Pål Møller
Impact in
- Pathology and Forensic Medicine top 0.2%
- Genetic factors in colorectal cancer
- Reproductive Medicine top 0.5%
- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 114
- BRCA gene mutations in cancer 99
- Genomic variations and chromosomal abnormalities 22
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- Genetic factors in colorectal cancer 53
- Co-authors
- Ketil Heimdal (35 shared papers)Ragnhild Husby (1 shared paper)Steven A. Narod (27 shared papers)Lovise Mæhle (38 shared papers)Jan Lubiński (26 shared papers)Henry T. Lynch (22 shared papers)Hans F. A. Vasen (22 shared papers)William D. Foulkes (21 shared papers)
- Journals
- Clinical Genetics (15 papers)Scandinavian Journal of Rheumatology (14 papers)Disease Markers (12 papers)Familial Cancer (10 papers)European Journal of Cancer (9 papers)
- Partner nations
- NorwayUnited StatesCanada
In The Last Decade
Pål Møller
176 papers receiving 6.5k citations
Pål Møller's Hit Papers
Peers
Comparison fields: 5 of 120
- Pathology and Forensic Medicine 2.6k
- Reproductive Medicine 1.2k
- Cancer Research 1.9k
- Genetics 3.3k
- Oncology 2.3k
Countries citing papers authored by Pål Møller
This map shows the geographic impact of Pål Møller'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 Pål Møller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pål Møller more than expected).
Fields of papers citing papers by Pål Møller
This network shows the impact of papers produced by Pål Møller. 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 Pål Møller. The network helps show where Pål Møller may publish in the future.
Co-authors
The 25 scholars most cited alongside Pål Møller, 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 181 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history. Hit paper breakdown → | 1993 | 673 |
| 2 | 2000 | 354 | |
| 3 | 2005 | 304 | |
| 4 | 2001 | 280 | |
| 5 | 2008 | 261 | |
| 6 | 1997 | 209 | |
| 7 | 2012 | 178 | |
| 8 | 1997 | 172 | |
| 9 | 2006 | 154 | |
| 10 | 2020 | 145 | |
| 11 | 2000 | 140 | |
| 12 | 2007 | 135 | |
| 13 | 2008 | 134 | |
| 14 | 2008 | 132 | |
| 15 | 2019 | 102 | |
| 16 | 2013 | 102 | |
| 17 | 2018 | 99 | |
| 18 | 2008 | 96 | |
| 19 | 1990 | 95 | |
| 20 | 2007 | 94 |
About Pål Møller
Pål Møller is a scholar working on Genetics, Pathology and Forensic Medicine, Cancer Research, Molecular Biology and Oncology, having authored 181 papers that have together received 6.8k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (99 papers), Genetic factors in colorectal cancer (53 papers), Cancer Genomics and Diagnostics (46 papers), Ovarian cancer diagnosis and treatment (30 papers), Spondyloarthritis Studies and Treatments (23 papers), Genomic variations and chromosomal abnormalities (22 papers), Colorectal Cancer Screening and Detection (16 papers) and DNA Repair Mechanisms (14 papers). The work is most often cited by research in Pathology and Forensic Medicine (2.6k citations), Reproductive Medicine (1.2k citations), Cancer Research (1.9k citations), Genetics (3.3k citations) and Oncology (2.3k citations). Pål Møller has collaborated with scholars based in Norway, United States and Canada. Frequent co-authors include Ketil Heimdal, Ragnhild Husby, Steven A. Narod, Lovise Mæhle, Jan Lubiński, Henry T. Lynch, Hans F. A. Vasen, William D. Foulkes, Ping Sun and Charmaine Kim‐Sing. Their work appears in journals such as Clinical Genetics, Scandinavian Journal of Rheumatology, Disease Markers, Familial Cancer and European Journal of Cancer.
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.