Cathy Sullivan
Impact in
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
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- Prenatal Screening and Diagnostics 5
- Fetal and Pediatric Neurological Disorders 2
- Genetics 4
- Genomic variations and chromosomal abnormalities 3
- BRCA gene mutations in cancer 2
- Co-authors
- Jennifer Hoskovec (2 shared papers)Chad A. Shaw (1 shared paper)Arthur L. Beaudet (1 shared paper)Xinyan Lu (1 shared paper)M. Lance Cooper (1 shared paper)Karen L. Wilson (1 shared paper)Carlos A. Bacino (1 shared paper)Claire N. Singletary (1 shared paper)
- Journals
- Prenatal Diagnosis (2 papers)Obstetrical & Gynecological Survey (1 paper)PLoS ONE (1 paper)Journal of Genetic Counseling (3 papers)
- Partner nations
- United StatesSwitzerlandFrance
In The Last Decade
Cathy Sullivan
6 papers receiving 270 citations
Peers
Comparison fields: 5 of 38
- Pediatrics, Perinatology and Child Health 153
- Genetics 150
- Infectious Diseases 19
- Genetics 10
- Molecular Biology 55
Countries citing papers authored by Cathy Sullivan
This map shows the geographic impact of Cathy Sullivan'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 Cathy Sullivan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cathy Sullivan more than expected).
Fields of papers citing papers by Cathy Sullivan
This network shows the impact of papers produced by Cathy Sullivan. 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 Cathy Sullivan. The network helps show where Cathy Sullivan may publish in the future.
Co-authors
The 25 scholars most cited alongside Cathy Sullivan, 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 | 2007 | 148 | |
| 2 | 2012 | 94 | |
| 3 | 2017 | 20 | |
| 4 | 2016 | 14 | |
| 5 | 2011 | 4 | |
| 6 | 2017 | 1 | |
| 7 | 2022 | 0 |
About Cathy Sullivan
Cathy Sullivan is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Public Health, Environmental and Occupational Health, Physiology and Infectious Diseases, having authored 7 papers that have together received 281 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Fetal and Pediatric Neurological Disorders (2 papers), BRCA gene mutations in cancer (2 papers), Biomedical Ethics and Regulation (1 paper) and Ethics in Clinical Research (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (153 citations), Genetics (150 citations), Infectious Diseases (19 citations), Genetics (10 citations) and Molecular Biology (55 citations). Cathy Sullivan has collaborated with scholars based in United States, Switzerland and France. Frequent co-authors include Jennifer Hoskovec, Chad A. Shaw, Arthur L. Beaudet, Xinyan Lu, M. Lance Cooper, Karen L. Wilson, Carlos A. Bacino, Claire N. Singletary, A. Craig Chinault and Sarah Noblin. Their work appears in journals such as Prenatal Diagnosis, Obstetrical & Gynecological Survey, PLoS ONE 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.