Emma Clement

6.6k total citations
37 papers, 1.3k citations indexed

About

Emma Clement is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Emma Clement has authored 37 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Genetics. Recurrent topics in Emma Clement's work include Muscle Physiology and Disorders (12 papers), Genomics and Rare Diseases (7 papers) and Ubiquitin and proteasome pathways (4 papers). Emma Clement is often cited by papers focused on Muscle Physiology and Disorders (12 papers), Genomics and Rare Diseases (7 papers) and Ubiquitin and proteasome pathways (4 papers). Emma Clement collaborates with scholars based in United Kingdom, United States and Italy. Emma Clement's co-authors include Caroline Godfrey, A. Reghan Foley, Francesco Muntoni, Stephen Abbs, Eugenio Mercuri, Francesco Muntoni, Caroline A. Sewry, C. Jimenez‐Mallebrera, R. Mein and Lucy Feng and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Development.

In The Last Decade

Emma Clement

33 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emma Clement United Kingdom 16 968 294 245 217 187 37 1.3k
Paola Prandini Italy 11 799 0.8× 212 0.7× 189 0.8× 71 0.3× 152 0.8× 15 1.0k
Claudio Graziano Italy 20 695 0.7× 325 1.1× 183 0.7× 118 0.5× 104 0.6× 77 1.2k
Chantal Thys Belgium 19 332 0.3× 194 0.7× 175 0.7× 166 0.8× 104 0.6× 45 1.1k
P. Gallano Spain 20 1.0k 1.0× 287 1.0× 261 1.1× 261 1.2× 213 1.1× 65 1.4k
Ikuya Nonaka Japan 18 1.6k 1.7× 131 0.4× 275 1.1× 173 0.8× 281 1.5× 49 1.8k
Genri Kawahara United States 22 1.4k 1.4× 115 0.4× 236 1.0× 219 1.0× 118 0.6× 33 1.6k
Andoni Urtizberea France 15 555 0.6× 108 0.4× 129 0.5× 155 0.7× 203 1.1× 27 796
Rosie Fisher United Kingdom 8 1.4k 1.4× 348 1.2× 202 0.8× 128 0.6× 279 1.5× 12 1.5k
Desirée du Sart Australia 26 888 0.9× 617 2.1× 130 0.5× 394 1.8× 130 0.7× 39 2.0k
Marco Savarese Finland 20 983 1.0× 197 0.7× 477 1.9× 271 1.2× 224 1.2× 72 1.3k

Countries citing papers authored by Emma Clement

Since Specialization
Citations

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

Fields of papers citing papers by Emma Clement

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Clement

This figure shows the co-authorship network connecting the top 25 collaborators of Emma Clement. A scholar is included among the top collaborators of Emma Clement 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 Emma Clement. Emma Clement 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.
Moosajee, Mariya, et al.. (2025). Retinal Degeneration Diagnosed at 12 and 13 Months and Sensorineural Hearing Loss in Two Unrelated Female Infants With PRS Deficiency. American Journal of Medical Genetics Part A. 200(1). 192–198.
2.
D’Arco, Felice, Sedat Giray Kandemirli, Hisham Dahmoush, et al.. (2024). Incomplete partition type II in its various manifestations: isolated, in association with EVA, syndromic, and beyond; a multicentre international study. Neuroradiology. 66(8). 1397–1403.
3.
Lewis, Martin, Amy F. Juliano, Caroline D. Robson, et al.. (2023). The spectrum of cochlear malformations in CHARGE syndrome and insights into the role of the CHD7 gene during embryogenesis of the inner ear. Neuroradiology. 65(4). 819–834. 4 indexed citations
4.
Juliano, Amy F., et al.. (2022). The Cochlea in Branchio-Oto-Renal Syndrome: An Objective Method for the Diagnosis of Offset Cochlear Turns. American Journal of Neuroradiology. 43(11). 1646–1652. 1 indexed citations
5.
D’Arco, Felice, et al.. (2022). Re-Examining the Cochlea in Branchio-Oto-Renal Syndrome: Genotype-Phenotype Correlation. American Journal of Neuroradiology. 43(2). 309–314. 7 indexed citations
6.
D’Arco, Felice, Asthik Biswas, Emma Clement, Kaukab Rajput, & Amy F. Juliano. (2022). Subtle Malformation of the Cochlear Apex and Genetic Abnormalities: Beyond the “Thorny” Cochlea. American Journal of Neuroradiology. 44(1). 79–81. 1 indexed citations
7.
Lewis, Celine, James Buchanan, Angus Clarke, et al.. (2021). Mixed-methods evaluation of the NHS Genomic Medicine Service for paediatric rare diseases: study protocol. SHILAP Revista de lepidopterología. 1. 23–23. 4 indexed citations
8.
Wortmann, Saskia B., Brigitte Meunier, Lamia Mestek, et al.. (2020). Bi-allelic Variants in TKFC Encoding Triokinase/FMN Cyclase Are Associated with Cataracts and Multisystem Disease. The American Journal of Human Genetics. 106(2). 256–263. 18 indexed citations
9.
Cerbone, Manuela, Emma Clement, Lamia Mestek, et al.. (2019). Sotos Syndrome Presenting with Neonatal Hyperinsulinaemic Hypoglycaemia, Extensive Thrombosis, and Multisystem Involvement. Hormone Research in Paediatrics. 92(1). 64–70. 4 indexed citations
10.
Mestek, Lamia, Emma Clement, Wendy D. Jones, et al.. (2018). Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children. Journal of Medical Genetics. 55(11). 721–728. 89 indexed citations
11.
Stabej, Polona Le Quesne, Chela James, Louise Ocaka, et al.. (2017). An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes. Orphanet Journal of Rare Diseases. 12(1). 24–24. 14 indexed citations
12.
Clement, Emma, L. Feng, R. Mein, et al.. (2012). Relative frequency of congenital muscular dystrophy subtypes: Analysis of the UK diagnostic service 2001–2008. Neuromuscular Disorders. 22(6). 522–527. 41 indexed citations
13.
Godfrey, Caroline, Emma Clement, Stephen Abbs, & Francesco Muntoni. (2011). Exclusion of WWP1 mutations in a cohort of dystroglycanopathy patients. Muscle & Nerve. 44(3). 388–392. 3 indexed citations
14.
Godfrey, Caroline, A. Reghan Foley, Emma Clement, & Francesco Muntoni. (2011). Dystroglycanopathies: coming into focus. Current Opinion in Genetics & Development. 21(3). 278–285. 172 indexed citations
15.
Geranmayeh, Fatemeh, Emma Clement, Lucy Feng, et al.. (2010). Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations. Neuromuscular Disorders. 20(4). 241–250. 133 indexed citations
16.
Mercuri, Eugenio, Emma Clement, Amaka C Offiah, et al.. (2009). Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine. Annals of Neurology. 67(2). 201–208. 103 indexed citations
17.
Clement, Emma, Caroline Godfrey, Jenny Tan, et al.. (2008). Mild POMGnT1 Mutations Underlie a Novel Limb-Girdle Muscular Dystrophy Variant. Archives of Neurology. 65(1). 137–41. 57 indexed citations
18.
Clement, Emma, E. Mercuri, Mary Rutherford, et al.. (2007). C.P.3.06 Spectrum of brain changes and genotype-phenotype correlations in secondary dystroglycanopathies. Neuromuscular Disorders. 17(9-10). 871–871. 1 indexed citations
19.
Klein, Andrea, Emma Clement, Eugenio Mercuri, & Francesco Muntoni. (2007). Differential diagnosis of congenital muscular dystrophies. European Journal of Paediatric Neurology. 12(5). 371–377. 10 indexed citations
20.
Godfrey, Caroline, Diana M. Escolar, Martin Brockington, et al.. (2006). Fukutin gene mutations in steroid‐responsive limb girdle muscular dystrophy. Annals of Neurology. 60(5). 603–610. 108 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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