester. (2005). Molecular defects in Sanfilippo syndrome type B (mucopolysaccharidosis IIIB). Journal of Inherited Metabolic Disease. 28(5). 759–767. 35 indexed citations
11.
Mills, Philippa B., Robert Surtees, M. P. Champion, et al.. (2005). Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5′-phosphate oxidase. Human Molecular Genetics. 14(8). 1077–1086. 211 indexed citations
12.
Beesley, Clare, Marina Moraitou, Bryan Winchester, et al.. (2004). Sanfilippo B syndrome: molecular defects in Greek patients. Clinical Genetics. 65(2). 143–149. 17 indexed citations
13.
Beesley, Clare, et al.. (2003). Sanfilippo syndrome type D: identification of the first mutation in the N-acetylglucosamine-6-sulphatase gene. Journal of Medical Genetics. 40(3). 192–194. 19 indexed citations
14.
Matte, Úrsula da Silveira, Gouri Yogalingam, Doug A. Brooks, et al.. (2003). Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patients. Molecular Genetics and Metabolism. 78(1). 37–43. 69 indexed citations
15.
Hermans, M M, Dik van Leenen, Marian A. Kroos, et al.. (2003). Twenty-two novel mutations in the lysosomal ?-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II. Human Mutation. 23(1). 47–56. 113 indexed citations
16.
Davies, Nigel P., Clare Beesley, Perry Elliott, et al.. (2002). Intronic and missense mutations within the LAMP-2 gene in Danon disease (X linked vacuolar cardiomyopathy and myopathy). UCL Discovery (University College London). 1 indexed citations
17.
Meaney, Cathy, Vanessa M. Adams, Ashok Vellodi, et al.. (2001). Mutational analysis of 85 mucopolysaccharidosis type I families: frequency of known mutations, identification of 17 novel mutations and in vitro expression of missense mutations. Human Genetics. 109(5). 503–511. 100 indexed citations
18.
Beesley, Clare, Anne H. Child, & Magdi H. Yacoub. (1998). The identification of five novel mutations in the lysosomal acid a-(1,4) glucosidase gene from patients with glycogen storage disease type II. Human Mutation. 11(5). 413–413. 28 indexed citations
19.
Beesley, Clare, Anne H. Child, & Magdi H. Yacoub. (1998). The identification of five novel mutations in the lysosomal acid a‐(1,4) glucosidase gene from patients with glycogen storage disease type II. Human Mutation. 11(5). 413–413. 2 indexed citations
20.
Beesley, Clare, Richard J. Smith, Stephen J. Temple, & Peter J. Lea. (1994). Cloning and nucleotide sequence of the gene encoding dinitrogenase reductase (nifH) from the cyanobacterium Nostoc 6720. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1219(2). 548–550. 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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