Peter Devilee
Impact in
- Cancer Research top 0.05%
- Cancer Genomics and Diagnostics
- Cancer, Hypoxia, and Metabolism
- Genetics top 0.05%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 130
- BRCA gene mutations in cancer 98
- Genomic variations and chromosomal abnormalities 44
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- DNA Repair Mechanisms 23
- Co-authors
- Fattaneh A. Tavassoli (1 shared paper)Cees J. Cornelisse (66 shared papers)Jean‐Pierre Bayley (24 shared papers)Cornelisse Cj (17 shared papers)Peter E.M. Taschner (9 shared papers)Bert Vogelstein (2 shared papers)Thomas W. Glover (1 shared paper)Stephen Baylin (1 shared paper)
- Journals
- European Journal of Human Genetics (10 papers)International Journal of Cancer (10 papers)Genes Chromosomes and Cancer (10 papers)Human Mutation (9 papers)Journal of Medical Genetics (8 papers)
- Partner nations
- NetherlandsUnited KingdomUnited States
In The Last Decade
Peter Devilee
217 papers receiving 18.1k citations
Peter Devilee's Hit Papers
Peers
Comparison fields: 5 of 154
- Cancer Research 6.6k
- Genetics 6.5k
- Pathology and Forensic Medicine 3.6k
- Oncology 5.2k
- Reproductive Medicine 1.3k
Countries citing papers authored by Peter Devilee
This map shows the geographic impact of Peter Devilee'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 Devilee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Devilee more than expected).
Fields of papers citing papers by Peter Devilee
This network shows the impact of papers produced by Peter Devilee. 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 Devilee. The network helps show where Peter Devilee may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Devilee, 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 220 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in the p53 gene occur in diverse human tumour types Hit paper breakdown → | 1989 | 2370 |
| 2 | Pathology and Genetics of Tumours of the Breast and Female Genital Organs Hit paper breakdown → | 2003 | 2215 |
| 3 | Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma Hit paper breakdown → | 2000 | 1264 |
| 4 | Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk Hit paper breakdown → | 2015 | 579 |
| 5 | SDH5 , a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma Hit paper breakdown → | 2009 | 541 |
| 6 | 1988 | 401 | |
| 7 | 1994 | 340 | |
| 8 | 1998 | 336 | |
| 9 | 1997 | 321 | |
| 10 | 1986 | 299 | |
| 11 | 1987 | 295 | |
| 12 | 1995 | 253 | |
| 13 | 2000 | 225 | |
| 14 | An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage Consortium. | 1995 | 210 |
| 15 | Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes. | 1988 | 207 |
| 16 | 2000 | 186 | |
| 17 | 1989 | 181 | |
| 18 | Amplification of genes within the chromosome 11q13 region is indicative of poor prognosis in patients with operable breast cancer. | 1992 | 175 |
| 19 | Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q. | 1991 | 173 |
| 20 | 1994 | 171 |
About Peter Devilee
Peter Devilee is a scholar working on Genetics, Molecular Biology, Cancer Research, Pathology and Forensic Medicine and Surgery, having authored 220 papers that have together received 18.6k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (98 papers), Genetic factors in colorectal cancer (51 papers), Cancer Genomics and Diagnostics (47 papers), Genomic variations and chromosomal abnormalities (44 papers), Adrenal and Paraganglionic Tumors (36 papers), Cancer, Hypoxia, and Metabolism (29 papers), DNA Repair Mechanisms (23 papers) and Cancer-related Molecular Pathways (21 papers). The work is most often cited by research in Cancer Research (6.6k citations), Genetics (6.5k citations), Pathology and Forensic Medicine (3.6k citations), Oncology (5.2k citations) and Reproductive Medicine (1.3k citations). Peter Devilee has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Fattaneh A. Tavassoli, Cees J. Cornelisse, Jean‐Pierre Bayley, Cornelisse Cj, Peter E.M. Taschner, Bert Vogelstein, Thomas W. Glover, Stephen Baylin, Curtis C. Harris and J. Milburn Jessup. Their work appears in journals such as European Journal of Human Genetics, International Journal of Cancer, Genes Chromosomes and Cancer, Human Mutation 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.