Gregory Costain
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 10%
- Congenital heart defects research
Papers in
- Genetics 37
- Genomics and Rare Diseases 28
- Genomic variations and chromosomal abnormalities 19
- Genetics and Neurodevelopmental Disorders 6
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- Congenital heart defects research 21
- RNA modifications and cancer 5
- RNA Research and Splicing 4
- Co-authors
- Anne S. Bassett (26 shared papers)Stephen W. Scherer (18 shared papers)Christian R. Marshall (26 shared papers)Candice K. Silversides (8 shared papers)Eva W.C. Chow (9 shared papers)Daniele Merico (7 shared papers)Nancy J. Butcher (5 shared papers)Anath C. Lionel (6 shared papers)
- Journals
- Genetics in Medicine (6 papers)European Journal of Human Genetics (4 papers)Journal of Medical Genetics (3 papers)npj Genomic Medicine (2 papers)International Journal of Cardiology (2 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Gregory Costain
68 papers receiving 1.9k citations
Peers
Comparison fields: 5 of 86
- Genetics 790
- Molecular Biology 1.1k
- Cardiology and Cardiovascular Medicine 201
- Epidemiology 291
- Cognitive Neuroscience 137
Countries citing papers authored by Gregory Costain
This map shows the geographic impact of Gregory Costain'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 Gregory Costain with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gregory Costain more than expected).
Fields of papers citing papers by Gregory Costain
This network shows the impact of papers produced by Gregory Costain. 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 Gregory Costain. The network helps show where Gregory Costain may publish in the future.
Co-authors
The 25 scholars most cited alongside Gregory Costain, 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 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 215 | |
| 2 | 2015 | 196 | |
| 3 | 2012 | 119 | |
| 4 | 2014 | 109 | |
| 5 | 2013 | 94 | |
| 6 | 2019 | 73 | |
| 7 | 2018 | 67 | |
| 8 | 2012 | 60 | |
| 9 | 2016 | 58 | |
| 10 | 2014 | 52 | |
| 11 | 2010 | 51 | |
| 12 | 2019 | 48 | |
| 13 | 2012 | 44 | |
| 14 | 2015 | 40 | |
| 15 | 2014 | 39 | |
| 16 | 2011 | 38 | |
| 17 | 2012 | 38 | |
| 18 | 2011 | 36 | |
| 19 | 2012 | 35 | |
| 20 | 2015 | 27 |
About Gregory Costain
Gregory Costain is a scholar working on Genetics, Molecular Biology, Epidemiology, Cancer Research and Pathology and Forensic Medicine, having authored 72 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (28 papers), Congenital heart defects research (21 papers), Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (6 papers), Congenital Heart Disease Studies (6 papers), RNA modifications and cancer (5 papers), Cancer Genomics and Diagnostics (4 papers) and RNA Research and Splicing (4 papers). The work is most often cited by research in Genetics (790 citations), Molecular Biology (1.1k citations), Cardiology and Cardiovascular Medicine (201 citations), Epidemiology (291 citations) and Cognitive Neuroscience (137 citations). Gregory Costain has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Anne S. Bassett, Stephen W. Scherer, Christian R. Marshall, Candice K. Silversides, Eva W.C. Chow, Daniele Merico, Nancy J. Butcher, Anath C. Lionel, Chelsea Lowther and Danielle M. Andrade. Their work appears in journals such as Genetics in Medicine, European Journal of Human Genetics, Journal of Medical Genetics, npj Genomic Medicine and International Journal of Cardiology.
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.