C Clow
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Biochemistry top 5%
- Amino Acid Enzymes and Metabolism
Papers in
-
- Metabolism and Genetic Disorders 14
-
- Biochemical and Molecular Research 5
- Co-authors
- C. R. Scriver (16 shared papers)John J. Mitchell (3 shared papers)Susan A. MacKenzie (2 shared papers)E. Delvin (1 shared paper)C R Scriver (9 shared papers)Eileen P. Treacy (3 shared papers)Feige Kaplan (2 shared papers)Orval Mamer (3 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (4 papers)Pediatric Research (3 papers)The Lancet (3 papers)The Journal of Pediatrics (1 paper)Human Genetics (1 paper)
- Partner nations
- CanadaUnited StatesIsrael
In The Last Decade
C Clow
27 papers receiving 691 citations
Peers
Comparison fields: 5 of 70
- Clinical Biochemistry 353
- Biochemistry 124
- Genetics 107
- Pediatrics, Perinatology and Child Health 113
- Rheumatology 80
Countries citing papers authored by C Clow
This map shows the geographic impact of C Clow'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 C Clow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C Clow more than expected).
Fields of papers citing papers by C Clow
This network shows the impact of papers produced by C Clow. 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 C Clow. The network helps show where C Clow may publish in the future.
Co-authors
The 25 scholars most cited alongside C Clow, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1971 | 122 | |
| 2 | Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schools. | 1996 | 122 |
| 3 | 1991 | 80 | |
| 4 | 1993 | 52 | |
| 5 | The Hartnup phenotype: Mendelian transport disorder, multifactorial disease. | 1987 | 49 |
| 6 | Beta-thalassemia disease prevention: genetic medicine applied. | 1984 | 43 |
| 7 | 1993 | 34 | |
| 8 | Feasibility of chemical screening of urine for neuroblastoma case finding in infancy in Quebec. | 1987 | 24 |
| 9 | Cystic fibrosis carrier screening by DNA analysis: a pilot study of attitudes among participants. | 1991 | 24 |
| 10 | 1985 | 22 | |
| 11 | 1988 | 18 | |
| 12 | 1974 | 18 | |
| 13 | Hereditary tyrosinemia and tyrosyluria: clinical report of four patients. | 1967 | 15 |
| 14 | 1987 | 14 | |
| 15 | 1982 | 13 | |
| 16 | 1973 | 13 | |
| 17 | 1991 | 12 | |
| 18 | 1993 | 11 | |
| 19 | 1966 | 11 | |
| 20 | Newborn screening for sickle cell and other hemoglobinopathies: a Canadian pilot study. | 1992 | 11 |
About C Clow
C Clow is a scholar working on Clinical Biochemistry, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Hematology, having authored 28 papers that have together received 735 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (14 papers), Hemoglobinopathies and Related Disorders (6 papers), Biochemical and Molecular Research (5 papers), Folate and B Vitamins Research (4 papers), Neonatal Health and Biochemistry (4 papers), Iron Metabolism and Disorders (4 papers), Amino Acid Enzymes and Metabolism (3 papers) and Blood groups and transfusion (3 papers). The work is most often cited by research in Clinical Biochemistry (353 citations), Biochemistry (124 citations), Genetics (107 citations), Pediatrics, Perinatology and Child Health (113 citations) and Rheumatology (80 citations). C Clow has collaborated with scholars based in Canada, United States and Israel. Frequent co-authors include C. R. Scriver, John J. Mitchell, Susan A. MacKenzie, E. Delvin, C R Scriver, Eileen P. Treacy, Feige Kaplan, Orval Mamer, David Chitayat and Claude Laberge. Their work appears in journals such as Journal of Inherited Metabolic Disease, Pediatric Research, The Lancet, The Journal of Pediatrics and Human 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.