Stephanie Groß
- Genetics top 2%
- Molecular Biology top 10%
- Pediatrics, Perinatology and Child Health top 2%
- Pathology and Forensic Medicine
- Surgery
- Co-authors
- Karin BuitingBernhard HorsthemkeBärbel DittrichShinji SaitohStuart SchwartzRobert D. NichollsChristina LichGabriele Gillessen‐Kaesbach
- Topics
- Genetic Syndromes and Imprinting (7 papers)Epigenetics and DNA Methylation (7 papers)Prenatal Screening and Diagnostics (4 papers)
- Partner nations
- GermanySwitzerlandNetherlands
In The Last Decade
Stephanie Groß
11 papers receiving 894 citations
Peers
Comparison fields: 5 of 58
- Genetics 812
- Molecular Biology 724
- Pediatrics, Perinatology and Child Health 433
- Pathology and Forensic Medicine 40
- Surgery 23
Countries citing papers authored by Stephanie Groß
This map shows the geographic impact of Stephanie Groß'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 Stephanie Groß with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie Groß more than expected).
Fields of papers citing papers by Stephanie Groß
This network shows the impact of papers produced by Stephanie Groß. 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 Stephanie Groß. The network helps show where Stephanie Groß may publish in the future.
Co-authorship network of co-authors of Stephanie Groß
This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie Groß. A scholar is included among the top collaborators of Stephanie Groß 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 Stephanie Groß. Stephanie Groß 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 | 8 | |
| 3 | 4 | |
| 4 | 30 | |
| 5 | 15 | |
| 6 | 57 | |
| 7 | 30 | |
| 8 | 208 | |
| 9 | 35 | |
| 10 | 471 | |
| 11 | 4 | |
| 12 | 72 |
About Stephanie Groß
Stephanie Groß is a scholar working on Genetics, Geriatrics and Gerontology and Pediatrics, Perinatology and Child Health, having authored 12 papers that have together received 934 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (7 papers), Epigenetics and DNA Methylation (7 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (812 citations), Pediatrics, Perinatology and Child Health (433 citations) and Molecular Biology (724 citations). Stephanie Groß has collaborated with scholars based in Germany, Switzerland and Netherlands. Frequent co-authors include Karin Buiting, Bernhard Horsthemke, Bärbel Dittrich, Shinji Saitoh, Stuart Schwartz, Robert D. Nicholls, Christina Lich, Gabriele Gillessen‐Kaesbach, Osman El‐Maarri and Jürgen Neesen. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular 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.