Udo Trautmann
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 43
- Genomic variations and chromosomal abnormalities 35
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
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- Congenital heart defects research 8
- Genomics and Chromatin Dynamics 7
- Co-authors
- Anita Rauch (28 shared papers)André Reis (11 shared papers)Cornelia Kraus (9 shared papers)Martin Zenker (8 shared papers)Christiane Zweier (7 shared papers)Christian T. Thiel (7 shared papers)Rudolf A. Pfeiffer (5 shared papers)Thomas Liehr (9 shared papers)
- Journals
- European Journal of Medical Genetics (5 papers)Clinical Genetics (5 papers)Prenatal Diagnosis (4 papers)International Journal of Oncology (4 papers)Journal of Medical Genetics (4 papers)
- Partner nations
- GermanySwitzerlandUnited Kingdom
In The Last Decade
Udo Trautmann
62 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 82
- Genetics 982
- Pediatrics, Perinatology and Child Health 267
- Molecular Biology 836
- Hematology 88
- Genetics 80
Countries citing papers authored by Udo Trautmann
This map shows the geographic impact of Udo Trautmann'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 Udo Trautmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Udo Trautmann more than expected).
Fields of papers citing papers by Udo Trautmann
This network shows the impact of papers produced by Udo Trautmann. 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 Udo Trautmann. The network helps show where Udo Trautmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Udo Trautmann, 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 65 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 290 | |
| 2 | 2009 | 99 | |
| 3 | 1994 | 91 | |
| 4 | 2011 | 85 | |
| 5 | 2001 | 84 | |
| 6 | 1992 | 74 | |
| 7 | 2003 | 66 | |
| 8 | 2017 | 59 | |
| 9 | 2007 | 56 | |
| 10 | 2018 | 56 | |
| 11 | 1996 | 51 | |
| 12 | 1998 | 51 | |
| 13 | 2001 | 42 | |
| 14 | 2007 | 41 | |
| 15 | 2000 | 32 | |
| 16 | 2000 | 29 | |
| 17 | 2007 | 29 | |
| 18 | 2006 | 28 | |
| 19 | 2003 | 24 | |
| 20 | 1992 | 24 |
About Udo Trautmann
Udo Trautmann is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Genetics, having authored 65 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (35 papers), Chromosomal and Genetic Variations (17 papers), Prenatal Screening and Diagnostics (12 papers), Congenital heart defects research (8 papers), Acute Lymphoblastic Leukemia research (8 papers), Acute Myeloid Leukemia Research (7 papers), Genomics and Chromatin Dynamics (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). The work is most often cited by research in Genetics (982 citations), Pediatrics, Perinatology and Child Health (267 citations), Molecular Biology (836 citations), Hematology (88 citations) and Genetics (80 citations). Udo Trautmann has collaborated with scholars based in Germany, Switzerland and United Kingdom. Frequent co-authors include Anita Rauch, André Reis, Cornelia Kraus, Martin Zenker, Christiane Zweier, Christian T. Thiel, Rudolf A. Pfeiffer, Thomas Liehr, R. Ulmer and Juliane Hoyer. Their work appears in journals such as European Journal of Medical Genetics, Clinical Genetics, Prenatal Diagnosis, International Journal of Oncology and Journal of Medical 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.