Uta Francke
Impact in
- Genetics top 0.01%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Molecular Biology top 0.05%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
Papers in
- Genetics 208
- Genomic variations and chromosomal abnormalities 54
- Genetics and Neurodevelopmental Disorders 47
- Genetic Syndromes and Imprinting 25
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- RNA modifications and cancer 36
- Genomics and Chromatin Dynamics 34
- Epigenetics and DNA Methylation 32
- Biochemical and Molecular Research 30
- RNA Research and Splicing 27
- Co-authors
- Teresa L. Yang‐FengHuda Y. ZoghbiMimi WanRuthie E. AmirIgnatia B. Van den VeyverLisa M. CoussensJonathan M.J. DerryAxel Ullrich
- Journals
- Cytogenetic and Genome Research (51 papers)Genomics (51 papers)Proceedings of the National Academy of Sciences (22 papers)Human Genetics (22 papers)Human Molecular Genetics (18 papers)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Uta Francke
500 papers receiving 40.3k citations
Hit Papers
Peers
Comparison fields: 5 of 182
- Genetics 14.5k
- Molecular Biology 24.1k
- Immunology and Allergy 2.0k
- Developmental Neuroscience 1.1k
- Cell Biology 4.0k
Countries citing papers authored by Uta Francke
This map shows the geographic impact of Uta Francke'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 Uta Francke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Uta Francke more than expected).
Fields of papers citing papers by Uta Francke
This network shows the impact of papers produced by Uta Francke. 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 Uta Francke. The network helps show where Uta Francke may publish in the future.
Co-authors
The 25 scholars most cited alongside Uta Francke, 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 | 2024 | 1 | |
| 2 | 2016 | 171 | |
| 3 | 2011 | 59 | |
| 4 | 1997 | 93 | |
| 5 | Ascending aortic aneurysm with or without features of Marfan syndrome and other fibrillinopathies: new insights. | 1997 | 26 |
| 6 | 1997 | 164 | |
| 7 | Dermal fibroblast culture as a model system for studies of fibrillin assembly and pathogenetic mechanisms: defects in distinct groups of individuals with Marfan's syndrome. | 1996 | 20 |
| 8 | A Gly1127Ser mutation in an EGF-like domain of the fibrillin-1 gene is a risk factor for ascending aortic aneurysm and dissection. | 1995 | 124 |
| 9 | Rett Syndrome—Clinical and Biological Aspects | 1994 | 1 |
| 10 | Deletions and candidate genes in Williams syndrome | 1994 | 2 |
| 11 | 1993 | 73 | |
| 12 | 1992 | 298 | |
| 13 | Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM. | 1992 | 31 |
| 14 | Mapping of the human tissue-type plasminogen-activator gene on chromosome (8p21-]q11.2) | 1986 | 1 |
| 15 | 1985 | 20 | |
| 16 | 1982 | 21 | |
| 17 | 1978 | 5 | |
| 18 | 1977 | 57 | |
| 19 | The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease. | 1976 | 86 |
| 20 | 1973 | 6 |
About Uta Francke
Uta Francke is a scholar working on Genetics, Molecular Biology, Developmental Neuroscience, Genetics and Developmental Biology, having authored 503 papers that have together received 41.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (54 papers), Genetics and Neurodevelopmental Disorders (47 papers), RNA modifications and cancer (36 papers), Genomics and Chromatin Dynamics (34 papers), Epigenetics and DNA Methylation (32 papers), Biochemical and Molecular Research (30 papers), RNA Research and Splicing (27 papers) and Genetic Syndromes and Imprinting (25 papers). The work is most often cited by research in Genetics (14.5k citations), Molecular Biology (24.1k citations), Immunology and Allergy (2.0k citations), Developmental Neuroscience (1.1k citations) and Cell Biology (4.0k citations). Uta Francke has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Teresa L. Yang‐Feng, Huda Y. Zoghbi, Mimi Wan, Ruthie E. Amir, Ignatia B. Van den Veyver, Lisa M. Coussens, Jonathan M.J. Derry, Axel Ullrich, Vincent M. Riccardi and Joseph Schlessinger. Their work appears in journals such as Cytogenetic and Genome Research, Genomics, Proceedings of the National Academy of Sciences, Human Genetics and Human Molecular 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.