Viola Freeman
Impact in
-
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetic Syndromes and Imprinting 1
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- Prenatal Screening and Diagnostics 4
- Assisted Reproductive Technology and Twin Pregnancy 3
- Co-authors
- Irene A. Uchida (7 shared papers)IreneA. Uchida (1 shared paper)Annette E. Cockwell (2 shared papers)R. Dwain Blackston (2 shared papers)Sallie B. Freeman (2 shared papers)Norma T. Takaesu (2 shared papers)Darrell J. Tomkins (2 shared papers)P. A. Jacobs (1 shared paper)
- Journals
- Clinical Genetics (1 paper)Human Genetics (1 paper)American Journal of Obstetrics and Gynecology (1 paper)European Journal of Human Genetics (1 paper)Prenatal Diagnosis (1 paper)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Viola Freeman
13 papers receiving 481 citations
Peers
Comparison fields: 5 of 29
- Pediatrics, Perinatology and Child Health 156
- Genetics 257
- Public Health, Environmental and Occupational Health 178
- Reproductive Medicine 36
- Cell Biology 38
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 | 90 | |
| 3 | 1985 | 60 | |
| 4 | 1996 | 53 | |
| 5 | Twinning rate in spontaneous abortions. | 1983 | 42 |
| 6 | 1999 | 34 | |
| 7 | Additional evidence for fragile X activity in heterozygous carriers. | 1983 | 33 |
| 8 | 2003 | 28 | |
| 9 | 1986 | 21 | |
| 10 | 2005 | 14 | |
| 11 | 1985 | 3 | |
| 12 | 2002 | 2 | |
| 13 | 2000 | 1 |
About Viola Freeman
Viola Freeman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, Nuclear Energy and Engineering and Waste Management and Disposal, having authored 13 papers that have together received 533 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers), Down syndrome and intellectual disability research (3 papers), Assisted Reproductive Technology and Twin Pregnancy (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (156 citations), Genetics (257 citations), Public Health, Environmental and Occupational Health (178 citations), Reproductive Medicine (36 citations) and Cell Biology (38 citations). Viola Freeman has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Irene A. Uchida, IreneA. Uchida, Annette E. Cockwell, R. Dwain Blackston, Sallie B. Freeman, Norma T. Takaesu, Darrell J. Tomkins, P. A. Jacobs, Stephanie L. Sherman and Donald T. Whelan. Their work appears in journals such as Clinical Genetics, Human Genetics, American Journal of Obstetrics and Gynecology, European Journal of Human Genetics and Prenatal Diagnosis.
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.