Dorothea Gadzicki

3.3k total citations
30 papers, 913 citations indexed

About

Dorothea Gadzicki is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Dorothea Gadzicki has authored 30 papers receiving a total of 913 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Hematology. Recurrent topics in Dorothea Gadzicki's work include BRCA gene mutations in cancer (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and DNA Repair Mechanisms (5 papers). Dorothea Gadzicki is often cited by papers focused on BRCA gene mutations in cancer (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and DNA Repair Mechanisms (5 papers). Dorothea Gadzicki collaborates with scholars based in Germany, United Kingdom and France. Dorothea Gadzicki's co-authors include Brigitte Schlegelberger, Alfons Meindl, Tim Ripperger, Manfred Stuhrmann, Kirsten Müller‐Vahl, Christoph Engel, Rita K. Schmutzler, Karin Kast, Ulrich Bick and Kerstin Rhiem and has published in prestigious journals such as Journal of Clinical Oncology, Blood and International Journal of Cancer.

In The Last Decade

Dorothea Gadzicki

29 papers receiving 892 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dorothea Gadzicki Germany 14 494 294 292 192 161 30 913
Omar Khalid United States 16 204 0.4× 183 0.6× 620 2.1× 216 1.1× 51 0.3× 22 930
Krishna Krithivas United States 10 466 0.9× 156 0.5× 1.0k 3.5× 184 1.0× 76 0.5× 14 1.6k
Agnès Hardouin France 13 333 0.7× 136 0.5× 392 1.3× 218 1.1× 117 0.7× 25 778
José Cláudio Casali da Rocha Brazil 13 139 0.3× 162 0.6× 295 1.0× 220 1.1× 126 0.8× 45 704
Yvonne Wallis United Kingdom 15 319 0.6× 170 0.6× 507 1.7× 198 1.0× 229 1.4× 26 1.1k
Paul Smyth Ireland 18 80 0.2× 479 1.6× 622 2.1× 141 0.7× 116 0.7× 36 1.0k
Ruthann I. Blough United States 13 187 0.4× 63 0.2× 388 1.3× 120 0.6× 66 0.4× 19 671
Din‐Lii Lin United States 9 183 0.4× 91 0.3× 381 1.3× 212 1.1× 36 0.2× 13 730
Monica Taborelli Italy 15 173 0.4× 92 0.3× 194 0.7× 189 1.0× 242 1.5× 23 753
Marius C. Jones United Kingdom 10 166 0.3× 155 0.5× 426 1.5× 76 0.4× 34 0.2× 10 908

Countries citing papers authored by Dorothea Gadzicki

Since Specialization
Citations

This map shows the geographic impact of Dorothea Gadzicki'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 Dorothea Gadzicki with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dorothea Gadzicki more than expected).

Fields of papers citing papers by Dorothea Gadzicki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dorothea Gadzicki. 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 Dorothea Gadzicki. The network helps show where Dorothea Gadzicki may publish in the future.

Co-authorship network of co-authors of Dorothea Gadzicki

This figure shows the co-authorship network connecting the top 25 collaborators of Dorothea Gadzicki. A scholar is included among the top collaborators of Dorothea Gadzicki 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 Dorothea Gadzicki. Dorothea Gadzicki 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.
Rhiem, Kerstin, Christoph Engel, Monika Graeser, et al.. (2012). The risk of contralateral breast cancer in patients from BRCA1/2 negative high risk families as compared to patients from BRCA1 or BRCA2 positive families: a retrospective cohort study. Breast Cancer Research. 14(6). R156–R156. 76 indexed citations
2.
Penkert, Judith, Brigitte Schlegelberger, Doris Steinemann, & Dorothea Gadzicki. (2012). No evidence for breast cancer susceptibility associated with variants of BRD7, a component of p53 and BRCA1 pathways. Familial Cancer. 11(4). 601–606. 10 indexed citations
3.
Skawran, Britta, Winfried Hofmann, Norbert Arnold, et al.. (2011). Human BRCA1-Associated Breast Cancer: No Increase in Numerical Chromosomal Instability Compared to Sporadic Tumors. Cytogenetic and Genome Research. 135(2). 84–92. 4 indexed citations
4.
Gadzicki, Dorothea, D. Gareth Evans, Hilary Harris, et al.. (2011). Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany. Journal of Community Genetics. 2(2). 53–69. 53 indexed citations
5.
Fischer, Christine, Christoph Engel, Christian Sutter, et al.. (2011). BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families. Clinical Genetics. 82(5). 478–483. 12 indexed citations
6.
Bohnhorst, Bettina, I. Luhmer, Susanne Morlot, et al.. (2010). Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome. European Journal of Medical Genetics. 53(5). 280–285. 14 indexed citations
7.
Gadzicki, Dorothea, Christine Fischer, Ulrich Lehmann, et al.. (2009). Histopathological criteria and selection algorithms for BRCA1 genetic testing. Cancer Genetics and Cytogenetics. 189(2). 105–111. 14 indexed citations
8.
Gadzicki, Dorothea, et al.. (2009). Recurrent involvement of heterochromatic regions in multiple myeloma—A multicolor FISH study. Leukemia Research. 34(8). 1002–1006. 9 indexed citations
9.
Ripperger, Tim, Dorothea Gadzicki, Alfons Meindl, & Brigitte Schlegelberger. (2008). Breast cancer susceptibility: current knowledge and implications for genetic counselling. European Journal of Human Genetics. 17(6). 722–731. 146 indexed citations
10.
Christgen, Matthias, Catarina Hadamitzky, Cornelia Rudolph, et al.. (2008). Comprehensive genetic and functional characterization of IPH‐926: a novel CDH1‐null tumour cell line from human lobular breast cancer. The Journal of Pathology. 217(5). 620–632. 27 indexed citations
11.
Buesche, Guntram, Arnold Ganser, Brigitte Schlegelberger, et al.. (2007). Marrow fibrosis and its relevance during imatinib treatment of chronic myeloid leukemia. Leukemia. 21(12). 2420–2427. 38 indexed citations
12.
Gerhardus, Ansgar, et al.. (2007). Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations: a systematic review. European Journal of Human Genetics. 15(6). 619–627. 54 indexed citations
13.
Pagenstecher, Constanze, Dorothea Gadzicki, Dietlinde Stienen, et al.. (2007). A Complex Rearrangement in the APC Gene Uncovered by Multiplex Ligation-Dependent Probe Amplification. Journal of Molecular Diagnostics. 9(1). 122–126. 7 indexed citations
14.
Gadzicki, Dorothea, Christoph M. Happel, Cornelia Rudolph, et al.. (2006). Jacobsen Syndrome and Beckwith‐Wiedemann Syndrome Caused by a Parental Pericentric Inversion inv(11)(p15q24). Annals of Human Genetics. 70(6). 958–964. 5 indexed citations
15.
Schmidtke, Jörg, et al.. (2005). Hereditary hemorrhagic telangiectasia is caused by the Q490X mutation of the ACVRL1 gene in a large Arab family: support of homozygous lethality. European Journal of Medical Genetics. 49(4). 323–330. 8 indexed citations
16.
Gadzicki, Dorothea, Nils von Neuhoff, Doris Steinemann, et al.. (2005). BCR-ABL gene amplification and overexpression in a patient with chronic myeloid leukemia treated with imatinib. Cancer Genetics and Cytogenetics. 159(2). 164–167. 26 indexed citations
17.
Wilkens, Ludwig, et al.. (2005). Standardised fluorescence in situ hybridisation in cytological and histological specimens. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 447(3). 586–592. 21 indexed citations
18.
Gadzicki, Dorothea, et al.. (2004). Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 127B(1). 97–103. 31 indexed citations
19.
Rudolph, Cornelia, Doris Steinemann, Nils von Neuhoff, et al.. (2004). Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519. Cancer Genetics and Cytogenetics. 153(2). 144–150. 34 indexed citations
20.
Schneider, Udo, Kirsten Müller‐Vahl, Manfred Stuhrmann, et al.. (2000). Die Bedeutung des endogenen Cannabinoidsystems bei verschiedenen neuro-psychiatrischen Erkrankungen. Fortschritte der Neurologie · Psychiatrie. 68(10). 433–438. 2 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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