Ann Strydom
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 13
- Genomics and Rare Diseases 8
- BRCA gene mutations in cancer 5
- Genomic variations and chromosomal abnormalities 4
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- Cancer Genomics and Diagnostics 6
- Co-authors
- Nazneen Rahman (13 shared papers)Sheila Seal (11 shared papers)Shazia Mahamdallie (10 shared papers)Angela Joy George (4 shared papers)Elise Ruark (10 shared papers)Zoe Kemp (2 shared papers)Ingrid Slade (2 shared papers)HELEN LOUISE HANSON (2 shared papers)
- Journals
- Wellcome Open Research (5 papers)F1000Research (3 papers)JAMA Network Open (1 paper)Familial Cancer (1 paper)Value in Health (1 paper)
- Partner nations
- United KingdomUnited StatesSingapore
In The Last Decade
Ann Strydom
15 papers receiving 545 citations
Peers
Comparison fields: 5 of 55
- Genetics 384
- Cancer Research 110
- Reproductive Medicine 34
- Oncology 91
- Pathology and Forensic Medicine 38
Countries citing papers authored by Ann Strydom
This map shows the geographic impact of Ann Strydom'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 Ann Strydom with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ann Strydom more than expected).
Fields of papers citing papers by Ann Strydom
This network shows the impact of papers produced by Ann Strydom. 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 Ann Strydom. The network helps show where Ann Strydom may publish in the future.
Co-authors
The 25 scholars most cited alongside Ann Strydom, 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 | 2016 | 185 | |
| 2 | 2019 | 93 | |
| 3 | 2016 | 82 | |
| 4 | 2017 | 60 | |
| 5 | 2015 | 49 | |
| 6 | 2016 | 29 | |
| 7 | 2015 | 21 | |
| 8 | 2017 | 9 | |
| 9 | 2018 | 7 | |
| 10 | 2018 | 5 | |
| 11 | 2022 | 4 | |
| 12 | 2016 | 3 | |
| 13 | 2018 | 3 | |
| 14 | The ICR1000 UK exome series: a resource of gene variation in an outbred population [version 1; referees: 2 approved] | 2015 | 2 |
| 15 | 1995 | 1 |
About Ann Strydom
Ann Strydom is a scholar working on Genetics, Cancer Research, Molecular Biology, Reproductive Medicine and Rheumatology, having authored 15 papers that have together received 553 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Cancer Genomics and Diagnostics (6 papers), BRCA gene mutations in cancer (5 papers), CRISPR and Genetic Engineering (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Phylogenetic Studies (2 papers), Folate and B Vitamins Research (1 paper) and Ovarian cancer diagnosis and treatment (1 paper). The work is most often cited by research in Genetics (384 citations), Cancer Research (110 citations), Reproductive Medicine (34 citations), Oncology (91 citations) and Pathology and Forensic Medicine (38 citations). Ann Strydom has collaborated with scholars based in United Kingdom, United States and Singapore. Frequent co-authors include Nazneen Rahman, Sheila Seal, Shazia Mahamdallie, Angela Joy George, Elise Ruark, Zoe Kemp, Ingrid Slade, HELEN LOUISE HANSON, Emma Ramsay and Matthew Clarke. Their work appears in journals such as Wellcome Open Research, F1000Research, JAMA Network Open, Familial Cancer and Value in Health.
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.