Wiltrud Coerdt
- Molecular Biology
- Genetics top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Surgery
- Public Health, Environmental and Occupational Health top 10%
- Co-authors
- Helga RehderE. SchwingerH MünteferingR. JohannissonA. GroppThomas HaafGalyna PliushchE. Schneider
- Topics
- Prenatal Screening and Diagnostics (13 papers)Congenital gastrointestinal and neural anomalies (6 papers)Genetic Syndromes and Imprinting (5 papers)
- Partner nations
- GermanyUnited KingdomDenmark
In The Last Decade
Wiltrud Coerdt
42 papers receiving 967 citations
Peers
Comparison fields: 5 of 82
- Molecular Biology 372
- Genetics 346
- Pediatrics, Perinatology and Child Health 345
- Surgery 271
- Public Health, Environmental and Occupational Health 150
Countries citing papers authored by Wiltrud Coerdt
This map shows the geographic impact of Wiltrud Coerdt'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 Wiltrud Coerdt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wiltrud Coerdt more than expected).
Fields of papers citing papers by Wiltrud Coerdt
This network shows the impact of papers produced by Wiltrud Coerdt. 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 Wiltrud Coerdt. The network helps show where Wiltrud Coerdt may publish in the future.
Co-authorship network of co-authors of Wiltrud Coerdt
This figure shows the co-authorship network connecting the top 25 collaborators of Wiltrud Coerdt. A scholar is included among the top collaborators of Wiltrud Coerdt 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 Wiltrud Coerdt. Wiltrud Coerdt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 70 | |
| 2 | 3 | |
| 3 | 48 | |
| 4 | 5 | |
| 5 | 94 | |
| 6 | 58 | |
| 7 | 2 | |
| 8 | 6 | |
| 9 | 35 | |
| 10 | 1 | |
| 11 | 4 | |
| 12 | 58 | |
| 13 | 103 | |
| 14 | 11 | |
| 15 | 16 | |
| 16 | 5 | |
| 17 | 1 | |
| 18 | 29 | |
| 19 | 32 | |
| 20 | 36 |
About Wiltrud Coerdt
Wiltrud Coerdt is a scholar working on Microbiology, Pediatrics, Perinatology and Child Health and Gastroenterology, having authored 42 papers that have together received 998 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (13 papers), Congenital gastrointestinal and neural anomalies (6 papers) and Genetic Syndromes and Imprinting (5 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (345 citations), Gastroenterology (71 citations) and Genetics (346 citations). Wiltrud Coerdt has collaborated with scholars based in Germany, United Kingdom and Denmark. Frequent co-authors include Helga Rehder, E. Schwinger, H Müntefering, R. Johannisson, A. Gropp, Thomas Haaf, Galyna Pliushch, E. Schneider, Nady El Hajj and Ulrich Zechner. Their work appears in journals such as Nucleic Acids Research, Gut and American Journal Of Pathology.
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.