R.‐D. Wegner

1.3k total citations
32 papers, 724 citations indexed

About

R.‐D. Wegner is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, R.‐D. Wegner has authored 32 papers receiving a total of 724 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in R.‐D. Wegner's work include Prenatal Screening and Diagnostics (9 papers), DNA Repair Mechanisms (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). R.‐D. Wegner is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), DNA Repair Mechanisms (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). R.‐D. Wegner collaborates with scholars based in Germany, United States and Netherlands. R.‐D. Wegner's co-authors include Rolf Becker, Karl Sperling, Markus Stümm, H. Riehm, G. Obe, André Reis, Michael Entezami, Martin Jung, Peter Wieacker and Susann Neubauer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cellular and Molecular Life Sciences and Osteoarthritis and Cartilage.

In The Last Decade

R.‐D. Wegner

31 papers receiving 683 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
R.‐D. Wegner Germany 14 399 222 179 155 115 32 724
Silvana Guerneri Italy 17 357 0.9× 112 0.5× 344 1.9× 406 2.6× 121 1.1× 50 902
Rolf‐Dieter Wegner Germany 16 270 0.7× 85 0.4× 227 1.3× 226 1.5× 60 0.5× 38 626
Patrik Asp United States 14 801 2.0× 81 0.4× 39 0.2× 141 0.9× 45 0.4× 22 1.2k
M.C. Baker United Kingdom 12 191 0.5× 92 0.4× 23 0.1× 145 0.9× 107 0.9× 17 469
Eunike Velleuer Germany 15 564 1.4× 169 0.8× 37 0.2× 236 1.5× 53 0.5× 30 873
Benjamin Rauwel France 13 353 0.9× 71 0.3× 47 0.3× 44 0.3× 71 0.6× 21 807
Shida Zhu China 13 276 0.7× 162 0.7× 29 0.2× 70 0.5× 32 0.3× 37 484
Sara Nouri Australia 11 221 0.6× 22 0.1× 93 0.5× 147 0.9× 38 0.3× 16 664
G. Bell United Kingdom 10 413 1.0× 20 0.1× 123 0.7× 254 1.6× 43 0.4× 15 879
Felix Moltzahn Switzerland 11 588 1.5× 454 2.0× 38 0.2× 26 0.2× 45 0.4× 23 847

Countries citing papers authored by R.‐D. Wegner

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of R.‐D. Wegner

This figure shows the co-authorship network connecting the top 25 collaborators of R.‐D. Wegner. A scholar is included among the top collaborators of R.‐D. Wegner 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 R.‐D. Wegner. R.‐D. Wegner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Stümm, Markus, Erich T. Boger, Christoph Gaissmaier, et al.. (2012). Genomic chondrocyte culture profiling by array-CGH, interphase-FISH and RT-PCR. Osteoarthritis and Cartilage. 20(9). 1039–1045. 9 indexed citations
2.
Schaftenaar, Willem, Teresa Fernandes, Guido Fritsch, et al.. (2010). Dystocia and Fetotomy Associated with Cerebral Aplasia in a Greater One‐horned Rhinoceros (Rhinoceros unicornis). Reproduction in Domestic Animals. 46(1). e97–101. 8 indexed citations
3.
Becker, Rolf, Denise Horn, Ute Knoll, et al.. (2010). First-Trimester Prenatal Diagnosis of Okihiro Syndrome. Fetal Diagnosis and Therapy. 27(4). 222–226. 4 indexed citations
4.
Staboulidou, I., Markus Stümm, R.‐D. Wegner, et al.. (2010). A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator dataset. Prenatal Diagnosis. 30(11). 1100–1106. 3 indexed citations
5.
Liehr, Thomas, Markus Stümm, R.‐D. Wegner, et al.. (2009). 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences. Cytogenetic and Genome Research. 124(1). 102–105. 27 indexed citations
6.
Stümm, Markus, et al.. (2006). Interphase M-FISH applications using commercial probes in prenatal and PGD diagnostics. Cytogenetic and Genome Research. 114(3-4). 296–301. 12 indexed citations
7.
Becker, Rolf & R.‐D. Wegner. (2006). Detailed screening for fetal anomalies and cardiac defects at the 11–13‐week scan. Ultrasound in Obstetrics and Gynecology. 27(6). 613–618. 117 indexed citations
8.
Sarioglu, Nanette, et al.. (2003). Epignathus: always a simple teratoma? Report of an exceptional case with two additional fetiforme bodies. Ultrasound in Obstetrics and Gynecology. 21(4). 397–403. 19 indexed citations
9.
Becker, Rolf, et al.. (2001). Prenatal diagnosis of familial absent pulmonary valve syndrome: case report and review of the literature. Ultrasound in Obstetrics and Gynecology. 17(3). 263–267. 29 indexed citations
10.
Becker, Rolf, et al.. (2000). Clinical variability of Larsen syndrome: diagnosis in a father after sonographic detection of a severely affected fetus. Clinical Genetics. 57(2). 148–150. 13 indexed citations
11.
Saar, Kathrin, Krystyńa Chrzańowska, Markus Stümm, et al.. (1997). The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.. PubMed. 60(3). 605–10. 85 indexed citations
12.
Wegner, R.‐D., Evelin Schröck, M. Obladen, et al.. (1996). PARTIAL TRISOMY/MONOSOMY 6q IN FETAL CELLS AND CVS LONG-TERM CULTURE NOT PRESENT IN CVS SHORT-TERM CULTURE. Prenatal Diagnosis. 16(8). 741–748. 13 indexed citations
13.
Wegner, H, et al.. (1994). [Mixed gonadal dysgenesis--a rare cause of primary infertility. Report of 2 cases and review of the literature].. PubMed. 33(4). 342–6. 2 indexed citations
14.
Becker, Rolf, et al.. (1991). Bakteriologische Befunde vor und bei transzervikaler Chorionzottenbiopsie und deren klinische Relevanz. Geburtshilfe und Frauenheilkunde. 51(9). 704–709. 3 indexed citations
15.
Stuhrmann, Manfred, H. Heilbronner, André Reis, et al.. (1991). Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita. Human Genetics. 86(4). 414–5. 15 indexed citations
16.
Wegner, R.‐D., et al.. (1989). Calla-Positive Acute Leukaemia with t(5q;14q) Translocation and Hypereosinophilia – A Unique Entity?. Acta Haematologica. 82(2). 85–90. 12 indexed citations
17.
Wegner, R.‐D., Marc J. Metzger, F. Hanefeld, et al.. (1988). AT‐related disorder. Clinical Genetics. 33(1). 20–32. 56 indexed citations
18.
Wegner, R.‐D., et al.. (1988). Trisomy 14 mosaicism leading to cytogenetic discrepancies in chorionic villi sampled at different times. Prenatal Diagnosis. 8(3). 239–243. 13 indexed citations
19.
Rodewald, A., U. Froster‐Iskenius, U. Langenbeck, et al.. (1986). Dermatoglyphic peculiarities in families with X‐linked mental retardation and fragile site Xq27: a collaborative study. Clinical Genetics. 30(1). 1–13. 12 indexed citations
20.
Wegner, R.‐D., et al.. (1982). The effects of diagnostic ultrasonography on the frequencies of sister chromatid exchanges in Chinese hamster cells and human lymphocytes.. Journal of Ultrasound in Medicine. 1(9). 355–358. 16 indexed citations

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.

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