Rolf‐Dieter Wegner
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
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- Prenatal Screening and Diagnostics 19
- Fetal and Pediatric Neurological Disorders 6
-
- DNA Repair Mechanisms 8
- Co-authors
- Markus Stümm (16 shared papers)Rolf Becker (8 shared papers)Ute Knoll (6 shared papers)Günter Obe (1 shared paper)Christine Lücke‐Huhle (1 shared paper)Jürgen Kunze (1 shared paper)Ludwig Hieber (1 shared paper)Mathias Ehrich (2 shared papers)
- Journals
- Prenatal Diagnosis (6 papers)Human Genetics (5 papers)Clinical Genetics (4 papers)Journal of Clinical Medicine (2 papers)Molecular Cytogenetics (2 papers)
- Partner nations
- GermanyUnited StatesNetherlands
In The Last Decade
Rolf‐Dieter Wegner
36 papers receiving 559 citations
Peers
Comparison fields: 5 of 69
- Pediatrics, Perinatology and Child Health 227
- Genetics 226
- Cancer Research 85
- Hematology 52
- Molecular Biology 270
Countries citing papers authored by Rolf‐Dieter Wegner
This map shows the geographic impact of Rolf‐Dieter Wegner'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 Rolf‐Dieter Wegner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rolf‐Dieter Wegner more than expected).
Fields of papers citing papers by Rolf‐Dieter Wegner
This network shows the impact of papers produced by Rolf‐Dieter Wegner. 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 Rolf‐Dieter Wegner. The network helps show where Rolf‐Dieter Wegner may publish in the future.
Co-authors
The 25 scholars most cited alongside Rolf‐Dieter Wegner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 83 | |
| 2 | 1999 | 55 | |
| 3 | 1995 | 46 | |
| 4 | 1999 | 41 | |
| 5 | 1986 | 38 | |
| 6 | 1983 | 31 | |
| 7 | 1980 | 30 | |
| 8 | 2003 | 29 | |
| 9 | 1981 | 29 | |
| 10 | 2002 | 24 | |
| 11 | 2014 | 23 | |
| 12 | 2012 | 22 | |
| 13 | 2012 | 22 | |
| 14 | 2003 | 21 | |
| 15 | 1998 | 17 | |
| 16 | 1994 | 15 | |
| 17 | 2009 | 14 | |
| 18 | 1980 | 11 | |
| 19 | 2007 | 10 | |
| 20 | 1982 | 10 |
About Rolf‐Dieter Wegner
Rolf‐Dieter Wegner is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics, Surgery and Cancer Research, having authored 38 papers that have together received 626 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (19 papers), DNA Repair Mechanisms (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Carcinogens and Genotoxicity Assessment (6 papers), Fetal and Pediatric Neurological Disorders (6 papers), Chromosomal and Genetic Variations (5 papers), Parvovirus B19 Infection Studies (4 papers) and Congenital Anomalies and Fetal Surgery (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (227 citations), Genetics (226 citations), Cancer Research (85 citations), Hematology (52 citations) and Molecular Biology (270 citations). Rolf‐Dieter Wegner has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Markus Stümm, Rolf Becker, Ute Knoll, Günter Obe, Christine Lücke‐Huhle, Jürgen Kunze, Ludwig Hieber, Mathias Ehrich, Sebastian Grömminger and Ulrike Schöck. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Clinical Genetics, Journal of Clinical Medicine and Molecular Cytogenetics.
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.