U Theile
Impact in
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- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Skin and Cellular Biology Research
Papers in
- Genetics 14
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- RNA modifications and cancer 3
- Sexual Differentiation and Disorders 3
- Protein Tyrosine Phosphatases 2
- Co-authors
- G. G. Wendt (3 shared papers)Christina Lich (1 shared paper)Stephanie Demuth (1 shared paper)Bernhard Horsthemke (1 shared paper)Gabriele Gillessen‐Kaesbach (1 shared paper)Hannelore Thiele (1 shared paper)M. Rister (2 shared papers)Peter Wieacker (3 shared papers)
- Journals
- Human Genetics (3 papers)Human Mutation (2 papers)Prenatal Diagnosis (2 papers)European Journal of Human Genetics (1 paper)Human Heredity (1 paper)
- Partner nations
- GermanyEstoniaUnited Kingdom
In The Last Decade
U Theile
22 papers receiving 231 citations
Peers
Comparison fields: 5 of 51
- Genetics 147
- Cell Biology 36
- Molecular Biology 144
- Pediatrics, Perinatology and Child Health 36
- Developmental Biology 3
Countries citing papers authored by U Theile
This map shows the geographic impact of U Theile'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 U Theile with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites U Theile more than expected).
Fields of papers citing papers by U Theile
This network shows the impact of papers produced by U Theile. 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 U Theile. The network helps show where U Theile may publish in the future.
Co-authors
The 25 scholars most cited alongside U Theile, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 62 | |
| 2 | 1974 | 39 | |
| 3 | 2003 | 22 | |
| 4 | 1997 | 18 | |
| 5 | 1996 | 16 | |
| 6 | 1963 | 16 | |
| 7 | 2004 | 10 | |
| 8 | 2000 | 10 | |
| 9 | 2000 | 10 | |
| 10 | [FAMILIAL STUDIES ON GAMMA GLOBULIN GROUPS; GM (A), GM (B), GM (X) AND GM (R)]. | 1963 | 6 |
| 11 | 2000 | 5 | |
| 12 | 1963 | 4 | |
| 13 | 1974 | 4 | |
| 14 | 1997 | 4 | |
| 15 | 1974 | 3 | |
| 16 | 1978 | 3 | |
| 17 | 1973 | 3 | |
| 18 | 2004 | 2 | |
| 19 | [Effect of heredity and environment in immune diseases. Presentation of twin data]. | 1994 | 2 |
| 20 | [Cardiac findings in Noonan syndrome]. | 1986 | 1 |
About U Theile
U Theile is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Plant Science and Clinical Biochemistry, having authored 23 papers that have together received 242 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (3 papers), RNA modifications and cancer (3 papers), Sexual Differentiation and Disorders (3 papers), Metabolism and Genetic Disorders (2 papers), Protein Tyrosine Phosphatases (2 papers), Skin and Cellular Biology Research (2 papers), Hormonal and reproductive studies (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Genetics (147 citations), Cell Biology (36 citations), Molecular Biology (144 citations), Pediatrics, Perinatology and Child Health (36 citations) and Developmental Biology (3 citations). U Theile has collaborated with scholars based in Germany, Estonia and United Kingdom. Frequent co-authors include G. G. Wendt, Christina Lich, Stephanie Demuth, Bernhard Horsthemke, Gabriele Gillessen‐Kaesbach, Hannelore Thiele, M. Rister, Peter Wieacker, Sabine Scherer and Vera Beyer. Their work appears in journals such as Human Genetics, Human Mutation, Prenatal Diagnosis, European Journal of Human Genetics and Human Heredity.
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.