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
-
- RNA Interference and Gene Delivery 2
- Peroxisome Proliferator-Activated Receptors 1
- Ion Transport and Channel Regulation 1
- Ion channel regulation and function 1
- Genetics 6
- Virus-based gene therapy research 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetics and Neurodevelopmental Disorders 1
- Co-authors
- Lies H. Hoefsloot (3 shared papers)Ben C.J. Hamel (2 shared papers)Irene B. M. Konings (1 shared paper)Marcel Nelen (1 shared paper)Jean‐Pierre Fryns (1 shared paper)Rainer Koch (1 shared paper)E Peeters (1 shared paper)Hannie Kremer (1 shared paper)
- Journals
- Nucleic Acids Research (2 papers)European Journal of Human Genetics (1 paper)Biochemical and Biophysical Research Communications (1 paper)Molecular Biology Reports (1 paper)Journal of Assisted Reproduction and Genetics (1 paper)
- Partner nations
- NetherlandsUnited KingdomPoland
In The Last Decade
F. Schoute
12 papers receiving 633 citations
Peers
Comparison fields: 5 of 63
- Reproductive Medicine 86
- Genetics 269
- Molecular Biology 451
- Clinical Biochemistry 40
- 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 | 253 | |
| 2 | 1997 | 104 | |
| 3 | 1994 | 70 | |
| 4 | Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data. | 1994 | 67 |
| 5 | 1990 | 63 | |
| 6 | 1995 | 57 | |
| 7 | 1997 | 16 | |
| 8 | 1992 | 13 | |
| 9 | 1988 | 9 | |
| 10 | The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region. | 1995 | 9 |
| 11 | 2001 | 6 | |
| 12 | 1987 | 6 |
About F. Schoute
F. Schoute is a scholar working on Molecular Biology, Genetics, Immunology, Cardiology and Cardiovascular Medicine and Pulmonary and Respiratory Medicine, having authored 12 papers that have together received 673 indexed citations. Recurring topics across this work include Virus-based gene therapy research (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), RNA Interference and Gene Delivery (2 papers), Peroxisome Proliferator-Activated Receptors (1 paper), Eicosanoids and Hypertension Pharmacology (1 paper), Ion Transport and Channel Regulation (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Ion channel regulation and function (1 paper). The work is most often cited by research in Reproductive Medicine (86 citations), Genetics (269 citations), Molecular Biology (451 citations), Clinical Biochemistry (40 citations) and Physiology (24 citations). F. Schoute has collaborated with scholars based in Netherlands, United Kingdom and Poland. Frequent co-authors include Lies H. Hoefsloot, Ben C.J. Hamel, Irene B. M. Konings, Marcel Nelen, Jean‐Pierre Fryns, Rainer Koch, E Peeters, Hannie Kremer, C. Geoffrey Woods and George W. Padberg. Their work appears in journals such as Nucleic Acids Research, European Journal of Human Genetics, Biochemical and Biophysical Research Communications, Molecular Biology Reports and Journal of Assisted Reproduction and 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.