Ingrid Winship
Impact in
- Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 86
- BRCA gene mutations in cancer 51
- Genomics and Rare Diseases 22
- Genomic variations and chromosomal abnormalities 11
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- Genetic factors in colorectal cancer 59
- Co-authors
- John L. Hopper (34 shared papers)Mark A. Jenkins (40 shared papers)Andrew N. Shelling (9 shared papers)Peter Beighton (12 shared papers)Melissa C. Southey (27 shared papers)Daniel D. Buchanan (36 shared papers)Julie McGaughran (3 shared papers)Graham G. Giles (30 shared papers)
- Journals
- Familial Cancer (19 papers)Australasian Journal of Dermatology (8 papers)Journal of Medical Genetics (7 papers)Genetics in Medicine (6 papers)European Journal of Human Genetics (6 papers)
- Partner nations
- AustraliaUnited StatesNew Zealand
In The Last Decade
Ingrid Winship
218 papers receiving 4.8k citations
Ingrid Winship's Hit Papers
Peers
Comparison fields: 5 of 135
- Pathology and Forensic Medicine 1.4k
- Cancer Research 829
- Genetics 1.4k
- Oncology 1.3k
- Genetics 344
Countries citing papers authored by Ingrid Winship
This map shows the geographic impact of Ingrid Winship'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 Winship with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingrid Winship more than expected).
Fields of papers citing papers by Ingrid Winship
This network shows the impact of papers produced by Ingrid Winship. 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 Winship. The network helps show where Ingrid Winship may publish in the future.
Co-authors
The 25 scholars most cited alongside Ingrid Winship, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 229 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia Hit paper breakdown → | 2001 | 518 |
| 2 | 2008 | 377 | |
| 3 | 2011 | 138 | |
| 4 | 2000 | 133 | |
| 5 | 2006 | 124 | |
| 6 | 2006 | 116 | |
| 7 | 2006 | 91 | |
| 8 | 2010 | 89 | |
| 9 | 2013 | 85 | |
| 10 | 1999 | 82 | |
| 11 | 2013 | 78 | |
| 12 | 2013 | 78 | |
| 13 | 2013 | 71 | |
| 14 | 2021 | 69 | |
| 15 | 2006 | 68 | |
| 16 | 2017 | 65 | |
| 17 | 1997 | 65 | |
| 18 | 1989 | 64 | |
| 19 | 2014 | 58 | |
| 20 | 2002 | 56 |
About Ingrid Winship
Ingrid Winship is a scholar working on Genetics, Pathology and Forensic Medicine, Molecular Biology, Oncology and Cancer Research, having authored 229 papers that have together received 5.0k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (59 papers), BRCA gene mutations in cancer (51 papers), Cancer Genomics and Diagnostics (30 papers), Colorectal Cancer Screening and Detection (29 papers), Genomics and Rare Diseases (22 papers), Genomic variations and chromosomal abnormalities (11 papers), Renal cell carcinoma treatment (9 papers) and Family Support in Illness (9 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.4k citations), Cancer Research (829 citations), Genetics (1.4k citations), Oncology (1.3k citations) and Genetics (344 citations). Ingrid Winship has collaborated with scholars based in Australia, United States and New Zealand. Frequent co-authors include John L. Hopper, Mark A. Jenkins, Andrew N. Shelling, Peter Beighton, Melissa C. Southey, Daniel D. Buchanan, Julie McGaughran, Graham G. Giles, Mark Clendenning and James G. Dowty. Their work appears in journals such as Familial Cancer, Australasian Journal of Dermatology, Journal of Medical Genetics, Genetics in Medicine and European Journal of Human 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.