Audrey Smith
Impact in
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- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
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- RNA modifications and cancer 1
- Congenital heart defects research 1
- Genetics 2
- Neurogenetic and Muscular Disorders Research 2
- Genomics and Rare Diseases 1
- Genomic variations and chromosomal abnormalities 1
- Co-authors
- Dian Donnai (1 shared paper)Shelagh Joss (1 shared paper)Alison Kraus (1 shared paper)Miranda Splitt (1 shared paper)Eamonn Sheridan (1 shared paper)Christopher M. Watson (1 shared paper)Mohnish Suri (1 shared paper)Sally M. Harrison (1 shared paper)
- Journals
- Neuromuscular Disorders (1 paper)Journal of Medical Genetics (1 paper)Molecular Genetics & Genomic Medicine (1 paper)Clinical Dysmorphology (1 paper)
- Partner nations
- United Kingdom
In The Last Decade
Audrey Smith
4 papers receiving 43 citations
Peers
Comparison fields: 5 of 17
- Aging 2
- Genetics 9
- Cell Biology 10
- Genetics 15
- Molecular Biology 27
Countries citing papers authored by Audrey Smith
This map shows the geographic impact of Audrey Smith'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 Audrey Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Audrey Smith more than expected).
Fields of papers citing papers by Audrey Smith
This network shows the impact of papers produced by Audrey Smith. 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 Audrey Smith. The network helps show where Audrey Smith may publish in the future.
Co-authors
The 25 scholars most cited alongside Audrey Smith, 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 | 2017 | 21 | |
| 2 | 2016 | 12 | |
| 3 | 2008 | 7 | |
| 4 | 2020 | 3 |
About Audrey Smith
Audrey Smith is a scholar working on Molecular Biology, Genetics, Hematology, Genetics and Infectious Diseases, having authored 4 papers that have together received 43 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (2 papers), Acute Myeloid Leukemia Research (1 paper), Genomics and Rare Diseases (1 paper), RNA modifications and cancer (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Congenital heart defects research (1 paper). The work is most often cited by research in Aging (2 citations), Genetics (9 citations), Cell Biology (10 citations), Genetics (15 citations) and Molecular Biology (27 citations). Audrey Smith has collaborated with scholars based in United Kingdom. Frequent co-authors include Dian Donnai, Shelagh Joss, Alison Kraus, Miranda Splitt, Eamonn Sheridan, Christopher M. Watson, Mohnish Suri, Sally M. Harrison, Meriel McEntagart and Agne Antanaviciute. Their work appears in journals such as Neuromuscular Disorders, Journal of Medical Genetics, Molecular Genetics & Genomic Medicine and Clinical Dysmorphology.
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.