S. Melançon
Impact in
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
- Biochemistry top 5%
Papers in
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- Mitochondrial Function and Pathology 14
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- Genetic Neurodegenerative Diseases 14
- Co-authors
- Louis Dallaire (16 shared papers)L. Mameli (2 shared papers)M. Bélisle (2 shared papers)M. Potier (1 shared paper)G. Geoffroy (14 shared papers)B. Lemieux (7 shared papers)A. Barbeau (12 shared papers)Henry L. Nadler (2 shared papers)
- Journals
- Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (16 papers)Journal of Medical Genetics (2 papers)Catalysis Letters (2 papers)Clinical Genetics (2 papers)The Journal of Pediatrics (1 paper)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
S. Melançon
40 papers receiving 1.4k citations
S. Melançon's Hit Papers
Peers
Comparison fields: 5 of 104
- Clinical Biochemistry 159
- Biochemistry 114
- Epidemiology 503
- Cellular and Molecular Neuroscience 199
- Molecular Biology 751
Countries citing papers authored by S. Melançon
This map shows the geographic impact of S. Melançon'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 S. Melançon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Melançon more than expected).
Fields of papers citing papers by S. Melançon
This network shows the impact of papers produced by S. Melançon. 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 S. Melançon. The network helps show where S. Melançon may publish in the future.
Co-authors
The 25 scholars most cited alongside S. Melançon, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Fluorometric assay of neuraminidase with a sodium (4-methylumbelliferyl-α-d-N-acetylneuraminate) substrate Hit paper breakdown → | 1979 | 737 |
| 2 | 2005 | 151 | |
| 3 | Genetic homogeneity at the Friedreich ataxia locus on chromosome 9. | 1989 | 61 |
| 4 | 1992 | 55 | |
| 5 | More than one mutant allele causes infantile Tay-Sachs disease in French-Canadians. | 1990 | 45 |
| 6 | 1973 | 43 | |
| 7 | 1976 | 42 | |
| 8 | 2011 | 35 | |
| 9 | 1976 | 35 | |
| 10 | 1980 | 34 | |
| 11 | 1976 | 26 | |
| 12 | 1988 | 25 | |
| 13 | 2001 | 21 | |
| 14 | 1979 | 20 | |
| 15 | 1988 | 18 | |
| 16 | 2002 | 15 | |
| 17 | 1978 | 12 | |
| 18 | 1972 | 11 | |
| 19 | 1979 | 10 | |
| 20 | 1985 | 10 |
About S. Melançon
S. Melançon is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Clinical Biochemistry, Cell Biology and Biochemistry, having authored 40 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (14 papers), Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (11 papers), Biochemical Acid Research Studies (10 papers), Aldose Reductase and Taurine (6 papers), Lysosomal Storage Disorders Research (4 papers), Diet, Metabolism, and Disease (2 papers) and Endoplasmic Reticulum Stress and Disease (2 papers). The work is most often cited by research in Clinical Biochemistry (159 citations), Biochemistry (114 citations), Epidemiology (503 citations), Cellular and Molecular Neuroscience (199 citations) and Molecular Biology (751 citations). S. Melançon has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Louis Dallaire, L. Mameli, M. Bélisle, M. Potier, G. Geoffroy, B. Lemieux, A. Barbeau, Henry L. Nadler, D. Shapcott and Guillaume Breton. Their work appears in journals such as Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, Journal of Medical Genetics, Catalysis Letters, Clinical Genetics and The Journal of Pediatrics.
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.