Sally Davies
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
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- Epigenetics and DNA Methylation
- Congenital heart defects research
Papers in
- Genetics 9
- Genetic Syndromes and Imprinting 3
- Connective tissue disorders research 2
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Helen E. Hughes (3 shared papers)David F. Griffiths (1 shared paper)Elizabeth D. Williams (1 shared paper)David W. Williams (1 shared paper)Gareth Williams (1 shared paper)Nazneen Rahman (1 shared paper)Sandra Hanks (1 shared paper)Susan Tomkins (1 shared paper)
- Journals
- Journal of Medical Genetics (6 papers)European Journal of Human Genetics (2 papers)Journal of Dental Education (1 paper)Human Mutation (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomItalyBelgium
In The Last Decade
Sally Davies
16 papers receiving 911 citations
Peers
Comparison fields: 5 of 105
- Genetics 563
- Molecular Biology 536
- Pathology and Forensic Medicine 97
- Endocrinology, Diabetes and Metabolism 78
- Cancer Research 67
Countries citing papers authored by Sally Davies
This map shows the geographic impact of Sally Davies'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 Sally Davies with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sally Davies more than expected).
Fields of papers citing papers by Sally Davies
This network shows the impact of papers produced by Sally Davies. 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 Sally Davies. The network helps show where Sally Davies may publish in the future.
Co-authors
The 25 scholars most cited alongside Sally Davies, 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 | 1993 | 211 | |
| 2 | 2003 | 210 | |
| 3 | 1988 | 139 | |
| 4 | 2003 | 75 | |
| 5 | 1999 | 59 | |
| 6 | 2005 | 52 | |
| 7 | 1999 | 46 | |
| 8 | 2014 | 34 | |
| 9 | 1994 | 29 | |
| 10 | 1996 | 29 | |
| 11 | 1999 | 14 | |
| 12 | 1996 | 13 | |
| 13 | 2000 | 10 | |
| 14 | 2022 | 9 | |
| 15 | 2021 | 5 | |
| 16 | 2009 | 2 |
About Sally Davies
Sally Davies is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Surgery and Public Health, Environmental and Occupational Health, having authored 16 papers that have together received 937 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (3 papers), Genetic Syndromes and Imprinting (3 papers), Connective tissue disorders research (2 papers), Innovations in Medical Education (2 papers), Oral and Maxillofacial Pathology (2 papers), Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Hereditary Neurological Disorders (1 paper). The work is most often cited by research in Genetics (563 citations), Molecular Biology (536 citations), Pathology and Forensic Medicine (97 citations), Endocrinology, Diabetes and Metabolism (78 citations) and Cancer Research (67 citations). Sally Davies has collaborated with scholars based in United Kingdom, Italy and Belgium. Frequent co-authors include Helen E. Hughes, David F. Griffiths, Elizabeth D. Williams, David W. Williams, Gareth Williams, Nazneen Rahman, Sandra Hanks, Susan Tomkins, Meena Upadhyaya and Alexandra Murray. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Journal of Dental Education, Human Mutation and The American Journal of Human 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.