Audrey Smith
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Epigenetics and DNA Methylation
- Congenital heart defects research
- RNA modifications and cancer
Papers in
- Genetics 12
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 4
- Neurogenetic and Muscular Disorders Research 2
-
- Congenital heart defects research 2
- Genomics and Chromatin Dynamics 2
- Co-authors
- Tabib Dabir (1 shared paper)Jill Clayton‐Smith (1 shared paper)Alison Kraus (1 shared paper)Janet M. Thornton (1 shared paper)Miranda P. Splitt (1 shared paper)Dian Donnai (1 shared paper)Jenny Morton (1 shared paper)Mohnish Suri (1 shared paper)
- Journals
- The American Journal of Human Genetics (3 papers)Nature Communications (2 papers)Nature Genetics (2 papers)Nature (1 paper)Frontiers in Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Audrey Smith
19 papers receiving 1.3k citations
Audrey Smith's Hit Papers
Peers
Comparison fields: 5 of 71
- Genetics 703
- Molecular Biology 626
- Psychiatry and Mental health 97
- Clinical Biochemistry 41
- Genetics 54
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 | Evidence for 28 genetic disorders discovered by combining healthcare and research data Hit paper breakdown → | 2020 | 402 |
| 2 | 2011 | 139 | |
| 3 | 2015 | 122 | |
| 4 | 2017 | 112 | |
| 5 | 2017 | 111 | |
| 6 | 2018 | 91 | |
| 7 | 2019 | 62 | |
| 8 | 2021 | 58 | |
| 9 | 2019 | 50 | |
| 10 | 2021 | 42 | |
| 11 | 2017 | 28 | |
| 12 | 2024 | 18 | |
| 13 | 2016 | 16 | |
| 14 | 2024 | 12 | |
| 15 | 2021 | 8 | |
| 16 | 2008 | 7 | |
| 17 | 2024 | 6 | |
| 18 | 2023 | 5 | |
| 19 | 2020 | 3 |
About Audrey Smith
Audrey Smith is a scholar working on Genetics, Genetics, Molecular Biology, Otorhinolaryngology and Hematology, having authored 19 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Neurogenetic and Muscular Disorders Research (2 papers), Congenital heart defects research (2 papers), Genomics and Chromatin Dynamics (2 papers), Acute Myeloid Leukemia Research (1 paper) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Genetics (703 citations), Molecular Biology (626 citations), Psychiatry and Mental health (97 citations), Clinical Biochemistry (41 citations) and Genetics (54 citations). Audrey Smith has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Tabib Dabir, Jill Clayton‐Smith, Alison Kraus, Janet M. Thornton, Miranda P. Splitt, Dian Donnai, Jenny Morton, Mohnish Suri, Dragana J. Josifova and Roman A. Laskowski. Their work appears in journals such as The American Journal of Human Genetics, Nature Communications, Nature Genetics, Nature and Frontiers in 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.