F Murton
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
- Childhood Cancer Survivors' Quality of Life
- Ethics and Legal Issues in Pediatric Healthcare
Papers in
- Genetics 10
- BRCA gene mutations in cancer 10
- Nutrition, Genetics, and Disease 3
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- Prenatal Screening and Diagnostics 2
- Co-authors
- Nina Hallowell (10 shared papers)Helen Statham (10 shared papers)Martin Richards (3 shared papers)Josephine Green (2 shared papers)Matt Richards (2 shared papers)MA Richards (1 shared paper)
- Journals
- Patient Education and Counseling (1 paper)Psychology Health & Medicine (1 paper)Child Care Health and Development (1 paper)Journal of Medical Genetics (1 paper)Journal of Genetic Counseling (5 papers)
- Partner nations
- United KingdomPortugal
In The Last Decade
F Murton
12 papers receiving 555 citations
Peers
Comparison fields: 5 of 73
- Genetics 410
- Pediatrics, Perinatology and Child Health 136
- General Decision Sciences 8
- Sociology and Political Science 189
- Pathology and Forensic Medicine 50
Countries citing papers authored by F Murton
This map shows the geographic impact of F Murton'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 Murton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F Murton more than expected).
Fields of papers citing papers by F Murton
This network shows the impact of papers produced by F Murton. 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 Murton. The network helps show where F Murton may publish in the future.
Co-authors
The 6 scholars most cited alongside F Murton, 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 | 1997 | 163 | |
| 2 | 1997 | 91 | |
| 3 | 1997 | 90 | |
| 4 | 1998 | 50 | |
| 5 | 1995 | 46 | |
| 6 | 1998 | 40 | |
| 7 | 1993 | 37 | |
| 8 | 1997 | 31 | |
| 9 | 1996 | 27 | |
| 10 | 1998 | 10 | |
| 11 | Genetic counselling for breast and ovarian cancer: Why do women attend? | 1997 | 3 |
| 12 | Family communication following genetic counselling for breast/ovarian cancer | 1997 | 2 |
About F Murton
F Murton is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Sociology and Political Science, Social Psychology and Neurology, having authored 12 papers that have together received 590 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Nutrition, Genetics, and Disease (3 papers), Prenatal Screening and Diagnostics (2 papers), Family Support in Illness (2 papers), Ovarian cancer diagnosis and treatment (1 paper), Fibromyalgia and Chronic Fatigue Syndrome Research (1 paper), Neurofibromatosis and Schwannoma Cases (1 paper) and Tuberous Sclerosis Complex Research (1 paper). The work is most often cited by research in Genetics (410 citations), Pediatrics, Perinatology and Child Health (136 citations), General Decision Sciences (8 citations), Sociology and Political Science (189 citations) and Pathology and Forensic Medicine (50 citations). F Murton has collaborated with scholars based in United Kingdom and Portugal. Frequent co-authors include Nina Hallowell, Helen Statham, Martin Richards, Josephine Green, Matt Richards and MA Richards. Their work appears in journals such as Patient Education and Counseling, Psychology Health & Medicine, Child Care Health and Development, Journal of Medical Genetics and Journal of Genetic Counseling.
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.