Thilo Dörk

34.5k total citations
161 papers, 4.7k citations indexed

About

Thilo Dörk is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Thilo Dörk has authored 161 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 83 papers in Molecular Biology, 53 papers in Pulmonary and Respiratory Medicine and 47 papers in Genetics. Recurrent topics in Thilo Dörk's work include DNA Repair Mechanisms (56 papers), BRCA gene mutations in cancer (34 papers) and Cystic Fibrosis Research Advances (32 papers). Thilo Dörk is often cited by papers focused on DNA Repair Mechanisms (56 papers), BRCA gene mutations in cancer (34 papers) and Cystic Fibrosis Research Advances (32 papers). Thilo Dörk collaborates with scholars based in Germany, United States and Belarus. Thilo Dörk's co-authors include Natalia Bogdanova, Michael Bremer, Peter Hillemanns, Johann H. Karstens, Manfred Stuhrmann, Martin F. Lavin, Manfred Stuhrmann, Olaf Dammann, Burkhard Tümmler and Britta Wieland and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nucleic Acids Research.

In The Last Decade

Thilo Dörk

153 papers receiving 4.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Thilo Dörk Germany 40 2.5k 1.3k 1.3k 1.0k 995 161 4.7k
Dietrich von Schweinitz Germany 46 3.2k 1.3× 596 0.5× 754 0.6× 1.5k 1.5× 1.3k 1.3× 189 6.8k
Tommy Martinsson Sweden 49 3.3k 1.3× 1.0k 0.8× 497 0.4× 1.1k 1.1× 1.3k 1.3× 202 6.3k
Susanne M. Gollin United States 48 4.4k 1.8× 1.3k 1.0× 549 0.4× 2.0k 2.0× 1.6k 1.6× 141 7.2k
Carl W. Miller United States 41 2.8k 1.1× 617 0.5× 569 0.5× 1.7k 1.6× 665 0.7× 90 4.7k
Jiexin Zhang United States 29 2.2k 0.9× 504 0.4× 603 0.5× 699 0.7× 704 0.7× 66 3.4k
Neil V. Morgan United Kingdom 42 3.0k 1.2× 1.0k 0.8× 1.2k 0.9× 505 0.5× 1.0k 1.0× 109 5.7k
Colin C. Pritchard United States 22 4.1k 1.7× 719 0.6× 716 0.6× 1.2k 1.2× 3.6k 3.6× 41 6.1k
Shai Izraeli Israel 42 2.6k 1.1× 583 0.5× 433 0.3× 885 0.9× 972 1.0× 176 5.7k
K. Czerwenka Austria 41 1.5k 0.6× 567 0.4× 557 0.4× 1.3k 1.2× 646 0.6× 179 4.6k
Kathleen Claes Belgium 34 1.6k 0.6× 836 0.7× 512 0.4× 516 0.5× 697 0.7× 124 3.5k

Countries citing papers authored by Thilo Dörk

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Thilo Dörk

This figure shows the co-authorship network connecting the top 25 collaborators of Thilo Dörk. A scholar is included among the top collaborators of Thilo Dörk based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Thilo Dörk. Thilo Dörk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ramachandran, Dhanya, Peter Schürmann, Robert Geffers, et al.. (2024). Germline variants of homology‐directed repair or mismatch repair genes in cervical cancer. International Journal of Cancer. 156(4). 700–710. 1 indexed citations
2.
3.
Qu, Dong, et al.. (2023). Revisiting the association of sudden infant death syndrome (SIDS) with polymorphisms of NHE3 and IL13. International Journal of Legal Medicine. 138(3). 743–749. 2 indexed citations
4.
Qu, Dong, Peter Schürmann, Thomas Rothämel, Thilo Dörk, & Michael Klintschar. (2022). Variants in genes encoding the SUR1-TRPM4 non-selective cation channel and sudden infant death syndrome (SIDS): potentially increased risk for cerebral edema. International Journal of Legal Medicine. 136(4). 1113–1120. 5 indexed citations
5.
Schürmann, Peter, et al.. (2021). Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS). International Journal of Legal Medicine. 135(4). 1499–1506. 5 indexed citations
6.
Schürmann, Peter, et al.. (2020). Genetic association study of fatal pulmonary embolism. International Journal of Legal Medicine. 135(1). 143–151. 5 indexed citations
7.
Schürmann, Peter, et al.. (2019). Evidence for an association of interferon gene variants with sudden infant death syndrome. International Journal of Legal Medicine. 133(3). 863–869. 10 indexed citations
8.
Schröder, Claudia, Georgios Sogkas, Manfred Fliegauf, et al.. (2019). Late-Onset Antibody Deficiency Due to Monoallelic Alterations in NFKB1. Frontiers in Immunology. 10. 2618–2618. 28 indexed citations
9.
Klapdor, Rüdiger, Shuo Wang, Ulrich Hacker, et al.. (2017). Improved Killing of Ovarian Cancer Stem Cells by Combining a Novel Chimeric Antigen Receptor–Based Immunotherapy and Chemotherapy. Human Gene Therapy. 28(10). 886–896. 81 indexed citations
10.
Rothämel, Thomas, Peter Schürmann, Matthias Arnold, et al.. (2016). Candidate gene variants of the immune system and sudden infant death syndrome. International Journal of Legal Medicine. 130(4). 1025–1033. 15 indexed citations
11.
Kostovska, Ivana Maleva, Jing Wang, Natalia Bogdanova, et al.. (2016). Rare ATAD5 missense variants in breast and ovarian cancer patients. Cancer Letters. 376(1). 173–177. 21 indexed citations
12.
Bogdanova, Natalia, Britta Wieland, Tjoung-Won Park-Simon, et al.. (2014). Functional deficiency of NBN, the Nijmegen breakage syndrome protein, in a p.R215W mutant breast cancer cell line. BMC Cancer. 14(1). 434–434. 11 indexed citations
13.
Hille, Ulrike E., Philipp Soergel, Liza Makowski, Thilo Dörk, & Peter Hillemanns. (2012). Lymphedema of the Breast as a Symptom of Internal Diseases or Side Effect of mTor Inhibitors. Lymphatic Research and Biology. 10(2). 63–73. 10 indexed citations
14.
Gatei, Magtouf, Burkhard Jakob, Philip Chen, et al.. (2011). ATM Protein-dependent Phosphorylation of Rad50 Protein Regulates DNA Repair and Cell Cycle Control. Journal of Biological Chemistry. 286(36). 31542–31556. 70 indexed citations
15.
Meyer, Andreas, Natalia Bogdanova, Natalia Dubrowinskaja, et al.. (2011). Apoptosis gene polymorphisms and risk of prostate cancer: A hospital-based study of German patients treated with brachytherapy. Urologic Oncology Seminars and Original Investigations. 31(1). 74–81. 24 indexed citations
16.
Schmalhorst, Philipp S., et al.. (2009). A Single UDP-galactofuranose Transporter Is Required for Galactofuranosylation in Aspergillus fumigatus. Journal of Biological Chemistry. 284(49). 33859–33868. 55 indexed citations
17.
Stanke, Frauke, Manfred Ballmann, Inez Bronsveld, et al.. (2008). Diversity of the basic defect of homozygous CFTR mutation genotypes in humans. Journal of Medical Genetics. 45(1). 47–54. 30 indexed citations
18.
Scott, Shaun P., et al.. (2002). Missense mutations but not allelic variants alter the function of ATM by dominant interference in patients with breast cancer. Proceedings of the National Academy of Sciences. 99(2). 925–930. 143 indexed citations
19.
Dörk, Thilo & Manfred Stuhrmann. (1998). Polymorphisms of the humanβ-defensin-1gene. Molecular and Cellular Probes. 12(3). 171–173. 49 indexed citations
20.
Dörk, Thilo, et al.. (1993). A donor splice mutation (405 + 1 G → A) in cystic fibrosis associated with exon skipping in epithelial CFTR mRNA. Human Molecular Genetics. 2(11). 1965–1966. 11 indexed citations

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.

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