Claude Laberge
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Biochemistry top 2%
- Amino Acid Enzymes and Metabolism
Papers in
-
- Metabolism and Genetic Disorders 29
- Genetics 26
- Genomics and Rare Diseases 9
- BRCA gene mutations in cancer 6
- Co-authors
- Jacques Letarte (10 shared papers)H. Guyda (9 shared papers)Jean H. Dussault (9 shared papers)R. Gagné (7 shared papers)Robert M. Tanguay (7 shared papers)A Grenier (11 shared papers)Bartha Maria Knoppers (8 shared papers)Khalil El Khoury (1 shared paper)
- Journals
- The Journal of Pediatrics (6 papers)Clinical Chemistry (5 papers)Pediatric Research (3 papers)Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (3 papers)Public Health Genomics (3 papers)
- Partner nations
- CanadaUnited StatesFrance
In The Last Decade
Claude Laberge
101 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 145
- Clinical Biochemistry 616
- Biochemistry 208
- Endocrinology, Diabetes and Metabolism 369
- Genetics 651
- Pediatrics, Perinatology and Child Health 277
Countries citing papers authored by Claude Laberge
This map shows the geographic impact of Claude Laberge'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 Claude Laberge with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Claude Laberge more than expected).
Fields of papers citing papers by Claude Laberge
This network shows the impact of papers produced by Claude Laberge. 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 Claude Laberge. The network helps show where Claude Laberge may publish in the future.
Co-authors
The 25 scholars most cited alongside Claude Laberge, 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 104 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1975 | 250 | |
| 2 | 1999 | 173 | |
| 3 | 2012 | 149 | |
| 4 | 2007 | 86 | |
| 5 | Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I). | 1990 | 84 |
| 6 | 1972 | 72 | |
| 7 | 1982 | 59 | |
| 8 | 1987 | 56 | |
| 9 | 1980 | 56 | |
| 10 | Recurrent mutation, gene conversion, or recombination at the human phenylalanine hydroxylase locus: evidence in French-Canadians and a catalog of mutations. | 1990 | 54 |
| 11 | [Thyroxine (T4) determination by radioimmunological method in dried blood eluate: new diagnostic method of neonatal hypothyroidism?]. | 1973 | 54 |
| 12 | 1976 | 52 | |
| 13 | 1971 | 50 | |
| 14 | The Hartnup phenotype: Mendelian transport disorder, multifactorial disease. | 1987 | 49 |
| 15 | 2004 | 47 | |
| 16 | Hereditary tyrosinemia in a French Canadian isolate. | 1969 | 47 |
| 17 | Novel PKU mutation on haplotype 2 in French-Canadians. | 1989 | 47 |
| 18 | 1978 | 43 | |
| 19 | 2005 | 42 | |
| 20 | 1973 | 37 |
About Claude Laberge
Claude Laberge is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health, having authored 104 papers that have together received 2.4k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (29 papers), Thyroid Disorders and Treatments (12 papers), Amino Acid Enzymes and Metabolism (9 papers), Genomics and Rare Diseases (9 papers), Ethics in Clinical Research (9 papers), Genetic Neurodegenerative Diseases (8 papers), Neonatal Health and Biochemistry (7 papers) and BRCA gene mutations in cancer (6 papers). The work is most often cited by research in Clinical Biochemistry (616 citations), Biochemistry (208 citations), Endocrinology, Diabetes and Metabolism (369 citations), Genetics (651 citations) and Pediatrics, Perinatology and Child Health (277 citations). Claude Laberge has collaborated with scholars based in Canada, United States and France. Frequent co-authors include Jacques Letarte, H. Guyda, Jean H. Dussault, R. Gagné, Robert M. Tanguay, A Grenier, Bartha Maria Knoppers, Khalil El Khoury, Pierre A. Coulombe and Béatrice Godard. Their work appears in journals such as The Journal of Pediatrics, Clinical Chemistry, Pediatric Research, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques and Public Health Genomics.
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.