Nicola Dikow
- Molecular Biology
- Genetics top 10%
- Pediatrics, Perinatology and Child Health
- Oncology
- Clinical Biochemistry top 10%
- Co-authors
- Johannes ZschockeKatrin HinderhoferChristina EversJan P. SchoutenBart JanssenChristine FischerChristian SutterUte Moog
- Topics
- BRCA gene mutations in cancer (10 papers)Genomic variations and chromosomal abnormalities (7 papers)Genomics and Rare Diseases (5 papers)
- Partner nations
- GermanyPolandUnited States
In The Last Decade
Nicola Dikow
25 papers receiving 422 citations
Peers
Comparison fields: 5 of 75
- Molecular Biology 226
- Genetics 219
- Pediatrics, Perinatology and Child Health 46
- Oncology 43
- Clinical Biochemistry 41
Countries citing papers authored by Nicola Dikow
This map shows the geographic impact of Nicola Dikow'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 Nicola Dikow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nicola Dikow more than expected).
Fields of papers citing papers by Nicola Dikow
This network shows the impact of papers produced by Nicola Dikow. 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 Nicola Dikow. The network helps show where Nicola Dikow may publish in the future.
Co-authorship network of co-authors of Nicola Dikow
This figure shows the co-authorship network connecting the top 25 collaborators of Nicola Dikow. A scholar is included among the top collaborators of Nicola Dikow 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 Nicola Dikow. Nicola Dikow is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 2 | |
| 3 | 9 | |
| 4 | 8 | |
| 5 | 10 | |
| 6 | 11 | |
| 7 | 8 | |
| 8 | 36 | |
| 9 | 7 | |
| 10 | 10 | |
| 11 | 8 | |
| 12 | 21 | |
| 13 | 29 | |
| 14 | 10 | |
| 15 | 28 | |
| 16 | 6 | |
| 17 | 35 | |
| 18 | 69 | |
| 19 | 43 | |
| 20 | 46 |
About Nicola Dikow
Nicola Dikow is a scholar working on Genetics, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 28 papers that have together received 441 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genomics and Rare Diseases (5 papers). The work is most often cited by research in Genetics (219 citations), Clinical Biochemistry (41 citations) and Molecular Biology (226 citations). Nicola Dikow has collaborated with scholars based in Germany, Poland and United States. Frequent co-authors include Johannes Zschocke, Katrin Hinderhofer, Christina Evers, Jan P. Schouten, Bart Janssen, Christine Fischer, Christian Sutter, Ute Moog, Sarah Schott and Anders O.H. Nygren. Their work appears in journals such as PLoS ONE, Human Molecular Genetics and Breast Cancer Research and Treatment.
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.