Thilo Dörk
Impact in
- Genetics top 0.05%
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Cancer Research top 0.5%
- Breast Cancer Treatment Studies
Papers in
- Genetics 169
- BRCA gene mutations in cancer 96
- Genetic Associations and Epidemiology 69
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- Ovarian cancer diagnosis and treatment 22
- Co-authors
- Francisco Ernesto Baralle (2 shared papers)Emanuele Buratti (2 shared papers)Natalia Viktorovna Bogdanova (40 shared papers)Regina Bendix (7 shared papers)Peter Hillemanns (30 shared papers)Franco Pagani (1 shared paper)Maurizio Romano (1 shared paper)Johann Hinrich Karstens (18 shared papers)
- Journals
- Nature Genetics (25 papers)Human Molecular Genetics (19 papers)Cancer Epidemiology Biomarkers & Prevention (17 papers)Human Mutation (15 papers)Journal of Medical Genetics (14 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
Thilo Dörk
397 papers receiving 27.4k citations
Thilo Dörk's Hit Papers
Peers
Comparison fields: 5 of 182
- Genetics 9.2k
- Cancer Research 1.4k
- Reproductive Medicine 1.0k
- Oncology 1.3k
- Pulmonary and Respiratory Medicine 1.9k
Countries citing papers authored by Thilo Dörk
This map shows the geographic impact of Thilo Dörk'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 Thilo Dörk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thilo Dörk more than expected).
Fields of papers citing papers by Thilo Dörk
This network shows the impact of papers produced by Thilo Dörk. 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 Thilo Dörk. The network helps show where Thilo Dörk may publish in the future.
Co-authors
The 25 scholars most cited alongside Thilo Dörk, 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 403 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genome-wide association study identifies novel breast cancer susceptibility loci Hit paper breakdown → | 2007 | 1919 |
| 2 | Association analysis identifies 65 new breast cancer risk loci Hit paper breakdown → | 2017 | 1040 |
| 3 | Large-scale genotyping identifies 41 new loci associated with breast cancer risk Hit paper breakdown → | 2013 | 913 |
| 4 | Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk Hit paper breakdown → | 2015 | 859 |
| 5 | Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes Hit paper breakdown → | 2018 | 775 |
| 6 | RAD51B in Familial Breast Cancer Hit paper breakdown → | 2016 | 641 |
| 7 | 2014 | 610 | |
| 8 | 2010 | 575 | |
| 9 | 2001 | 536 | |
| 10 | Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer Hit paper breakdown → | 2015 | 489 |
| 11 | 2007 | 486 | |
| 12 | Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer Hit paper breakdown → | 2013 | 468 |
| 13 | Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants Hit paper breakdown → | 2015 | 450 |
| 14 | 2009 | 408 | |
| 15 | Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer Hit paper breakdown → | 2017 | 368 |
| 16 | 2009 | 354 | |
| 17 | 2013 | 349 | |
| 18 | Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer Hit paper breakdown → | 2015 | 349 |
| 19 | 2015 | 324 | |
| 20 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses Hit paper breakdown → | 2020 | 321 |
About Thilo Dörk
Thilo Dörk is a scholar working on Genetics, Reproductive Medicine, Pulmonary and Respiratory Medicine, Oncology and Endocrine and Autonomic Systems, having authored 403 papers that have together received 27.9k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (96 papers), Genetic Associations and Epidemiology (69 papers), Cystic Fibrosis Research Advances (42 papers), Ovarian cancer diagnosis and treatment (22 papers), DNA Repair Mechanisms (16 papers), Cancer Risks and Factors (9 papers), Cervical Cancer and HPV Research (8 papers) and Neuroscience of respiration and sleep (7 papers). The work is most often cited by research in Genetics (9.2k citations), Cancer Research (1.4k citations), Reproductive Medicine (1.0k citations), Oncology (1.3k citations) and Pulmonary and Respiratory Medicine (1.9k citations). Thilo Dörk has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Francisco Ernesto Baralle, Emanuele Buratti, Natalia Viktorovna Bogdanova, Regina Bendix, Peter Hillemanns, Franco Pagani, Maurizio Romano, Johann Hinrich Karstens, Manfred Stuhrmann and Burkhard Tümmler. Their work appears in journals such as Nature Genetics, Human Molecular Genetics, Cancer Epidemiology Biomarkers & Prevention, 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.