Scott Gurd
Impact in
- Genetics top 5%
- Genetic Associations and Epidemiology
- Clinical Biochemistry top 5%
Papers in
-
- Genomics and Chromatin Dynamics 5
- Epigenetics and DNA Methylation 4
- RNA Research and Splicing 3
- RNA and protein synthesis mechanisms 2
- RNA modifications and cancer 2
- Genetics 6
- Genetic Associations and Epidemiology 4
- Co-authors
- Thomas J. Hudson (8 shared papers)Robert Sladek (6 shared papers)Bing Ge (7 shared papers)Eef Harmsen (7 shared papers)Tomi Pastinen (7 shared papers)Marie‐Claude Vohl (2 shared papers)Tony Kwan (3 shared papers)Denis Richard (1 shared paper)
- Journals
- Genome Research (3 papers)PLoS Genetics (2 papers)Physiological Genomics (2 papers)Human Mutation (1 paper)Nature Genetics (1 paper)
- Partner nations
- CanadaSwedenUnited States
In The Last Decade
Scott Gurd
12 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 89
- Genetics 439
- Clinical Biochemistry 98
- Molecular Biology 918
- Rheumatology 154
- Cancer Research 146
Countries citing papers authored by Scott Gurd
This map shows the geographic impact of Scott Gurd'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 Gurd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Scott Gurd more than expected).
Fields of papers citing papers by Scott Gurd
This network shows the impact of papers produced by Scott Gurd. 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 Gurd. The network helps show where Scott Gurd may publish in the future.
Co-authors
The 25 scholars most cited alongside Scott Gurd, 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 | 2004 | 262 | |
| 2 | 2008 | 231 | |
| 3 | 2004 | 209 | |
| 4 | 2008 | 179 | |
| 5 | 2009 | 145 | |
| 6 | 2005 | 103 | |
| 7 | 2007 | 91 | |
| 8 | 2005 | 77 | |
| 9 | 2008 | 61 | |
| 10 | 2007 | 30 | |
| 11 | 2008 | 26 | |
| 12 | 2005 | 5 |
About Scott Gurd
Scott Gurd is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Cardiology and Cardiovascular Medicine and Epidemiology, having authored 12 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (5 papers), Genetic Associations and Epidemiology (4 papers), Epigenetics and DNA Methylation (4 papers), RNA Research and Splicing (3 papers), RNA and protein synthesis mechanisms (2 papers), RNA modifications and cancer (2 papers), Metabolism and Genetic Disorders (1 paper) and Bone health and osteoporosis research (1 paper). The work is most often cited by research in Genetics (439 citations), Clinical Biochemistry (98 citations), Molecular Biology (918 citations), Rheumatology (154 citations) and Cancer Research (146 citations). Scott Gurd has collaborated with scholars based in Canada, Sweden and United States. Frequent co-authors include Thomas J. Hudson, Robert Sladek, Bing Ge, Eef Harmsen, Tomi Pastinen, Marie‐Claude Vohl, Tony Kwan, Denis Richard, Julie Robitaille and Picard Marceau. Their work appears in journals such as Genome Research, PLoS Genetics, Physiological Genomics, Human Mutation and Nature Genetics.
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.