D.E. Saunders
Impact in
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- Metabolism and Genetic Disorders
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- Radiomics and Machine Learning in Medical Imaging
Papers in
- Genetics 2
- Glioma Diagnosis and Treatment 1
- Hemoglobinopathies and Related Disorders 1
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- Fetal and Pediatric Neurological Disorders 1
- Co-authors
- Carlos de Sousa (1 shared paper)Stephanie Grünewald (1 shared paper)Matthew C. Pitt (1 shared paper)Shamima Rahman (1 shared paper)Emma E Glamuzina (1 shared paper)Fenella Jane Kirkham (1 shared paper)Isabelle Russell‐Eggitt (1 shared paper)
- Journals
- UCL Discovery (University College London) (3 papers)
In The Last Decade
D.E. Saunders
2 papers receiving 4 citations
Peers
Comparison fields: 3 of 3
- Clinical Biochemistry 2
- Radiology, Nuclear Medicine and Imaging 2
- Molecular Biology 2
Countries citing papers authored by D.E. Saunders
This map shows the geographic impact of D.E. Saunders'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 D.E. Saunders with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D.E. Saunders more than expected).
Fields of papers citing papers by D.E. Saunders
This network shows the impact of papers produced by D.E. Saunders. 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 D.E. Saunders. The network helps show where D.E. Saunders may publish in the future.
Co-authors
The 7 scholars most cited alongside D.E. Saunders, 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 | THE CHILDREN'S CANCER AND LEUKAEMIA GROUP (CCLG) FUNCTIONAL IMAGING E-REPOSITORY FOR CLINICAL TRIALS OF CHILDHOOD BRAIN TUMOURS | 2010 | 2 |
| 2 | Further delineation of pontocerebellar hypoplasia type 6 due to mutations in the gene encoding mitochondrial arginyl-tRNA synthetase, RARS2 | 2012 | 2 |
| 3 | Change of cerebral blood flow over time in children with sickle cell disease | 2004 | 0 |
About D.E. Saunders
D.E. Saunders is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Nuclear Energy and Engineering, Waste Management and Disposal and Infectious Diseases, having authored 3 papers that have together received 4 indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (1 paper), Hemoglobinopathies and Related Disorders (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). The work is most often cited by research in Clinical Biochemistry (2 citations), Radiology, Nuclear Medicine and Imaging (2 citations), Molecular Biology (2 citations), Nuclear Energy and Engineering (0 citations) and Waste Management and Disposal (0 citations). Frequent co-authors include Carlos de Sousa, Stephanie Grünewald, Matthew C. Pitt, Shamima Rahman, Emma E Glamuzina, Fenella Jane Kirkham and Isabelle Russell‐Eggitt. Their work appears in journals such as UCL Discovery (University College London).
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.