Uta Francke
Impact in
- Genetics top 0.02%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genetic Syndromes and Imprinting
- Molecular Biology top 0.05%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Muscle Physiology and Disorders
Papers in
- Genetics 222
- Genomic variations and chromosomal abnormalities 54
- Genetics and Neurodevelopmental Disorders 50
- Connective tissue disorders research 35
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- Genomics and Chromatin Dynamics 34
- RNA modifications and cancer 34
- Biochemical and Molecular Research 31
- Epigenetics and DNA Methylation 29
- RNA Research and Splicing 28
- Co-authors
- Teresa L. Yang‐Feng (23 shared papers)Huda Yahya Zoghbi (3 shared papers)Mimi Wan (3 shared papers)Ruthie E. Amir (2 shared papers)Ignatia B. Van den Veyver (1 shared paper)Lisa M. Coussens (5 shared papers)Jonathan M.J. Derry (8 shared papers)Axel Ullrich (6 shared papers)
- Journals
- Genomics (52 papers)Human Genetics (23 papers)Proceedings of the National Academy of Sciences (22 papers)Human Molecular Genetics (18 papers)The American Journal of Human Genetics (16 papers)
- Partner nations
- United StatesGermanyFrance
In The Last Decade
Uta Francke
502 papers receiving 43.5k citations
Uta Francke's Hit Papers
Peers
Comparison fields: 5 of 183
- Genetics 15.8k
- Molecular Biology 24.7k
- Immunology and Allergy 1.9k
- Developmental Neuroscience 1.3k
- Cell Biology 4.1k
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
Showing the 20 most-cited of 526 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 Hit paper breakdown → | 1999 | 4063 |
| 2 | Tyrosine Kinase Receptor with Extensive Homology to EGF Receptor Shares Chromosomal Location with neu Oncogene Hit paper breakdown → | 1985 | 1594 |
| 3 | Human proto‐oncogene c‐kit: a new cell surface receptor tyrosine kinase for an unidentified ligand. Hit paper breakdown → | 1987 | 1445 |
| 4 | Structure of the receptor for platelet-derived growth factor helps define a family of closely related growth factor receptors Hit paper breakdown → | 1986 | 1130 |
| 5 | Multiple, Distinct Forms of Bovine and Human Protein Kinase C Suggest Diversity in Cellular Signaling Pathways Hit paper breakdown → | 1986 | 968 |
| 6 | Isolation of a novel gene mutated in Wiskott-Aldrich syndrome Hit paper breakdown → | 1994 | 873 |
| 7 | The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. Hit paper breakdown → | 1989 | 830 |
| 8 | Wiskott–Aldrich Syndrome Protein, a Novel Effector for the GTPase CDC42Hs, Is Implicated in Actin Polymerization Hit paper breakdown → | 1996 | 750 |
| 9 | Cloning, Sequencing, and Expression of the Gene Coding for the Human Platelet α 2 -Adrenergic Receptor Hit paper breakdown → | 1987 | 726 |
| 10 | The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome Hit paper breakdown → | 1993 | 720 |
| 11 | Chromosomal Imbalance in the Aniridia-Wilms' Tumor Association: 11p Interstitial Deletion Hit paper breakdown → | 1978 | 626 |
| 12 | cDNA for the human beta 2-adrenergic receptor: a protein with multiple membrane-spanning domains and encoded by a gene whose chromosomal location is shared with that of the receptor for platelet-derived growth factor. Hit paper breakdown → | 1987 | 603 |
| 13 | NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21 Hit paper breakdown → | 2006 | 589 |
| 14 | 1997 | 494 | |
| 15 | 1987 | 471 | |
| 16 | 2007 | 449 | |
| 17 | 2011 | 445 | |
| 18 | 1985 | 444 | |
| 19 | 1992 | 436 | |
| 20 | 1991 | 430 |
About Uta Francke
Uta Francke is a scholar working on Genetics, Molecular Biology, Cell Biology, Genetics and Cancer Research, having authored 526 papers that have together received 46.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (54 papers), Genetics and Neurodevelopmental Disorders (50 papers), Connective tissue disorders research (35 papers), Genomics and Chromatin Dynamics (34 papers), RNA modifications and cancer (34 papers), Biochemical and Molecular Research (31 papers), Epigenetics and DNA Methylation (29 papers) and RNA Research and Splicing (28 papers). The work is most often cited by research in Genetics (15.8k citations), Molecular Biology (24.7k citations), Immunology and Allergy (1.9k citations), Developmental Neuroscience (1.3k citations) and Cell Biology (4.1k citations). Uta Francke has collaborated with scholars based in United States, Germany and France. Frequent co-authors include Teresa L. Yang‐Feng, Huda Yahya Zoghbi, Mimi Wan, Ruthie E. Amir, Ignatia B. Van den Veyver, Lisa M. Coussens, Jonathan M.J. Derry, Axel Ullrich, Hans D. Ochs and Joseph Schlessinger. Their work appears in journals such as Genomics, Human Genetics, Proceedings of the National Academy of Sciences, Human Molecular Genetics and The American Journal of Human 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.