Sofie E. Ashford
Impact in
- Genetics top 2%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Immunology top 5%
- Immunodeficiency and Autoimmune Disorders
Papers in
- Genetics 14
- Genomics and Rare Diseases 5
- Genetic Associations and Epidemiology 5
- Genomic variations and chromosomal abnormalities 2
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- Platelet Disorders and Treatments 3
Sofie E. Ashford
30 papers receiving 3.8k citations
Sofie E. Ashford's Hit Papers
Peers
Comparison fields: 5 of 131
- Genetics 1.2k
- Immunology 621
- Molecular Biology 1.6k
- Cancer Research 323
- Hematology 245
Countries citing papers authored by Sofie E. Ashford
This map shows the geographic impact of Sofie E. Ashford'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 Sofie E. Ashford with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sofie E. Ashford more than expected).
Fields of papers citing papers by Sofie E. Ashford
This network shows the impact of papers produced by Sofie E. Ashford. 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 Sofie E. Ashford. The network helps show where Sofie E. Ashford may publish in the future.
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All Works
Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells Hit paper breakdown → | 2016 | 462 |
| 2 | Common genetic variation drives molecular heterogeneity in human iPSCs Hit paper breakdown → | 2017 | 432 |
| 3 | 2016 | 379 | |
| 4 | 2010 | 353 | |
| 5 | 2008 | 294 | |
| 6 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. Hit paper breakdown → | 2021 | 290 |
| 7 | 2020 | 174 | |
| 8 | 2018 | 173 | |
| 9 | 2019 | 172 | |
| 10 | 2013 | 155 | |
| 11 | 2016 | 131 | |
| 12 | 2016 | 120 | |
| 13 | 2020 | 98 | |
| 14 | 2020 | 60 | |
| 15 | 2019 | 60 | |
| 16 | 2017 | 58 | |
| 17 | 2018 | 53 | |
| 18 | 2019 | 50 | |
| 19 | 2018 | 50 | |
| 20 | 2017 | 46 |
About Sofie E. Ashford
Sofie E. Ashford is a scholar working on Genetics, Hematology, Pathology and Forensic Medicine, Immunology and Physiology, having authored 30 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genetic Associations and Epidemiology (5 papers), Genetic factors in colorectal cancer (4 papers), Immunodeficiency and Autoimmune Disorders (3 papers), Platelet Disorders and Treatments (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Retinal Development and Disorders (2 papers) and Single-cell and spatial transcriptomics (2 papers). The work is most often cited by research in Genetics (1.2k citations), Immunology (621 citations), Molecular Biology (1.6k citations), Cancer Research (323 citations) and Hematology (245 citations). Sofie E. Ashford has collaborated with scholars based in United Kingdom, United States and Netherlands. Their work appears in journals such as The American Journal of Human Genetics, Cell, Scientific Reports, Journal of Allergy and Clinical Immunology and Nature Communications.
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.