Helga Rehder
- Genetics top 1%
- Molecular Biology top 10%
- Pediatrics, Perinatology and Child Health top 1%
- Surgery top 10%
- Oncology top 10%
- Co-authors
- E. SchwingerWiltrud CoerdtBárbara FritzVera M. KalscheuerA. GroppMarga SchepensEdwin C.M. MarimanHarald Rieder
- Topics
- Prenatal Screening and Diagnostics (42 papers)Genomic variations and chromosomal abnormalities (24 papers)Genetic Syndromes and Imprinting (14 papers)
In The Last Decade
Helga Rehder
115 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 103
- Genetics 1.2k
- Molecular Biology 906
- Pediatrics, Perinatology and Child Health 777
- Surgery 408
- Oncology 352
Countries citing papers authored by Helga Rehder
This map shows the geographic impact of Helga Rehder'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 Helga Rehder with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Helga Rehder more than expected).
Fields of papers citing papers by Helga Rehder
This network shows the impact of papers produced by Helga Rehder. 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 Helga Rehder. The network helps show where Helga Rehder may publish in the future.
Co-authorship network of co-authors of Helga Rehder
This figure shows the co-authorship network connecting the top 25 collaborators of Helga Rehder. A scholar is included among the top collaborators of Helga Rehder 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 Helga Rehder. Helga Rehder is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 2 | |
| 3 | 2 | |
| 4 | 13 | |
| 5 | 14 | |
| 6 | 2 | |
| 7 | 21 | |
| 8 | 3 | |
| 9 | 24 | |
| 10 | 103 | |
| 11 | Disruptive anomalies in a newborn with focal dermalhypoplasia (Goltz syndrome) | 3 |
| 12 | 14 | |
| 13 | 11 | |
| 14 | 22 | |
| 15 | 2 | |
| 16 | 19 | |
| 17 | 38 | |
| 18 | 31 | |
| 19 | 6 | |
| 20 | [Pathological and embryological studies on abortion cases related to the Seveso accident]. | 11 |
About Helga Rehder
Helga Rehder is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Developmental Biology, having authored 119 papers that have together received 2.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (42 papers), Genomic variations and chromosomal abnormalities (24 papers) and Genetic Syndromes and Imprinting (14 papers). The work is most often cited by research in Genetics (1.2k citations), Pediatrics, Perinatology and Child Health (777 citations) and Developmental Biology (70 citations). Helga Rehder has collaborated with scholars based in Germany, Austria and Denmark. Frequent co-authors include E. Schwinger, Wiltrud Coerdt, Bárbara Fritz, Vera M. Kalscheuer, A. Gropp, Marga Schepens, Edwin C.M. Mariman, Harald Rieder, Wolfgang Holzgreve and R. Johannisson. Their work appears in journals such as Nature Genetics, Gastroenterology and JNCI Journal of the National Cancer Institute.
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.