T. M. Schroeder-Kurth
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- Genomic variations and chromosomal abnormalities 4
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- Chromosomal and Genetic Variations 2
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- Carcinogens and Genotoxicity Assessment 1
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- DNA Repair Mechanisms 2
- Pluripotent Stem Cells Research 1
- DNA and Nucleic Acid Chemistry 1
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- Prenatal Screening and Diagnostics 3
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- Down syndrome and intellectual disability research 1
- Co-authors
- Caspar Grond‐GinsbachHarry ScherthanCarolin DäumerPeter LichterJan MurkenThomas CremerA. JauchHolger Hoehn
- Cited by
- GeneticsPlant ScienceCancer Research
- Partner nations
- GermanyNetherlandsItaly
In The Last Decade
T. M. Schroeder-Kurth
10 papers receiving 324 citations
Peers
Comparison fields: 5 of 45
- Genetics 143
- Plant Science 135
- Cancer Research 54
- Molecular Biology 227
- Pediatrics, Perinatology and Child Health 47
Countries citing papers authored by T. M. Schroeder-Kurth
This map shows the geographic impact of T. M. Schroeder-Kurth'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 T. M. Schroeder-Kurth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. M. Schroeder-Kurth more than expected).
Fields of papers citing papers by T. M. Schroeder-Kurth
This network shows the impact of papers produced by T. M. Schroeder-Kurth. 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 T. M. Schroeder-Kurth. The network helps show where T. M. Schroeder-Kurth may publish in the future.
Co-authorship network
The 25 scholars most cited alongside T. M. Schroeder-Kurth, 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 | 2005 | 2 | |
| 2 | 1998 | 6 | |
| 3 | 1995 | 77 | |
| 4 | [Risk assessment for familial occurrence of breast cancer]. | 1995 | 4 |
| 5 | 1994 | 24 | |
| 6 | 1991 | 74 | |
| 7 | 1990 | 76 | |
| 8 | Fanconi Anemia : Clinical, Cytogenetic and Experimental Aspects | 1989 | 36 |
| 9 | [Prenatal sonographic diagnosis of a case of Desbuquois familial osseous dysplasia]. | 1989 | 1 |
| 10 | 1982 | 30 |
About T. M. Schroeder-Kurth
T. M. Schroeder-Kurth is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 10 papers that have together received 330 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers), DNA Repair Mechanisms (2 papers), Chromosomal and Genetic Variations (2 papers), Down syndrome and intellectual disability research (1 paper), Pluripotent Stem Cells Research (1 paper), DNA and Nucleic Acid Chemistry (1 paper) and Carcinogens and Genotoxicity Assessment (1 paper). The work is most often cited by research in Genetics (143 citations), Plant Science (135 citations) and Cancer Research (54 citations). T. M. Schroeder-Kurth has collaborated with scholars based in Germany, Netherlands and Italy. Frequent co-authors include Caspar Grond‐Ginsbach, Harry Scherthan, Carolin Däumer, Peter Lichter, Jan Murken, Thomas Cremer, A. Jauch, Holger Hoehn, G. Obe and Arleen D. Auerbach. Their work appears in journals such as Blood, Human Genetics and American 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.