Jane Carpenter
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Nutrition, Genetics, and Disease
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 16
- BRCA gene mutations in cancer 14
- Genetic Associations and Epidemiology 5
- Genomic variations and chromosomal abnormalities 3
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- Cancer Genomics and Diagnostics 3
- Co-authors
- Christine L. Clarke (4 shared papers)Jan Lubiński (1 shared paper)Rodney J. Scott (1 shared paper)Michelle W. Wong‐Brown (1 shared paper)Cliff J. Meldrum (1 shared paper)Anna Jakubowska (1 shared paper)Steven Alexander Narod (1 shared paper)Helena Rudnicka (1 shared paper)
- Journals
- Breast Cancer Research (4 papers)Nature Communications (3 papers)Nature Genetics (2 papers)Scientific Reports (2 papers)Human Molecular Genetics (2 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
Jane Carpenter
25 papers receiving 2.2k citations
Jane Carpenter's Hit Papers
Peers
Comparison fields: 5 of 88
- Genetics 1.2k
- Cancer Research 521
- Oncology 457
- Pathology and Forensic Medicine 254
- Molecular Biology 764
Countries citing papers authored by Jane Carpenter
This map shows the geographic impact of Jane Carpenter'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 Jane Carpenter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jane Carpenter more than expected).
Fields of papers citing papers by Jane Carpenter
This network shows the impact of papers produced by Jane Carpenter. 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 Jane Carpenter. The network helps show where Jane Carpenter may publish in the future.
Co-authors
The 13 scholars most cited alongside Jane Carpenter, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants Hit paper breakdown → | 2015 | 446 |
| 2 | 2013 | 348 | |
| 3 | 2011 | 265 | |
| 4 | 2016 | 175 | |
| 5 | 2012 | 149 | |
| 6 | 2013 | 130 | |
| 7 | 2015 | 108 | |
| 8 | 2011 | 104 | |
| 9 | 2014 | 101 | |
| 10 | 2016 | 90 | |
| 11 | 2019 | 88 | |
| 12 | 2020 | 42 | |
| 13 | 2016 | 31 | |
| 14 | 2021 | 29 | |
| 15 | 2022 | 18 | |
| 16 | 2021 | 14 | |
| 17 | 2014 | 12 | |
| 18 | 2013 | 11 | |
| 19 | 2022 | 10 | |
| 20 | 2021 | 10 |
About Jane Carpenter
Jane Carpenter is a scholar working on Genetics, Cancer Research, Pathology and Forensic Medicine, Molecular Biology and Information Systems and Management, having authored 26 papers that have together received 2.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (14 papers), Genomics and Chromatin Dynamics (6 papers), Genetic Associations and Epidemiology (5 papers), Genetic factors in colorectal cancer (4 papers), Cancer Genomics and Diagnostics (3 papers), DNA Repair Mechanisms (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cancer-related Molecular Pathways (2 papers). The work is most often cited by research in Genetics (1.2k citations), Cancer Research (521 citations), Oncology (457 citations), Pathology and Forensic Medicine (254 citations) and Molecular Biology (764 citations). Jane Carpenter has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Christine L. Clarke, Jan Lubiński, Rodney J. Scott, Michelle W. Wong‐Brown, Cliff J. Meldrum, Anna Jakubowska, Steven Alexander Narod, Helena Rudnicka, Matloob Khushi and Rosemary L. Balleine. Their work appears in journals such as Breast Cancer Research, Nature Communications, Nature Genetics, Scientific Reports and Human Molecular 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.