Senno Verhoef
Impact in
- Genetics top 1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 38
- BRCA gene mutations in cancer 29
- Genomic variations and chromosomal abnormalities 14
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- Cancer Genomics and Diagnostics 18
- Co-authors
- Frans B.L. Hogervorst (10 shared papers)Petra M. Nederlof (6 shared papers)Dick Lindhout (10 shared papers)Dicky Halley (7 shared papers)Margreet G.E.M. Ausems (17 shared papers)Mark Nellist (7 shared papers)Laura J. van’t Veer (8 shared papers)Bernard A. Zonnenberg (3 shared papers)
- Journals
- Familial Cancer (8 papers)Journal of Medical Genetics (8 papers)European Journal of Human Genetics (6 papers)Breast Cancer Research and Treatment (5 papers)Psycho-Oncology (2 papers)
- Partner nations
- NetherlandsUnited KingdomUnited States
In The Last Decade
Senno Verhoef
67 papers receiving 3.0k citations
Peers
Comparison fields: 5 of 126
- Genetics 1.3k
- Cancer Research 629
- Oncology 907
- Reproductive Medicine 268
- Physiology 696
Countries citing papers authored by Senno Verhoef
This map shows the geographic impact of Senno Verhoef'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 Senno Verhoef with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Senno Verhoef more than expected).
Fields of papers citing papers by Senno Verhoef
This network shows the impact of papers produced by Senno Verhoef. 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 Senno Verhoef. The network helps show where Senno Verhoef may publish in the future.
Co-authors
The 25 scholars most cited alongside Senno Verhoef, 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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 344 | |
| 2 | Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method. | 2003 | 247 |
| 3 | 2005 | 178 | |
| 4 | 2015 | 133 | |
| 5 | 2005 | 124 | |
| 6 | 1999 | 121 | |
| 7 | 2008 | 109 | |
| 8 | 1994 | 105 | |
| 9 | 1999 | 105 | |
| 10 | 2005 | 101 | |
| 11 | 1999 | 82 | |
| 12 | 2009 | 77 | |
| 13 | 2010 | 75 | |
| 14 | 2006 | 73 | |
| 15 | 2001 | 71 | |
| 16 | 2009 | 66 | |
| 17 | 2010 | 63 | |
| 18 | 2013 | 62 | |
| 19 | 2005 | 60 | |
| 20 | 2010 | 53 |
About Senno Verhoef
Senno Verhoef is a scholar working on Genetics, Cancer Research, Molecular Biology, Oncology and Pathology and Forensic Medicine, having authored 67 papers that have together received 3.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (29 papers), Cancer Genomics and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (14 papers), Tuberous Sclerosis Complex Research (13 papers), Genetic factors in colorectal cancer (11 papers), Cancer-related Molecular Pathways (7 papers), Polyomavirus and related diseases (5 papers) and Epigenetics and DNA Methylation (5 papers). The work is most often cited by research in Genetics (1.3k citations), Cancer Research (629 citations), Oncology (907 citations), Reproductive Medicine (268 citations) and Physiology (696 citations). Senno Verhoef has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Frans B.L. Hogervorst, Petra M. Nederlof, Dick Lindhout, Dicky Halley, Margreet G.E.M. Ausems, Mark Nellist, Laura J. van’t Veer, Bernard A. Zonnenberg, Ans van den Ouweland and Simon A. Joosse. Their work appears in journals such as Familial Cancer, Journal of Medical Genetics, European Journal of Human Genetics, Breast Cancer Research and Treatment and Psycho-Oncology.
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.