Simon Ramsden
Impact in
- Genetics top 1%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Connective tissue disorders research
- Ocular Disorders and Treatments
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 46
- Genomics and Rare Diseases 28
- Genetic Syndromes and Imprinting 6
- Genetics and Neurodevelopmental Disorders 5
- Ocular Disorders and Treatments 4
- Connective tissue disorders research 3
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- Retinal Development and Disorders 28
- Co-authors
- Graeme Charles M. Black (37 shared papers)Jill Clayton‐Smith (15 shared papers)Sanjeev S. Bhaskar (9 shared papers)James O’Sullivan (6 shared papers)Andrew R. Webster (11 shared papers)Jamie M. Ellingford (15 shared papers)Panagiotis I. Sergouniotis (17 shared papers)Peter Hamilton Watson (1 shared paper)
- Journals
- European Journal of Human Genetics (13 papers)Journal of Medical Genetics (9 papers)The Lancet (4 papers)Human Mutation (4 papers)Clinical Chemistry (4 papers)
- Partner nations
- United KingdomGermanyUnited States
In The Last Decade
Simon Ramsden
85 papers receiving 3.7k citations
Simon Ramsden's Hit Papers
Peers
Comparison fields: 5 of 99
- Genetics 1.6k
- Pediatrics, Perinatology and Child Health 576
- Molecular Biology 1.4k
- Ophthalmology 135
- Clinical Biochemistry 62
Countries citing papers authored by Simon Ramsden
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
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.
All Works
Showing the 20 most-cited of 86 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study Hit paper breakdown → | 2019 | 510 |
| 2 | 2001 | 171 | |
| 3 | Recommendations for clinical interpretation of variants found in non-coding regions of the genome Hit paper breakdown → | 2022 | 171 |
| 4 | 2000 | 156 | |
| 5 | 2014 | 153 | |
| 6 | 2016 | 137 | |
| 7 | 2019 | 137 | |
| 8 | 2012 | 135 | |
| 9 | 2006 | 120 | |
| 10 | 2016 | 117 | |
| 11 | 2001 | 101 | |
| 12 | 2011 | 93 | |
| 13 | 2017 | 89 | |
| 14 | 2010 | 88 | |
| 15 | 2017 | 77 | |
| 16 | 2011 | 64 | |
| 17 | 2014 | 63 | |
| 18 | 2017 | 59 | |
| 19 | 2014 | 57 | |
| 20 | 2017 | 57 |
About Simon Ramsden
Simon Ramsden is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Physiology and Pharmacology, having authored 86 papers that have together received 3.8k indexed citations. Recurring topics across this work include Retinal Development and Disorders (28 papers), Genomics and Rare Diseases (28 papers), Clinical Laboratory Practices and Quality Control (8 papers), Genetic Syndromes and Imprinting (6 papers), Prenatal Screening and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Ocular Disorders and Treatments (4 papers) and Connective tissue disorders research (3 papers). The work is most often cited by research in Genetics (1.6k citations), Pediatrics, Perinatology and Child Health (576 citations), Molecular Biology (1.4k citations), Ophthalmology (135 citations) and Clinical Biochemistry (62 citations). Simon Ramsden has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Graeme Charles M. Black, Jill Clayton‐Smith, Sanjeev S. Bhaskar, James O’Sullivan, Andrew R. Webster, Jamie M. Ellingford, Panagiotis I. Sergouniotis, Peter Hamilton Watson, Stephanie Barton and Ian Christopher Lloyd. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, The Lancet, Human Mutation and Clinical Chemistry.
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.