Thilo Dörk
Impact in
- Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
- Genetics top 2%
- BRCA gene mutations in cancer
Papers in
-
- DNA Repair Mechanisms 47
-
- Cystic Fibrosis Research Advances 33
- Neonatal Respiratory Health Research 18
- Tracheal and airway disorders 13
- Co-authors
- Francisco E. Baralle (2 shared papers)Emanuele Buratti (2 shared papers)Natalia Bogdanova (36 shared papers)Maurizio Romano (1 shared paper)Peter Hillemanns (26 shared papers)Michael Bremer (19 shared papers)Johann H. Karstens (16 shared papers)Manfred Stuhrmann (10 shared papers)
- Journals
- Human Mutation (11 papers)Breast Cancer Research and Treatment (8 papers)International Journal of Legal Medicine (7 papers)Human Genetics (5 papers)Human Molecular Genetics (5 papers)
- Partner nations
- GermanyUnited StatesBelarus
In The Last Decade
Thilo Dörk
157 papers receiving 5.1k citations
Thilo Dörk's Hit Papers
Peers
Comparison fields: 5 of 125
- Cancer Research 769
- Genetics 432
- Genetics 1.1k
- Pulmonary and Respiratory Medicine 1.1k
- Molecular Biology 2.3k
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 162 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Nuclear factor TDP‐43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping Hit paper breakdown → | 2001 | 517 |
| 2 | 1997 | 190 | |
| 3 | 2009 | 190 | |
| 4 | 2002 | 176 | |
| 5 | 2002 | 144 | |
| 6 | 2003 | 125 | |
| 7 | Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients. | 2001 | 123 |
| 8 | 2007 | 110 | |
| 9 | 2009 | 110 | |
| 10 | A novel donor splice site in intron 11 of the CFTR gene, created by mutation 1811+1.6kbA-->G, produces a new exon: high frequency in Spanish cystic fibrosis chromosomes and association with severe phenotype. | 1995 | 98 |
| 11 | 2019 | 90 | |
| 12 | 2017 | 84 | |
| 13 | 1993 | 79 | |
| 14 | 2004 | 75 | |
| 15 | 2005 | 73 | |
| 16 | 1994 | 72 | |
| 17 | 2004 | 70 | |
| 18 | 2011 | 70 | |
| 19 | 2002 | 68 | |
| 20 | 2000 | 68 |
About Thilo Dörk
Thilo Dörk is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine, Genetics, Cancer Research and Oncology, having authored 162 papers that have together received 5.1k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (47 papers), Cystic Fibrosis Research Advances (33 papers), BRCA gene mutations in cancer (30 papers), Neonatal Respiratory Health Research (18 papers), Carcinogens and Genotoxicity Assessment (15 papers), Tracheal and airway disorders (13 papers), Cancer Genomics and Diagnostics (12 papers) and Cancer-related Molecular Pathways (12 papers). The work is most often cited by research in Cancer Research (769 citations), Genetics (432 citations), Genetics (1.1k citations), Pulmonary and Respiratory Medicine (1.1k citations) and Molecular Biology (2.3k citations). Thilo Dörk has collaborated with scholars based in Germany, United States and Belarus. Frequent co-authors include Francisco E. Baralle, Emanuele Buratti, Natalia Bogdanova, Maurizio Romano, Peter Hillemanns, Michael Bremer, Johann H. Karstens, Manfred Stuhrmann, Martin F. Lavin and Manfred Stuhrmann. Their work appears in journals such as Human Mutation, Breast Cancer Research and Treatment, International Journal of Legal Medicine, Human Genetics and Human Molecular 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.