Simon Ramsden

5.2k citations
68 papers · 2.1k · h-index 27

Impact in

    • Retinal Diseases and Treatments
  • Genetics top 2%
    • Genomics and Rare Diseases
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Ocular Disorders and Treatments

Papers in

    • Retinal Development and Disorders 17
    • Molecular Biology Techniques and Applications 5
    • Genomics and Rare Diseases 12
    • Genetic Syndromes and Imprinting 6
    • BRCA gene mutations in cancer 5
    • Ocular Disorders and Treatments 5
    • Genetic and Kidney Cyst Diseases 4

Simon Ramsden

65 papers receiving 2.1k citations

Peers

Simon Ramsden
Comparison fields: 5 of 104
  • Ophthalmology 362
  • Genetics 770
  • Molecular Biology 1.3k
  • Immunology and Allergy 61
  • Pediatrics, Perinatology and Child Health 168
Replace Mohammed A. Aldahmesh with:
Mohammed A. Aldahmesh Saudi Arabia
Claudia Ruivenkamp Netherlands
Gavin Arno United Kingdom
Susmito Biswas United Kingdom
A Churchill United Kingdom
Marta Cortón Spain
Shagufta Khaliq Pakistan
Ariana Kariminejad Iran
Xiaoyun Jia China
I. Christopher Lloyd United Kingdom
Simon Ramsden relative to Mohammed A. Aldahmesh Saudi Arabia Mohammed A. Aldahmesh's profile →
Citations per field
00.5×3.2×
Mohammed A. Aldahmesh · 1×
Citations per year

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

20 of 20 papers shown

Showing the 20 most-cited of 68 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2014141
2 2012131
3 2006119
4 2016116
5 2016102
6 201192
7 200190
8 201085
9 201785
10 201764
11 201162
12 201460
13 200548
14 201748
15 201747
16 201944
17 201441
18 201940
19 200636
20 201336

About Simon Ramsden

Simon Ramsden is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cell Biology and Cellular and Molecular Neuroscience, having authored 68 papers that have together received 2.1k indexed citations. Recurring topics across this work include Retinal Development and Disorders (17 papers), Genomics and Rare Diseases (12 papers), Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (6 papers), BRCA gene mutations in cancer (5 papers), Molecular Biology Techniques and Applications (5 papers), Ocular Disorders and Treatments (5 papers) and Genetic and Kidney Cyst Diseases (4 papers). The work is most often cited by research in Ophthalmology (362 citations), Genetics (770 citations), Molecular Biology (1.3k citations), Immunology and Allergy (61 citations) and Pediatrics, Perinatology and Child Health (168 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, Panagiotis I. Sergouniotis, Anna O’Grady and Stephanie Barton. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Human Mutation, Clinical Chemistry and Ophthalmology.

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.

Explore authors with similar magnitude of impact