Simon Ramsden

5.1k citations

67 papers · 2.0k indexed · h-index 26

Impact in

Ophthalmology top 1%
- Retinal Diseases and Treatments
Genetics top 2%
- Genomics and Rare Diseases
- Ocular Disorders and Treatments
- Genomic variations and chromosomal abnormalities

Papers in ⓘ

Genetics 40
- Genomics and Rare Diseases 13
- Ocular Disorders and Treatments 11
- Genetic Syndromes and Imprinting 6
Ophthalmology 12
- Retinal Diseases and Treatments 10

Co-authors: Graeme C. Black (33 shared papers)Jill Clayton‐Smith (11 shared papers)Sanjeev S. Bhaskar (8 shared papers)Georgina Hall (12 shared papers)James O’Sullivan (6 shared papers)Andrew R. Webster (9 shared papers)Jamie M. Ellingford (14 shared papers)Anna O’Grady (5 shared papers)
Journals: European Journal of Human Genetics (12 papers)Journal of Medical Genetics (8 papers)Human Mutation (5 papers)Clinical Chemistry (4 papers)European Journal of Medical Genetics (3 papers)
Partner nations: United Kingdom Germany United States

In The Last Decade

Simon Ramsden

64 papers receiving 1.9k citations

Peers

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-authors

The 25 scholars most cited alongside Simon Ramsden, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Simon Ramsden Line = papers co-authored together Simon Ramsden links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 67 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Personalized Diagnosis and Management of Congenital Cataract by Next-Generation Sequencing Ophthalmology ·Rachel Gillespie, James O’Sullivan, Jane Ashworth, Sanjeev S. Bhaskar, Simon G. Williams, Susmito Biswas, Elias Kehdi, Simon Ramsden, Jill Clayton‐Smith, Graeme C. Black, I. Christopher Lloyd	2014	130
2	A paradigm shift in the delivery of services for diagnosis of inherited retinal disease Journal of Medical Genetics ·James O’Sullivan, Brendan G Mullaney, Sanjeev S. Bhaskar, Jonathan E. Dickerson, Georgina Hall, Anna O’Grady, Andrew R. Webster, Simon Ramsden, Graeme C. Black	2012	124
3	RPGRmutation analysis and disease: an update Human Mutation ·Xinhua Shu, Graeme C. Black, Jacqueline M. Rice, Niki Hart‐Holden, Alison Jones, Anna O’Grady, Simon Ramsden, Alan F. Wright	2006	117
4	Molecular findings from 537 individuals with inherited retinal disease Journal of Medical Genetics ·Jamie M. Ellingford, Stephanie Barton, Sanjeev S. Bhaskar, James O’Sullivan, Simon G. Williams, Janine A. Lamb, Binay Panda, Panagiotis I. Sergouniotis, Rachel Gillespie, Stephen P. Daiger, Georgina Hall, Theodora Gale, I. Christopher Lloyd, (unknown), Simon Ramsden, Graeme C. Black	2016	112
5	Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease Ophthalmology ·Jamie M. Ellingford, Stephanie Barton, Sanjeev S. Bhaskar, Simon G. Williams, Panagiotis I. Sergouniotis, James O’Sullivan, Janine A. Lamb, Rahat Perveen, Georgina Hall, William G. Newman, Richard D. Unwin, Stephen A. Roberts, Rick Leach, Rick Tearle, S. C. Bayliss, Simon Ramsden, Andrea H. Németh, Graeme C. Black	2016	93
6	Codon-Optimized RPGR Improves Stability and Efficacy of AAV8 Gene Therapy in Two Mouse Models of X-Linked Retinitis Pigmentosa Molecular Therapy ·M. Dominik Fischer, Michelle E. McClements, Cristina Martínez-Fernández de la Cámara, Julia-Sophia Bellingrath, Daniyar Dauletbekov, Simon Ramsden, Doron G. Hickey, Alun R. Barnard, Robert E. MacLaren	2017	83
7	Pseudoachondroplasia and multiple epiphyseal dysplasia: A 7‐year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution Human Mutation ·Gail C. Jackson, Lauréane Mittaz‐Crettol, Jacqueline Taylor, Geert Mortier, J Spranger, Bernhard Zabel, Martine Le Merrer, Valérie Cormier‐Daire, Christine M Hall, Amaka C Offiah, Michael Wright, Ravi Savarirayan, Gen Nishimura, Simon Ramsden, Rob Elles, Luisa Bonafé, Andrea Superti‐Furga, Sheila Unger, Andreas Zankl, Michael D. Briggs	2011	81
8	Quality control in molecular genetic testing Nature Reviews Genetics ·Elisabeth Dequeker, Simon Ramsden, Wayne W. Grody, Timothy T. Stenzel, David Barton	2001	75
9	Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes BMC Medical Genetics ·Simon Ramsden, Jill Clayton‐Smith, Rachael Birch, Karin Buiting	2010	75
10	Validation of copy number variation analysis for next-generation sequencing diagnostics European Journal of Human Genetics ·Jamie M. Ellingford, Christopher Campbell, Stephanie Barton, Sanjeev S. Bhaskar, Saurabh Gupta, Rachel L. Taylor, Panagiotis I. Sergouniotis, Bradley Horn, Janine A. Lamb, Michel Michaelides, Andrew R. Webster, William G. Newman, Binay Panda, Simon Ramsden, Graeme C. Black	2017	64
11	The Phenotypic Variability of Retinal Dystrophies Associated With Mutations in CRX, With Report of a Novel Macular Dystrophy Phenotype Investigative Ophthalmology & Visual Science ·Sarah Hull, Gavin Arno, Vincent Plagnol, Sarah Chamney, I Russell‐Eggitt, Dorothy Thompson, Simon Ramsden, Graeme C. Black, Anthony G. Robson, G.E. Holder, Anthony T. Moore, A. R. Webster	2014	57
12	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 ·Jason Kennedy, Gail C. Jackson, Simon Ramsden, Jacky Taylor, William G. Newman, Michael Wright, Dian Donnai, Rob Elles, Michael D. Briggs	2005	47
13	Panel-Based Clinical Genetic Testing in 85 Children with Inherited Retinal Disease Ophthalmology ·Rachel L. Taylor, Neil R. A. Parry, Stephanie Barton, Christopher Campbell, Claire Delaney, Jamie M. Ellingford, Georgina Hall, Claire Hardcastle, Jiten Morarji, Elisabeth J. Nichol, Lindsi C. Williams, Sofia Douzgou, Jill Clayton‐Smith, Simon Ramsden, Vinod Sharma, Susmito Biswas, Iva Lloyd, Jane Ashworth, Graeme C. Black, Panagiotis I. Sergouniotis	2017	46
14	Assessment of the incorporation of CNV surveillance into gene panel next-generation sequencing testing for inherited retinal diseases Journal of Medical Genetics ·Jamie M. Ellingford, Bradley Horn, Christopher Campbell, Gavin Arno, Stephanie Barton, Catriona Tate, Sanjeev S. Bhaskar, Panagiotis I. Sergouniotis, Rachel L. Taylor, Keren Carss, Lucy F. Raymond, Michel Michaelides, Simon Ramsden, Andrew R. Webster, Graeme C. Black	2017	46
15	Genotype to phenotype correlations in cartilage oligomeric matrix protein associated chondrodysplasias European Journal of Human Genetics ·Michael D. Briggs, Joanne Brock, Simon Ramsden, Peter A. Bell	2014	40
16	Clinical utility of genetic testing in 201 preschool children with inherited eye disorders Genetics in Medicine ·Eva Lenassi, Jill Clayton‐Smith, Sofia Douzgou, Simon Ramsden, Stuart Ingram, Georgina Hall, Claire Hardcastle, Tracy Fletcher, Rachel L. Taylor, Jamie M. Ellingford, William Newman, Cecilia Fenerty, Vinod Sharma, Iva Lloyd, Susmito Biswas, Jane Ashworth, Graeme C. Black, Panagiotis I. Sergouniotis	2019	40
17	Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes European Journal of Human Genetics ·Jasmin Beygo, Karin Buiting, Simon Ramsden, Rachael Ellis, Jill Clayton‐Smith, Deniz Kanber	2019	38
18	Clinical utility gene card for: Choroideremia European Journal of Human Genetics ·Mariya Moosajee, Simon Ramsden, Graeme C. Black, Miguel C. Seabra, Andrew R. Webster	2013	36
19	EQUAL-quant: An International External Quality Assessment Scheme for Real-Time PCR Clinical Chemistry ·Simon Ramsden, Sarah B. Daly, Wolf‐Jochen Geilenkeuser, Graeme Duncan, Fabienne Hermitte, Ettore Marubini, Michael Neumaier, Claudio Orlando, Vladimír Palička, Angelo Paradiso, Mario Pazzagli, Sara Pizzamiglio, Paolo Verderio	2006	36
20	Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis Journal of Medical Genetics ·Majlinda Lako, Simon Ramsden, R. Duncan Campbell, Tom Strachan	1999	36

About Simon Ramsden

Simon Ramsden is a scholar working on Genetics, Ophthalmology, Molecular Biology, Cell Biology and Pediatrics, Perinatology and Child Health, having authored 67 papers that have together received 2.0k indexed citations. Recurring topics across this work include Retinal Development and Disorders (24 papers), Genomics and Rare Diseases (13 papers), Ocular Disorders and Treatments (11 papers), Retinal Diseases and Treatments (10 papers), RNA regulation and disease (6 papers), Genetic Syndromes and Imprinting (6 papers), Connexins and lens biology (6 papers) and Prenatal Screening and Diagnostics (6 papers). The work is most often cited by research in Ophthalmology (547 citations), Genetics (871 citations), Molecular Biology (1.4k citations), Immunology and Allergy (68 citations) and Cancer Research (134 citations). Simon Ramsden has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Graeme C. Black, Jill Clayton‐Smith, Sanjeev S. Bhaskar, Georgina Hall, James O’Sullivan, Andrew R. Webster, Jamie M. Ellingford, Anna O’Grady, Panagiotis I. Sergouniotis and Stephanie Barton. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Human Mutation, Clinical Chemistry and European Journal of Medical Genetics.

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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