R.‐D. Wegner
- Cancer Research top 10%
- Carcinogens and Genotoxicity Assessment 5
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- Prenatal Screening and Diagnostics 9
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- DNA Repair Mechanisms 7
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- Genomic variations and chromosomal abnormalities 6
- Genetic Syndromes and Imprinting 2
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- Congenital Anomalies and Fetal Surgery 5
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- Chromosomal and Genetic Variations 5
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- Eosinophilic Disorders and Syndromes 2
- Journals
- Human Genetics (5 papers)Cytogenetic and Genome Research (4 papers)Prenatal Diagnosis (3 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
R.‐D. Wegner
31 papers receiving 683 citations
Peers
Comparison fields: 5 of 68
- Cancer Research 222
- Pediatrics, Perinatology and Child Health 179
- Molecular Biology 399
- Genetics 155
- Oncology 102
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 9 | |
| 2 | 2010 | 8 | |
| 3 | 2010 | 4 | |
| 4 | 2010 | 3 | |
| 5 | 2009 | 27 | |
| 6 | 2006 | 12 | |
| 7 | 2006 | 117 | |
| 8 | 2003 | 19 | |
| 9 | 2001 | 29 | |
| 10 | 2001 | 28 | |
| 11 | 2000 | 13 | |
| 12 | The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. | 1997 | 85 |
| 13 | 1996 | 13 | |
| 14 | [Mixed gonadal dysgenesis--a rare cause of primary infertility. Report of 2 cases and review of the literature]. | 1994 | 2 |
| 15 | 1991 | 3 | |
| 16 | 1991 | 15 | |
| 17 | 1989 | 12 | |
| 18 | 1988 | 13 | |
| 19 | 1988 | 56 | |
| 20 | 1986 | 12 |
About R.‐D. Wegner
R.‐D. Wegner is a scholar working on Chemical Health and Safety, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 32 papers that have together received 724 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (9 papers), DNA Repair Mechanisms (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Carcinogens and Genotoxicity Assessment (5 papers), Congenital Anomalies and Fetal Surgery (5 papers), Chromosomal and Genetic Variations (5 papers), Genetic Syndromes and Imprinting (2 papers) and Eosinophilic Disorders and Syndromes (2 papers). The work is most often cited by research in Cancer Research (222 citations), Pediatrics, Perinatology and Child Health (179 citations) and Molecular Biology (399 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, Martin Jung, Kathrin Saar and Rolf Sauer. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Prenatal Diagnosis, Ultrasound in Obstetrics and Gynecology 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.