R.‐D. Wegner
Impact in
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- Prenatal Screening and Diagnostics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Blood disorders and treatments
Papers in
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- Prenatal Screening and Diagnostics 10
- Genetics 16
- Genomic variations and chromosomal abnormalities 9
- Co-authors
- Karl Sperling (11 shared papers)Markus Stümm (10 shared papers)Cordula U. Kirchgessner (1 shared paper)André Reis (4 shared papers)H. Riehm (1 shared paper)Guenter Obe (1 shared paper)Fré Arwert (1 shared paper)Carola G.M. van Berkel (1 shared paper)
- Journals
- Human Genetics (6 papers)Cytogenetic and Genome Research (4 papers)Clinical Genetics (3 papers)Ultrasound in Obstetrics and Gynecology (3 papers)Prenatal Diagnosis (3 papers)
- Partner nations
- GermanyUnited StatesNetherlands
In The Last Decade
R.‐D. Wegner
41 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 71
- Pediatrics, Perinatology and Child Health 205
- Genetics 382
- Molecular Biology 494
- Developmental Biology 16
- Cancer Research 79
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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 150 | |
| 2 | 2006 | 140 | |
| 3 | 1983 | 137 | |
| 4 | The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. | 1997 | 96 |
| 5 | 1992 | 74 | |
| 6 | 1994 | 74 | |
| 7 | Characterization of cell cycle checkpoint responses after ionizing radiation in Nijmegen breakage syndrome cells. | 1998 | 65 |
| 8 | 1988 | 64 | |
| 9 | 1975 | 63 | |
| 10 | 2001 | 57 | |
| 11 | 1991 | 35 | |
| 12 | 2001 | 31 | |
| 13 | 1982 | 30 | |
| 14 | 2001 | 29 | |
| 15 | 2009 | 29 | |
| 16 | 1982 | 19 | |
| 17 | 2003 | 19 | |
| 18 | 1991 | 17 | |
| 19 | 1988 | 16 | |
| 20 | 2000 | 16 |
About R.‐D. Wegner
R.‐D. Wegner is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Cancer Research, Molecular Biology and Developmental Biology, having authored 43 papers that have together received 1.3k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (11 papers), Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Carcinogens and Genotoxicity Assessment (5 papers), Down syndrome and intellectual disability research (3 papers), Congenital Anomalies and Fetal Surgery (2 papers), Radioactive contamination and transfer (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (205 citations), Genetics (382 citations), Molecular Biology (494 citations), Developmental Biology (16 citations) and Cancer Research (79 citations). R.‐D. Wegner has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Karl Sperling, Markus Stümm, Cordula U. Kirchgessner, André Reis, H. Riehm, Guenter Obe, Fré Arwert, Carola G.M. van Berkel, Manuel Buchwald and Hans Joenje. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Clinical Genetics, Ultrasound in Obstetrics and Gynecology and Prenatal Diagnosis.
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.