Scott E. Hickey
Impact in
- Emergency Medicine top 5%
- Cardiac Arrest and Resuscitation
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 20
- Genomic variations and chromosomal abnormalities 12
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Neurogenetic and Muscular Disorders Research 2
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- Congenital heart defects research 6
- RNA modifications and cancer 4
- Co-authors
- Helga V. Toriello (1 shared paper)Cynthia J. Curry (1 shared paper)Dean C. Williams (1 shared paper)R G Powell (1 shared paper)Al M. Best (1 shared paper)D. P. Edwards (1 shared paper)Harinder Dhindsa (1 shared paper)Joseph P. Ornato (1 shared paper)
- Journals
- European Journal of Medical Genetics (7 papers)Molecular Case Studies (6 papers)Genetics in Medicine (4 papers)Journal of Medical Systems (2 papers)Journal of Pediatric and Adolescent Gynecology (1 paper)
- Partner nations
- United StatesItalyCanada
In The Last Decade
Scott E. Hickey
39 papers receiving 693 citations
Peers
Comparison fields: 5 of 88
- Emergency Medicine 154
- Genetics 241
- Internal Medicine 18
- Hematology 54
- Pediatrics, Perinatology and Child Health 63
Countries citing papers authored by Scott E. Hickey
This map shows the geographic impact of Scott E. Hickey'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 Scott E. Hickey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Scott E. Hickey more than expected).
Fields of papers citing papers by Scott E. Hickey
This network shows the impact of papers produced by Scott E. Hickey. 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 Scott E. Hickey. The network helps show where Scott E. Hickey may publish in the future.
Co-authors
The 25 scholars most cited alongside Scott E. Hickey, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 163 | |
| 2 | 2013 | 122 | |
| 3 | 2020 | 56 | |
| 4 | 2018 | 46 | |
| 5 | 2021 | 34 | |
| 6 | 2018 | 30 | |
| 7 | 2022 | 28 | |
| 8 | 2016 | 28 | |
| 9 | 1999 | 25 | |
| 10 | 2023 | 23 | |
| 11 | 2013 | 17 | |
| 12 | 2013 | 17 | |
| 13 | 2014 | 15 | |
| 14 | 2019 | 14 | |
| 15 | 2000 | 13 | |
| 16 | 2020 | 11 | |
| 17 | 2019 | 11 | |
| 18 | 2003 | 11 | |
| 19 | 2022 | 9 | |
| 20 | 2016 | 8 |
About Scott E. Hickey
Scott E. Hickey is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 41 papers that have together received 733 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (8 papers), Congenital heart defects research (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Prenatal Screening and Diagnostics (4 papers), RNA modifications and cancer (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). The work is most often cited by research in Emergency Medicine (154 citations), Genetics (241 citations), Internal Medicine (18 citations), Hematology (54 citations) and Pediatrics, Perinatology and Child Health (63 citations). Scott E. Hickey has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Helga V. Toriello, Cynthia J. Curry, Dean C. Williams, R G Powell, Al M. Best, D. P. Edwards, Harinder Dhindsa, Joseph P. Ornato, Marcus Eng Hock Ong and Mary Ann Peberdy. Their work appears in journals such as European Journal of Medical Genetics, Molecular Case Studies, Genetics in Medicine, Journal of Medical Systems and Journal of Pediatric and Adolescent Gynecology.
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.