kConFab
Impact in
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- BRCA gene mutations in cancer
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 9
- BRCA gene mutations in cancer 8
- Genomic variations and chromosomal abnormalities 2
- Genetic Associations and Epidemiology 1
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- DNA Repair Mechanisms 3
- CRISPR and Genetic Engineering 2
- RNA modifications and cancer 1
- Co-authors
- Georgia Chenevix‐Trench (5 shared papers)Alison H. Trainer (2 shared papers)Ian Campbell (2 shared papers)Ella R. Thompson (2 shared papers)Paul A. James (2 shared papers)Sarah Sawyer (2 shared papers)Melissa C. Southey (5 shared papers)Gillian Mitchell (2 shared papers)
- Journals
- Human Mutation (3 papers)Familial Cancer (2 papers)Reproduction Fertility and Development (1 paper)International Journal of Molecular Sciences (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- AustraliaUnited StatesFrance
In The Last Decade
kConFab
10 papers receiving 158 citations
Peers
Comparison fields: 5 of 26
- Genetics 106
- Cancer Research 49
- Pathology and Forensic Medicine 48
- Reproductive Medicine 14
- Molecular Biology 111
Countries citing papers authored by kConFab
This map shows the geographic impact of kConFab'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 kConFab with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites kConFab more than expected).
Fields of papers citing papers by kConFab
This network shows the impact of papers produced by kConFab. 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 kConFab. The network helps show where kConFab may publish in the future.
Co-authors
The 25 scholars most cited alongside kConFab, 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 | 53 | |
| 2 | 2005 | 39 | |
| 3 | 2013 | 30 | |
| 4 | 2021 | 16 | |
| 5 | 2003 | 7 | |
| 6 | 2010 | 6 | |
| 7 | 2007 | 5 | |
| 8 | 2005 | 2 | |
| 9 | 2006 | 2 | |
| 10 | 2004 | 1 |
About kConFab
kConFab is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Cancer Research and Reproductive Medicine, having authored 10 papers that have together received 161 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (8 papers), Cancer Genomics and Diagnostics (3 papers), Genetic factors in colorectal cancer (3 papers), DNA Repair Mechanisms (3 papers), CRISPR and Genetic Engineering (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genetic Associations and Epidemiology (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (106 citations), Cancer Research (49 citations), Pathology and Forensic Medicine (48 citations), Reproductive Medicine (14 citations) and Molecular Biology (111 citations) kConFab has collaborated with scholars based in Australia, United States and France. Frequent co-authors include Georgia Chenevix‐Trench, Alison H. Trainer, Ian Campbell, Ella R. Thompson, Paul A. James, Sarah Sawyer, Melissa C. Southey, Gillian Mitchell, John L. Hopper and Ee Ming Wong. Their work appears in journals such as Human Mutation, Familial Cancer, Reproduction Fertility and Development, International Journal of Molecular Sciences 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.