Karin Wadt
Impact in
- Ophthalmology top 1%
- Ocular Oncology and Treatments
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
-
- DNA Repair Mechanisms 8
- Genetics 23
- BRCA gene mutations in cancer 11
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Nicholas K. Hayward (14 shared papers)Anne‐Marie Gerdes (28 shared papers)Lauren G. Aoude (9 shared papers)J Read (1 shared paper)Steffen Heegaard (9 shared papers)Jens Folke Kiilgaard (7 shared papers)Antonia L. Pritchard (5 shared papers)Thomas Mandrup‐Poulsen (2 shared papers)
- Journals
- Familial Cancer (7 papers)PLoS ONE (5 papers)Pigment Cell & Melanoma Research (3 papers)Journal of Medical Genetics (3 papers)Psycho-Oncology (2 papers)
- Partner nations
- DenmarkAustraliaUnited States
In The Last Decade
Karin Wadt
59 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 83
- Ophthalmology 361
- Cancer Research 319
- Oncology 528
- Immunology 298
- Cell Biology 173
Countries citing papers authored by Karin Wadt
This map shows the geographic impact of Karin Wadt'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 Karin Wadt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin Wadt more than expected).
Fields of papers citing papers by Karin Wadt
This network shows the impact of papers produced by Karin Wadt. 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 Karin Wadt. The network helps show where Karin Wadt may publish in the future.
Co-authors
The 25 scholars most cited alongside Karin Wadt, 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 65 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 215 | |
| 2 | 2015 | 143 | |
| 3 | 1998 | 140 | |
| 4 | 2019 | 139 | |
| 5 | 2014 | 99 | |
| 6 | 2012 | 76 | |
| 7 | 2019 | 54 | |
| 8 | 2013 | 46 | |
| 9 | 2015 | 43 | |
| 10 | 1998 | 37 | |
| 11 | 2022 | 36 | |
| 12 | 2015 | 33 | |
| 13 | 2020 | 24 | |
| 14 | 2019 | 20 | |
| 15 | 2020 | 19 | |
| 16 | 2018 | 19 | |
| 17 | 2015 | 18 | |
| 18 | 2022 | 18 | |
| 19 | Novel high risk genes of melanoma | 2017 | 17 |
| 20 | 2019 | 15 |
About Karin Wadt
Karin Wadt is a scholar working on Molecular Biology, Genetics, Cancer Research, Oncology and Pathology and Forensic Medicine, having authored 65 papers that have together received 1.4k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (16 papers), BRCA gene mutations in cancer (11 papers), Cutaneous Melanoma Detection and Management (10 papers), Genetic factors in colorectal cancer (10 papers), Ocular Oncology and Treatments (9 papers), DNA Repair Mechanisms (8 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). The work is most often cited by research in Ophthalmology (361 citations), Cancer Research (319 citations), Oncology (528 citations), Immunology (298 citations) and Cell Biology (173 citations). Karin Wadt has collaborated with scholars based in Denmark, Australia and United States. Frequent co-authors include Nicholas K. Hayward, Anne‐Marie Gerdes, Lauren G. Aoude, J Read, Steffen Heegaard, Jens Folke Kiilgaard, Antonia L. Pritchard, Thomas Mandrup‐Poulsen, Claus M. Larsen and Göran Jönsson. Their work appears in journals such as Familial Cancer, PLoS ONE, Pigment Cell & Melanoma Research, Journal of Medical Genetics 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.