Thilo Dörk

34.5k citations

161 papers · 4.7k indexed · h-index 40

Impact in

Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
- Cancer Genomics and Diagnostics
Genetics top 1%
- BRCA gene mutations in cancer

Papers in ⓘ

Cancer Research 39
- Carcinogens and Genotoxicity Assessment 18
- Cancer Genomics and Diagnostics 14
Genetics 47
- BRCA gene mutations in cancer 34

Co-authors: Natalia Bogdanova (36 shared papers)Michael Bremer (19 shared papers)Peter Hillemanns (26 shared papers)Johann H. Karstens (16 shared papers)Manfred Stuhrmann (10 shared papers)Martin F. Lavin (7 shared papers)Manfred Stuhrmann (5 shared papers)Olaf Dammann (8 shared papers)
Journals: Human Mutation (11 papers)Breast Cancer Research and Treatment (8 papers)International Journal of Legal Medicine (7 papers)Radiotherapy and Oncology (6 papers)International Journal of Cancer (5 papers)
Partner nations: Germany United States Belarus

In The Last Decade

Thilo Dörk

153 papers receiving 4.6k citations

Peers

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-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.

Border = papers with Thilo Dörk Line = papers co-authored together Thilo Dörk links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 161 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens Human Genetics ·Thilo Dörk, Bernd Dworniczak, C. Aulehla‐Scholz, Dagmar Wieczorek, Ingolf Böhm, A Mayerová, H. H. Seydewitz, Eberhard Nieschlag, Dieter Meschede, Jürgen Horst, Hans-Jürgen Pander, H. Sperling, Félix Ratjen, Eberhard Passarge, Jörg Schmidtke, Manfred Stuhrmann	1997	190
2	Human RAD50 Deficiency in a Nijmegen Breakage Syndrome-like Disorder The American Journal of Human Genetics ·Regina Waltes, Reinhard Kalb, Magtouf Gatei, Amanda W. Kijas, Markus Stümm, Alexandra Sobeck, Britta Wieland, Raymonda Varon, Yaniv Lerenthal, Martin F. Lavin, Detlev Schindler, Thilo Dörk	2009	189
3	A new type of mutation causes a splicing defect in ATM Nature Genetics ·(unknown), Emanuele Buratti, Cristiana Stuani, Regina Bendix, Thilo Dörk, Francisco E. Baralle	2002	175
4	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 ·Shaun P. Scott, Regina Bendix, Philip Chen, Raymond Clark, Thilo Dörk, Martin F. Lavin	2002	143
5	Spectrum of ATM gene mutations in a hospital-based series of unselected breast cancer patients. PubMed ·Thilo Dörk, Regina Bendix, M. Bremer, Dirk Rades, Karin Klöpper, Marion Nicke, Britta Skawran, Andreas Hector, P Yamini, Diana Steinmann, Susanne Weise, Manfred Stuhrmann, Johann H. Karstens	2001	123
6	Nonclassical splicing mutations in the coding and noncoding regions of the ATM Gene: Maximum entropy estimates of splice junction strengths Human Mutation ·Laura Eng, Gabriela Coutinho, Shareef Nahas, G Yeo, Robert Tanouye, Mahnoush Babaei, Thilo Dörk, Christopher B. Burge, Richard A. Gatti	2003	122
7	Nijmegen Breakage Syndrome mutations and risk of breast cancer International Journal of Cancer ·Natalia Bogdanova, Sergei Feshchenko, Peter Schürmann, Regina Waltes, Britta Wieland, Peter Hillemanns, Yuriy Rogov, Olaf Dammann, Michael Bremer, Johann H. Karstens, Christof Sohn, Raymonda Varon, Thilo Dörk	2007	110
8	Immaturity, perinatal inflammation, and retinopathy of prematurity: A multi-hit hypothesis Early Human Development ·Olaf Dammann, Maria-Jantje Brinkhaus, Dorothee B. Bartels, Michael Dördelmann, Frank Dressler, Julia Kerk, Thilo Dörk, Christiane E.L. Dammann	2009	109
9	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. PubMed ·Miguel Chillón, Thilo Dörk, Teresa Casals, Juliette Gimenez, Núria Fonknechten, Katrin Will, Daniela Fernandes Ramos, Virginia Nunes, Xavier Estivill	1995	98
10	Indicators of late normal tissue response after radiotherapy for head and neck cancer: fibroblasts, lymphocytes, genetics, DNA repair, and chromosome aberrations Radiotherapy and Oncology ·Kerstin Borgmann, Barbara Röper, R A El-Awady, Sophie Brackrock, Maika Bigalke, Thilo Dörk, Winfried Alberti, Ekkehard Dikomey, Jochen Dahm‐Daphi	2002	91
11	Characterization of a Novel Third-Generation Anti-CD24-CAR against Ovarian Cancer International Journal of Molecular Sciences ·Rüdiger Klapdor, Shuo Wang, Michael Morgan, Thilo Dörk, Ulrich Hacker, Peter Hillemanns, Hildegard Büning, Axel Schambach	2019	87
12	Improved Killing of Ovarian Cancer Stem Cells by Combining a Novel Chimeric Antigen Receptor–Based Immunotherapy and Chemotherapy Human Gene Therapy ·Rüdiger Klapdor, Shuo Wang, Ulrich Hacker, Hildegard Büning, Michael Morgan, Thilo Dörk, Peter Hillemanns, Axel Schambach	2017	81
13	Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis The Lancet ·Peter Kubesch, Thilo Dörk, Ulrich Wulbrand, Nanette Kälin, Thomas Neumann, Brigitte Wulf, B. Tümmler, Heinz Geerlings, H. Weißbrodt, H. von der Hardt	1993	79
14	ATM polymorphisms as risk factors for prostate cancer development British Journal of Cancer ·Sandra Angèle, Alison Falconer, S M Edwards, Thilo Dörk, M. Bremer, Norman Moullan, Brigitte Chapot, Kenneth Muir, Richard S. Houlston, A. Norman, Sarah Bullock, Questa Hope, J.C. Meitz-Hopkins, David Dearnaley, Anna Dowe, Christine Southgate, Audrey Ardern‐Jones, Douglas F. Easton, Rosalind A. Eeles, J. Hall	2004	75
15	Association of two mutations in the CHEK2 gene with breast cancer International Journal of Cancer ·Natalia Bogdanova, Natalia Enβen‐Dubrowinskaja, Sergei Feshchenko, G. I. Lazjuk, Yuriy Rogov, Olaf Dammann, Michael Bremer, Johann H. Karstens, Christof Sohn, Thilo Dörk	2005	73
16	Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients Human Genetics ·Thilo Dörk, Frauke Mekus, Karen Schmidt, Jutta Boßhammer, Rainer Fislage, Thomas Heuer, Violetta Dziadek, Thomas Neumann, Nanette Kälin, Ulrich Wulbrand, Brigitte Wulf, H. von der Hardt, Günther Maaß, Burkhard Tümmler	1994	71
17	ATM Protein-dependent Phosphorylation of Rad50 Protein Regulates DNA Repair and Cell Cycle Control Journal of Biological Chemistry ·Magtouf Gatei, Burkhard Jakob, Philip Chen, Amanda W. Kijas, Olivier J. Bécherel, Nuri Gueven, Geoffrey W. Birrell, Ji‐Hoon Lee, Tanya T. Paull, Yaniv Lerenthal, Shazrul Fazry, G. Taucher-Scholz, Reinhard Kalb, Detlev Schindler, Regina Waltes, Thilo Dörk, Martin F. Lavin	2011	70
18	Functional consequences of ATM sequence variants for chromosomal radiosensitivity Genes Chromosomes and Cancer ·Sara Gutiérrez‐Enríquez, Marie Fernet, Thilo Dörk, Michael Bremer, Anthony Laugé, Dominique Stoppa‐Lyonnet, Norman Moullan, Sandra Angèle, Janet Hall	2004	70
19	CFTR gene mutations and male infertility Andrologia ·Manfred Stuhrmann, Thilo Dörk	2000	68
20	Radiosensitivity of Ataxia Telangiectasia and Nijmegen Breakage Syndrome Homozygotes and Heterozygotes as Determined by Three-Color FISH Chromosome Painting Radiation Research ·Susann Neubauer, Rouben Arutyunyan, Markus Stümm, Thilo Dörk, Regina Bendix, Michael Bremer, Raymonda Varon, Rolf Sauer, Erich Gebhart	2002	68

About Thilo Dörk

Thilo Dörk is a scholar working on Cancer Research, Genetics, Pulmonary and Respiratory Medicine, Endocrine and Autonomic Systems and Molecular Biology, having authored 161 papers that have together received 4.7k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (56 papers), BRCA gene mutations in cancer (34 papers), Cystic Fibrosis Research Advances (32 papers), Neonatal Respiratory Health Research (24 papers), Carcinogens and Genotoxicity Assessment (18 papers), Cancer-related Molecular Pathways (16 papers), Tracheal and airway disorders (15 papers) and Cancer Genomics and Diagnostics (14 papers). The work is most often cited by research in Cancer Research (995 citations), Genetics (1.3k citations), Pulmonary and Respiratory Medicine (1.3k citations), Oncology (1.0k citations) and Molecular Biology (2.5k citations). Thilo Dörk has collaborated with scholars based in Germany, United States and Belarus. Frequent 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. Their work appears in journals such as Human Mutation, Breast Cancer Research and Treatment, International Journal of Legal Medicine, Radiotherapy and Oncology and International 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.

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