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 8
- BRCA gene mutations in cancer 6
- Genomics and Rare Diseases 5
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- Cancer Genomics and Diagnostics 2
- Co-authors
- Nazneen Rahman (5 shared papers)HELEN LOUISE HANSON (3 shared papers)Hilary Burton (2 shared papers)Angela Joy George (2 shared papers)Ann Strydom (2 shared papers)Sheila Seal (1 shared paper)Sabrina Talukdar (1 shared paper)Shazia Mahamdallie (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)Clinical Medicine (1 paper)Drug Safety (1 paper)Familial Cancer (1 paper)Nature Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Ingrid Slade
14 papers receiving 835 citations
Peers
Comparison fields: 5 of 82
- Genetics 299
- Cancer Research 101
- Reproductive Medicine 55
- Surgery 179
- Pulmonary and Respiratory Medicine 117
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 | 2011 | 282 | |
| 2 | 2016 | 185 | |
| 3 | 2012 | 66 | |
| 4 | 2019 | 60 | |
| 5 | 2010 | 54 | |
| 6 | 2009 | 43 | |
| 7 | 2015 | 39 | |
| 8 | 2019 | 36 | |
| 9 | 2016 | 29 | |
| 10 | 2016 | 24 | |
| 11 | 2009 | 21 | |
| 12 | 2016 | 20 | |
| 13 | 2019 | 7 | |
| 14 | 2022 | 3 | |
| 15 | 2025 | 0 |
About Ingrid Slade
Ingrid Slade is a scholar working on Genetics, Cancer Research, Immunology and Allergy, Economics and Econometrics and Reproductive Medicine, having authored 15 papers that have together received 869 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (6 papers), Genomics and Rare Diseases (5 papers), Cancer Genomics and Diagnostics (2 papers), Renal and related cancers (2 papers), Health Systems, Economic Evaluations, Quality of Life (2 papers), CRISPR and Genetic Engineering (1 paper), Contact Dermatitis and Allergies (1 paper) and Congenital Diaphragmatic Hernia Studies (1 paper). The work is most often cited by research in Genetics (299 citations), Cancer Research (101 citations), Reproductive Medicine (55 citations), Surgery (179 citations) and Pulmonary and Respiratory Medicine (117 citations). Ingrid Slade has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Nazneen Rahman, HELEN LOUISE HANSON, Hilary Burton, Angela Joy George, Ann Strydom, Sheila Seal, Sabrina Talukdar, Shazia Mahamdallie, Elise Ruark and Zoe Kemp. Their work appears in journals such as Journal of Medical Genetics, Clinical Medicine, Drug Safety, Familial Cancer and Nature 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.