Ryan E. Lamont
Impact in
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
- Genetics top 5%
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
Papers in
- Genetics 26
- Genomics and Rare Diseases 17
- Genetics and Neurodevelopmental Disorders 8
- Genetic and Kidney Cyst Diseases 5
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- Fetal and Pediatric Neurological Disorders 4
- Co-authors
- Sarah J. Childs (8 shared papers)Allan Micheil Innes (19 shared papers)Jillian S. Parboosingh (21 shared papers)François P. Bernier (16 shared papers)Teresa A. Zelinski (3 shared papers)Marion E. Reid (1 shared paper)Lennart Lögdberg (1 shared paper)Christopher Smith (3 shared papers)
- Journals
- The American Journal of Human Genetics (6 papers)European Journal of Human Genetics (4 papers)Genetics in Medicine (4 papers)Clinical Genetics (3 papers)JAMA Network Open (2 papers)
- Partner nations
- CanadaUnited StatesGermany
In The Last Decade
Ryan E. Lamont
54 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 78
- Clinical Biochemistry 110
- Genetics 556
- Molecular Biology 685
- Developmental Neuroscience 29
- Cell Biology 118
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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 206 | |
| 2 | 2017 | 167 | |
| 3 | 2014 | 110 | |
| 4 | 2009 | 104 | |
| 5 | 2013 | 101 | |
| 6 | 2017 | 99 | |
| 7 | 2014 | 93 | |
| 8 | 2004 | 63 | |
| 9 | 2017 | 61 | |
| 10 | 2014 | 58 | |
| 11 | 2019 | 55 | |
| 12 | 2006 | 49 | |
| 13 | 2005 | 46 | |
| 14 | 2018 | 43 | |
| 15 | 2015 | 38 | |
| 16 | 2016 | 37 | |
| 17 | 2010 | 35 | |
| 18 | 2009 | 34 | |
| 19 | 2019 | 31 | |
| 20 | 2019 | 29 |
About Ryan E. Lamont
Ryan E. Lamont is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry, having authored 55 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (17 papers), Genetics and Neurodevelopmental Disorders (8 papers), Traumatic Brain Injury Research (5 papers), Genetic and Kidney Cyst Diseases (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Mitochondrial Function and Pathology (4 papers), Developmental Biology and Gene Regulation (4 papers) and Axon Guidance and Neuronal Signaling (3 papers). The work is most often cited by research in Clinical Biochemistry (110 citations), Genetics (556 citations), Molecular Biology (685 citations), Developmental Neuroscience (29 citations) and Cell Biology (118 citations). Ryan E. Lamont has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Sarah J. Childs, Allan Micheil Innes, Jillian S. Parboosingh, François P. Bernier, Teresa A. Zelinski, Marion E. Reid, Lennart Lögdberg, Christopher Smith, Kym M. Boycott and Cheryl R. Greenberg. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Genetics in Medicine, Clinical Genetics and JAMA Network Open.
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.