Jutta Müller‐Navia
- Genetics top 10%
- Molecular Biology
- Plant Science
- Pediatrics, Perinatology and Child Health
- Cancer Research
- Co-authors
- Harry ScherthanMirella L. Meyer‐FiccaLutz FrönickeAnnette MüllerEkkehard VollmerTorsten GoldmannYasmin MehraeinJ. Olert
- Topics
- Chromosomal and Genetic Variations (8 papers)Genomic variations and chromosomal abnormalities (8 papers)Molecular Biology Techniques and Applications (4 papers)
In The Last Decade
Jutta Müller‐Navia
13 papers receiving 383 citations
Peers
Comparison fields: 5 of 68
- Genetics 227
- Molecular Biology 201
- Plant Science 168
- Pediatrics, Perinatology and Child Health 76
- Cancer Research 31
Countries citing papers authored by Jutta Müller‐Navia
This map shows the geographic impact of Jutta Müller‐Navia'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 Jutta Müller‐Navia with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jutta Müller‐Navia more than expected).
Fields of papers citing papers by Jutta Müller‐Navia
This network shows the impact of papers produced by Jutta Müller‐Navia. 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 Jutta Müller‐Navia. The network helps show where Jutta Müller‐Navia may publish in the future.
Co-authorship network of co-authors of Jutta Müller‐Navia
This figure shows the co-authorship network connecting the top 25 collaborators of Jutta Müller‐Navia. A scholar is included among the top collaborators of Jutta Müller‐Navia 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 Jutta Müller‐Navia. Jutta Müller‐Navia is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 12 | |
| 3 | 4 | |
| 4 | 115 | |
| 5 | 72 | |
| 6 | 64 | |
| 7 | 58 | |
| 8 | Tetrasomy 18p caused by paternal meiotic nondisjunction. | 16 |
| 9 | 16 | |
| 10 | 2 | |
| 11 | 16 | |
| 12 | 17 | |
| 13 | 1 |
About Jutta Müller‐Navia
Jutta Müller‐Navia is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health, having authored 13 papers that have together received 396 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Molecular Biology Techniques and Applications (4 papers). The work is most often cited by research in Genetics (227 citations), Plant Science (168 citations) and Pediatrics, Perinatology and Child Health (76 citations). Jutta Müller‐Navia has collaborated with scholars based in Germany and Poland. Frequent co-authors include Harry Scherthan, Mirella L. Meyer‐Ficca, Lutz Frönicke, Annette Müller, Ekkehard Vollmer, Torsten Goldmann, Yasmin Mehraein, J. Olert, Can Apacik and Thomas Eggermann. Their work appears in journals such as Journal of Cell Science, The American Journal of Human Genetics and Human 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.