Peter Kraft
Impact in
- Genetics top 0.1%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- BRCA gene mutations in cancer
- Cancer Research top 1%
Papers in
- Genetics 136
- Genetic Associations and Epidemiology 99
- BRCA gene mutations in cancer 33
- Genetic Mapping and Diversity in Plants and Animals 32
- Genetic and phenotypic traits in livestock 21
- Nutrition, Genetics, and Disease 15
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- Bioinformatics and Genomic Networks 21
- Epigenetics and DNA Methylation 14
- Gene expression and cancer classification 13
- Co-authors
- David J. Hunter (65 shared papers)Edward L. Giovannucci (46 shared papers)Stephen J. Chanock (25 shared papers)Charles S. Fuchs (28 shared papers)Susan E. Hankinson (21 shared papers)Marilyn C. Cornelis (9 shared papers)Brian M. Wolpin (28 shared papers)Immaculata De Vivo (18 shared papers)
- Journals
- Cancer Epidemiology Biomarkers & Prevention (29 papers)Genetic Epidemiology (22 papers)Journal of Clinical Oncology (13 papers)The American Journal of Human Genetics (13 papers)Human Molecular Genetics (13 papers)
- Partner nations
- United StatesUnited KingdomSweden
In The Last Decade
Peter Kraft
346 papers receiving 16.5k citations
Peter Kraft's Hit Papers
Peers
Comparison fields: 5 of 192
- Genetics 5.2k
- Cancer Research 1.3k
- Aging 150
- Oncology 1.7k
- Hematology 719
Countries citing papers authored by Peter Kraft
This map shows the geographic impact of Peter Kraft'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 Peter Kraft with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Kraft more than expected).
Fields of papers citing papers by Peter Kraft
This network shows the impact of papers produced by Peter Kraft. 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 Peter Kraft. The network helps show where Peter Kraft may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Kraft, 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 351 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 429 | |
| 2 | Methodological Challenges in Mendelian Randomization Hit paper breakdown → | 2014 | 357 |
| 3 | 2008 | 345 | |
| 4 | The NLRP3 inflammasome drives inflammation in ischemia/reperfusion injury after transient middle cerebral artery occlusion in mice Hit paper breakdown → | 2020 | 297 |
| 5 | 2014 | 296 | |
| 6 | 2007 | 294 | |
| 7 | 2009 | 290 | |
| 8 | 2009 | 285 | |
| 9 | 2009 | 280 | |
| 10 | 2012 | 274 | |
| 11 | 2007 | 269 | |
| 12 | 2009 | 251 | |
| 13 | 2009 | 213 | |
| 14 | 2009 | 188 | |
| 15 | 2009 | 185 | |
| 16 | 2009 | 183 | |
| 17 | 2008 | 178 | |
| 18 | 2013 | 168 | |
| 19 | 2015 | 155 | |
| 20 | 2009 | 148 |
About Peter Kraft
Peter Kraft is a scholar working on Genetics, Molecular Biology, Oncology, Epidemiology and Pulmonary and Respiratory Medicine, having authored 351 papers that have together received 16.8k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (99 papers), BRCA gene mutations in cancer (33 papers), Genetic Mapping and Diversity in Plants and Animals (32 papers), Genetic and phenotypic traits in livestock (21 papers), Bioinformatics and Genomic Networks (21 papers), Nutrition, Genetics, and Disease (15 papers), Epigenetics and DNA Methylation (14 papers) and Gene expression and cancer classification (13 papers). The work is most often cited by research in Genetics (5.2k citations), Cancer Research (1.3k citations), Aging (150 citations), Oncology (1.7k citations) and Hematology (719 citations). Peter Kraft has collaborated with scholars based in United States, United Kingdom and Sweden. Frequent co-authors include David J. Hunter, Edward L. Giovannucci, Stephen J. Chanock, Charles S. Fuchs, Susan E. Hankinson, Marilyn C. Cornelis, Brian M. Wolpin, Immaculata De Vivo, Sara Lindström and Constance Chen. Their work appears in journals such as Cancer Epidemiology Biomarkers & Prevention, Genetic Epidemiology, Journal of Clinical Oncology, The American Journal of Human Genetics 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.