Viola Freeman
Impact in
-
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 2
- Genetic Syndromes and Imprinting 2
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- Prenatal Screening and Diagnostics 7
- Co-authors
- Irene A. Uchida (7 shared papers)Annette E. Cockwell (2 shared papers)R. Dwain Blackston (2 shared papers)Sallie B. Freeman (2 shared papers)Norma T. Takaesu (2 shared papers)Stephanie L. Sherman (1 shared paper)P. A. Jacobs (1 shared paper)Darrell J. Tomkins (2 shared papers)
- Journals
- European Journal of Human Genetics (1 paper)Clinical Genetics (1 paper)American Journal of Obstetrics and Gynecology (1 paper)American Journal of Medical Genetics (4 papers)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Viola Freeman
11 papers receiving 435 citations
Peers
Comparison fields: 5 of 47
- Pediatrics, Perinatology and Child Health 242
- Genetics 289
- Public Health, Environmental and Occupational Health 109
- Reproductive Medicine 32
- Plant Science 90
Countries citing papers authored by Viola Freeman
This map shows the geographic impact of Viola Freeman'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 Viola Freeman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Viola Freeman more than expected).
Fields of papers citing papers by Viola Freeman
This network shows the impact of papers produced by Viola Freeman. 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 Viola Freeman. The network helps show where Viola Freeman may publish in the future.
Co-authors
The 25 scholars most cited alongside Viola Freeman, 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 | Trisomy 21: association between reduced recombination and nondisjunction. | 1991 | 152 |
| 2 | 1985 | 89 | |
| 3 | 1996 | 50 | |
| 4 | Twinning rate in spontaneous abortions. | 1983 | 39 |
| 5 | 1999 | 34 | |
| 6 | Additional evidence for fragile X activity in heterozygous carriers. | 1983 | 33 |
| 7 | 2003 | 27 | |
| 8 | 1986 | 24 | |
| 9 | 2005 | 15 | |
| 10 | 1985 | 4 | |
| 11 | 2000 | 1 |
About Viola Freeman
Viola Freeman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, Molecular Biology and Plant Science, having authored 11 papers that have together received 468 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Gestational Trophoblastic Disease Studies (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic Syndromes and Imprinting (2 papers), Chromosomal and Genetic Variations (2 papers), Genomics and Chromatin Dynamics (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (242 citations), Genetics (289 citations), Public Health, Environmental and Occupational Health (109 citations), Reproductive Medicine (32 citations) and Plant Science (90 citations). Viola Freeman has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Irene A. Uchida, Annette E. Cockwell, R. Dwain Blackston, Sallie B. Freeman, Norma T. Takaesu, Stephanie L. Sherman, P. A. Jacobs, Darrell J. Tomkins, Charlotte Phillips and John S. Waye. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, American Journal of Obstetrics and Gynecology, American Journal of Medical Genetics and American Journal of Medical Genetics Part A.
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.