Reinhard Ullmann
- Molecular Biology top 5%
- Genetics top 0.5%
- Pediatrics, Perinatology and Child Health top 2%
- Plant Science top 5%
- Oncology top 10%
- Co-authors
- D.M. KolbT. WillHans‐Hilger RopersFikret ErdoganWei ChenAndreas TzschachVera M. KalscheuerNiels Tommerup
- Topics
- Genomic variations and chromosomal abnormalities (59 papers)Genetics and Neurodevelopmental Disorders (24 papers)Chromosomal and Genetic Variations (20 papers)
- Partner nations
- GermanyDenmarkUnited States
In The Last Decade
Reinhard Ullmann
129 papers receiving 4.6k citations
Peers
Comparison fields: 5 of 140
- Molecular Biology 2.3k
- Genetics 2.2k
- Pediatrics, Perinatology and Child Health 433
- Plant Science 398
- Oncology 349
Countries citing papers authored by Reinhard Ullmann
This map shows the geographic impact of Reinhard Ullmann'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 Reinhard Ullmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Reinhard Ullmann more than expected).
Fields of papers citing papers by Reinhard Ullmann
This network shows the impact of papers produced by Reinhard Ullmann. 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 Reinhard Ullmann. The network helps show where Reinhard Ullmann may publish in the future.
Co-authorship network of co-authors of Reinhard Ullmann
This figure shows the co-authorship network connecting the top 25 collaborators of Reinhard Ullmann. A scholar is included among the top collaborators of Reinhard Ullmann 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 Reinhard Ullmann. Reinhard Ullmann 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 | 7 | |
| 3 | 6 | |
| 4 | 13 | |
| 5 | 5 | |
| 6 | 68 | |
| 7 | 36 | |
| 8 | 62 | |
| 9 | 15 | |
| 10 | 22 | |
| 11 | 49 | |
| 12 | 4 | |
| 13 | 168 | |
| 14 | 202 | |
| 15 | 102 | |
| 16 | 112 | |
| 17 | 185 | |
| 18 | 24 | |
| 19 | 6 | |
| 20 | 46 |
About Reinhard Ullmann
Reinhard Ullmann is a scholar working on Genetics, Molecular Biology and Developmental Biology, having authored 132 papers that have together received 4.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (59 papers), Genetics and Neurodevelopmental Disorders (24 papers) and Chromosomal and Genetic Variations (20 papers). The work is most often cited by research in Genetics (2.2k citations), Developmental Biology (96 citations) and Molecular Biology (2.3k citations). Reinhard Ullmann has collaborated with scholars based in Germany, Denmark and United States. Frequent co-authors include D.M. Kolb, T. Will, Hans‐Hilger Ropers, Fikret Erdogan, Wei Chen, Andreas Tzschach, Vera M. Kalscheuer, Niels Tommerup, Eva Klopocki and Helmut Popper. Their work appears in journals such as Science, Nature Genetics and The Journal of Experimental Medicine.
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.