Simon Ramsden

5.1k total citations
67 papers, 2.0k citations indexed

About

Simon Ramsden is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Simon Ramsden has authored 67 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 40 papers in Genetics and 12 papers in Ophthalmology. Recurrent topics in Simon Ramsden's work include Retinal Development and Disorders (24 papers), Genomics and Rare Diseases (13 papers) and Ocular Disorders and Treatments (11 papers). Simon Ramsden is often cited by papers focused on Retinal Development and Disorders (24 papers), Genomics and Rare Diseases (13 papers) and Ocular Disorders and Treatments (11 papers). Simon Ramsden collaborates with scholars based in United Kingdom, Germany and United States. Simon Ramsden's co-authors include Graeme C. Black, Jill Clayton‐Smith, Sanjeev S. Bhaskar, Georgina Hall, James O’Sullivan, Andrew R. Webster, Jamie M. Ellingford, Panagiotis I. Sergouniotis, Anna O’Grady and Stephanie Barton and has published in prestigious journals such as The Lancet, Nature Reviews Genetics and Scientific Reports.

In The Last Decade

Simon Ramsden

64 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simon Ramsden United Kingdom 26 1.4k 871 547 174 145 67 2.0k
Pierre Bitoun France 17 1.4k 1.0× 818 0.9× 239 0.4× 144 0.8× 123 0.8× 39 1.9k
Mohammed A. Aldahmesh Saudi Arabia 32 1.2k 0.9× 815 0.9× 591 1.1× 68 0.4× 213 1.5× 61 2.0k
Arif O. Khan Saudi Arabia 24 845 0.6× 610 0.7× 669 1.2× 115 0.7× 145 1.0× 131 1.8k
Mais Hashem Saudi Arabia 23 1.1k 0.8× 544 0.6× 192 0.4× 97 0.6× 152 1.0× 51 1.8k
Robyn V. Jamieson Australia 27 1.3k 0.9× 844 1.0× 616 1.1× 72 0.4× 229 1.6× 88 2.1k
Áslaug Jónasdóttir Iceland 14 989 0.7× 825 0.9× 345 0.6× 50 0.3× 89 0.6× 19 1.9k
I. Christopher Lloyd United Kingdom 23 807 0.6× 482 0.6× 735 1.3× 153 0.9× 95 0.7× 47 1.7k
Claudia Ruivenkamp Netherlands 31 1.8k 1.3× 1.8k 2.1× 268 0.5× 393 2.3× 112 0.8× 79 3.4k
Gavin Arno United Kingdom 29 1.7k 1.2× 714 0.8× 818 1.5× 31 0.2× 288 2.0× 113 2.3k
Shagufta Khaliq Pakistan 23 920 0.7× 504 0.6× 309 0.6× 33 0.2× 113 0.8× 64 1.6k

Countries citing papers authored by Simon Ramsden

Since Specialization
Citations

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

Fields of papers citing papers by Simon Ramsden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simon Ramsden

This figure shows the co-authorship network connecting the top 25 collaborators of Simon Ramsden. A scholar is included among the top collaborators of Simon Ramsden 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 Simon Ramsden. Simon Ramsden 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.
Sergouniotis, Panagiotis I., Vincent Michaud, Eulalie Lasseaux, et al.. (2023). A multilayered approach to the analysis of genetic data from individuals with suspected albinism. Journal of Medical Genetics. 60(12). 1245–1249. 1 indexed citations
2.
Lenassi, Eva, Ana Carolina de Carvalho, Anja Thormann, et al.. (2023). EyeG2P: an automated variant filtering approach improves efficiency of diagnostic genomic testing for inherited ophthalmic disorders. Journal of Medical Genetics. 60(8). 810–818. 3 indexed citations
3.
Sergouniotis, Panagiotis I., Simon Ramsden, Andrew Lotery, et al.. (2022). Assessing the Pathogenicity of In-Frame CACNA1F Indel Variants Using Structural Modeling. Journal of Molecular Diagnostics. 24(12). 1232–1239. 1 indexed citations
4.
Ellingford, Jamie M., Panagiotis I. Sergouniotis, Simon Ramsden, et al.. (2021). Improving the clinical interpretation of missense variants in X linked genes using structural analysis. Journal of Medical Genetics. 59(4). 385–392. 3 indexed citations
5.
Sergouniotis, Panagiotis I., Stephanie Barton, Simon Ramsden, et al.. (2020). Using an integrative machine learning approach utilising homology modelling to clinically interpret genetic variants: CACNA1F as an exemplar. European Journal of Human Genetics. 28(9). 1274–1282. 15 indexed citations
6.
Campbell, Patrick, Jamie M. Ellingford, Neil R. A. Parry, et al.. (2019). Clinical and genetic variability in children with partial albinism. Scientific Reports. 9(1). 16576–16576. 30 indexed citations
7.
Beygo, Jasmin, Karin Buiting, Simon Ramsden, et al.. (2019). Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes. European Journal of Human Genetics. 27(9). 1326–1340. 38 indexed citations
8.
Fischer, M. Dominik, Michelle E. McClements, Cristina Martínez-Fernández de la Cámara, et al.. (2017). Codon-Optimized RPGR Improves Stability and Efficacy of AAV8 Gene Therapy in Two Mouse Models of X-Linked Retinitis Pigmentosa. Molecular Therapy. 25(8). 1854–1865. 83 indexed citations
9.
Ellingford, Jamie M., Panagiotis I. Sergouniotis, Rachel Lennon, et al.. (2015). Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome. The Lancet. 385(9980). 1916–1916. 21 indexed citations
10.
Ramsden, Simon, Anna O’Grady, Tracy Fletcher, et al.. (2013). A clinical molecular genetic service for United Kingdom families with choroideraemia. European Journal of Medical Genetics. 56(8). 432–438. 16 indexed citations
11.
Combs, Ryan, Georgina Hall, Katherine Payne, et al.. (2013). Understanding the expectations of patients with inherited retinal dystrophies. British Journal of Ophthalmology. 97(8). 1057–1061. 23 indexed citations
12.
Combs, Ryan, Marion McAllister, Katherine Payne, et al.. (2013). Understanding the impact of genetic testing for inherited retinal dystrophy. European Journal of Human Genetics. 21(11). 1209–1213. 27 indexed citations
13.
Sullivan, William F., D. Gareth Evans, William G. Newman, et al.. (2012). Developing National Guidance on Genetic Testing for Breast Cancer Predisposition: The Role of Economic Evidence?. Genetic Testing and Molecular Biomarkers. 16(6). 580–591. 7 indexed citations
14.
Ramsden, Simon, Alice E. Davidson, Bart P. Leroy, et al.. (2012). Clinical utility gene card for: BEST1-related dystrophies (Bestrophinopathies). European Journal of Human Genetics. 20(5). 4–4. 2 indexed citations
15.
Higgs, Jenny, et al.. (2009). Pharmacogenetic Testing in the United Kingdom Genetics and Immunogenetics Laboratories. Genetic Testing and Molecular Biomarkers. 14(1). 121–125. 15 indexed citations
16.
Ramsden, Simon, Zandra C. Deans, David Robinson, et al.. (2006). Monitoring Standards for Molecular Genetic Testing in the United Kingdom, The Netherlands, and Ireland. Genetic Testing. 10(3). 147–156. 27 indexed citations
17.
Shu, Xinhua, Graeme C. Black, Niki Hart‐Holden, et al.. (2006). RPGRmutation analysis and disease: an update. Human Mutation. 28(4). 322–328. 117 indexed citations
18.
Kennedy, Jason, Gail C. Jackson, Simon Ramsden, et al.. (2005). COMP mutation screening as an aid for the clinical diagnosis and counselling of patients with a suspected diagnosis of pseudoachondroplasia or multiple epiphyseal dysplasia. European Journal of Human Genetics. 13(5). 547–555. 47 indexed citations
19.
Elles, R, et al.. (2002). The National Genetics Reference Laboratories. ePrints Soton (University of Southampton). 1 indexed citations
20.
Dequeker, Elisabeth, Simon Ramsden, Wayne W. Grody, Timothy T. Stenzel, & David Barton. (2001). Quality control in molecular genetic testing. Nature Reviews Genetics. 2(9). 717–723. 75 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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