F. Schoute
Impact in
- Reproductive Medicine top 10%
- Sperm and Testicular Function
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Virus-based gene therapy research
Papers in
-
- Sexual Differentiation and Disorders 2
- RNA Interference and Gene Delivery 2
- Ion channel regulation and function 1
- Ubiquitin and proteasome pathways 1
- Genetics 6
- Virus-based gene therapy research 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Co-authors
- Lies H. Hoefsloot (3 shared papers)Ben C.J. Hamel (2 shared papers)Jean‐Pierre Fryns (1 shared paper)Irene B. M. Konings (1 shared paper)Hannie Kremer (1 shared paper)Rainer Koch (1 shared paper)Marcel Nelen (1 shared paper)George W. Padberg (1 shared paper)
- Journals
- Nucleic Acids Research (2 papers)Journal of Assisted Reproduction and Genetics (1 paper)European Journal of Human Genetics (1 paper)Journal of Autoimmunity (1 paper)Journal of Biological Chemistry (1 paper)
- Partner nations
- NetherlandsSloveniaUnited Kingdom
In The Last Decade
F. Schoute
12 papers receiving 595 citations
Peers
Comparison fields: 5 of 69
- Reproductive Medicine 98
- Genetics 263
- Molecular Biology 455
- Clinical Biochemistry 37
- Physiology 24
Countries citing papers authored by F. Schoute
This map shows the geographic impact of F. Schoute'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 F. Schoute with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. Schoute more than expected).
Fields of papers citing papers by F. Schoute
This network shows the impact of papers produced by F. Schoute. 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 F. Schoute. The network helps show where F. Schoute may publish in the future.
Co-authors
The 25 scholars most cited alongside F. Schoute, 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 | 1999 | 234 | |
| 2 | 1997 | 99 | |
| 3 | 1994 | 68 | |
| 4 | Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data. | 1994 | 64 |
| 5 | 1990 | 60 | |
| 6 | 1995 | 44 | |
| 7 | 1997 | 15 | |
| 8 | 1988 | 9 | |
| 9 | 1992 | 9 | |
| 10 | The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region. | 1995 | 8 |
| 11 | 2001 | 6 | |
| 12 | 1987 | 6 |
About F. Schoute
F. Schoute is a scholar working on Molecular Biology, Genetics, Immunology, Reproductive Medicine and Cardiology and Cardiovascular Medicine, having authored 12 papers that have together received 622 indexed citations. Recurring topics across this work include Virus-based gene therapy research (3 papers), Sperm and Testicular Function (2 papers), Sexual Differentiation and Disorders (2 papers), RNA Interference and Gene Delivery (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Hemophilia Treatment and Research (1 paper), Ion channel regulation and function (1 paper) and Ubiquitin and proteasome pathways (1 paper). The work is most often cited by research in Reproductive Medicine (98 citations), Genetics (263 citations), Molecular Biology (455 citations), Clinical Biochemistry (37 citations) and Physiology (24 citations). F. Schoute has collaborated with scholars based in Netherlands, Slovenia and United Kingdom. Frequent co-authors include Lies H. Hoefsloot, Ben C.J. Hamel, Jean‐Pierre Fryns, Irene B. M. Konings, Hannie Kremer, Rainer Koch, Marcel Nelen, George W. Padberg, E Peeters and C. Geoffrey Woods. Their work appears in journals such as Nucleic Acids Research, Journal of Assisted Reproduction and Genetics, European Journal of Human Genetics, Journal of Autoimmunity and Journal of Biological Chemistry.
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.