Ingrid Slade
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Reproductive Medicine top 10%
- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 7
- BRCA gene mutations in cancer 6
- Genomics and Rare Diseases 4
- Genetic Associations and Epidemiology 1
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- Hedgehog Signaling Pathway Studies 2
- Co-authors
- Nazneen Rahman (5 shared papers)Helen Hanson (3 shared papers)Angela George (2 shared papers)Ann Strydom (2 shared papers)Shazia Mahamdallie (1 shared paper)Michael Dunn (1 shared paper)Sabrina Talukdar (1 shared paper)Sheela Upadhyaya (1 shared paper)
- Journals
- Scientific Reports (1 paper)Drug Safety (1 paper)Familial Cancer (1 paper)European Journal of Human Genetics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomCanadaUnited States
In The Last Decade
Ingrid Slade
10 papers receiving 424 citations
Peers
Comparison fields: 5 of 73
- Genetics 238
- Reproductive Medicine 47
- Cancer Research 72
- Oncology 106
- Immunology and Allergy 16
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 | 54 | |
| 3 | 2010 | 47 | |
| 4 | 2009 | 42 | |
| 5 | 2015 | 30 | |
| 6 | 2016 | 29 | |
| 7 | 2019 | 28 | |
| 8 | 2016 | 21 | |
| 9 | 2009 | 16 | |
| 10 | 2019 | 7 |
About Ingrid Slade
Ingrid Slade is a scholar working on Genetics, Molecular Biology, Cancer Research, Pathology and Forensic Medicine and Dermatology, having authored 10 papers that have together received 431 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (6 papers), Genomics and Rare Diseases (4 papers), Cancer Genomics and Diagnostics (3 papers), Hedgehog Signaling Pathway Studies (2 papers), Genetic Associations and Epidemiology (1 paper), Allergic Rhinitis and Sensitization (1 paper), Health Systems, Economic Evaluations, Quality of Life (1 paper) and Healthcare cost, quality, practices (1 paper). The work is most often cited by research in Genetics (238 citations), Reproductive Medicine (47 citations), Cancer Research (72 citations), Oncology (106 citations) and Immunology and Allergy (16 citations). Ingrid Slade has collaborated with scholars based in United Kingdom, Canada and United States. Frequent co-authors include Nazneen Rahman, Helen Hanson, Angela George, Ann Strydom, Shazia Mahamdallie, Michael Dunn, Sabrina Talukdar, Sheela Upadhyaya, Elise Ruark and Martin Gore. Their work appears in journals such as Scientific Reports, Drug Safety, Familial Cancer, European Journal of Human Genetics and Journal of Medical 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.