R.‐D. Wegner
Impact in
- Cancer Research top 10%
- Carcinogens and Genotoxicity Assessment
-
- Prenatal Screening and Diagnostics
Papers in
-
- DNA Repair Mechanisms 9
- Sexual Differentiation and Disorders 2
- Genetics 12
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Rolf Becker (6 shared papers)Karl Sperling (9 shared papers)Markus Stümm (10 shared papers)H. Riehm (1 shared paper)G. Obe (1 shared paper)André Reis (3 shared papers)Michael Entezami (3 shared papers)Krystyńa Chrzańowska (1 shared paper)
- Journals
- Human Genetics (5 papers)Cytogenetic and Genome Research (4 papers)Ultrasound in Obstetrics and Gynecology (3 papers)Prenatal Diagnosis (3 papers)Clinical Genetics (3 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
R.‐D. Wegner
34 papers receiving 729 citations
Peers
Comparison fields: 5 of 68
- Cancer Research 229
- Pediatrics, Perinatology and Child Health 160
- Genetics 178
- Molecular Biology 423
- Oncology 99
Countries citing papers authored by R.‐D. Wegner
This map shows the geographic impact of R.‐D. 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 R.‐D. Wegner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R.‐D. Wegner more than expected).
Fields of papers citing papers by R.‐D. Wegner
This network shows the impact of papers produced by R.‐D. 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 R.‐D. Wegner. The network helps show where R.‐D. Wegner may publish in the future.
Co-authors
The 25 scholars most cited alongside R.‐D. 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 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 135 | |
| 2 | The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. | 1997 | 90 |
| 3 | 1975 | 63 | |
| 4 | 1988 | 62 | |
| 5 | Characterization of cell cycle checkpoint responses after ionizing radiation in Nijmegen breakage syndrome cells. | 1998 | 62 |
| 6 | 2001 | 55 | |
| 7 | 1982 | 31 | |
| 8 | 2001 | 31 | |
| 9 | 2001 | 29 | |
| 10 | 2009 | 29 | |
| 11 | 2003 | 19 | |
| 12 | 1982 | 19 | |
| 13 | 2006 | 16 | |
| 14 | 1991 | 16 | |
| 15 | 1988 | 15 | |
| 16 | 2000 | 14 | |
| 17 | 1986 | 14 | |
| 18 | 1996 | 14 | |
| 19 | 1991 | 12 | |
| 20 | 1983 | 10 |
About R.‐D. Wegner
R.‐D. Wegner is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 36 papers that have together received 803 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (9 papers), Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (6 papers), Carcinogens and Genotoxicity Assessment (6 papers), Chromosomal and Genetic Variations (6 papers), Congenital Anomalies and Fetal Surgery (4 papers), Sexual Differentiation and Disorders (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). The work is most often cited by research in Cancer Research (229 citations), Pediatrics, Perinatology and Child Health (160 citations), Genetics (178 citations), Molecular Biology (423 citations) and Oncology (99 citations). R.‐D. Wegner has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Rolf Becker, Karl Sperling, Markus Stümm, H. Riehm, G. Obe, André Reis, Michael Entezami, Krystyńa Chrzańowska, Gudrun Nürnberg and Martin Jung. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Ultrasound in Obstetrics and Gynecology, Prenatal Diagnosis and Clinical 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.