Ingrid Slade
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 6
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 3
- Genetic and rare skin diseases. 1
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- Hedgehog Signaling Pathway Studies 1
- Co-authors
- Nazneen Rahman (5 shared papers)Helen Hanson (3 shared papers)Angela George (2 shared papers)Ann Strydom (2 shared papers)Leah Z. Rand (1 shared paper)Sheila Seal (1 shared paper)Shazia Mahamdallie (1 shared paper)Zoe Kemp (1 shared paper)
- Journals
- Cost Effectiveness and Resource Allocation (1 paper)European Journal of Human Genetics (1 paper)Clinical Medicine (1 paper)Drug Safety (1 paper)Scientific Reports (1 paper)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
Ingrid Slade
10 papers receiving 435 citations
Peers
Comparison fields: 5 of 71
- Genetics 224
- Cancer Research 52
- Reproductive Medicine 23
- Oncology 63
- Health Informatics 3
Countries citing papers authored by Ingrid Slade
This map shows the geographic impact of Ingrid Slade'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 Ingrid Slade with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingrid Slade more than expected).
Fields of papers citing papers by Ingrid Slade
This network shows the impact of papers produced by Ingrid Slade. 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 Ingrid Slade. The network helps show where Ingrid Slade may publish in the future.
Co-authors
The 25 scholars most cited alongside Ingrid Slade, 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 | 157 | |
| 2 | 2019 | 55 | |
| 3 | 2010 | 49 | |
| 4 | 2009 | 44 | |
| 5 | 2019 | 31 | |
| 6 | 2015 | 30 | |
| 7 | 2016 | 29 | |
| 8 | 2016 | 23 | |
| 9 | 2009 | 17 | |
| 10 | 2019 | 8 |
About Ingrid Slade
Ingrid Slade is a scholar working on Genetics, Molecular Biology, Cancer Research, Dermatology and Physiology, having authored 10 papers that have together received 443 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (3 papers), Cancer Genomics and Diagnostics (2 papers), Contact Dermatitis and Allergies (1 paper), Food Allergy and Anaphylaxis Research (1 paper), Allergic Rhinitis and Sensitization (1 paper), Hedgehog Signaling Pathway Studies (1 paper) and Genetic and rare skin diseases. (1 paper). The work is most often cited by research in Genetics (224 citations), Cancer Research (52 citations), Reproductive Medicine (23 citations), Oncology (63 citations) and Health Informatics (3 citations). Ingrid Slade has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Nazneen Rahman, Helen Hanson, Angela George, Ann Strydom, Leah Z. Rand, Sheila Seal, Shazia Mahamdallie, Zoe Kemp, Elise Ruark and Michael Dunn. Their work appears in journals such as Cost Effectiveness and Resource Allocation, European Journal of Human Genetics, Clinical Medicine, Drug Safety and Scientific Reports.
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.