Ryan E. Lamont
Impact in
-
- RNA modifications and cancer
- RNA Research and Splicing
- Angiogenesis and VEGF in Cancer
- RNA and protein synthesis mechanisms
- Peroxisome Proliferator-Activated Receptors
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
Papers in
-
- RNA modifications and cancer 6
- Angiogenesis and VEGF in Cancer 5
- Renal and related cancers 4
- Congenital heart defects research 4
- Genetics 12
- Genomics and Rare Diseases 7
- Co-authors
- Sarah J. Childs (8 shared papers)A. Micheil Innes (19 shared papers)Jillian S. Parboosingh (21 shared papers)François P. Bernier (16 shared papers)Teresa Zelinski (3 shared papers)Marion E. Reid (1 shared paper)Kym M. Boycott (6 shared papers)Cheryl R. Greenberg (3 shared papers)
- Journals
- The American Journal of Human Genetics (5 papers)European Journal of Human Genetics (3 papers)Developmental Biology (2 papers)Developmental Dynamics (2 papers)Clinical Genetics (2 papers)
- Partner nations
- CanadaUnited StatesGermany
In The Last Decade
Ryan E. Lamont
33 papers receiving 890 citations
Peers
Comparison fields: 5 of 82
- Molecular Biology 583
- Clinical Biochemistry 55
- Cell Biology 136
- Cellular and Molecular Neuroscience 131
- Genetics 55
Countries citing papers authored by Ryan E. Lamont
This map shows the geographic impact of Ryan E. Lamont'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 Ryan E. Lamont with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryan E. Lamont more than expected).
Fields of papers citing papers by Ryan E. Lamont
This network shows the impact of papers produced by Ryan E. Lamont. 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 Ryan E. Lamont. The network helps show where Ryan E. Lamont may publish in the future.
Co-authors
The 25 scholars most cited alongside Ryan E. Lamont, 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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 103 | |
| 2 | 2014 | 101 | |
| 3 | 2014 | 85 | |
| 4 | 2004 | 57 | |
| 5 | 2019 | 48 | |
| 6 | 2006 | 48 | |
| 7 | 2005 | 45 | |
| 8 | 2016 | 36 | |
| 9 | 2018 | 35 | |
| 10 | 2010 | 35 | |
| 11 | 2009 | 33 | |
| 12 | 2015 | 32 | |
| 13 | 2019 | 26 | |
| 14 | 2016 | 26 | |
| 15 | 2019 | 24 | |
| 16 | 2007 | 22 | |
| 17 | 2018 | 17 | |
| 18 | 2016 | 14 | |
| 19 | 2016 | 14 | |
| 20 | 2016 | 13 |
About Ryan E. Lamont
Ryan E. Lamont is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Cell Biology and Genetics, having authored 35 papers that have together received 906 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Metabolism and Genetic Disorders (6 papers), RNA modifications and cancer (6 papers), Angiogenesis and VEGF in Cancer (5 papers), Renal and related cancers (4 papers), Congenital heart defects research (4 papers), Axon Guidance and Neuronal Signaling (4 papers) and Zebrafish Biomedical Research Applications (4 papers). The work is most often cited by research in Molecular Biology (583 citations), Clinical Biochemistry (55 citations), Cell Biology (136 citations), Cellular and Molecular Neuroscience (131 citations) and Genetics (55 citations). Ryan E. Lamont has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Sarah J. Childs, A. Micheil Innes, Jillian S. Parboosingh, François P. Bernier, Teresa Zelinski, Marion E. Reid, Kym M. Boycott, Cheryl R. Greenberg, Klaus Wrogemann and Christopher Smith. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Developmental Biology, Developmental Dynamics and Clinical 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.