Sarah Ramsden
Impact in
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- Neuroscience and Neuropharmacology Research
- Photoreceptor and optogenetics research
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- Neuroinflammation and Neurodegeneration Mechanisms
Papers in
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- Chemical Synthesis and Analysis 1
- Ion channel regulation and function 1
- Receptor Mechanisms and Signaling 1
- Genetics 3
- Genetic Syndromes and Imprinting 2
- Co-authors
- Kirsten Harvey (3 shared papers)Hermann Schindelin (2 shared papers)Verena Tretter (2 shared papers)Stephen J. Moss (2 shared papers)Hans Michael Maric (2 shared papers)Antoine Triller (1 shared paper)Karla Kretschmannova (1 shared paper)Géraldine Gouzer (1 shared paper)
- Journals
- Journal of Biological Chemistry (2 papers)Journal of Neuroscience (1 paper)The Lancet (1 paper)European Journal of Medical Genetics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Sarah Ramsden
9 papers receiving 300 citations
Peers
Comparison fields: 5 of 54
- Cellular and Molecular Neuroscience 203
- Neurology 25
- Molecular Biology 191
- Cognitive Neuroscience 53
- Cell Biology 43
Countries citing papers authored by Sarah Ramsden
This map shows the geographic impact of Sarah 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 Sarah Ramsden with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah Ramsden more than expected).
Fields of papers citing papers by Sarah Ramsden
This network shows the impact of papers produced by Sarah 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 Sarah Ramsden. The network helps show where Sarah Ramsden may publish in the future.
Co-authors
The 25 scholars most cited alongside Sarah 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
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 132 | |
| 2 | 2011 | 87 | |
| 3 | Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophy. | 2009 | 20 |
| 4 | Lesion sites that predict the ability to gesture how an object is used. | 2010 | 18 |
| 5 | 2010 | 15 | |
| 6 | 2020 | 13 | |
| 7 | 2006 | 12 | |
| 8 | Somatic mutation in the MECP2 gene may be a cause of non-lethal neurodevelopmental diosrder in males. | 2000 | 6 |
| 9 | Angelman syndrome phenotype associated with mutations in MECP2. | 2001 | 1 |
| 10 | 2023 | 1 |
About Sarah Ramsden
Sarah Ramsden is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Radiology, Nuclear Medicine and Imaging and Cell Biology, having authored 10 papers that have together received 305 indexed citations. Recurring topics across this work include Cellular transport and secretion (2 papers), Neuroscience and Neuropharmacology Research (2 papers), Genetic Syndromes and Imprinting (2 papers), Chemical Synthesis and Analysis (1 paper), Ion channel regulation and function (1 paper), Gestational Trophoblastic Disease Studies (1 paper), Receptor Mechanisms and Signaling (1 paper) and Action Observation and Synchronization (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (203 citations), Neurology (25 citations), Molecular Biology (191 citations), Cognitive Neuroscience (53 citations) and Cell Biology (43 citations). Sarah Ramsden has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Kirsten Harvey, Hermann Schindelin, Verena Tretter, Stephen J. Moss, Hans Michael Maric, Antoine Triller, Karla Kretschmannova, Géraldine Gouzer, Paul Davies and Jayanta Mukherjee. Their work appears in journals such as Journal of Biological Chemistry, Journal of Neuroscience, The Lancet, European Journal of Medical Genetics and 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.